Michael Owen

Q: What Schools Are Affiliated With Michael Owen

Michael Owen is affiliated with the following schools: University of Oxford, Cardiff University, University of Birmingham, University of Toronto, King's College London

Michael Owen 's AcademicInfluence.com Rankings

Michael Owen

Biology

#3424

World Rank

#5239

Historical Rank

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Biology

Michael Owen 's Degrees

Bachelors Medicine University of Oxford

Why Is Michael Owen Influential?

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According to Wikipedia, Sir Michael John Owen FRCPsych FMedSci FLSW is a Welsh research scientist in the area of psychiatry, currently the head of the Division of Psychological Medicine and Clinical Neurosciences at Cardiff University.

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Michael Owen 's Published Works

Number of citations in a given year to any of this author's works

Total number of citations to an author for the works they published in a given year. This highlights publication of the most important work(s) by the author

Published Works

Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls (2007) (9208)
Biological Insights From 108 Schizophrenia-Associated Genetic Loci (2014) (6445)
Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease (2013) (3484)
Synaptic, transcriptional, and chromatin genes disrupted in autism (2014) (2080)
Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs (2013) (2011)
Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression (2018) (1816)
Common variants in ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer’s disease (2011) (1701)
Genome-wide association study identifies five new schizophrenia loci (2011) (1680)
Letter abstract - Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's Disease (2009) (1644)
Rare chromosomal deletions and duplications increase risk of schizophrenia (2008) (1506)
Genome-wide Association Analysis Identifies 14 New Risk Loci for Schizophrenia (2013) (1455)
De novo mutations in schizophrenia implicate synaptic networks (2014) (1454)
Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease, and shows evidence for additional susceptibility genes (2009) (1441)
Association scan of 14,500 nonsynonymous SNPs in four diseases identifies autoimmunity variants (2007) (1421)
Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease (2013) (1388)
Analysis of shared heritability in common disorders of the brain (2016) (1385)
Gene-Wide Analysis Detects Two New Susceptibility Genes for Alzheimer's Disease (2014) (1230)
Genome scan meta-analysis of schizophrenia and bipolar disorder, part II: Schizophrenia. (2003) (1195)
Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder (2008) (1189)
Genome-wide analysis of genetic loci associated with Alzheimer disease. (2010) (1177)
A contribution of novel CNVs to schizophrenia from a genome-wide study of 41,321 subjects: CNV Analysis Group and the Schizophrenia Working Group of the Psychiatric Genomics Consortium (2016) (1125)
Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection (2018) (1124)
Genetic meta-analysis of diagnosed Alzheimer’s disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing (2019) (1073)
Identification of loci associated with schizophrenia by genome-wide association and follow-up (2008) (1069)
High rates of schizophrenia in adults with velo-cardio-facial syndrome (VCFS) (1999) (1035)
Genome-wide association study identifies 30 Loci Associated with Bipolar Disorder (2017) (998)
The genetic basis of complex human behaviors. (1994) (975)
Large-scale genome-wide association analysis of bipolar disorder identifies a new susceptibility locus near ODZ4 (2011) (929)
The UK10K project identifies rare variants in health and disease (2015) (926)
Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects (2016) (736)
Genomic Relationships, Novel Loci, and Pleiotropic Mechanisms across Eight Psychiatric Disorders (2019) (724)
Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease (2017) (693)
Microduplications of 16p11.2 are Associated with Schizophrenia (2009) (685)
Psychiatric genome-wide association study analyses implicate neuronal, immune and histone pathways (2015) (676)
The genetics of schizophrenia and bipolar disorder: dissecting psychosis (2005) (606)
Psychiatric disorders from childhood to adulthood in 22q11.2 deletion syndrome: results from the International Consortium on Brain and Behavior in 22q11.2 Deletion Syndrome. (2014) (601)
Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls (2010) (600)
Meta-analysis shows significant association between dopamine system genes and attention deficit hyperactivity disorder (ADHD). (2006) (591)
Genetic Evidence Implicates the Immune System and Cholesterol Metabolism in the Aetiology of Alzheimer's Disease (2010) (587)
DNA Pooling: a tool for large-scale association studies (2002) (560)
Rare chromosomal deletions and duplications in attention-deficit hyperactivity disorder: a genome-wide analysis (2010) (530)
Schizophrenia (2016) (526)
Candidate single-nucleotide polymorphisms from a genomewide association study of Alzheimer disease. (2008) (522)
Definition and description of schizophrenia in the DSM-5 (2013) (521)
Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes (2017) (517)
Genes for schizophrenia and bipolar disorder? Implications for psychiatric nosology. (2005) (509)
The Kraepelinian dichotomy – going, going... but still not gone (2010) (509)
Discovery and statistical genotyping of copy-number variation from whole-exome sequencing depth. (2012) (496)
Genome-wide association study of copy number variation in 16,000 cases of eight common diseases and 3,000 shared controls (2010) (465)
Integrative functional genomic analysis of human brain development and neuropsychiatric risks (2018) (464)
Meta-analysis of genome-wide association studies of attention-deficit/hyperactivity disorder. (2010) (459)
Genetic identification of brain cell types underlying schizophrenia (2017) (424)
Gene ontology analysis of GWA study data sets provides insights into the biology of bipolar disorder. (2009) (412)
Support for the involvement of large copy number variants in the pathogenesis of schizophrenia. (2009) (409)
Susceptibility locus for Alzheimer's disease on chromosome 10. (2000) (397)
A structural variation reference for medical and population genetics (2020) (394)
The Role of Genes, Stress, and Dopamine in the Development of Schizophrenia (2017) (394)
Comparative genome hybridization suggests a role for NRXN1 and APBA2 in schizophrenia. (2007) (390)
Altering the course of schizophrenia: progress and perspectives (2016) (390)
The beginning of the end for the Kraepelinian dichotomy (2005) (390)
Analysis of copy number variations at 15 schizophrenia-associated loci (2014) (387)
A full genome scan for late onset Alzheimer's disease (1999) (383)
Rare loss-of-function variants in SETD1A are associated with schizophrenia and developmental disorders (2016) (363)
Mapping genomic loci implicates genes and synaptic biology in schizophrenia (2022) (361)
A haplotype implicated in schizophrenia susceptibility is associated with reduced COMT expression in human brain. (2003) (359)
Genome-Wide Association Identifies a Common Variant in the Reelin Gene That Increases the Risk of Schizophrenia Only in Women (2008) (343)
Schizophrenia: genes at last? (2005) (326)
The molecular genetics of schizophrenia: new findings promise new insights (2004) (326)
The Penetrance of Copy Number Variations for Schizophrenia and Developmental Delay (2014) (317)
Tbx1 haploinsufficiency is linked to behavioral disorders in mice and humans: Implications for 22q11 deletion syndrome (2006) (310)
Strong evidence that KIAA0319 on chromosome 6p is a susceptibility gene for developmental dyslexia. (2005) (306)
Improved imputation of low-frequency and rare variants using the UK10K haplotype reference panel (2015) (296)
Genetic overlap between autism, schizophrenia and bipolar disorder (2009) (294)
Neurodevelopmental hypothesis of schizophrenia (2011) (294)
The genetic deconstruction of psychosis. (2007) (294)
Evaluating Historical Candidate Genes for Schizophrenia (2015) (293)
Genome-wide association study identifies genetic variation in neurocan as a susceptibility factor for bipolar disorder. (2011) (286)
Genetics of schizophrenia (2005) (272)
Evidence for novel susceptibility genes for late-onset Alzheimer's disease from a genome-wide association study of putative functional variants. (2007) (271)
Variation in DCP1, encoding ACE, is associated with susceptibility to Alzheimer disease (1999) (267)
PREDISPOSING LOCUS FOR ALZHEIMER'S DISEASE ON CHROMOSOME 21 (1989) (267)
The GDP-GTP Exchange Factor Collybistin: An Essential Determinant of Neuronal Gephyrin Clustering (2004) (265)
A family based association study of T102C polymorphism in 5HT2A and schizophrenia plus identification of new polymorphisms in the promoter (1998) (257)
Cis-acting variation in the expression of a high proportion of genes in human brain (2003) (257)
Operation of the schizophrenia susceptibility gene, neuregulin 1, across traditional diagnostic boundaries to increase risk for bipolar disorder. (2005) (255)
Genetic Risk for Schizophrenia: Convergence on Synaptic Pathways Involved in Plasticity (2015) (248)
Genome-Wide Analysis of Copy Number Variants in Attention Deficit Hyperactivity Disorder: The Role of Rare Variants and Duplications at 15q13.3 (2012) (245)
Genome-wide association study of over 40,000 bipolar disorder cases provides new insights into the underlying biology (2021) (240)
A combined analysis of D22S278 marker alleles in affected sib-pairs: support for a susceptibility locus for schizophrenia at chromosome 22q12. Schizophrenia Collaborative Linkage Group (Chromosome 22). (1996) (235)
Genetics of psychosis; insights from views across the genome (2009) (227)
Neurexin 1 (NRXN1) deletions in schizophrenia. (2009) (227)
The catechol-O-methyl transferase (COMT) gene as a candidate for psychiatric phenotypes: evidence and lessons (2006) (222)
Psychosis genetics: modeling the relationship between schizophrenia, bipolar disorder, and mixed (or "schizoaffective") psychoses. (2009) (218)
Evidence for association between polymorphisms in the promoter and coding regions of the 5-HT2A receptor gene and response to clozapine (1998) (216)
Mutations in the gene encoding GlyT2 (SLC6A5) define a presynaptic component of human startle disease (2006) (215)
A replicated molecular genetic basis for subtyping antisocial behavior in children with attention-deficit/hyperactivity disorder. (2008) (214)
Identifying gene-environment interactions in schizophrenia: contemporary challenges for integrated, large-scale investigations. (2014) (210)
Common variants at VRK2 and TCF4 conferring risk of schizophrenia. (2011) (210)
Recent advances in the genetics of schizophrenia. (2003) (209)
Full genome screen for Alzheimer disease: stage II analysis. (2002) (209)
Identification of genetic variants associated with Huntington's disease progression: a genome-wide association study (2017) (208)
Rethinking psychosis: the disadvantages of a dichotomous classification now outweigh the advantages. (2007) (206)
Joint Analysis of Psychiatric Disorders Increases Accuracy of Risk Prediction for Schizophrenia, Bipolar Disorder, and Major Depressive Disorder (2015) (206)
Association of the dopamine D4 receptor gene 7-repeat allele with neuropsychological test performance of children with ADHD. (2004) (205)
Pre-morbid Adjustment and Personality in Psychosis (1991) (204)
Phenotypic Manifestation of Genetic Risk for Schizophrenia During Adolescence in the General Population. (2016) (204)
Expanded CAG repeats in schizophrenia and bipolar disorder (1995) (202)
Genomewide linkage scan in schizoaffective disorder: significant evidence for linkage at 1q42 close to DISC1, and suggestive evidence at 22q11 and 19p13. (2005) (201)
Identification in 2 independent samples of a novel schizophrenia risk haplotype of the dystrobrevin binding protein gene (DTNBP1). (2004) (200)
Haplotypes at the dystrobrevin binding protein 1 (DTNBP1) gene locus mediate risk for schizophrenia through reduced DTNBP1 expression. (2005) (199)
Most genome-wide significant susceptibility loci for schizophrenia and bipolar disorder reported to date cross-traditional diagnostic boundaries. (2011) (196)
Genotype effects of CHRNA7, CNR1 and COMT in schizophrenia: interactions with tobacco and cannabis use (2007) (193)
Genetic relationships between schizophrenia, bipolar disorder, and schizoaffective disorder. (2014) (193)
Investigating the Contribution of Common Genetic Variants to the Risk and Pathogenesis of ADHD (2012) (192)
Rare copy number variants: a point of rarity in genetic risk for bipolar disorder and schizophrenia. (2010) (192)
Evidence that interaction between neuregulin 1 and its receptor erbB4 increases susceptibility to schizophrenia (2006) (190)
Logic and justification for dimensional assessment of symptoms and related clinical phenomena in psychosis: Relevance to DSM-5 (2013) (186)
Structure of the psychotic disorders classification in DSM‐5 (2013) (186)
A genome-wide association study for late-onset Alzheimer's disease using DNA pooling (2008) (185)
Genetic disruption of voltage-gated calcium channels in psychiatric and neurological disorders (2015) (183)
Serotonergic system and attention deficit hyperactivity disorder (ADHD): a potential susceptibility locus at the 5-HT1B receptor gene in 273 nuclear families from a multi-centre sample (2001) (183)
Genome-wide Association for Major Depression Through Age at Onset Stratification: Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium☆ (2017) (183)
The contribution of rare variants to risk of schizophrenia in individuals with and without intellectual disability (2017) (182)
Endophenotypes in psychiatric genetics (2007) (181)
Genomic insights into the overlap between psychiatric disorders: implications for research and clinical practice (2014) (181)
Schizophrenia and the neurodevelopmental continuum:evidence from genomics (2017) (181)
Universal, robust, highly quantitative SNP allele frequency measurement in DNA pools (2002) (180)
Adolescent clinical outcomes for young people with attention-deficit hyperactivity disorder (2010) (178)
Low activity allele of catechol-O-methyltransferase gene associated with rapid cycling bipolar disorder (1998) (176)
Relationship between homozygosity at the dopamine D3 receptor gene and schizophrenia. (1994) (176)
A genome-wide association study in 574 schizophrenia trios using DNA pooling (2009) (175)
Catechol O-methyltransferase gene variant and birth weight predict early-onset antisocial behavior in children with attention-deficit/hyperactivity disorder. (2005) (175)
Catatonia in DSM-5 (2013) (174)
Defining the Effect of the 16p11.2 Duplication on Cognition, Behavior, and Medical Comorbidities. (2016) (174)
Meta-analysis of genome-wide association data of bipolar disorder and major depressive disorder (2011) (173)
Is COMT a susceptibility gene for schizophrenia? (2007) (172)
Strong evidence for association between the dystrobrevin binding protein 1 gene (DTNBP1) and schizophrenia in 488 parent-offspring trios from Bulgaria (2004) (172)
Convergent genetic and expression data implicate immunity in Alzheimer's disease (2014) (172)
Cheap, accurate and rapid allele frequency estimation of single nucleotide polymorphisms by primer extension and DHPLC in DNA pools (2000) (169)
Agreement between maternal report and antenatal records for a range of pre and peri-natal factors: the influence of maternal and child characteristics. (2007) (167)
A family-based and case-control association study of the dopamine D4 receptor gene and dopamine transporter gene in attention deficit hyperactivity disorder (2000) (167)
Structural brain abnormalities associated with deletion at chromosome 22q11 (2001) (166)
Whole genome linkage scan of recurrent depressive disorder from the depression network study. (2005) (164)
Novel Findings from CNVs Implicate Inhibitory and Excitatory Signaling Complexes in Schizophrenia (2015) (164)
Meta-analysis of the association between variants in SORL1 and Alzheimer disease. (2011) (159)
Genetic variation of brain-derived neurotrophic factor (BDNF) in bipolar disorder (2006) (157)
A scan of chromosome 10 identifies a novel locus showing strong association with late-onset Alzheimer disease. (2006) (156)
Paternal age and risk for schizophrenia (2003) (156)
Attenuated psychosis syndrome in DSM-5 (2013) (156)
No evidence for allelic association between schizophrenia and a polymorphism determining high or low catechol O-methyltransferase activity. (1996) (154)
Rare coding variants in ten genes confer substantial risk for schizophrenia (2022) (154)
Association of Per1 and Npas2 with autistic disorder: support for the clock genes/social timing hypothesis (2007) (153)
Hyperekplexia associated with compound heterozygote mutations in the beta-subunit of the human inhibitory glycine receptor (GLRB). (2002) (153)
An update on the genetics of schizophrenia (2006) (151)
Genome-Wide Association Study Implicates HLA-C*01:02 as a Risk Factor at the Major Histocompatibility Complex Locus in Schizophrenia (2012) (151)
Psychiatric Genetics and Genomics (2002) (150)
Variation at the DAOA/G30 locus influences susceptibility to major mood episodes but not psychosis in schizophrenia and bipolar disorder. (2006) (148)
A network of dopaminergic gene variations implicated as risk factors for schizophrenia. (2008) (148)
Replication of bipolar disorder susceptibility alleles and identification of two novel genome-wide significant associations in a new bipolar disorder case–control sample (2013) (145)
Psychosis susceptibility gene ZNF804A and cognitive performance in schizophrenia. (2010) (145)
GWAS of Suicide Attempt in Psychiatric Disorders and Association With Major Depression Polygenic Risk Scores. (2019) (144)
Association of late-onset Alzheimer's disease with genetic variation in multiple members of the GAPD gene family. (2004) (143)
A two-stage genome scan for schizophrenia susceptibility genes in 196 affected sibling pairs. (1999) (143)
Velo-cardio-facial syndrome: a model for understanding the genetics and pathogenesis of schizophrenia (2001) (141)
Evidence for recessive as well as dominant forms of startle disease (hyperekplexia) caused by mutations in the alpha 1 subunit of the inhibitory glycine receptor. (1994) (141)
Cognitive Performance Among Carriers of Pathogenic Copy Number Variants: Analysis of 152,000 UK Biobank Subjects (2017) (140)
Brain anatomy in adults with velocardiofacial syndrome with and without schizophrenia: preliminary results of a structural magnetic resonance imaging study. (2004) (138)
A Quantitative Trait Locus Associated With Cognitive Ability in Children (1998) (138)
Support for RGS4 as a susceptibility gene for schizophrenia (2004) (138)
High Loading of Polygenic Risk for ADHD in Children With Comorbid Aggression (2013) (137)
A promoter polymorphism in the monoamine oxidase A gene and its relationships to monoamine metabolite concentrations in CSF of healthy volunteers. (2000) (137)
Confirmation of association between expanded CAG/CTG repeats and both schizophrenia and bipolar disorder (1996) (136)
A Genetic Investigation of Sex Bias in the Prevalence of Attention-Deficit/Hyperactivity Disorder (2017) (136)
Strong genetic evidence for a selective influence of GABAA receptors on a component of the bipolar disorder phenotype (2008) (135)
Gene expression imputation across multiple brain regions provides insights into schizophrenia risk (2019) (134)
The genetics of attention deficit hyperactivity disorder. (2005) (134)
Schizophrenia susceptibility alleles are enriched for alleles that affect gene expression in adult human brain (2012) (132)
Examining for association between candidate gene polymorphisms in the dopamine pathway and attention-deficit hyperactivity disorder: a family-based study. (2001) (132)
Corrigendum: TCTEX1D2 mutations underlie Jeune asphyxiating thoracic dystrophy with impaired retrograde intraflagellar transport (2016) (131)
A systematic genomewide linkage study in 353 sib pairs with schizophrenia. (2003) (131)
Suggestion of roles for both common and rare risk variants in genome-wide studies of schizophrenia. (2010) (131)
Four Components Describe Behavioral Symptoms in 1,120 Individuals with Late‐Onset Alzheimer's Disease (2006) (130)
Age of onset in Huntington disease: sex specific influence of apolipoprotein E genotype and normal CAG repeat length (1999) (129)
Genome-wide association study of borderline personality disorder reveals genetic overlap with bipolar disorder, major depression and schizophrenia (2017) (129)
Finding schizophrenia genes. (2005) (129)
SNPs Associated with Cerebrospinal Fluid Phospho-Tau Levels Influence Rate of Decline in Alzheimer's Disease (2010) (128)
New Approaches to Psychiatric Diagnostic Classification (2014) (128)
Charting the landscape of priority problems in psychiatry, part 1: classification and diagnosis. (2016) (127)
Convergent evidence that oligodendrocyte lineage transcription factor 2 (OLIG2) and interacting genes influence susceptibility to schizophrenia (2006) (125)
Medical disorders in people with recurrent depression (2008) (124)
Association between genetic variation in a region on chromosome 11 and schizophrenia in large samples from Europe (2012) (124)
Isoform Heterogeneity of the Human Gephyrin Gene (GPHN), Binding Domains to the Glycine Receptor, and Mutation Analysis in Hyperekplexia* (2003) (124)
Association of the paternally transmitted copy of common Valine allele of the Val66Met polymorphism of the brain-derived neurotrophic factor (BDNF) gene with susceptibility to ADHD (2005) (123)
An investigation of the neuropsychological profile in adults with velo-cardio-facial syndrome (VCFS) (2000) (122)
Schizoaffective Disorder in the DSM-5 (2013) (121)
DAPK1 variants are associated with Alzheimer's disease and allele-specific expression. (2006) (121)
Candidate-gene association studies of schizophrenia. (1999) (119)
Convergent evidence for 2',3'-cyclic nucleotide 3'-phosphodiesterase as a possible susceptibility gene for schizophrenia. (2006) (117)
The implications of the shared genetics of psychiatric disorders (2016) (117)
Genome-wide Association Study of Alzheimer’s disease with Psychotic Symptoms (2011) (114)
Support for Neuregulin 1 as a Susceptibility Gene for Bipolar Disorder and Schizophrenia (2008) (114)
Advances in genetic findings on attention deficit hyperactivity disorder (2007) (113)
Case–control association study of 59 candidate genes reveals the DRD2 SNP rs6277 (C957T) as the only susceptibility factor for schizophrenia in the Bulgarian population (2009) (113)
Mental health resilience in the adolescent offspring of parents with depression: a prospective longitudinal study (2016) (112)
Association studies in psychiatric genetics (1997) (111)
Familiality of symptom dimensions in depression. (2004) (111)
Catechol‐O‐methyltransferase polymorphisms and schizophrenia: a transmission disequilibrium study in multiply affected families (1997) (109)
Is the dysbindin gene (DTNBP1) a susceptibility gene for schizophrenia? (2005) (109)
Large-scale mapping of cortical alterations in 22q11.2 deletion syndrome: Convergence with idiopathic psychosis and effects of deletion size (2018) (109)
Genetic relationships between suicide attempts, suicidal ideation and major psychiatric disorders: A genome-wide association and polygenic scoring study (2014) (108)
Association analysis of monoamine oxidase A and attention deficit hyperactivity disorder (2003) (108)
Genetic correlation between amyotrophic lateral sclerosis and schizophrenia (2017) (107)
Dynamic mutations and psychiatric genetics (1996) (107)
Bipolar disorder and polymorphisms in the dysbindin gene (DTNBP1) (2005) (107)
Copy Number Variation in Schizophrenia in the Japanese Population (2010) (106)
Suggestive evidence for linkage of schizophrenia to markers on chromosome 13q14.1‐q32 (1995) (106)
Genetic studies on chromosome 12 in late-onset Alzheimer disease. (1998) (105)
Expression quantitative trait loci in the developing human brain and their enrichment in neuropsychiatric disorders (2018) (105)
Cognitive deficits associated with schizophrenia in velo-cardio-facial syndrome (2004) (104)
Distribution and Expression of Picalm in Alzheimer Disease (2010) (104)
Analysis of Intellectual Disability Copy Number Variants for Association With Schizophrenia. (2016) (104)
Genomewide Association Scan of Suicidal Thoughts and Behaviour in Major Depression (2011) (103)
Evaluation of a Susceptibility Gene for Schizophrenia: Genotype Based Meta-Analysis of RGS4 Polymorphisms from Thirteen Independent Samples (2006) (101)
Effects of Differential Genotyping Error Rate on the Type I Error Probability of Case-Control Studies (2006) (100)
Aggressive behaviour in patients with schizophrenia is associated with catechol-O-methyltransferase genotype (2001) (99)
The Genetics of the Mood Disorder Spectrum: Genome-wide Association Analyses of More Than 185,000 Cases and 439,000 Controls (2018) (99)
Low birth weight and a family history of schizophrenia predict poor premorbid functioning in psychosis (1991) (98)
Seminars in Psychiatric Genetics (1994) (98)
Obstetric complications and schizophrenia: a computed tomographic study (1988) (97)
Genotyping single nucleotide polymorphisms by primer extension and high performance liquid chromatography (1999) (97)
Schizophrenia and functional polymorphisms in the MAOA and COMT genes: no evidence for association or epistasis. (2002) (97)
Genetic utility of broadly defined bipolar schizoaffective disorder as a diagnostic concept (2009) (96)
Biological Overlap of Attention-Deficit/Hyperactivity Disorder and Autism Spectrum Disorder: Evidence From Copy Number Variants (2014) (96)
European Multicentre Association Study of Schizophrenia: a study of the DRD2 Ser311Cys and DRD3 Ser9Gly polymorphisms. (1998) (96)
Shared polygenic contribution between childhood attention-deficit hyperactivity disorder and adult schizophrenia† (2013) (95)
Substantial linkage disequilibrium across the insulin-degrading enzyme locus but no association with late-onset Alzheimer's disease (2001) (95)
DRD2 Ser311/Cys311 polymorphism in schizophrenia (1994) (95)
Psychopathy trait scores in adolescents with childhood ADHD: the contribution of genotypes affecting MAOA, 5HTT and COMT activity (2009) (95)
Association of Genetic Liability to Psychotic Experiences With Neuropsychotic Disorders and Traits (2019) (95)
Maternally derived microduplications at 15q11-q13: implication of imprinted genes in psychotic illness. (2011) (94)
Premature mortality among people with severe mental illness — New evidence from linked primary care data (2018) (94)
HTR2A: Association and expression studies in neuropsychiatric genetics (2005) (93)
De Novo Rates and Selection of Schizophrenia-Associated Copy Number Variants (2011) (93)
Complement genes contribute sex-biased vulnerability in diverse illnesses (2020) (92)
Evidence of Common Genetic Overlap Between Schizophrenia and Cognition (2015) (92)
A mitochondrial DNA sequence variant associated with schizophrenia and oxidative stress (2003) (92)
Alzheimer's disease genetics: current knowledge and future challenges (2011) (92)
No association between schizophrenia and polymorphisms in COMT in two large samples. (2005) (92)
Schizophrenia genetics: emerging themes for a complex disorder (2014) (92)
Genome-Wide Association Study of Schizophrenia in a Japanese Population (2011) (91)
Psychiatric genetics: back to the future (2000) (90)
SGCE mutations cause psychiatric disorders: clinical and genetic characterization. (2013) (90)
Identification of Novel Candidate Genes for Treatment Response to Risperidone and Susceptibility for Schizophrenia: Integrated Analysis Among Pharmacogenomics, Mouse Expression, and Genetic Case-Control Association Approaches (2010) (90)
Refining the attention deficit hyperactivity disorder phenotype for molecular genetic studies (2006) (90)
Medical consequences of pathogenic CNVs in adults: analysis of the UK Biobank (2018) (89)
Transcript expression-aware annotation improves rare variant interpretation (2020) (89)
Phenotypic and genetic complexity of psychosis (2007) (87)
Does Childhood Trauma Moderate Polygenic Risk for Depression? A Meta-analysis of 5765 Subjects From the Psychiatric Genomics Consortium (2017) (87)
Shared Genetic Influences Between Attention-Deficit/Hyperactivity Disorder (ADHD) Traits in Children and Clinical ADHD (2015) (86)
Evaluating drug targets through human loss-of-function genetic variation (2019) (86)
Linkage studies on chromosome 22 in familial schizophrenia. (1995) (86)
Psychiatric disorders in children with 16p11.2 deletion and duplication (2019) (85)
Family aggregation of high myopia: estimation of the sibling recurrence risk ratio. (2004) (85)
Association Between Schizophrenia-Related Polygenic Liability and the Occurrence and Level of Mood-Incongruent Psychotic Symptoms in Bipolar Disorder (2017) (84)
Further evidence for high rates of schizophrenia in 22q11.2 deletion syndrome (2014) (83)
Linkage analysis of the genetic loci for high myopia on 18p, 12q, and 17q in 51 U.K. families. (2004) (83)
CNV analysis in a large schizophrenia sample implicates deletions at 16p12.1 and SLC1A1 and duplications at 1p36.33 and CGNL1 (2013) (83)
A Population-Based Study of Genetic Variation and Psychotic Experiences in Adolescents (2013) (82)
De novo mutations identified by exome sequencing implicate rare missense variants in SLC6A1 in schizophrenia (2019) (82)
Pooled DNA genotyping on Affymetrix SNP genotyping arrays (2006) (82)
Follow-up of genetic linkage findings on chromosome 16p13: evidence of association of N-methyl-D aspartate glutamate receptor 2A gene polymorphism with ADHD (2004) (82)
Family-based association studies of bipolar disorder with candidate genes involved in dopamine neurotransmission: DBH, DAT1, COMT, DRD2, DRD3 and DRD5 (1999) (81)
Stressful life events, 5-HTT genotype and risk of depression (2006) (81)
Psychopathology and cognition in children with 22q11.2 deletion syndrome (2014) (80)
No support for association between the dopamine transporter (DAT1) gene and ADHD (2005) (80)
SORL1 variants and risk of late-onset Alzheimer’s disease (2008) (80)
Genome screen for loci influencing age at onset and rate of decline in late onset Alzheimer's disease (2005) (79)
Schizophrenia: a genetic disorder of the synapse? (2005) (79)
Polymorphisms in the MAOA, MAOB, and COMT genes and aggressive behavior in schizophrenia (2004) (79)
Schizophrenia genetics: advancing on two fronts. (2009) (79)
Reasons for discontinuing clozapine: A cohort study of patients commencing treatment (2016) (78)
Characterising the loss-of-function impact of 5’ untranslated region variants in 15,708 individuals (2019) (78)
Schizophrenia genetics: new insights from new approaches. (2009) (78)
No Major Schizophrenia Locus Detected on Chromosome 1q in a Large Multicenter Sample (2002) (78)
Independent estimation of the frequency of rare CNVs in the UK population confirms their role in schizophrenia (2012) (77)
Tryptophan hydroxylase and catechol-O-methyltransferase gene polymorphisms: relationships to monoamine metabolite concentrations in CSF of healthy volunteers (2008) (77)
Association of Rare Copy Number Variants With Risk of Depression (2019) (76)
Confirmation of association between the e4 allele of apolipoprotein E and Alzheimer's disease. (1994) (76)
Rare Genome-Wide Copy Number Variation and Expression of Schizophrenia in 22q11.2 Deletion Syndrome. (2017) (76)
A cross-sectional and a prospective study of thyroid disorders in lithium-treated patients. (2005) (75)
Analysis of 10 independent samples provides evidence for association between schizophrenia and a SNP flanking fibroblast growth factor receptor 2 (2009) (75)
Strong evidence that GNB1L is associated with schizophrenia. (2008) (75)
Genetic risk of Alzheimer's disease: advising relatives (2001) (74)
Compound heterozygosity and nonsense mutations in the α1-subunit of the inhibitory glycine receptor in hyperekplexia (2001) (74)
Alzheimer's disease: The amyloid hypothesis on trial (2016) (74)
TCF4, schizophrenia, and Pitt-Hopkins Syndrome. (2010) (74)
An international collaborative family-based whole-genome linkage scan for high-grade myopia. (2009) (73)
DNA pooling as a tool for large‐scale association studies in complex traits (2004) (73)
The Wellcome trust UK–Irish bipolar affective disorder sibling-pair genome screen: first stage report (2002) (73)
Cognitive performance and functional outcomes of carriers of pathogenic copy number variants: analysis of the UK Biobank (2019) (73)
No evidence for allelic association between bipolar disorder and monoamine oxidase A gene polymorphisms. (1995) (72)
Genome-wide association studies in psychiatry: lessons from early studies of non-psychiatric and psychiatric phenotypes (2008) (72)
De novo CNVs in bipolar affective disorder and schizophrenia (2014) (72)
Testing for gene × environment interaction effects in attention deficit hyperactivity disorder and associated antisocial behavior (2008) (72)
Genome-wide gene-environment analyses of major depressive disorder and reported lifetime traumatic experiences in UK Biobank (2019) (72)
A Population-Based Cohort Study Examining the Incidence and Impact of Psychotic Experiences From Childhood to Adulthood, and Prediction of Psychotic Disorder. (2020) (71)
Chromosome 22q11 deletions, velo-cardio-facial syndrome and early-onset psychosis (2003) (71)
Cannabis, COMT and psychotic experiences (2011) (70)
A Multiple Indicators Multiple Causes (MIMIC) model of Behavioural and Psychological Symptoms in Dementia (BPSD) (2011) (70)
Polygenic dissection of the bipolar phenotype (2011) (70)
Reciprocal Duplication of the Williams-Beuren Syndrome Deletion on Chromosome 7q11.23 Is Associated with Schizophrenia (2014) (70)
A rare variant in APOC3 is associated with plasma triglyceride and VLDL levels in Europeans (2014) (69)
The Relationship Between Polygenic Risk Scores and Cognition in Schizophrenia (2019) (69)
Phenotypic variations on the theme of CNVs (2008) (69)
The effect of LRRK2 loss-of-function variants in humans (2020) (69)
The role of the major histocompatibility complex region in cognition and brain structure: a schizophrenia GWAS follow-up. (2013) (68)
Further support for an association between a polymorphic CAG repeat in the hKCa3 gene and schizophrenia (1998) (68)
Association analysis of NOTCH4 loci in schizophrenia using family and population-based controls (2001) (67)
Genotype link with extreme antisocial behavior: the contribution of cognitive pathways. (2010) (67)
Dissecting the Shared Genetic Architecture of Suicide Attempt, Psychiatric Disorders, and Known Risk Factors (2020) (66)
Association of DISC1 and TSNAX genes and affective disorders in the depression case–control (DeCC) and bipolar affective case–control (BACCS) studies (2010) (66)
Implication of a rare deletion at distal 16p11.2 in schizophrenia. (2013) (66)
Association and linkage: complementary strategies for complex disorders. (1993) (66)
Genome-wide association study of multiplex schizophrenia pedigrees. (2012) (66)
No association with the 5,10‐methylenetetrahydrofolate reductase gene and major depressive disorder: Results of the depression case control (DeCC) study and a meta‐analysis (2008) (66)
Dimensions of psychosis in affected sibling pairs (1998) (65)
Association analysis of AKT1 and schizophrenia in a UK case control sample (2007) (65)
Relationship between obesity and the risk of clinically significant depression: Mendelian randomisation study (2014) (64)
Erratum: Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease (2009) (64)
A genome-wide significant linkage for severe depression on chromosome 3: the depression network study. (2011) (64)
Intellectual disability and major psychiatric disorders: a continuum of neurodevelopmental causality. (2012) (64)
α-2 macroglobulin gene and Alzheimer disease (1999) (64)
COL1A1 and COL2A1 genes and myopia susceptibility: evidence of association and suggestive linkage to the COL2A1 locus. (2009) (64)
Genetic contributors to risk of schizophrenia in the presence of a 22q11.2 deletion (2020) (64)
Depression Case Control (DeCC) Study fails to support involvement of the muscarinic acetylcholine receptor M2 (CHRM2) gene in recurrent major depressive disorder. (2009) (63)
Mutation screening of the Homer gene family and association analysis in schizophrenia (2003) (63)
A population-based study of shared genetic variation between premorbid IQ and psychosis among male twin pairs and sibling pairs from Sweden. (2012) (63)
Analysis of genome-wide association studies of Alzheimer disease and of Parkinson disease to determine if these 2 diseases share a common genetic risk. (2013) (63)
Using common genetic variation to examine phenotypic expression and risk prediction in 22q11.2 deletion syndrome (2020) (62)
Glycogen synthase kinase‐3β and tau genes interact in Alzheimer's disease (2008) (62)
Implications of genetic findings for understanding schizophrenia. (2012) (62)
Positional cloning, association analysis and expression studies provide convergent evidence that the cadherin gene FAT contains a bipolar disorder susceptibility allele (2006) (62)
The role of variation at AβPP, PSEN1, PSEN2, and MAPT in late onset Alzheimer's disease. (2012) (61)
Comparative performances of machine learning methods for classifying Crohn Disease patients using genome-wide genotyping data (2019) (61)
Searching for schizophrenia genes. (2001) (60)
A Comparison of Ten Polygenic Score Methods for Psychiatric Disorders Applied Across Multiple Cohorts (2020) (60)
Genotype-phenotype associations in children with copy number variants associated with high neuropsychiatric risk in the UK (IMAGINE-ID): a case-control cohort study. (2019) (59)
Enhanced maternal origin of the 22q11.2 deletion in velocardiofacial and DiGeorge syndromes. (2013) (58)
The Depression Network (DeNT) Study: methodology and sociodemographic characteristics of the first 470 affected sibling pairs from a large multi-site linkage genetic study (2004) (58)
Risk of psychopathology in adolescent offspring of mothers with psychopathology and recurrent depression (2013) (58)
Association of ABCA1 with late-onset Alzheimer’s disease is not observed in a case-control study (2004) (58)
A neurogenetic model for the study of schizophrenia spectrum disorders: the International 22q11.2 Deletion Syndrome Brain Behavior Consortium (2017) (58)
New data and an old puzzle: the negative association between schizophrenia and rheumatoid arthritis. (2015) (58)
Linkage, association and mutational analysis of the dopamine D3 receptor gene in schizophrenia. (1996) (57)
A genetic risk score combining 32 SNPs is associated with body mass index and improves obesity prediction in people with major depressive disorder (2015) (57)
Further evidence of autosomal dominant congenital zonular pulverulent cataracts linked to 13q11 (CZP3) and a novel mutation in connexin 46 (GJA3). (2000) (57)
Minor Physical Anomalies and their Relationship to the Aetiology of Schizophrenia (1996) (57)
Fine mapping of ZNF 804 A and genome-wide significant evidence for its involvement in schizophrenia and bipolar disorder (2011) (57)
A genomewide linkage study of age at onset in schizophrenia. (2001) (57)
Chromosome 22qII deletions. An under-recognised cause of idiopathic learning disability. (1998) (57)
Failure to find linkage between a functional polymorphism in the dopamine D4 receptor gene and schizophrenia. (1994) (57)
Candidate gene association study of insulin signaling genes and Alzheimer's disease: Evidence for SOS2, PCK1, and PPARγ as susceptibility loci (2007) (56)
A large replication study and meta-analysis in European samples provides further support for association of AHI1 markers with schizophrenia. (2010) (55)
Charting the landscape of priority problems in psychiatry, part 2: pathogenesis and aetiology. (2016) (55)
A linkage study of schizophrenia with DNA markers from the long arm of chromosome 11 (1992) (55)
Effects of a functional COMT polymorphism on brain anatomy and cognitive function in adults with velo-cardio-facial syndrome (2007) (55)
Lack of support for a genetic association of the XBP1 promoter polymorphism with bipolar disorder in probands of European origin (2004) (55)
Association between PRODH and schizophrenia is not confirmed (2003) (55)
Localization of bipolar susceptibility locus by molecular genetic analysis of the chromosome 12q23-q24 region in two pedigrees with bipolar disorder and Darier's disease. (2005) (55)
Dysbindin-1 and schizophrenia: from genetics to neuropathology. (2004) (55)
Shared genetic contribution to ischemic stroke and Alzheimer's disease (2016) (55)
No evidence of association of two 5HT transporter gene polymorphisms and attention deficit hyperactivity disorder (2003) (55)
No Evidence for a Pseudoautosomal Locus for Schizophrenia (1992) (54)
Long repeat tracts at SCA8 in major psychosis. (2000) (54)
APOE ε4 influences the manifestation of Alzheimer's disease in adults with Down's syndrome (2000) (54)
No evidence for association between polymorphisms in GRM3 and schizophrenia (2005) (53)
Genome-wide linkage analysis of 723 affected relative pairs with late-onset Alzheimer's disease. (2007) (53)
Variation in tau isoform expression in different brain regions and disease states (2013) (53)
Pooled genotyping of microsatellite markers in parent-offspring trios. (2000) (53)
The synapse in schizophrenia (2014) (53)
Genome-wide common and rare variant analysis provides novel insights into clozapine-associated neutropenia (2016) (53)
Familial influence on variation in age of onset and behavioural phenotype in Alzheimer's disease. (2000) (52)
Modern molecular genetic approaches to psychiatric disease. (1996) (51)
Suggestive synergy between genetic variants in TF and HFE as risk factors for Alzheimer's disease (2009) (51)
Effects of pathogenic CNVs on physical traits in participants of the UK Biobank (2018) (51)
De novo mutation in schizophrenia. (2012) (51)
Association of serotonin and dopamine gene pathways with behavioral subphenotypes in dementia (2012) (51)
Trajectories of change in self-reported psychotic-like experiences in childhood and adolescence (2012) (51)
Allelic expression of APOE in human brain: effects of epsilon status and promoter haplotypes. (2004) (51)
Genome Wide Association Analysis of Copy Number Variation in Recurrent Depressive Disorder (2011) (51)
Exome arrays capture polygenic rare variant contributions to schizophrenia (2016) (51)
SGCE and myoclonus dystonia: motor characteristics, diagnostic criteria and clinical predictors of genotype (2014) (51)
Common schizophrenia alleles are enriched in mutation-intolerant genes and maintained by background selection (2016) (50)
Detailed analysis of PRODH and PsPRODH reveals no association with schizophrenia (2003) (50)
Neuropsychological effects of the CSMD1 genome‐wide associated schizophrenia risk variant rs10503253 (2013) (50)
Genetics of schizophrenia: A consensus paper of the WFSBP Task Force on Genetics (2017) (50)
Analysis of ProDH, COMT and ZDHHC8 risk variants does not support individual or interactive effects on schizophrenia susceptibility (2006) (49)
Interaction between the FTO gene, body mass index and depression: meta-analysis of 13701 individuals† (2017) (49)
Molecular genetic contribution to the developmental course of attention-deficit hyperactivity disorder (2008) (49)
Formalising recall by genotype as an efficient approach to detailed phenotyping and causal inference (2018) (49)
Schizophrenia aetiology: Do gene-environment interactions hold the key? (2008) (49)
Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depressive disorder (2017) (47)
Influence of NOS1 on verbal intelligence and working memory in both patients with schizophrenia and healthy control subjects. (2009) (47)
Examining cognition across the bipolar/schizophrenia diagnostic spectrum. (2018) (47)
Altered white matter microstructure in 22q11.2 deletion syndrome: a multisite diffusion tensor imaging study (2019) (47)
Association of Copy Number Variation of the 15q11.2 BP1-BP2 Region With Cortical and Subcortical Morphology and Cognition. (2020) (47)
Translating insights from neuropsychiatric genetics and genomics for precision psychiatry (2020) (46)
Bipolar disorder and the serotonin transporter gene: a family-based association study (1999) (46)
Psychopathy traits in adolescents with childhood attention-deficit hyperactivity disorder (2009) (46)
Localisation of a Susceptibility Locus for Schizophrenia on Chromosome 5 (1990) (46)
Exclusion of the Darier's disease gene, ATP2A2, as a common susceptibility gene for bipolar disorder (2001) (45)
Further evidence of autosomal dominant congenital zonular pulverulent cataracts linked to 13q11 (CZP3) and a novel mutation in connexin 46 (GJA3) (2000) (45)
No Association Between the Putative Functional ZDHHC8 Single Nucleotide Polymorphism rs175174 and Schizophrenia in Large European Samples (2005) (45)
Defective Processing Speed and Nonclinical Psychotic Experiences in Children: Longitudinal Analyses in a Large Birth Cohort (2013) (45)
Novel Insight Into the Etiology of Autism Spectrum Disorder Gained by Integrating Expression Data With Genome-wide Association Statistics (2019) (45)
Processing facial emotions in adults with velo-cardio-facial syndrome: functional magnetic resonance imaging (2006) (45)
Genetic variability at the amyloid-β precursor protein locus may contribute to the risk of late-onset Alzheimer's disease (1999) (45)
Steroid sulfatase is a potential modifier of cognition in attention deficit hyperactivity disorder (2011) (44)
A single nucleotide polymorphism in CHAT influences response to acetylcholinesterase inhibitors in Alzheimer's disease (2006) (44)
Psychiatric disorders, myoclonus dystonia, and the epsilon‐sarcoglycan gene: A systematic review (2011) (44)
Investigating the genetic architecture of general and specific psychopathology in adolescence (2018) (43)
Parental Origin of Interstitial Duplications at 15q11.2-q13.3 in Schizophrenia and Neurodevelopmental Disorders (2016) (43)
Genetic Differences between Five European Populations (2010) (43)
Psychiatric disorders, myoclonus dystonia and SGCE: an international study (2015) (43)
Rare Variant Analysis of Human and Rodent Obesity Genes in Individuals with Severe Childhood Obesity (2017) (43)
Evidence that common variation in NEDD9 is associated with susceptibility to late-onset Alzheimer's and Parkinson's disease. (2008) (43)
Misconceptions about gene-environment interactions in psychiatry. (2011) (42)
Cyfip1 haploinsufficient rats show white matter changes, myelin thinning, abnormal oligodendrocytes and behavioural inflexibility (2019) (42)
No consistent evidence for association between mtDNA variants and Alzheimer disease (2012) (42)
A multi-center study of ACE and the risk of late-onset Alzheimer's disease. (2011) (42)
Clinical indicators of treatment-resistant psychosis (2019) (42)
No association between the alpha-2 macroglobulin I1000V polymorphism and Alzheimer's disease (1999) (42)
Linkage Study of Schizophrenia Candidate Regions on Chromosomes 5 q , 6 q , 10 p , and 13 q : Schizophrenia Linkage Collaborative Group III * (41)
Stage 2 of the Wellcome Trust UK–Irish bipolar affective disorder sibling-pair genome screen: evidence for linkage on chromosomes 6q16–q21, 4q12–q21, 9p21, 10p14–p12 and 18q22 (2005) (41)
Mutation screening of SCN2A in schizophrenia and identification of a novel loss-of-function mutation (2016) (41)
Genetic variants in the ErbB4 gene are associated with white matter integrity (2011) (41)
Hyperekplexia: abnormal startle response due to glycine receptor mutations (1997) (41)
Diagnosis of functional psychoses: time to face the future (2009) (40)
Case-control association study of 65 candidate genes revealed a possible association of a SNP of HTR5A to be a factor susceptible to bipolar disease in Bulgarian population. (2009) (40)
Mapping Subcortical Brain Alterations in 22q11.2 Deletion Syndrome: Effects of Deletion Size and Convergence With Idiopathic Neuropsychiatric Illness. (2020) (39)
Genetic abnormalities of chromosome 22 and the development of psychosis (2004) (39)
A Genetics-First Approach to Dissecting the Heterogeneity of Autism: Phenotypic Comparison of Autism Risk Copy Number Variants. (2020) (39)
Genetic association of the APP binding protein 2 gene (APBB2) with late onset Alzheimer disease (2005) (39)
A comparison of four clustering methods for brain expression microarray data (2008) (39)
Will schizophrenia become a graveyard for molecular geneticists? (1992) (39)
Presenilin-1 polymorphism and Alzheimer's disease (1996) (39)
Schizophrenia and genetics (2003) (38)
Association studies between risk for late‐onset Alzheimer's disease and variants in insulin degrading enzyme (2005) (38)
Sibling pairs with schizophrenia or schizoaffective disorder: associations of subtypes, symptoms and demographic variables (1998) (38)
No evidence of association between Catechol-O-Methyltransferase (COMT) Val158Met genotype and performance on neuropsychological tasks in children with ADHD: A case-control study (2004) (38)
Ubiquilin 1 polymorphisms are not associated with late‐onset Alzheimer's disease (2006) (37)
Association of polygenic score for major depression with response to lithium in patients with bipolar disorder (2020) (37)
Cognitive analysis of schizophrenia risk genes that function as epigenetic regulators of gene expression (2016) (37)
Chromosome 22 markers demonstrate transmission disequilibrium with schizophrenia (1995) (37)
Complete Sequence of the 22q11.2 Allele in 1,053 Subjects with 22q11.2 Deletion Syndrome Reveals Modifiers of Conotruncal Heart Defects. (2019) (36)
Repeat length variation in the dopamine D4 receptor gene shows no evidence of association with schizophrenia. (1994) (36)
New findings from genetic association studies of schizophrenia (2009) (36)
Pharmacogenomic Variants and Drug Interactions Identified Through the Genetic Analysis of Clozapine Metabolism. (2019) (36)
Conditional GWAS analysis to identify disorder-specific SNPs for psychiatric disorders (2020) (35)
Association and haplotype analysis at the tyrosine hydroxylase locus in a combined German‐British sample of manic depressive patients and controls (1994) (35)
The dopamine D3 receptor gene: no association with bipolar affective disorder. (1993) (35)
Molecular investigation of TBP allele length: a SCA17 cellular model and population study (2003) (35)
Sustained and selective attention as measures of genetic liability to schizophrenia (2001) (35)
Alzheimer's disease risk variant in CLU is associated with neural inefficiency in healthy individuals (2015) (35)
Linked polymorphisms upstream of exons 1 and 2 of the human cholecystokinin gene are not associated with schizophrenia or bipolar disorder (1998) (35)
Sequence variation in the CHAT locus shows no association with late-onset Alzheimer's disease (2003) (34)
An association study of common variation at the MAPT locus with late‐onset Alzheimer's disease (2009) (34)
EVIDENCE THAT PUTATIVE ADHD LOW RISK ALLELES AT SNAP25 MAY INCREASE THE RISK OF SCHIZOPHRENIA (2009) (34)
Association study of bipolar disorder using a functional polymorphism (Ser311→Cys) in the dopamine D2 receptor gene (1995) (34)
Whole Genome Association Study in a Homogenous Population in Shandong Peninsula of China Reveals JARID2 as a Susceptibility Gene for Schizophrenia (2009) (34)
Stage 2 of the Wellcome Trust UK–Irish bipolar affective disorder sibling-pair genome screen: evidence for linkage on chromosomes 6q16–q21, 4q12–q21, 9p21, 10p14–p12 and 18q22 (2006) (34)
Analysis of exome sequence in 604 trios for recessive genotypes in schizophrenia (2015) (34)
Physical mapping around the Alzheimer disease locus on the proximal long arm of chromosome 21. (1990) (34)
Expansion of 50 CAG/CTG repeats excluded in schizophrenia by application of a highly efficient approach using repeat expansion detection and a PCR screening set. (1996) (34)
Bipolar disorder and variation at a common polymorphism (A1832G) within exon 8 of the Wolfram gene. (2000) (34)
The clinical presentation of attention deficit‐hyperactivity disorder (ADHD) in children with 22q11.2 deletion syndrome (2015) (33)
Clinical and cognitive characteristics of children with attention-deficit hyperactivity disorder, with and without copy number variants (2011) (33)
Dissecting the Genetic Heterogeneity of Depression Through Age at Onset (2012) (33)
A Regulatory Monoamine Oxidase A Promoter Polymorphism and Personality Traits (2003) (33)
Associations between polygenic risk for schizophrenia and brain function during probabilistic learning in healthy individuals (2015) (32)
Tryptophan hydroxylase gene and manic-depressive illness. (1999) (32)
Association study of myo-inositol monophosphatase 2 (IMPA2) polymorphisms with bipolar affective disorder and response to lithium treatment (2005) (32)
Reciprocal White Matter Changes Associated With Copy Number Variation at 15q11.2 BP1-BP2: A Diffusion Tensor Imaging Study (2019) (32)
A genome-wide association study in individuals of African ancestry reveals the importance of the Duffy-null genotype in the assessment of clozapine-related neutropenia (2019) (32)
A Family Based Study Implicates Solute Carrier Family 1–Member 3 (SLC1A3) Gene in Attention-Deficit/Hyperactivity Disorder (2005) (32)
Pathogenic copy number variants and SCN1A mutations in patients with intellectual disability and childhood-onset epilepsy (2016) (32)
The butyrylcholinesterase K variant and susceptibility to Alzheimer's disease. (1998) (32)
Screening the human protocadherin 8 (PCDH8) gene in schizophrenia (2002) (32)
Dynamic expression of genes associated with schizophrenia and bipolar disorder across development (2019) (31)
A polygenic resilience score moderates the genetic risk for schizophrenia (2019) (31)
Developmental coordination disorder, psychopathology and IQ in 22q11.2 deletion syndrome (2018) (31)
The Bipolar Association Case–Control Study (BACCS) and meta‐analysis: No association with the 5,10‐Methylenetetrahydrofolate reductase gene and bipolar disorder (2010) (31)
Allelic variation of a BalI polymorphism in the DRD3 gene does not influence susceptibility to bipolar disorder: results of analysis and meta-analysis. (2001) (31)
A family based study of catechol‐O‐methyltransferase (COMT) and attention deficit hyperactivity disorder (ADHD) (2005) (31)
A genome-wide study shows a limited contribution of rare copy number variants to Alzheimer's disease risk (2012) (31)
Steroid receptor coactivator-1 modulates the function of Pomc neurons and energy homeostasis (2019) (31)
Childhood cognitive development in 22q11.2 deletion syndrome: case–control study (2017) (30)
Reduced burden of very large and rare CNVs in bipolar affective disorder. (2013) (30)
Targeted Sequencing of 10,198 Samples Confirms Abnormalities in Neuronal Activity and Implicates Voltage-Gated Sodium Channels in Schizophrenia Pathogenesis (2019) (30)
A transcriptome-wide association study implicates specific pre- and post-synaptic abnormalities in schizophrenia (2019) (30)
Searching for susceptibility genes in schizophrenia (1995) (30)
The molecular genetics of schizophrenia. (1992) (30)
Visuospatial working memory in children and adolescents with 22q11.2 deletion syndrome; an fMRI study (2009) (30)
Association study in the 5q31-32 linkage region for schizophrenia using pooled DNA genotyping (2008) (30)
Bipolar disorder among an isolated island community in Ethiopia. (2004) (29)
TBP, a polyglutamine tract containing protein, accumulates in Alzheimer's disease. (2004) (29)
Family History and Cerebral Ventricular Enlargement in Schizophrenia (1989) (29)
Clusterin mRNA and protein in Alzheimer's disease. (2012) (29)
Association between a PS‐1 intronic polymorphism and late onset Alzheimer's disease (1996) (29)
DCLK1 Variants Are Associated across Schizophrenia and Attention Deficit/Hyperactivity Disorder (2012) (29)
Streamlined analysis of pooled genotype data in SNP‐based association studies (2005) (29)
Genomic approaches to schizophrenia. (2005) (28)
Candidate gene association studies of the alpha 4 (CHRNA4) and beta 2 (CHRNB2) neuronal nicotinic acetylcholine receptor subunit genes in Alzheimer's disease. (2004) (28)
Linkage disequilibrium mapping of bipolar affective disorder at 12q23‐q24 provides evidence for association at CUX2 and FLJ32356 (2005) (28)
Mood-incongruent psychosis in bipolar disorder: conditional linkage analysis shows genome-wide suggestive linkage at 1q32.3, 7p13 and 20q13.31. (2009) (28)
The molecular genetics of Alzheimer's disease (1994) (28)
Association study of bipolar disorder at the phospholipase A2 gene (PLA2A) in the Darier's disease (DAR) region of chromosome 12q23‐q24.1 (1996) (27)
Comparison of Genetic Liability for Sleep Traits Among Individuals With Bipolar Disorder I or II and Control Participants (2019) (27)
Phenotypic Association Analyses With Copy Number Variation in Recurrent Depressive Disorder (2016) (26)
Epilepsy and seizures in young people with 22q11.2 deletion syndrome: Prevalence and links with other neurodevelopmental disorders (2019) (26)
Author Correction: Genetic meta-analysis of diagnosed Alzheimer’s disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing (2019) (26)
Candidate gene association studies of the α4 (CHRNA4) and β2 (CHRNB2) neuronal nicotinic acetylcholine receptor subunit genes in Alzheimer's disease (2004) (26)
α-T-catenin is expressed in human brain and interacts with the Wnt signaling pathway but is not responsible for linkage to chromosome 10 in Alzheimer’s disease (2007) (26)
Evidence to suggest biased phenotypes in children with Attention Deficit Hyperactivity Disorder from completely ascertained trios (2002) (26)
Cognitive Characterization of Schizophrenia Risk Variants Involved in Synaptic Transmission: Evidence of CACNA1C's Role in Working Memory (2017) (26)
The effect of age and the H1c MAPT haplotype on MAPT expression in human brain (2009) (26)
Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection (2018) (25)
Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection (2018) (25)
Complement genes contribute sex-biased vulnerability in diverse disorders (2020) (25)
Schizophrenia, autism spectrum disorders and developmental disorders share specific disruptive coding mutations (2020) (25)
The high affinity neurotensin receptor gene (NTSR1): comparative sequencing and association studies in schizophrenia (2000) (25)
No evidence that common allelic variation in the Amyloid Precursor Protein (APP) gene confers susceptibility to Alzheimer's disease. (1995) (25)
Variation in the urokinase‐plasminogen activator gene does not explain the chromosome 10 linkage signal for late onset AD (2004) (25)
Schizophrenia two‐hit hypothesis in velo‐cardio facial syndrome (2013) (25)
Alpha-T-catenin is expressed in human brain and interacts with the Wnt signaling pathway but is not responsible for linkage to chromosome 10 in Alzheimer's disease. (2004) (25)
Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection (2018) (25)
Genome wide significant linkage in schizophrenia conditioning on occurrence of depressive episodes (2005) (24)
Dopamine receptors and schizophrenia: contribution of molecular genetics and clinical neuropsychology. (1999) (24)
Permutation-based approaches do not adequately allow for linkage disequilibrium in gene-wide multi-locus association analysis (2012) (24)
Linkage studies of bipolar disorder with chromosome 18 markers. (1999) (24)
Structural and Functional Neuroimaging of Polygenic Risk for Schizophrenia: A Recall-by-Genotype–Based Approach (2018) (24)
A functional polymorphism in the promoter of monoamine oxidase A gene and bipolar affective disorder. (1999) (24)
Modern molecular genetic approaches to complex traits: implications for psychiatric disorders. (1996) (24)
Association between schizophrenia and a microsatellite polymorphism at the dopamine D5 receptor gene (1997) (24)
Exome sequencing in bipolar disorder identifies AKAP11 as a risk gene shared with schizophrenia (2022) (24)
A Transcriptome Wide Association Study implicates specific pre- and post-synaptic abnormalities in Schizophrenia (2018) (24)
Meta-analysis of the Association Between Variants in SORL 1 and Alzheimer Disease (2011) (23)
Schizophrenia and a high-resolution map of the three-dimensional chromatin interactome of adult and fetal cortex (2018) (23)
Linkage studies in bipolar affective disorder with markers on chromosome 21. (1996) (23)
Haplotype Analysis and a Novel Allele-Sharing Method Refines a Chromosome 4p Locus Linked to Bipolar Affective Disorder (2007) (23)
Association of copy number variation across the genome with neuropsychiatric traits in the general population (2018) (23)
Schizophrenia risk variants modulate white matter volume across the psychosis spectrum: Evidence from two independent cohorts (2015) (23)
Interaction Testing and Polygenic Risk Scoring to Estimate the Association of Common Genetic Variants With Treatment Resistance in Schizophrenia (2022) (23)
Variation at the DAOA / G 30 Locus Influences Susceptibility to Major Mood Episodes but Not Psychosis in Schizophrenia and Bipolar Disorder (2006) (23)
Defining the Effect of the 16 p 11 . 2 Duplication on Cognition , Behavior , andMedical Comorbidities (2015) (23)
Complement Factor H Y402H Polymorphism is not Associated with Late-onset Alzheimer’s Disease (2007) (23)
Mutation screening and LD mapping in the VCFS deleted region of chromosome 22q11 in schizophrenia using a novel DNA pooling approach (2002) (23)
Cis-effects on gene expression in the human prenatal brain associated with genetic risk for neuropsychiatric disorders (2020) (22)
Molecular genetic studies of schizophrenia (2000) (22)
Genome scans and microarrays: converging on genes for schizophrenia? (2002) (22)
Chromosome 22 deletion syndrome and schizophrenia. (2006) (22)
Genome-wide association study identifies 30 loci associated with bipolar disorder (2019) (22)
Low-frequency variation in TP53 has large effects on head circumference and intracranial volume (2018) (22)
Investigating the genetic variation underlying episodicity in major depressive disorder: suggestive evidence for a bipolar contribution. (2014) (22)
The interaction between child maltreatment, adult stressful life events and the 5-HTTLPR in major depression. (2013) (22)
Predictive modeling of schizophrenia from genomic data: Comparison of polygenic risk score with kernel support vector machines approach (2018) (21)
A neuropsychological investigation of the genome wide associated schizophrenia risk variant NRGN rs12807809 (2011) (21)
Genome-wide association study of dietary intake in the UK biobank study and its associations with schizophrenia and other traits (2020) (21)
The internet is parents' main source of information about psychiatric manifestations of 22q11.2 deletion syndrome (22q11.2DS)☆ (2013) (21)
Exclusion of CAG/CTG trinucleotide repeat loci which map to chromosome 4 in bipolar disorder and schizophrenia. (1997) (21)
Polygenic risk for schizophrenia and season of birth within the UK Biobank cohort (2018) (21)
Cis- and trans- loci influence expression of the schizophrenia susceptibility gene DTNBP1. (2008) (21)
No evidence for allelic association between schizophrenia and a functional variant of the human dopamine beta-hydroxylase gene (DBH). (1999) (21)
Autosome search for schizophrenia susceptibility genes in multiply affected families (1999) (21)
Associations Between Schizophrenia Polygenic Liability, Symptom Dimensions, and Cognitive Ability in Schizophrenia (2021) (20)
Classical Human Leukocyte Antigen Alleles and C4 Haplotypes Are Not Significantly Associated With Depression (2020) (20)
No association between a polymorphic CAG repeat in the human potassium channel gene hKCa3 and bipolar disorder. (1999) (20)
No evidence for association between a non-synonymous polymorphism in the gene encoding human metabotropic glutamate receptor 7 and schizophrenia. (2000) (20)
1q21.1 distal copy number variants are associated with cerebral and cognitive alterations in humans (2021) (20)
Genetic Variation in the Psychiatric Risk Gene CACNA1C Modulates Reversal Learning Across Species (2018) (20)
Variance of IQ is partially dependent on deletion type among 1,427 22q11.2 deletion syndrome subjects (2018) (20)
IGF1, growth pathway polymorphisms and schizophrenia: A pooling study (2007) (19)
EXOME SEQUENCING IN BIPOLAR DISORDER REVEALS SHARED RISK GENE AKAP11 WITH SCHIZOPHRENIA (2021) (19)
Genome-wide Burden of Rare Short Deletions Is Enriched in Major Depressive Disorder in Four Cohorts (2019) (19)
Alpha-2 macroglobulin gene and Alzheimer disease. (1999) (19)
Convergent Evidence That ZNF804A Is a Regulator of Pre-messenger RNA Processing and Gene Expression (2018) (18)
Increasing the Clinical Psychiatric Knowledge Base About Pathogenic Copy Number Variation. (2020) (18)
Fine‐mapping reveals novel alternative splicing of the dopamine transporter (2010) (18)
Sleep problems and associations with psychopathology and cognition in young people with 22q11.2 deletion syndrome (22q11.2DS) (2019) (18)
COMT Val158met genotype and striatal D2/3 receptor binding in adults with 22q11 deletion syndrome (2011) (18)
Association of Whole-Genome and NETRIN1 Signaling Pathway–Derived Polygenic Risk Scores for Major Depressive Disorder and White Matter Microstructure in the UK Biobank (2019) (18)
No evidence that extended tracts of homozygosity are associated with Alzheimer's disease (2011) (18)
CTG18.1 and ERDA-1 CAG/CTG Repeat Size in Bipolar Disorder (1999) (17)
Area deprivation, urbanicity, severe mental illness and social drift — A population-based linkage study using routinely collected primary and secondary care data (2020) (17)
Genetic association of FMRP targets with psychiatric disorders (2020) (17)
Genetic risk for schizophrenia and developmental delay is associated with shape and microstructure of midline white-matter structures (2019) (17)
Investigation of rare non-synonymous variants at ABCA13 in schizophrenia and bipolar disorder (2011) (17)
A national population-based e-cohort of people with psychosis (PsyCymru) linking prospectively ascertained phenotypically rich and genetic data to routinely collected records: Overview, recruitment and linkage (2015) (17)
Mutation intolerant genes and targets of FMRP are enriched for nonsynonymous alleles in schizophrenia (2017) (17)
Cognitive deficits in childhood, adolescence and adulthood in 22q11.2 deletion syndrome and association with psychopathology (2020) (17)
Genome-wide association study of co-occurring anxiety in major depression (2013) (17)
Genetic liability to schizophrenia is negatively associated with educational attainment in UK Biobank (2019) (17)
Variation at the GABAA receptor gene, Rho 1 (GABRR1) associated with susceptibility to bipolar schizoaffective disorder (2010) (17)
Linkage study of chromosome 6p in sib-pairs with schizophrenia. (1997) (16)
The health informatics cohort enhancement project (HICE): using routinely collected primary care data to identify people with a lifetime diagnosis of psychotic disorder (2012) (16)
Chromosome 22gl1 deletions—An under-recognized cause of idiopathic learning disability? (1998) (16)
Association between TCF4 and schizophrenia does not exert its effect by common nonsynonymous variation or by influencing cis‐acting regulation of mRNA expression in adult human brain (2011) (16)
Phenotype evaluation and genomewide linkage study of clinical variables in schizophrenia (2011) (16)
Eleven trinucleotide repeat loci that map to chromosome 12 excluded from involvement in the pathogenesis of bipolar disorder. (1999) (16)
Schizophrenia: complex genetics, not fairy tales (2008) (16)
Erratum: Genome-wide common and rare variant analysis provides novel insights into clozapine-associated neutropenia (2016) (16)
The behavioural phenotype in velo-cardio-facial syndrome (1998) (16)
Investigating rare pathogenic/likely pathogenic exonic variation in bipolar disorder (2021) (16)
Exclusion of expansion of 50 CAG/CTG trinucleotide repeats in bipolar disorder. (1997) (15)
CUX2, a potential regulator of NCAM expression: genomic characterization and analysis as a positional candidate susceptibility gene for bipolar disorder. (2001) (15)
Polygenic risk for circulating reproductive hormone levels and their influence on hippocampal volume and depression susceptibility (2019) (15)
Mosaic copy number variation in schizophrenia (2013) (15)
Association analysis of the glial cell line-derived neurotrophic factor (GDNF) gene in schizophrenia (2007) (15)
Evidence of association between DRD4 and ADHD with conduct disturbance. (2000) (15)
Debrisoquine 4-hydroxylase (CYP2D) locus and possible susceptibility to schizophrenia (1992) (15)
No evidence for linkage between the X-chromosome marker DXS7 and schizophrenia. (1995) (15)
The emergence of psychotic experiences in the early adolescence of 22q11.2 Deletion Syndrome (2019) (15)
Convergent patterns of association between phenylalanine hydroxylase variants and schizophrenia in four independent samples (2009) (14)
Molecular genetic studies of cognitive ability. (1998) (14)
Rare Copy Number Variants Are Associated With Poorer Cognition in Schizophrenia (2020) (14)
A brief report: de novo copy number variants in children with attention deficit hyperactivity disorder (2019) (14)
Molecular genetic studies of schizophrenia. (1996) (14)
Bioethics and genetic research in psychiatry. (2000) (14)
Neurotrophin receptor activation rescues cognitive and synaptic abnormalities caused by hemizygosity of the psychiatric risk gene Cacna1c (2021) (14)
Linkage analysis of the fragile X gene FMR‐1 and schizophrenia: no evidence for linkage but report of a family with schizophrenia and an unstable triplet repeat (1996) (14)
Explaining the missing heritability of psychiatric disorders (2021) (13)
Variation in the protocadherin gamma A gene cluster. (2003) (13)
Data and clinical utility should be the drivers of changes to psychiatric classification (2010) (13)
CNV analysis in a large schizophrenia sample implicates deletions at 16 p 12 . 1 and SLC 1 A 1 and duplications at 1 p 36 . 33 and CGNL 1 (2014) (13)
No evidence for an allelic association between schizophrenia and markers D22S278 and D22S283. (1997) (13)
Analysis of copy number variation using quantitative interspecies competitive PCR (2008) (13)
Association analysis of the HOPA12bp polymorphism in schizophrenia and manic depressive illness (2003) (13)
Failure to confirm association between PIK4CA and psychosis in 22q11.2 deletion syndrome (2010) (13)
Characterization of Single Gene Copy Number Variants in Schizophrenia (2019) (13)
What can we learn from the high rates of schizophrenia in people with 22q11.2 deletion syndrome? (2016) (13)
Introducing Selfcite 2.0—career enhancing software (1996) (13)
Candidate gene association studies in psychiatric genetics: a SERTain future? (1996) (13)
Corrigendum: Genome-wide common and rare variant analysis provides novel insights into clozapine-associated neutropenia (Molecular Psychiatry (2017) 22 (1502-1508) DOI: 10.1038/mp.2016.97) (2018) (13)
Analysis of neurogranin (NRGN) in schizophrenia (2011) (13)
Molecular genetics and the relationship between epilepsy and psychosis (2010) (13)
Linkage analysis between bipolar affective disorder and markers on chromosome X (1998) (13)
Erratum: Genome-wide common and rare variant analysis provides novel insights into clozapine-associated neutropenia (2017) (13)
Memory for new information as a cognitive marker of liability to Alzheimer's disease in a high risk group: a research note (2003) (12)
Is there a schizophrenia to diagnose? (2011) (12)
Birth order and the severity of illness in schizophrenia (2007) (12)
Attention deficit hyperactivity disorder symptoms as antecedents of later psychotic outcomes in 22q11.2 deletion syndrome (2019) (12)
Polymorphic DNA markers and mental disease (1988) (12)
Variation in the protocadherin γ A gene cluster (2003) (12)
The Research Domain Criteria: moving the goalposts to change the game (2014) (12)
Pharmacogenomics: A road ahead for precision medicine in psychiatry (2021) (12)
Molecular genetic studies of manic-depression and schizophrenia (1990) (12)
A review of psychiatric co-morbidity described in genetic and immune mediated movement disorders (2017) (12)
DISC1 mRNA expression is not influenced by common Cis‐acting regulatory polymorphisms or imprinting (2008) (12)
Advances and retreats in the molecular genetics of major mental illness. (1992) (11)
Major psychiatric disorders and the serotonin transporter gene (SLC6A4): family-based association studies (2002) (11)
Striatal dopaminergic alterations in individuals with copy number variants at the 22q11.2 genetic locus and their implications for psychosis risk: a [18F]-DOPA PET study (2021) (11)
Mutation screening of the DTNBP1 exonic sequence in 669 schizophrenics and 710 controls using high‐resolution melting analysis (2009) (11)
Genetics of mental retardation. (2005) (11)
Mutational analysis of two positional candidate susceptibility genes for bipolar disorder on chromosome 12q23‐q24: phenylalanine hydroxylase and human LIM‐homeobox LHX5 (2003) (11)
Gender differences in CNV burden do not confound schizophrenia CNV associations (2016) (11)
Clozapine Metabolism is Associated With Absolute Neutrophil Count in Individuals With Treatment-Resistant Schizophrenia (2021) (11)
Role of amyloid beta-protein in Alzheimer's disease. (1992) (11)
Gene expression imputation across multiple brain regions reveals schizophrenia risk throughout development (2017) (11)
Effects of eight neuropsychiatric copy number variants on human brain structure (2021) (11)
Associations between schizophrenia genetic risk, anxiety disorders and manic/hypomanic episode in a longitudinal population cohort study (2018) (11)
Publisher Correction: Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection (2019) (10)
Influence of NOS 1 on Verbal Intelligence and Working Memory in Both Patients With Schizophrenia and Healthy Control Subjects (2009) (10)
The future of psychiatric genetics (2003) (10)
A case‐control study of family history and cerebral cortical abnormalities in schizophrenia (1993) (10)
Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease (vol 41, pg 1088, 2009) (2013) (10)
An Examination of Single Nucleotide Polymorphism Selection Prioritization Strategies for Tests of Gene–Gene Interaction (2011) (10)
Lack of Support for the Genes by Early Environment Interaction Hypothesis in the Pathogenesis of Schizophrenia (2021) (10)
Does APOE explain the linkage of Alzheimer's disease to chromosome 19q13? (2008) (10)
Modelling the occurrence and pathology of Alzheimer's disease (1989) (10)
Promoting measured genes and measured environments: on the importance of careful statistical analyses and biological relevance - reply (2007) (9)
Genome-wide Association Study of Clinical Features in the Schizophrenia Psychiatric Genomics Consortium: Confirmation of Polygenic Effect on Negative Symptoms (2017) (9)
Mononucleotide repeat polymorphism in the APP gene. (1991) (9)
Movement Disorder Phenotypes in Children With 22q11.2 Deletion Syndrome (2020) (9)
It Is Time to Take a Stand for Medical Research and Against Terrorism Targeting Medical Scientists (2008) (9)
Molecular Genetics and the Kraepelinian Dichotomy: One Disorder, Two Disorders, or Do We Need to Start Thinking Afresh? (2010) (9)
Genetic risk for schizophrenia and developmental delay is associated with shape and microstructure of midline white matter structures (2018) (9)
Repeat sizes at CAG/CTG loci CTG18.1, ERDA1 and TGC13-7a in schizophrenia. (2000) (9)
A data‐driven investigation of relationships between bipolar psychotic symptoms and schizophrenia genome‐wide significant genetic loci (2018) (9)
Obstetric complications and cerebral abnormalities in schizophrenia (1987) (9)
Premature Mortality among People with Severe Mental Illness – New Evidence from Linked Primary Care Data (2018) (9)
A neurodevelopmental perspective on some epiphenomena of schizophrenia (1990) (9)
Prioritizing Genetic Contributors to Cortical Alterations in 22q11.2 Deletion Syndrome Using Imaging Transcriptomics (2021) (9)
Effects of MiR‐137 genetic risk score on brain volume and cortical measures in patients with schizophrenia and controls (2018) (9)
Symptom dimensions and the Kraepelinian dichotomy (2007) (9)
Association of genetic liability for psychiatric disorders with accelerometer-assessed physical activity in the UK Biobank (2021) (9)
No evidence for association between polymorphisms in GRM 3 and schizophrenia (2005) (8)
Schizophrenia and the androgen receptor gene: report of a sibship showing co-segregation with Reifenstein syndrome but no evidence for linkage in 23 multiply affected families. (1995) (8)
The relationship between season of birth and biological variables in schizophrenia (1989) (8)
A molecular genetic study of hyperkinetic disorder/attention deficit hyperactivity disorder (1998) (8)
Clinical evaluation of patients with a neuropsychiatric risk copy number variant (2021) (8)
A shared polygenic contribution between childhood ADHD and adult schizophrenia (2013) (8)
Conditional GWAS analysis identifies putative disorder-specific SNPs for psychiatric disorders (2019) (8)
Misconceptions about gene–environment interactions in psychiatry (2010) (8)
A normative chart for cognitive development in a genetically selected population (2021) (8)
Schizophrenia Genetics: Building the Foundations of the Future (2014) (8)
The Duffy-null genotype and risk of infection (2020) (8)
Psychiatric classification – a developmental perspective (2015) (7)
Characterisation of age and polarity at onset in bipolar disorder (2021) (7)
The Relationship Between Common Variant Schizophrenia Liability and Number of Offspring in the UK Biobank. (2019) (7)
Haploinsufficiency of the schizophrenia and autism risk gene Cyfip1 causes abnormal postnatal hippocampal neurogenesis through microglial and Arp2/3 mediated actin dependent mechanisms (2021) (7)
Correction: Psychiatric disorders in children with 16p11.2 deletion and duplication (2019) (7)
Genome-wide analysis of copy number variants in attention deficit hyperactivity disorder (2012) (7)
Strong genetic evidence for a selective influence of GABAA receptors on a component of the bipolar disorder phenotype [Corrigendum] (2010) (7)
Identifying schizophrenia patients who carry pathogenic genetic copy number variants using standard clinical assessment: retrospective cohort study (2020) (7)
Molecular and population genetics of schizophrenia (2002) (7)
Rare schizophrenia risk variants are enriched in genes shared with neurodevelopmental disorders (2016) (7)
Assocation between schizophrenia and T102C polymorphism of the 5-hydroxytryptamine type 2A receptor gene (1996) (7)
Developmental Profile of Psychiatric Risk Associated With Voltage-Gated Cation Channel Activity (2020) (7)
Complement C3 and C3aR mediate different aspects of emotional behaviours; relevance to risk for psychiatric disorder (2019) (7)
The molecular genetics of schizophrenia. (2007) (7)
Genome-wide association study of suicide attempt in psychiatric disorders identifies association with major depression polygenic risk scores (2018) (6)
The psychiatric phenotypes of 1q21 distal deletion and duplication (2021) (6)
Polymorphisms in the phosphate and tensin homolog gene are not associated with late-onset Alzheimer's disease (2006) (6)
Genetic variation in the seven‐pass transmembrane cadherin CELSR1: lack of association with schizophrenia (2003) (6)
The role of rare copy number variants in depression (2018) (6)
Familial schizophrenia shows no gender difference in age of onset (1993) (6)
An examination of MUTED as a schizophrenia susceptibility gene (2009) (6)
Mental health resilience in at-risk adolescents (2017) (6)
No significant association between a PS-1 intronic polymorphism and dementia in Down's syndrome (1998) (6)
Genes and behavior: nature-nurture interplay explained (2006) (6)
No evidence for linkage between schizophrenia and eight microsatellite markers on chromosome 19. (1996) (6)
Electrophysiological network alterations in adults with copy number variants associated with high neurodevelopmental risk (2019) (6)
Genome-wide analyses of smoking behaviors in schizophrenia: Findings from the Psychiatric Genomics Consortium. (2021) (6)
Molecular Genetics and its Application to the Study of Psychiatric Disorders (1989) (6)
Risk Factors in Schizophrenia (1988) (6)
Neuropsychiatric risk in children with intellectual disability of genetic origin: IMAGINE, a UK national cohort study (2022) (5)
Phenotypic variation between parent-offspring trios and non-trios in genetic studies of schizophrenia. (2006) (5)
Genetic Associations in Schizophrenia (2011) (5)
Structural variations in attention-deficit hyperactivity disorder – Authors' reply (2011) (5)
Examining pathways between genetic liability for schizophrenia and patterns of tobacco and cannabis use in adolescence (2020) (5)
Absence of de novo point mutations in exons of GRIN2B in a large schizophrenia trio sample (2012) (5)
Post-partum psychosis and its association with bipolar disorder in the UK: a case-control study using polygenic risk scores. (2021) (5)
Neuropsychiatric risk in children with intellectual disability of genetic origin: IMAGINE, a UK national cohort study (2022) (5)
7 A GENETIC FIRST APPROACH TO DISSECTING THE HETEROGENEITY OF AUTISM: PHENOTYPIC COMPARISON OF AUTISM RISK COPY NUMBER VARIANTS (2019) (5)
Further evidence of familial cosegregation of major affective disorder and Darier's disease (1999) (5)
Specific parental depression symptoms as risk markers for new-onset depression in high-risk offspring. (2013) (5)
Coordination difficulties, IQ and psychopathology in children with high-risk copy number variants (2019) (5)
Cognitive deficits associated with schizophrenia in adults with velocardio-facial syndrome (2003) (5)
Linkage analysis in an autosomal dominant ‘zonular nuclear pulverulent’ congenital cataract, mapped to chromosome 13q11-13 (2000) (5)
The Relationship Between Common Variant Schizophrenia Liability and Number of Offspring in the UK Biobank: Response to Lawn et al. (2019) (5)
A replicated molecular genetic basis for subtyping antisocial behavior in ADHD (2007) (5)
A full genome scan for late onset Alzheimers disease (2000) (5)
Intellectual Disability and Psychiatric Comorbidity: Challenges and Clinical Issues (2015) (5)
Structure of the Psychotic Disorders Classification in DSM-5. (2016) (5)
Meta-analysis of Scandinavian Schizophrenia Exomes (2019) (5)
pathogenesis of schizophrenia (2009) (4)
Genetic Heterogeneity Shapes Brain Connectivity in Psychiatry (2022) (4)
Genetic association study of psychotic experiences in UK Biobank (2019) (4)
The Wellcome Trust UK-Irish Bipolar Sib-pair Study: Chromosome 21 (1998) (4)
Genetics and the brain: many pathways to enlightenment (2009) (4)
Using induced pluripotent stem cells to investigate human neuronal phenotypes in 1q21.1 deletion and duplication syndrome (2021) (4)
Population‐based identity‐by‐descent mapping combined with exome sequencing to detect rare risk variants for schizophrenia (2019) (4)
Large-Scale Genomics: A Paradigm Shift in Psychiatry? (2021) (4)
A Mendelian randomization study of the causal association between anxiety phenotypes and schizophrenia. (2020) (4)
No Evidence for Enrichment in Schizophrenia for Common Allelic Associations at Imprinted Loci (2015) (4)
Publisher Correction: Gene expression imputation across multiple brain regions provides insights into schizophrenia risk (2019) (4)
Neurodevelopment and the Chronological Curiosities of Schizophrenia (1991) (4)
Chromosome 11 workshop. (1998) (4)
No evidence of association between HLA-DRB1 and attention deficit hyperactivity disorder (2003) (4)
Effects of pathogenic CNVs on biochemical markers: a study on the UK Biobank (2019) (4)
Using kinematic analyses to explore sensorimotor control impairments in children with 22q11.2 deletion syndrome (2019) (4)
Global Brain Flexibility During Working Memory is reduced in a High Genetic Risk Group for Schizophrenia. (2021) (4)
Transcriptional programs regulating neuronal differentiation are disrupted in DLG2 knockout human embryonic stem cells and enriched for schizophrenia and related disorders risk variants (2022) (4)
Genomic Stratification of Clozapine Prescription Patterns Using Schizophrenia Polygenic Scores (2022) (4)
Automated genotyping of single-nucleotide polymorphisms by extension of fluorescently labelled primers: analysis of individual and pooled DNA samples (2000) (4)
Psychosis and the level of mood incongruence in Bipolar Disorder are related to genetic liability for Schizophrenia (2017) (4)
Genome-wide association study of age at onset of Alzheimer's disease (2009) (4)
Alternative diffusion anisotropy measures for the investigation of white matter alterations in 22q11.2 deletion syndrome (2018) (4)
Role of amyloid β-protein in Alzheimer's disease (1992) (3)
Susceptibility to schizophrenia and the dopamine d3 receptor gene (1993) (3)
General discussion II (2008) (3)
Chromosome 22q11 deletions and severe learning disability (2001) (3)
Exclusion of close linkage between GABA a receptor subunit 1a gene and schizophrenia using a microsatellite repeat marker (1991) (3)
A quantitative trait loci study of attention deficit hyperactivity disorder (1999) (3)
The effect of age and the H1c MAPT haplotype on MAPT expression (2009) (3)
Genetic risk for schizophrenia is associated with altered visually-induced gamma band activity: evidence from a population sample stratified polygenic risk (2021) (3)
A phenome-wide association and Mendelian Randomisation study of polygenic risk for depression in UK Biobank (2020) (3)
Cognitive profile of children with velo-cardio-facial syndrome (VCFS) (2002) (3)
Autism: A model of neurodevelopmental diversity informed by genomics (2022) (3)
Analyses of rare and common alleles in parent-proband trios implicate rare missense variants in SLC6A1 in schizophrenia and confirm the involvement of loss of function intolerant and neurodevelopmental disorder genes (2019) (3)
Direct analysis of the genes encoding G proteins GαT2, Gαo, GαZ in ADHD (2004) (3)
Genetic Liabilities Differentiating Bipolar Disorder, Schizophrenia, and Major Depressive Disorder, and Phenotypic Heterogeneity in Bipolar Disorder (2022) (3)
Causal analyses, statistical efficiency and phenotypic precision through Recall-by-Genotype study design (2017) (3)
Molecular genetic research on IQ: can it be done? Should it be done? (1996) (3)
Manipulating immune pathways differentially impact emotionality: dissociable effects of complement C3 and C3aR on learned fear and innate anxiety (2019) (3)
Assessment of emotions and behaviour by the Developmental Behaviour Checklist in young people with neurodevelopmental CNVs (2020) (3)
Genotype-phenotype relationships in children with copy number variants associated with high neuropsychiatric risk: Findings from the Intellectual Disability & Mental Health: Assessing the Genomic Impact on Neurodevelopment (IMAGINE-ID) study (2019) (3)
IMAGING GENETICS IN PSYCHIATRY: DISEASE PATH OR GARDEN PATH? (2010) (3)
No evidence of association from transmission disequilibrium analysis of the hKCa3 gene in bipolar disorder. (2000) (3)
No association between polymorphisms of catechol-o-methyltransferase (COMT) or monoamine oxidase (MAO) genes and schizophrenia in adults with velo-cardio-facial syndrome (2000) (3)
Major depression ’ in Ethiopia : validity is the problem (2007) (3)
No association between RFLPs at the porphobilinogen deaminase gene and schizophrenia (1992) (3)
Cis-and trans-loci influence expression of the schizophrenia susceptibility gene DTNBP 1 (2008) (3)
Haploinsufficiency of the schizophrenia risk gene Cyfip1 causes abnormal postnatal hippocampal neurogenesis through a novel microglia dependent mechanism (2018) (3)
The Uk Biobank: A Resource For Cnv Analysis (2017) (3)
Developmental coordination disorder , psychopathology and IQ in 22 q 11 . 2 deletion syndrome (2017) (3)
The Epidemiology of Schizophrenia: Molecular genetics and epidemiology in schizophrenia: a necessary partnership (2002) (3)
Cyfip1 haploinsufficiency is associated with white matter changes, myelin thinning, reduction of mature oligodendrocytes and behavioural inflexibility: (2018) (3)
The molecular genetics of Alzheimer's disease. (1989) (3)
Family-based association studies of candidate genes in bipolar disorder (1998) (3)
Psychopathology in adults with copy number variants. (2022) (3)
Brain anatomy in psychotic and non-psychotic adults with chromosome 22q11 deletion (2002) (3)
Author Correction: The mutational constraint spectrum quantified from variation in 141,456 humans (2021) (3)
Neuropsychiatric copy number variants exert shared effects on human brain structure (2020) (3)
Pharmacokinetics and pharmacogenomics of clozapine in an ancestrally diverse sample: a longitudinal analysis and genome-wide association study using UK clinical monitoring data. (2023) (2)
Brain functional connectivity mirrors genetic pleiotropy in psychiatric conditions. (2022) (2)
Molecular genetic studies in familial Rett syndrome (1997) (2)
Gene expression imputation across multiple brain regions provides insights into schizophrenia risk (2019) (2)
Risk Factors, Clinical Features, and Polygenic Risk Scores in Schizophrenia and Schizoaffective Disorder Depressive-Type (2021) (2)
Genome-wide Significant Associations for Cannabis Dependence Severity: Relevance to Psychiatric Disorders. (2016) (2)
S178. SHOULD SCHIZOAFFECTIVE DISORDER DEPRESSED-TYPE BE DISTINCT FROM SCHIZOPHRENIA? ANALYSIS OF GENETIC LIABILITY AND LIFETIME CLINICAL CHARACTERISTICS (2020) (2)
Correction: Genetic Evidence Implicates the Immune System and Cholesterol Metabolism in the Aetiology of Alzheimer's Disease (2011) (2)
Association analysis of the proneurotensin gene and bipolar disorder. (2000) (2)
Atlas of functional connectivity relationships across rare and common genetic variants, traits, and psychiatric conditions (2021) (2)
Psychiatric profile of children with velo-cardio-faclial syndrome (VCFS) (2005) (2)
Brain abnormalities associated with deletions at 22q11: Implications for psychosis (2000) (2)
ADHD children with and without the dopamine D4 receptor 7-repeat allele: Evidence of differences in performance on neuropsychological tests (2003) (2)
Association between functional psychosis and expanded CAG/CTG repeats is not explained by health stratification (1998) (2)
Correction: Striatal dopaminergic alterations in individuals with copy number variants at the 22q11.2 genetic locus and their implications for psychosis risk: a [18F]-DOPA PET study (2021) (2)
Autism-associated SNPs in the clock genes npas2 , per1 and the homeobox gene en2 alter DNA sequences that show characteristics of microRNA genes. (2008) (2)
Schizophrenia scepticism (1992) (2)
Association between schizophrenia and both loss of function and missense mutations in paralog conserved sites of voltage-gated sodium channels (2018) (2)
Genetics: The implications for forensic psychiatry (2004) (2)
Rare Variant Analysis of Human and Rodent Obesity Genes in Individuals with Severe Childhood Obesity (2017) (2)
32-1 Molecular genetic studies of schizophrenia (1997) (2)
Expression quantitative trait loci in the developing human brain and their enrichment in neuropsychiatric disorders (2018) (2)
Ultrarare Coding Variants and Cognitive Function in Schizophrenia (2022) (2)
Gene expression imputation across multiple brain regions provides insights into schizophrenia risk (2019) (2)
A transient hyperekplexia phenotype associated with compound heterozygote mutations in the human beta-subunit of the inhibitory glycine receptor (GLRB). (2000) (2)
Processing facial emotions in adults with velo-cardio-facial syndrome: an fMRI study. (2006) (2)
Machine learning for prediction of schizophrenia using genetic and demographic factors in the UK biobank (2022) (2)
The Genetic Aetiology of Alzheimer's Disease (1989) (2)
A family based candidate gene association study of Attention Deficit Hyperactivity Disorder (2000) (2)
Alzheimer's disease (1994) (2)
Convergent functional genomics, association and linkage analysis suggests 2 ',3 '-cyclic nucleotide 3 '-phosphodiesterase (CNP) as a potential susceptibility gene for schizophrenia [Conference Abstract] (2004) (2)
Pathogenic mis-splicing of CPEB4 in schizophrenia (2022) (2)
Rare CNVs and phenome-wide profiling highlight brain structural divergence and phenotypical convergence. (2023) (2)
Genotype-phenotype relationships in children with Copy Number Variants associated with high neuropsychiatric risk: Findings from the case-control IMAGINE-ID cohort in the United Kingdom (2019) (2)
Linkage studies of schizophrenia with markers of chromosome-11q (1991) (2)
Sleep EEG in young people with 22q11.2 deletion syndrome: A cross-sectional study of slow-waves, spindles and correlations with memory and neurodevelopmental symptoms (2022) (2)
Association of ABCA 1 with late-onset Alzheimer ' s disease is not observed in a case-control study (2016) (2)
Molecular genetics and the relationship between epilepsy and psychosis. Authors' reply (2010) (1)
Exploring the indirect effects of catechol‐O‐methyltransferase (COMT) genotype on psychotic experiences through cognitive function and anxiety disorders in a large birth cohort of children (2014) (1)
Genome-wide association for major depression through age at onset stratificationGenomic analysis of age at onset in depression (2016) (1)
The continuum of psychosis and the gene. (1987) (1)
The contribution of Neanderthal introgression and natural selection to neurodegenerative diseases (2023) (1)
Sleep disturbance as a transdiagnostic marker of psychiatric risk in children with neurodevelopmental risk genetic conditions (2023) (1)
APP promotor variability as a risk factor for AD (2002) (1)
Sleep disturbance as a transdiagnostic marker of psychiatric risk in children with neurodevelopmental risk genetic conditions (2023) (1)
The rate of de novo CNVs in healthy controls (2019) (1)
Association between a functional promoter MAOA variant and schizophrenia (2002) (1)
A Developmental Perspective on the Convergence of Genetic Risk Factors for Neuropsychiatric Disorders (2020) (1)
A two-stage sib-pair genome scan for schizophrenia susceptibility genes (1998) (1)
Genome search for schizophrenia susceptibility genes using a two-stage sib-pair approach (1996) (1)
Rare CNVs and phenome-wide profiling: a tale of brain-structural divergence and phenotypical convergence (2022) (1)
Emotional and behavioural phenotypes in young people with neurodevelopmental CNVs (2020) (1)
Hair Cortisol in Twins: Heritability and Genetic Overlap with Psychological Variables and Stress-System Genes (2017) (1)
The effect of deletion 22q11 on brain anatomy: A structural imaging study of children and adolescents with velo-cardio-facial syndrome (VCFS) (2004) (1)
LOOKING FOR GENES IN SCHIZOPHRENIA (1992) (1)
T128. THE ASSOCIATION BETWEEN GENETIC RISK FOR SCHIZOPHRENIA AND PATTERNS OF CIGARETTE AND CANNABIS USE IN ADOLESCENCE (2018) (1)
DLG2 knockout reveals neurogenic transcriptional programs underlying neuropsychiatric disorders and cognition (2020) (1)
The prevalence of chromosome 22q11 deletions in an adult congenital heart disease population (1999) (1)
Meta-analysis of the association between SORL1 variants and Alzheimer's disease (2010) (1)
Investigating familiality of subtypes in schizophrenia (2000) (1)
Factor derived sub-syndromes of schizophrenia and familial morbid risks (1996) (1)
Linkage analysis of schizophrenia on chromosome 22 (1992) (1)
The General Impact of Haploinsufficiency on Brain Connectivity Underlies the Pleiotropic Effect of Neuropsychiatric CNVS (2020) (1)
Identification of a polymorphism in the human NURR1 gene and investigation of an association with schizophrenia (2000) (1)
Author Correction: Landscape of multi-nucleotide variants in 125,748 human exomes and 15,708 genomes (2021) (1)
Reply to Bertram et al. (2006) (1)
F29INVESTIGATING SUPERVISED MACHINE LEARNING METHODS FOR PREDICTION OF SCHIZOPHRENIA IN UK BIOBANK (2019) (1)
Correction: Genome-wide gene-environment analyses of major depressive disorder and reported lifetime traumatic experiences in UK Biobank (2020) (1)
High rates of schizophrenia in velo-cardio-facial syndrome (1999) (1)
No association of polymorphisms in the chat locus with late-onset Alzheimer's disease (2002) (1)
9. DOES BIOLOGY READ THE DSM? TRANSDIAGNOSTIC FINDINGS IN PSYCHOSIS AND IMPLICATIONS FOR TREATMENT (2018) (1)
Paternal age and risk for schizophrenia Paternal age and risk for schizophrenia (2003) (1)
Mental health impact of autism on families of children with intellectual and developmental disabilities of genetic origin (2023) (1)
1 – The cell, molecular biology and the new genetics (1991) (1)
and diagnosis Pre-morbid adjustment and personality in psychosis. Effects of sex (2011) (1)
The nature and nurture of depression: towards a new synthesis? (1996) (1)
DNA-and classical genetic markers in schizophrenia (2005) (1)
Psychiatric profile of children with velo-cardio-facial syndrome-preliminary findings (2002) (1)
Associations between polygenic liability for schizophrenia and level of psychosis and mood-incongruence in bipolar disorder (2017) (1)
Characterization of Age and Polarity at Onset in Bipolar Disorder (2021) (1)
Synaptic protein DLG2 controls neurogenic transcriptional programs disrupted in schizophrenia and related disorders (2020) (1)
Chromosome 22qll deletions and aggressive behaviour (1998) (1)
P1-331 Familiality and linkage analysis of behavioral symptoms and age at disease onset in late-onset Alzheimer’s disease (2006) (1)
Low-frequency variation in TP53 has large effects on head circumference and intracranial volume (2019) (1)
Neurogenetics of Schizophrenia (2002) (1)
Synaptic protein DLG2 controls neurogenic transcriptional programs disrupted in schizophrenia and related disorders (2020) (1)
SCHIZOPHRENIA TCF 4 , Schizophrenia , and Pitt-Hopkins Syndrome (2010) (1)
Impact of schizophrenia genetic liability on the association between schizophrenia and physical illness: data-linkage study (2020) (1)
DRAGON-Data: a platform and protocol for integrating genomic and phenotypic data across large psychiatric cohorts (2022) (1)
An MRI and fMRI study on the effect of deletions on chromosome 22 on brain (1999) (1)
Novel Insight into the Aetiology of Autism Spectrum Disorder Gained by Integrating Expression Data with Genome-wide Association Statistics (2018) (1)
Effects of pathogenic CNVs on physical traits in participants of the UK Biobank (2018) (1)
Erratum: Enhanced maternal origin of the 22q11.2 deletion in velocardiofacial and digeorge syndromes (American Journal of Human Genetics (2013) 92 (439-447)) (2013) (1)
P3-196: A genome-wide association study for late-onset Alzheimer's disease using DNA pooling (2008) (1)
The nature of schizophrenia: As broad as it is long (2021) (1)
Tau expression varies in different brain regions and disease state (2013) (1)
Neuropsychological profile of children with Velo-cardio-facial syndrome (VCFS) (2001) (1)
The health informatics cohort enhancement project (HICE): using routinely collected primary care data to identify people with a lifetime diagnosis of psychotic disorder (2012) (1)
Non-random mating, parent-of-origin, and maternal–fetal incompatibility effects in schizophrenia (2013) (1)
Letter to the Editor: Strong evidence for multiple psychosis susceptibility genes – a rejoinder to Crow (2008) (1)
Transcript expression-aware annotation improves rare variant interpretation (2020) (1)
Genome-wide linkage analysis using additional families from the Depression Network Study (2006) (1)
SA118LONGITUDINAL COGNITIVE DEVELOPMENT AND ASSOCIATION WITH PRODROMAL PSYCHOTIC SYMPTOMS IN ADOLESCENTS WITH 22Q11.2 DELETION SYNDROME (2019) (0)
withbipolar affective disorder (2011) (0)
Genetic meta-analysis of diagnosed Alzheimer’s disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing (2019) (0)
Schizophrenia Polygenic Risk and Experiences of Childhood Adversity: A Systematic Review and Meta-analysis (2022) (0)
Genomic Syndromes in Schizophrenia (2013) (0)
An examination of SNP selection prioritisation strategies for tests of gene-gene interaction (2011) (0)
Pre-pulse inhibition in the functional psychoses (1999) (0)
9.1 GENOMICS AND PSYCHIATRIC DIAGNOSIS (2018) (0)
Bipolar disorder and polymorphisms in the dystobrevin binding protein gene (2004) (0)
number variants attention-deficit hyperactivity disorder, with and without copy Clinical and cognitive characteristics of children with (2011) (0)
Simple and complex genetics of Alzheimer's disease (2001) (0)
schizophrenia-associated loci Analysis of copy number variations at 15 (2014) (0)
Author Correction: A structural variation reference for medical and population genetics (2021) (0)
ADARB1, a brain specific member of the RNA-specific adenosine deaminase family and bipolar affective disorder (2001) (0)
Examining the 4p16 region for association with bipolar disorder using DNA pooling (2000) (0)
Integrated analysis of environmental and genetic influences on cord blood DNA methylation in new-borns (2019) (0)
Polymorphisms in the glucocorticoid receptor gene and susceptibility to major affective disorders (2006) (0)
POMD10 Do psychiatric disorders form part of the myoclonus-dystonia syndrome phenotype? A systematic review of published literature (2010) (0)
Publisher Correction: Gene expression imputation across multiple brain regions provides insights into schizophrenia risk (2019) (0)
Publisher Correction: Gene expression imputation across multiple brain regions provides insights into schizophrenia risk (2019) (0)
Duffy-null genotype in clozapine-associated neutropenia (2019) (0)
Title Genomewide association scan of suicidal thoughts andbehaviour in major depression (2011) (0)
DCLK1Variants Are Associated across Schizophrenia and Attention Deficit/Hyperactivity Disorder (0)
THE EUROPEAN UNION GENE ENVIRONMENT INTERACTION (EUGEI) DATASET - A PAN-EUROPEAN PSYCHOSIS COHORT WITH PHENOTYPE AND ENVIRONMENT DATA AND COMMON AND RARE GENOTYPES (2017) (0)
Embryonic NCAM and schizophrenia: Genetic analysis of regulatory enzymes (1999) (0)
Association analysis of TBX1 and schizophrenia (2001) (0)
Background Velo-cardio-facial syndrome (VCFS) is associatedwith interstitial deletions of chromosome 22q11.About 30% of patientswithVCFS (2003) (0)
Genetic identification of brain cell types underlying schizophrenia (2018) (0)
SA99 TARGETED SEQUENCING OF 187 PUTATIVE SCHIZOPHRENIA RISK GENES IN 5,207 CASES AND 4,991 CONTROLS (2019) (0)
Neuropathology of Alzheimer ’ s disease : towards an understanding of the pathogenesis (2009) (0)
F138. INVESTIGATING A CAUSAL ASSOCIATION BETWEEN NEUROTICISM AND SCHIZOPHRENIA USING TWO-SAMPLE MENDELIAN RANDOMIZATION (2018) (0)
Genetic mapping on chromosome 22 (1993) (0)
Title : Examining cognition across the bipolar / schizophrenia diagnostic spectrum Running Title : Cognition in schizophrenia and bipolar disorder (2017) (0)
CHAPTER 5.4 Finding liability genes for schizophrenia (1999) (0)
P017 Differences in genetic risk for insomnia, hypersomnia and chronotype in bipolar disorder subtypes (2019) (0)
44A TWO-SAMPLE MENDELIAN RANDOMIZATION STUDY ASSESSING A CAUSAL ASSOCIATION BETWEEN NEUROTICISM AND SCHIZOPHRENIA (2019) (0)
Association of the muscarinic acetylcholine receptor M2 (CHRM2) gene with major depressive disorder (2006) (0)
No association between a promoter polymorphism of the UFD1L gene and schizophrenia in individuals with or without velo-cardio-facial syndrome (VCFS) (2001) (0)
Area Deprivation, Urbanicity and Severe Mental Illness – A Population-Based Linkage Study Using Routinely Collected Primary and Secondary Care Data (2019) (0)
Genome-wide association analyses identify 44 risk variants and refine the genetic architecture ofmajor depressive disorder (2018) (0)
Differences in Genetic Liability for Insomnia and Hypersomnia in Bipolar Disorder Subtypes (2019) (0)
Genome-wide association study of borderline personality disorder reveals genetic overlap with the bipolar disorder, schizophrenia and major depression (2017) (0)
Genetic dissection of behavioural abnormalities in mouse models of DiGeorge/velocardiofacial syndrome (2006) (0)
Genome‐wide significant locus for Research Diagnostic Criteria Schizoaffective Disorder Bipolar type (2017) (0)
Dynamic expression of risk genes for schizophrenia and bipolar disorder across development (2018) (0)
PSYCHIATRIC GENETICS '99 Candidate-Gene Association Studies of Schizophrenia (1999) (0)
Formalising recall by genotype as an efficient approach to detailed phenotyping and causal inference (2018) (0)
Kings Schizotypy Questionnaire (2014) (0)
Association studies between bipolar disorder and a polymorphism in the Wolfram gene (1999) (0)
Genes for schizophrenia and beyond (2006) (0)
P1-346 Evidence for independent effects of intra- and inter-gene variation at APOE on age at onset and disease risk (2006) (0)
Copy Number Variants increasing risk for schizophrenia: shared and distinct effects on brain morphometry and cognitive performance (2022) (0)
What can velo-cardio-facial syndrome tell us about the genetics of schizophrenia? (2004) (0)
Using rare genetic mutations to revisit structural brain asymmetry (2023) (0)
Mental Health Research, shared goals. (2021) (0)
Polymorphism screening and association studies of the Wolfram syndrome gene in schizophrenia (1999) (0)
UK 10 K Consortium (2019) (0)
The Contribution of the Rüdin School to Psychiatric Genetics: The Light and the Darkness. (2022) (0)
Schizophrenia: Molecular Genetics (2006) (0)
Screening the protocadherin 8 (PCDH8) gene in schizophrenia [Conference Abstract] (2002) (0)
Advising Relatives of Risk Advising Relatives of Risk of Alzheimer's Disease of Alzheimer's Disease (0)
Sib-pairs with psychosis (1996) (0)
Genomic insights into schizophrenia (2023) (0)
The Contribution of Cognitive Pathways (2015) (0)
Chromosome 22q, velo-cardio-facial syndrome (VCFS) and schizophrenia (2000) (0)
A genome screen to identify loci that modify the age-of-onset of Alzheimer's disease (2002) (0)
Publisher Correction: Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection (2019) (0)
Title: Neurotrophin receptor activation rescues cognitive and synaptic abnormalities caused by hemizygosity of the psychiatric risk gene Cacna1c Running title: Neurophysiological effects of low Cacna1c dosage (2020) (0)
Publisher Correction: Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection (2019) (0)
Using kinematic analyses to explore sensorimotor control impairments in children with 22q11.2 deletion syndrome (2019) (0)
Polymorphism screening of the human type 1 sigma (sigma) receptor (a candidate gene for schizophrenia) using a modified dideoxy fingerprinting technique. (1998) (0)
Different complement immune pathways mediate innate and learned aversion (2020) (0)
Psychotic Disorders and the Neurodevelopmental Continuum (2021) (0)
Clinical and genetic spectrum of myoclonus dystonia syndrome (2011) (0)
Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression (2018) (0)
5:00 PM DOPAMINE OR GLUTAMATE: USING GENETIC COPY NUMBER VARIANT PATHWAY ANALYSIS AND TREATMENT RESISTANCE TO ADJUDICATE SCHIZOPHRENIA HYPOTHESES (2014) (0)
Genomic insights into the overlap between psychiatric disorders: implications for research and clinical practice (2014) (0)
A structural variation reference for medical and population genetics (2020) (0)
Characterising the loss-of-function impact of 5’ untranslated region variants in 15,708 individuals (2020) (0)
PsycheMap - An interactive Internet-based database of psychiatric genetics linkage, association, and genome mapping projects (1998) (0)
No association of polymorphisms in the cholinergic locus with late-onset Alzheimer's disease. (2002) (0)
Genome wide association scan of co-morbid anxiety in major depressive disorder (MDD) [Abstract] (2010) (0)
Further suggestive evidence for linkage of schizophrenia to markers on chromosome 13 (1996) (0)
MYOCLONUS DYSTONIA: A CLINICAL AND GENETIC DESCRIPTION (2012) (0)
Linkage disequilibrium mapping of chromosome 22 in schizophrenia using DNA pooling on Chinese and Scottish populations (1998) (0)
1624 Myoclonus dystonia: a clinical and genetic description (2012) (0)
S139. INVESTIGATING THE GENETIC ARCHITECTURE OF GENERAL AND SPECIFIC PSYCHOPATHOLOGY IN ADOLESCENCE USING SCHIZOPHRENIA POLYGENIC SCORES (2018) (0)
Convergent evidence that oligodendrocyte lineage transcription factor 2 (OLIG2) and interacting genes influence susceptibility to schizophrenia [Conference Abstract] (2007) (0)
4 Neurodevelopmental Disorders What Is to Be Done ? (2015) (0)
Analysis of G proteins in ADHD (2001) (0)
Chapter 2.1.5 DNA pooling in allelic association studies (1999) (0)
Genetic findings in psychotic disorders (2003) (0)
Delusions in dementia - An investigation into their persistence and predictive value (2002) (0)
Design of the Depression Network (DeNt) study to identify susceptibility genes for unipolar depression (2002) (0)
Authors' reply. (2014) (0)
Further analysis of KIAA0027 in schizophrenic patients (2001) (0)
Screening of three candidate genes in the bipolar candidate region on chromosome 21q22.3 (2001) (0)
depression: Mendelian randomisation study Relationship between obesity and the risk of clinically significant (2014) (0)
Myoclonus dystonia syndrome: SGCE mutations and psychiatric disease [Abstract] (2012) (0)
What can the neurodevelopmental model explain? (1989) (0)
Is Psychiatric Disease a Core Phenotype of Myoclonus Dystonia Syndrome Caused by SGCE Mutations (2012) (0)
CDC2 as a candidate for late-onset Alzheimer's disease (2004) (0)
Analyses of de novo and common alleles implicate rare missense variants in SLC6A1 in schizophrenia (2019) (0)
Summary Studies of howgenetic and environmental exposures interactmaybe essential for understanding the aetiology of complexpsychiatric disorders (0)
Genetic Risk Factors for Schizophrenia (2000) (0)
Kraepelinian dichotomy - Author's reply (2005) (0)
Universitet Low-frequency variation in TP 53 has large effects on head circumference and intracranial (2019) (0)
Evaluating drug targets through human loss-of-function genetic variation (2020) (0)
A National Population-Based E-cohort of People with Psychosis (PsyCymru) Linkage of Phenotypical and Genetic Data to Routinely Collected Records (2018) (0)
Mutational analysis of purinergic receptor, P2X4: A positional candidate susceptibility gene for bipolar disorder. (2000) (0)
Visuospatial working memory in children and adolescents with velo-cardio-facial syndrome; An fMRI study (2005) (0)
An association study of ADHD and two MAOA polymorphisms: Examining comorbidity and subtypes (2001) (0)
RARE VARIANTSOF LARGE EFFECTAND COMMON VARIANTSOF SMALL EFFECT Theory (2007) (0)
Molecular characterisation of congenital hypothyroidism (2002) (0)
Large-scale candidate gene association analysis in psychiatric disorders (2002) (0)
Familial aggregation of clinical variables in a sibling pair study of schizophrenia (1999) (0)
Detection of cis-acting polymorphisms and epigenetic modification affecting gene expression [Conference Abstracts] (2002) (0)
Evidence of novel loci in late onset Alzheimer's disease (1999) (0)
Authors' reply (2001) (0)
The mutational constraint spectrum quantified from variation in 141,456 humans (2020) (0)
Progress in the search for expanded CAG/CTG repeats associated with psychosis (1996) (0)
Parkinson ’ s Disease α-Catenin and Wnt Signaling Ox-Phose Genes and Alzheimer ’ s Disease NO and Tardive Dyskinesia Homocysteine and Oxyradical-Induced Cognitive Impairment (2004) (0)
No association of the -277A variant allele of the UFD1L promoter polymorphism and schizophrenia (2000) (0)
Neuropsychological functioning in adults with velocardio-facial syndrome with and without schizophrenia (2003) (0)
Invited commentary on . . . Schizophrenia: a common disease Invited commentary on . . . Schizophrenia: a common disease caused by multiple rare alleles caused by multiple rare alleles { (2007) (0)
A cognitive investigation of children and adolescents with velo-cardio-facial syndrome (VCFS) (2003) (0)
The Genetics of Mood Disorders (1991) (0)
Cis- and trans-acting loci influence expression of DTNBP1, a susceptibility gene for schizophrenia (2006) (0)
A missense mutation of human Gephyrin (GPHN) is associated with Hyperekplexia and transcript isoform analysis re-defines the genomic structure of GPHN. (2001) (0)
Further evidence that KIAA0319 is associated with developmental dyslexia (2006) (0)
Sustained and selective attention as quantitative measures of schizophrenia liability (1999) (0)
Is schizophrenia linked to chromosome 1q? Response (2002) (0)
Parental age difference and schizophrenia - Reply (2004) (0)
Expression and population studies of the TATA-box binding protein polyglutamine region at normal and expanded lengths. (2001) (0)
Fine mapping of Alzheimers disease linkage region on chromosome 10 (2002) (0)
Genomic characterisation and mutational analysis of CUX2, a potential regulator of NCAM expression, mapping to chromosome 12q23-q24.1. (2000) (0)
Author's reply (2005) (0)
Genomic structure of postsynaptic organizational protein, Gephyrin, and mutation analysis in hyperekplexia and startle phenotypes (2000) (0)
Dysregulation of NRSF/REST via EHMT1 is associated with psychiatric disorders (2021) (0)
Testing and model for Alzheimer's disease (1992) (0)
Genomewide SNP linkage scan of schizophrenia in a large multicenter sample (2006) (0)
Allelic variation in the expression of neuropsychiatric candidate genes [Conference Abstract] (2004) (0)
Psychosis in velo-cardio-facial (22q11 deletion) syndrome (2005) (0)
Presence of the Apolipoprotein E e4 allele is associated with the manifestation of Alzheimer dementia in adults with Down syndrome (2000) (0)
No evidence for association between schizophrenia and MAO-A promoter polymorphism (1999) (0)
The effect of deletion 22q11 on brain anatomy and behaviour: A structural imaging study of children with velo-cardio-facial syndrome (VCFS) (2005) (0)
Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder (2018) (0)
Response to letter to editor: “Knowing when and how to use epilepsy screening questionnaires” (2020) (0)
Interaction between neuregulin 1 and its receptor ERBB4 increases susceptibility to schizophrenia [Conference Abstract] (2004) (0)
Bipolar disorder and unipolar depression: what is the genetic relationship? (2009) (0)
A multi-centre study of ACE and the risk of late-onset Alzheimer ’ s disease (2013) (0)
Authors' reply (2004) (0)
Stratification of bipolar disorder by psychotic features and a genome- (2017) (0)
P1-328 Association analysis of 22 positional/functional candidate genes on chromosome 10 with late onset Alzheimer’s disease (2006) (0)
Psychiatric disorders in Wolfram syndrome heterozygotes (1998) (0)
The Psychobiology of Down Syndrome . Edited by L. Nadel. (Pp. 484; illustrated; £31.50.) MIT press: Cambridge, Mass. 1988. (1990) (0)
Monoamine oxidase a promoter polymorphism and relationships to monoamine metabolite concentrations in CSF (1999) (0)
Comparative performances of machine learning methods for classifying Crohn Disease patients using genome-wide genotyping data (2019) (0)
P1-073 Protein profiling of the hippocampus of the Tg2576 transgenic AD mouse model (2006) (0)
Is dopa decarboxylase (DDC) a minor susceptibility gene for bipolar affective disorder (2000) (0)
Schizophrenia and Bipolar Disorder (2013) (0)
Identification of common genetic risk variants for autism spectrum disorder (2019) (0)
Neurotrophin receptor activation rescues cognitive and synaptic abnormalities caused by mutation of the psychiatric risk gene Cacna1c (2020) (0)
ARE PSYCHIATRIC SYMPTOMS A CORE PHENOTYPE OF MYOCLONUS DYSTONIA SYNDROME CAUSED BY SGCE MUTATIONS? (2013) (0)
S134. INCIDENCE, IMPACT AND TRAJECTORIES OF PSYCHOTIC EXPERIENCES FROM CHILDHOOD TO ADULTHOOD, AND PREDICTION OF PSYCHOTIC DISORDER (2020) (0)
P.4.016 Follow-up of schizophrenia genome-wide association studies implicates the MHC region in cognition (2011) (0)
Genetics and Alzheimer's Disease (1989) (0)
Psychopathology in mothers of children with pathogenic Copy Number Variants (2020) (0)
Correction: The psychiatric phenotypes of 1q21 distal deletion and duplication (2021) (0)
Using common genetic variation to examine phenotypic expression and risk prediction in 22q11.2 deletion syndrome (2020) (0)
Searching for the Causes of Schizophrenia (1994) (0)
The Origins of Schizophrenia (2012) (0)
S.16.02 Schizophrenia and the neurodevelopmental continuum; new support from genomics (2019) (0)
Publishing & Business Staff (2015) (0)
Landscape of multi-nucleotide variants in 125,748 human exomes and 15,708 genomes (2020) (0)
A functional and positional candidate gene for schizophrenia (2000) (0)
Symptom patterns and sibling correlations in the depression network (DeNt) study (2002) (0)
Contiguous gene deletions involving the SGCE gene: A clinical description (2012) (0)
Translating insights from neuropsychiatric genetics and genomics for precision psychiatry (2020) (0)
Age of onset in depression: Evidence for two subgroups showing familiality (2004) (0)
Running title : Psychopathology in 16 p 11 . 2 deletion / duplication (2018) (0)
Familial Alzheimer's Disease. Molecular Genetics and Clinical Perspectives (1990) (0)
Early onset antisocial behaviour in children with ADHD is associated with a functional variant in the catechol-O-methyltransferase (COMT) gene [Abstract] (2004) (0)
Author Correction: Characterising the loss-of-function impact of 5’ untranslated region variants in 15,708 individuals (2021) (0)
A rare deletion at distal 16 p 11 . 2 is implicated in schizophrenia (2013) (0)
VKučinskas-2001-2016 (2016) (0)
Genomewide linkage study of clinical variables in schizophrenia (2011) (0)
Molecular Neuropathology. Edited By Gareth W. Roberts and Julia M. Polak. Cambridge: Cambridge University Press. 1995. 189 pp. £24.95 (US$37.95). (1996) (0)
S0033291720001798jra 132..139 (2021) (0)
S.27.01 Finding susceptibility genes for schizophrenia (1996) (0)
DRD2 (TGn) repeat polymorphism in a large family data set (1992) (0)
Genes of the serotonergic and dopaminergic pathways and their interaction affect the expression of Behavioural and Psychological Symptoms in Dementia (BPSD). (2009) (0)
Author Correction: Evaluating drug targets through human loss-of-function genetic variation (2021) (0)
Applying polygenic risk scoring for psychiatric disorders to a large family with bipolar disorder and major depressive disorder (2018) (0)
Intra-pair correlations of symptom dimensions in a sibling pair study of schizophrenia (1999) (0)
Chapter 1.3 PsycheMap — An online database of psychiatric genetics linkage, association, and genome mapping projects (1999) (0)
Mutational analysis of 2 positional candidate susceptibility genes for bipolar disorder: PAH and LHX5 (2001) (0)
Neurodevelopmental Disorders and Schizophrenia: Recent Developments (2020) (0)
THE IMPACT OF THE DUFFY-NULL GENOTYPE IN CLOZAPINE-ASSOCIATED NEUTROPENIA: A GENOME-WIDE ASSOCIATION STUDY IN INDIVIDUALS OF AFRICAN ANCESTRY (2019) (0)
MAIN PLENARY ADDRESS - GENETICS (2010) (0)
Author Correction: Transcript expression-aware annotation improves rare variant interpretation (2021) (0)
Apolipoprotein E, Alzheimer's disease and Down's syndrome - Reply (2000) (0)
De novo mutations identified by exome sequencing implicate rare missense variants in SLC6A1 in schizophrenia (2020) (0)
Neurodevelopmental dimensional assessment of young children at high genomic risk of neuropsychiatric conditions (2023) (0)
Linkage Analysis of 18p, 12q and 17q High Myopia Loci in 51 UK Families (2003) (0)
Family-based analysis of the contribution of rare and common genetic variants to school performance in schizophrenia. (2023) (0)
A linkage study of chromosome 22q in sib-pairs with schizophrenia (1998) (0)
Chromatin regulators in the TBX1 network confer risk for conotruncal heart defects in 22q11.2DS and sporadic congenital heart disease (2022) (0)
Identifying loci that modify Alzheimer's disease development: A genome screen (2002) (0)
ANALYSIS OF DE NOVO COPY NUMBER VARIATIONS IN A LARGE, NEW SCHIZOPHRENIA SAMPLE (2017) (0)
Letters to the Editor (1993) (0)
Characterization, mutational analysis, and association of the human proline oxidase gene: A candidate gene for schizophrenia. (1999) (0)
The retained ability to display affection and emotion in Alzheimer's disease (2002) (0)
schizophrenia?and anticipation. Are they relevant to genetic studies of (2012) (0)
Complement C3 and C3aR differentially impact on learned fear and innate anxiety (2019) (0)
Molecular genetic research into Alzheimer's disease (1992) (0)
Authors' reply (2010) (0)
TITLE Genes of the serotonergic and dopaminergic pathways and their interaction affect the expression of Behavioural and Psychological Symptoms in Dementia (BPSD): A Multiple Indicators Multiple Causes (MIMIC) approach. (2009) (0)
Addendum: The mutational constraint spectrum quantified from variation in 141,456 humans (2021) (0)
Utilising machine-learning algorithms to uncovercomplex genetic interactions in schizophrenia [Conference Abstract] (2015) (0)
Evaluating an association of RGS4 polymorphisms with schizophrenia: Mega-analysis of over 12,000 individuals from 11 international sites (2004) (0)
Positional cloning, association analysis, and expression studies provide convergent evidence that the cadherin gene fat contains a bipolar disorder susceptibility allele (2005) (0)
P1-029: The Tg2576 mouse hippocampus shows early changes in the mitochondrial proteome that parallel those in models of other neurodegenerative diseases (2008) (0)
The effect of LRRK2 loss-of-function variants in humans (2020) (0)
Screening the critical region on chromosome 4p with DNA pooling for association with bipolar disorder (1998) (0)
Molecular genetic studies of dopamine and serotonin receptor genes in schizophrenia (1998) (0)
Schizophrenia risk conferred by rare protein-truncating variants is conserved across diverse human populations (2023) (0)
Allelic expression of APOE in brain [Conference Abstract] (2004) (0)
Rare coding variants as risk modifiers of the 22q11.2 deletion implicate postnatal cortical development in syndromic schizophrenia (2023) (0)
No association between the SER9/GLY polymorphism of the DRD3 gene and Attention Deficit Hyperactivity Disorder in a family-based sample (2003) (0)
Subject Index Vol. 46, 2002 (2003) (0)
49 MOLECULAR AND POPULATION GENETICS OF SCHIZOPHRENIA (2002) (0)
S0033291718000454jra 2499..2504 (2019) (0)
Combined whole genome linkage analysis of extraversion (2005) (0)
Linkage studies in schizophrenia: New findings promise new insights (2005) (0)
Association studies of polymorphisms in the promoter region of the dopamine D4 receptor and the D2 receptor [Abstract] (2000) (0)
Mitochondrial Genome-Wide association study of Alzheimer's disease (2010) (0)
O2-07-04 COPY NUMBER POLYMORPHISM AT CHROMOSOME 19 LOCUS ASSOCIATED WITH LATE-ONSET ALZHEIMER’S DISEASE (2010) (0)
P1-014 Principal components analysis of the neuropsychiatric inventory in Alzheimer's disease (2004) (0)
P3-245: Association analysis of tau and progranulin with late-onset Alzheimer's disease in a large caucasian U.K. sample (2008) (0)
P3-265: Testing for association between Alzheimer's disease with psychosis and variants identified as influencing risk of schizophrenia (2008) (0)
O2-02-05 Novel candidate genes for late-onset Alzheimer’s disease from a large scale association study of 20K functional variants (2006) (0)
Testing for association between Alzheimer's disease and known susceptibility variants for type 2 diabetes (2009) (0)
Haplotype structure of the 17 q 21 region in progressive supranuclear palsy and corticobasal degeneration (0)
P4-122 Genetic association of an APP binding protein gene with late onset Alzheimer's disease (2004) (0)
CLINICAL RELEVANCE OF GENOTYPE-PHENOTYPE ANALYSES WITHIN BIPOLAR DISORDER AND ACROSS THE MOOD AND PSYCHOSIS SPECTRUM (2021) (0)
M91 POLYGENIC RISK FOR SCHIZOPHRENIA AND SEASON OF BIRTH WITHIN THE UK BIOBANK COHORT (2019) (0)
T23 Polygenic Risk Scores Derived From Largest Schizophrenia Gwas Are Associated With The Presence Of Psychosis And Level Of Mood Incongruent Psychosis In Bipolar Disorder (2017) (0)
P4-058 Searching chromosome 10 for an AD risk factor — Analysis of a positional and biological candidate (2004) (0)
Genetic Risk Variants Interacting With MIR137: Effects On Cognition, Brain Structure And Brain Function In Patients And Healthy Participants (2019) (0)
Publisher Correction: Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection (2019) (0)
43RARE COPY NUMBER VARIATIONS ARE ASSOCIATED WITH POORER COGNITION IN SCHIZOPHRENIA (2019) (0)
P1-219 Three components describe behavioural symptoms in 1120 individuals with late-onset Alzheimer’s disease (2006) (0)
90. NEW EXOME SEQUENCING DATA PROVIDES PRELIMINARY EVIDENCE FOR 5 NOVEL SCHIZOPHRENIA RISK GENES (2022) (0)
SA127THE ASSOCIATION OF FRAGILE X MENTAL RETARDATION PROTEIN TARGETS WITH PSYCHIATRIC DISORDERS (2019) (0)
THE KINESIN LIGHT CHAIN 1 POLYMORPHISM rs 8702 IS ASSOCIATED WITH ELEVATED CSF LEVELS OF SECRETED FORMS OF AMYLOID PRECURSOR PROTEIN (2008) (0)
P4-106 Evidence for association of the calcium/calmodulin-dependent protein kinase type II gamma isoform (CAMKII γ) with late onset Alzheimer's disease (2004) (0)
SU25USING POLYGENIC RISK SCORE APPROACHES TO INVESTIGATE THE COMMON-VARIANT GENETIC ARCHITECTURE OF COGNITION IN SCHIZOPHRENIA (2019) (0)
53CONTROLLING TYPE 1 ERROR RATE IN CNV GENE-SET ENRICHMENT TESTS (2019) (0)
UPDATE ON THE ANALYSES OF THE LARGEST BIPOLAR CASE-CONTROL EXOME SEQUENCING DATASET TO DATE (2019) (0)
SA26 SPARSE CANONICAL CORRELATION IN APPLICATION TO BIPOLAR PSYCHOTIC PHENOTYPES AND SCHIZOPHRENIA GENOME-WIDE SIGNIFICANT GENETIC LOCI (2019) (0)
O2-06-01: A powerful, genome-wide association scan for susceptibility genes for late-onset Alzheimer's disease (2008) (0)
P.1.034 Copy number variants in CYP450 psychotropic drug metabolising enzymes in a large study of recurrent depressive disorder (2011) (0)
A PHENOTYPIC AND GENETIC COMPARISON OF SCHIZOPHRENIA IN UK BIOBANK AND OTHER GWAS SAMPLES (2022) (0)
83. DAMAGING RARE CODING VARIANTS IDENTIFIED BY EXOME SEQUENCING ARE ASSOCIATED WITH REDUCED COGNITIVE FUNCTION IN SCHIZOPHRENIA (2021) (0)
P4-067 Genetic association studies of insulin-degrading enzyme (IDE) with late onset Alzheimer's disease (LOAD) - Equivocal results from two large case-control studies (2004) (0)
Genome-wide association study of Alzheimer's with psychotic symptoms (2009) (0)
47TRANSCRIPTOME-WIDE ASSOCIATION ANALYSIS OF SCHIZOPHRENIA IMPLICATES PROCESSES INVOLVED IN SYNAPTIC DEVELOPMENT AND PLASTICITY, AND IMPAIRED LONG-TERM POTENTIATION (2019) (0)
4. POLYGENIC AND CLINICAL ASSOCIATIONS WITH SYMPTOM DIMENSIONS AND COGNITIVE ABILITY IN SCHIZOPHRENIA (2021) (0)
Investigating psychosis candidate genes in Alzheimer's disease with psychosis using genome-wide association studies (2009) (0)
SU25 TARGETED NEXT GENERATION SEQUENCING OF 187 GENES IN A BULGARIAN PSYCHOSIS SAMPLE (2019) (0)
PHARMACOGENOMIC ARCHITECTURE OF CLOZAPINE PLASMA CONCENTRATIONS (2019) (0)
On genetic pleiotropy between Alzheimer's disease and cardiovascular risk factors (2012) (0)
P4-046 Association of late onset Alzheimer's disease with genetic variation in multiple members of a gene family involved in neuronal apoptosis (2004) (0)
2788 – Large-Scale Mutation Screening of the Putative Autism Susceptibility Gene SCN2A in Schizophrenia (2013) (0)
P1-332 Glycogen synthase kinase -3 beta polymorphisms interact with Tau haplotypes in Alzheimer’s disease (2006) (0)
Correction: Investigating rare pathogenic/likely pathogenic exonic variation in bipolar disorder (2021) (0)
P4-101 Allelic expression of APOE in brain (2004) (0)
3 NRXN1 DELETION CARRIERS’ PHENOTYPES IN THE UK BIOBANK (2019) (0)
Evaluating Natural Selection In Schizophrenia Using Data From Genome-Wide Association Studies (2019) (0)
1. LATENT CLASS ANALYSIS IDENTIFIES BIOLOGICALLY-MEANINGFUL CLUSTERS OF INDIVIDUALS ACROSS THE SCHIZOPHRENIA-BIPOLAR SPECTRUM (2021) (0)
P1-327 Testing for association between Alzheimer’s disease with psychosis and functional gene candidates (2006) (0)
P1-275 A single nucleotide polymorphism in CHAT influences response to acetylcholinesterase inhibitors in Alzheimer’s disease (2006) (0)
F11EMPLOYING-TARGETED NEXT GENERATION SEQUENCING TO REVEAL THE GENETIC ARCHITECTURE OF BIPOLAR DISORDER AND SCHIZOPHRENIA IN BULGARIAN PATIENTS (2019) (0)
P4-110 A systematic scan of chromosome 10 single nucleotide polymorphisms identifies novel candidate genes showing strong association to Alzheimer's disease (2004) (0)
An examination of previously reported Alzheimer candidate genes within a large genome-wide association dataset (2009) (0)
P1-326 Statistical and genetic studies on the psychosis sub-phenotype in Alzheimer’s disease (2006) (0)
P1-335 A powerful association analysis of 496 SNPs in 80 positional candidate genes in a linked region on chromosome 10 for association with late onset Alzheimer’s disease (2006) (0)
F133INVESTIGATING THE PHENOTYPIC MANIFESTATION OF SCHIZOPHRENIA WITH REGARDS TO GENERAL AND SPECIFIC PSYCHOPATHOLOGY IN ADOLESCENCE USING A BIFACTOR MODELLING APPROACH (2019) (0)
79. IDENTIFICATION OF DISORDER-SPECIFIC LOCI AND GENES THROUGH CASE-CASE GENOME-WIDE ASSOCIATION STUDIES: AN APPLICATION TO SCHIZOPHRENIA AND BIPOLAR DISORDER (2021) (0)
50DE NOVO LOF AND DAMAGING MISSENSE VARIANTS ASSOCIATED WITH SCHIZOPHRENIA ARE CONCENTRATED IN LOF INTOLERANT GENES (2019) (0)
IDENTIFYING HIGH IMPACT CODING VARIANTS CONTRIBUTING TO REDUCED COGNITIVE ABILITY IN SCHIZOPHRENIA: A TRIO-BASED ANALYSIS (2022) (0)
P4-059 CDC2 as a candidate for late-onset Alzheimer's disease (2004) (0)
P1-284 Interaction between ADAM12 and SH3MD1 may confer susceptibility to late-onset Alzheimer’s disease (2006) (0)
P3-016: The APOE-ϵ4 allele does not affect rate of cognitive and functional decline in late-onset Alzheimer's disease (AD): Findings from the U.K. Medical Research Council (MRC) genetic resource for AD (2008) (0)
COMBINING EXOME SEQUENCING AND MICROARRAY DATA TO IDENTIFY RARE CNVS IMPACTING COGNITION IN SCHIZOPHRENIA (2022) (0)
F119EXPLORING THE UTILITY OF BIOLOGICALLY INFORMED POLYGENIC RISK SCORES IN SCHIZOPHRENIA (2019) (0)
T106. ASSESSING THE VALIDITY OF METHODS TO REPORT A SCHIZOPHRENIA DIAGNOSIS (2022) (0)
5:15 PM NOVEL GENETIC RISK VARIANTS FOR CLOZAPINE-ASSOCIATED NEUTROPENIA (2014) (0)
5THE ROLE OF NEURODEVELOPMENTAL COPY NUMBER VARIANTS IN DEPRESSION (2019) (0)
O2-02-07 Genetic variants on chromosome 9 are associated with late-onset Alzheimer’s disease, variation in allele-specific gene expression, and differential apoptotic response (2006) (0)
SU32GENETICS OF SLEEP DURATION AND BIPOLAR DISORDER (2019) (0)
Genetic influences on the psychotic symptomatology of Alzheimer's disease (2005) (0)
ZNF804A DELINEATES A SCHIZOPHRENIA SUBTYPE CHARACTERISED BY RELATIVELY SPARED COGNITIVE PERFORMANCE AND BRAIN VOLUME (2010) (0)
M25 Investigation of Relationships Between Bipolar Disorder Phenotypes And Genome-Wide Significant Loci From PGC2 Schizophrenia (2017) (0)
Screening of candidate genes related to myelination for mutations associated with schizophrenia (2001) (0)
Rare Variants in Pharmacogenes Influence Clozapine Metabolism in Individuals with Schizophrenia (2023) (0)
S.06.01 Copy number variations as risk and protective factors for schizophrenia in 22q11.2DS (2015) (0)
Clinical Indicators of Symptom Dimensions and Cognitive Ability in Schizophrenia (2022) (0)
Linkage disequilibrium mapping and candidate gene screening of the VCFS deleted region for mutations associated with schizophrenia (2000) (0)
P.1.j.006 Examining cognition across the bipolar/schizophrenia diagnostic spectrum (2017) (0)
Identification and characterisation of SNPs in candidate genes for schizophrenia (2000) (0)
Rare Maternally Inherited Coding Variants on Chromosome X Carry Predominantly Male Risk in Autism, Tourette Syndrome, and Attention-deficit/Hyperactivity Disorder (2022) (0)
Pharmacokinetics and pharmacogenomics of clozapine in an ancestrally diverse sample: A longitudinal analysis and GWAS using clinical monitoring data from the UK (2022) (0)
Finding susceptibility genes for schizophrenia (2020) (0)
Alterations in resting-state activity and functional connectivity in children with 22q11.2 deletion syndrome (2021) (0)
Genetic risk for schizophrenia is associated with increased proportion of indirect connections in brain networks revealed by a semi-metric analysis: evidence from population sample stratified for polygenic risk (2022) (0)
189. The Effect of Penetrance of CNVs for Intellectual Disability and Schizophrenia on Brain Structural Phenotypes (2019) (0)
O4.8. VULNERABLE PERIODS FOR COGNITIVE DEVELOPMENT IN INDIVIDUALS AT HIGH GENOMIC RISK OF SCHIZOPHRENIA (2018) (0)
SA85RESTING-STATE BRAIN CONNECTIVITY IN 22Q11.2 DELETION SYNDROME: A MAGNETOENCEPHALOGRAPHY STUDY (2019) (0)
Is there a link between schizophrenia and mutations at the fragile-X gene, FMR-1? (1993) (0)
INVESTIGATING THE SPECIFICITY OF GENOTYPE-PHENOTYPE RELATIONSHIPS IN CHILDREN WITH NEUROPSYCHIATRIC RISK COPY VARIANTS (2021) (0)
NREM sleep signatures of memory disruption and psychiatric symptoms in young people with 22q11.2 deletion syndrome (2021) (0)
SA103SLEEP IN YOUNG PEOPLE WITH 22Q11.2 DELETION SYNDROME (2019) (0)
SA97COMPUTATIONAL PSYCHIATRY MEETS GENETICS: REINFORCEMENT LEARNING IN EARLY PSYCHOSIS AND IN RELATION TO CLINICAL AND MOLECULAR GENETIC RISK FOR SCHIZOPHRENIA (2019) (0)
M104 EXAMINING ATTENTION DEFICIT HYPERACTIVITY DISORDER (ADHD) INATTENTION SYMPTOMS AS ANTECEDENTS OF PSYCHOSIS RISK IN 22Q11.2 DELETION SYNDROME (22Q11.2DS) (2019) (0)
Altered White Matter Microstructure in 22q11.2 Deletion Syndrome: A Multi-Site Diffusion Tensor Imaging Study Running Title: DTI in 22q11.2 Deletion Syndrome (2019) (0)
NRSF/REST lies at the intersection between epigenetic regulation, miRNA-mediated gene control and neurodevelopmental pathways associated with Intellectual disability (ID) and Schizophrenia (2022) (0)
Neurodevelopmental dimensional assessment of young children at high genomic risk of neuropsychiatric conditions (2023) (0)

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