David Andrew Collier

David Andrew Collier's AcademicInfluence.com Rankings

Biology

#9570

World Rank

#12792

Historical Rank

Genetics

#979

World Rank

#1075

Historical Rank

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Biology

David Andrew Collier's Degrees

PhD Genetics University of Oxford

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David Andrew Collier'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)
Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs (2013) (2011)
Large recurrent microdeletions associated with schizophrenia (2008) (1790)
Genome-wide association study identifies five new schizophrenia loci (2011) (1680)
Common variants conferring risk of schizophrenia (2009) (1653)
Genome-wide Association Analysis Identifies 14 New Risk Loci for Schizophrenia (2013) (1455)
Association scan of 14,500 nonsynonymous SNPs in four diseases identifies autoimmunity variants (2007) (1421)
Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder (2008) (1189)
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)
Large-scale genome-wide association analysis of bipolar disorder identifies a new susceptibility locus near ODZ4 (2011) (929)
The same sequence variant on 9p21 associates with myocardial infarction, abdominal aortic aneurysm and intracranial aneurysm (2008) (765)
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)
A novel functional polymorphism within the promoter of the serotonin transporter gene: possible role in susceptibility to affective disorders. (1996) (710)
Psychiatric genome-wide association study analyses implicate neuronal, immune and histone pathways (2015) (676)
Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes (2017) (517)
Disruption of the neurexin 1 gene is associated with schizophrenia. (2009) (469)
Meta-analysis of the association of urbanicity with schizophrenia. (2012) (376)
Genetic and Functional Analyses of SHANK2 Mutations Suggest a Multiple Hit Model of Autism Spectrum Disorders (2012) (371)
The frequency and distribution of thiopurine methyltransferase alleles in Caucasian and Asian populations. (1999) (368)
Rare loss-of-function variants in SETD1A are associated with schizophrenia and developmental disorders (2016) (363)
Is impaired set-shifting an endophenotype of anorexia nervosa? (2005) (348)
Pharmacogenetic prediction of clozapine response (2000) (345)
Genome-Wide Association Identifies a Common Variant in the Reelin Gene That Increases the Risk of Schizophrenia Only in Women (2008) (343)
Association between clozapine response and allelic variation in 5-HT2A receptor gene (1995) (332)
Short-term effects of antipsychotic treatment on cerebral function in drug-naive first-episode schizophrenia revealed by "resting state" functional magnetic resonance imaging. (2010) (329)
Improved imputation of low-frequency and rare variants using the UK10K haplotype reference panel (2015) (296)
Common variants near CAV1 and CAV2 are associated with primary open-angle glaucoma (2010) (296)
Meta-analysis shows strong positive association of the neuregulin 1 (NRG1) gene with schizophrenia. (2006) (295)
A genome-wide association study of anorexia nervosa (2014) (284)
Set shifting in anorexia nervosa: an examination before and after weight gain, in full recovery and relationship to childhood and adult OCPD traits. (2004) (269)
Cognitive flexibility in anorexia nervosa and bulimia nervosa (2004) (260)
Meta-analysis of studies on genetic variation in 5-HT2A receptors and clozapine response (1998) (254)
Copy number variations of chromosome 16p13.1 region associated with schizophrenia (2011) (253)
An integrated genetic-epigenetic analysis of schizophrenia: evidence for co-localization of genetic associations and differential DNA methylation (2016) (249)
Common variants on 8p12 and 1q24.2 confer risk of schizophrenia (2011) (243)
Association of cerebral deficits with clinical symptoms in antipsychotic-naive first-episode schizophrenia: an optimized voxel-based morphometry and resting state functional connectivity study. (2009) (240)
Systematic meta-analyses and field synopsis of genetic association studies of violence and aggression (2013) (238)
Association between schizophrenia and homozygosity at the dopamine D3 receptor gene. (1992) (236)
Association of BDNF with anorexia, bulimia and age of onset of weight loss in six European populations. (2004) (236)
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)
Prevalence and heritability of compulsive hoarding: a twin study. (2009) (231)
Neurexin 1 (NRXN1) deletions in schizophrenia. (2009) (227)
Evidence for association between polymorphisms in the promoter and coding regions of the 5-HT2A receptor gene and response to clozapine (1998) (216)
Gene variants associated with schizophrenia in a Norwegian genome-wide study are replicated in a large European cohort. (2010) (215)
Failure to Detect the Novel Retrovirus XMRV in Chronic Fatigue Syndrome (2010) (214)
Association between 5-HT2A gene promoter polymorphism and anorexia nervosa (1997) (212)
Common variants at VRK2 and TCF4 conferring risk of schizophrenia. (2011) (210)
Joint Analysis of Psychiatric Disorders Increases Accuracy of Risk Prediction for Schizophrenia, Bipolar Disorder, and Major Depressive Disorder (2015) (206)
5-HT2A and 5-HT2C receptor polymorphisms and psychopathology in late onset Alzheimer's disease. (1998) (199)
Rare deletions at the neurexin 3 locus in autism spectrum disorder. (2012) (198)
The serotonin transporter is a potential susceptibility factor for bipolar affective disorder. (1996) (198)
Genome-wide association study identifies a sequence variant within the DAB2IP gene conferring susceptibility to abdominal aortic aneurysm (2010) (197)
Clinical and molecular genetic analysis of 19 Wolfram syndrome kindreds demonstrating a wide spectrum of mutations in WFS1. (1999) (189)
Association between BDNF val66 met genotype and episodic memory (2005) (187)
A dopamine transporter gene functional variant associated with cocaine abuse in a Brazilian sample. (2006) (184)
Association between clozapine response and allelic variation in the 5-HT2C receptor gene (1995) (183)
Low activity allele of catechol-O-methyltransferase gene associated with rapid cycling bipolar disorder (1998) (176)
Additional support for schizophrenia linkage on chromosomes 6 and 8: a multicenter study. Schizophrenia Linkage Collaborative Group for Chromosomes 3, 6 and 8. (1996) (175)
Copy number variations in neurodevelopmental disorders (2012) (163)
Identification of a novel neuregulin 1 at-risk haplotype in Han schizophrenia Chinese patients, but no association with the Icelandic/Scottish risk haplotype (2004) (160)
Meta‐Analysis of Genome‐wide Linkage Studies in BMI and Obesity (2007) (159)
Therapygenetics: The 5HTTLPR and response to psychological therapy (2011) (152)
Family-based linkage disequilibrium mapping using SNP marker haplotypes: application to a potential locus for schizophrenia at chromosome 22q11 (2000) (151)
Dopamine D4 receptor subtypes and response to clozapine (1993) (148)
Association of BDNF with restricting anorexia nervosa and minimum body mass index: a family-based association study of eight European populations (2005) (147)
Meta-Analysis of the Alzheimer’s Disease Human Brain Transcriptome and Functional Dissection in Mouse Models (2020) (140)
Preferential transmission of the high activity allele of COMT in schizophrenia (1996) (139)
Penetrance for copy number variants associated with schizophrenia. (2010) (138)
Individual-specific risk factors for anorexia nervosa: a pilot study using a discordant sister-pair design (2001) (135)
Strong genetic evidence for a selective influence of GABAA receptors on a component of the bipolar disorder phenotype (2008) (135)
Corrigendum: TCTEX1D2 mutations underlie Jeune asphyxiating thoracic dystrophy with impaired retrograde intraflagellar transport (2016) (131)
Effect of BDNF val66met polymorphism on declarative memory and its neural substrate: A meta-analysis (2012) (130)
Altered Social Behaviours in Neurexin 1α Knockout Mice Resemble Core Symptoms in Neurodevelopmental Disorders (2013) (130)
Analysis of a structural polymorphism in the 5-HT2A receptor and clinical response to clozapine (1996) (129)
High and low activity alleles of catechol-O-methyltransferase gene: ethnic difference and possible association with Parkinson's disease (1997) (128)
Haplotype transmission disequilibrium and evidence for linkage of the CHRNA7 gene region to schizophrenia in Southern African Bantu families. (2000) (126)
Association between the neuregulin 1 gene and schizophrenia: a systematic review. (2005) (126)
Dopamine-beta hydroxylase polymorphism and cocaine addiction (2008) (123)
The quantification of COMT mRNA in post mortem cerebellum tissue: diagnosis, genotype, methylation and expression (2006) (123)
Metabolic Syndrome and Autoimmune Diabetes: Action LADA 3 (2009) (121)
Identification and validation of biomarkers for autism spectrum disorders (2015) (119)
Preliminary report of biological basis of sensitivity to the effects of cannabis on psychosis: AKT1 and DAT1 genotype modulates the effects of δ-9-tetrahydrocannabinol on midbrain and striatal function (2012) (117)
Lifetime course of eating disorders: design and validity testing of a new strategy to define the eating disorders phenotype (2008) (113)
Translating genome-wide association findings into new therapeutics for psychiatry (2016) (113)
Male-Biased Autosomal Effect of 16p13.11 Copy Number Variation in Neurodevelopmental Disorders (2013) (111)
No evidence for an association of affective disorders with high- or low-activity allele of catechol-o-methyltransferase gene (1997) (110)
At-Risk Variant in TCF7L2 for Type II Diabetes Increases Risk of Schizophrenia (2011) (109)
Catechol‐O‐methyltransferase polymorphisms and schizophrenia: a transmission disequilibrium study in multiply affected families (1997) (109)
Psychosis and aggression in Alzheimer's disease: the effect of dopamine receptor gene variation (2001) (108)
The aetiology of eating disorders (2004) (106)
Association analysis of the DRD4 and COMT genes in methamphetamine abuse (2004) (106)
Suggestive evidence for linkage of schizophrenia to markers on chromosome 13q14.1‐q32 (1995) (106)
Initial evidence for the role of CACNA1C on subcortical brain morphology in patients with bipolar disorder (2011) (105)
Analysis of Intellectual Disability Copy Number Variants for Association With Schizophrenia. (2016) (104)
The genetics of schizophrenia: glutamate not dopamine? (2003) (104)
Influence of X Chromosome and Hormones on Human Brain Development: A Magnetic Resonance Imaging and Proton Magnetic Resonance Spectroscopy Study of Turner Syndrome (2006) (102)
Aberrant intrinsic brain activity and cognitive deficit in first-episode treatment-naive patients with schizophrenia (2012) (101)
Evaluation of a Susceptibility Gene for Schizophrenia: Genotype Based Meta-Analysis of RGS4 Polymorphisms from Thirteen Independent Samples (2006) (101)
Association analysis of the dopamine D4 gene exon III VNTR and heroin abuse in Chinese subjects (1997) (101)
A 3-Mb map of a large Segmental duplication overlapping the alpha7-nicotinic acetylcholine receptor gene (CHRNA7) at human 15q13-q14. (2002) (100)
Catechol-O-methyltransferase Val158Met polymorphism: frequency analysis in Han Chinese subjects and allelic association of the low activity allele with bipolar affective disorder. (1997) (99)
The effects of gender and COMT Val158Met polymorphism on fearful facial affect recognition: a fMRI study. (2009) (98)
The 5-HT2A −1438G/A polymorphism in anorexia nervosa: a combined analysis of 316 trios from six European centres (2001) (98)
Association study of the INPP1, 5HTT, BDNF, AP-2β and GSK-3β GENE variants and restrospectively scored response to lithium prophylaxis in bipolar disorder (2006) (97)
Performance deficit of α7 nicotinic receptor knockout mice in a delayed matching‐to‐place task suggests a mild impairment of working/episodic‐like memory (2006) (97)
Genetic utility of broadly defined bipolar schizoaffective disorder as a diagnostic concept (2009) (96)
Epistasis between the DAT 3′ UTR VNTR and the COMT Val158Met SNP on cortical function in healthy subjects and patients with schizophrenia (2009) (95)
DRD2 Ser311/Cys311 polymorphism in schizophrenia (1994) (95)
Association analysis of the 5‐HT5A gene in depression, psychosis and antipsychotic response (2000) (95)
Dissociable Brain Structural Changes Associated with Predisposition, Resilience, and Disease Expression in Bipolar Disorder (2009) (95)
Maternally derived microduplications at 15q11-q13: implication of imprinted genes in psychotic illness. (2011) (94)
Suggestive evidence for linkage of schizophrenia to markers on chromosome 13 in Caucasian but not Oriental populations (1997) (94)
Complement genes contribute sex-biased vulnerability in diverse illnesses (2020) (92)
Genetic Markers of Human Evolution Are Enriched in Schizophrenia (2016) (91)
The impact of the CACNA1C gene polymorphism on frontolimbic function in bipolar disorder (2011) (90)
Evidence for association between novel polymorphisms in the PRODH gene and schizophrenia in a Chinese population (2004) (89)
Allelic association between a Ser-9-Gly polymorphism in the dopamine D3 receptor gene and schizophrenia (1996) (89)
No association between Parkinson's disease and low-activity alleles of catechol O-methyltransferase. (1996) (88)
Serotonin Transporter Gene and Risk for Bipolar Affective Disorder: An Association Study in a Spanish Population (1998) (87)
Hypermethylation in the ZBTB20 gene is associated with major depressive disorder (2014) (86)
Linkage studies on chromosome 22 in familial schizophrenia. (1995) (86)
An examination of decision making in bulimia nervosa (2009) (85)
Molecular and genetic evidence for abnormalities in the nodes of Ranvier in schizophrenia. (2012) (84)
Present and lifetime comorbidity of tobacco, alcohol and drug use in eating disorders: a European multicenter study. (2008) (84)
The effect of COMT, BDNF, 5-HTT, NRG1 and DTNBP1 genes on hippocampal and lateral ventricular volume in psychosis (2009) (83)
White-matter microstructure in previously drug-naive patients with schizophrenia after 6 weeks of treatment (2013) (82)
Low social interactions in eating disorder patients in childhood and adulthood: A multi-centre European case control study (2013) (81)
The Schizophrenia Risk Allele C of the TCF4 rs9960767 Polymorphism Disrupts Sensorimotor Gating in Schizophrenia Spectrum and Healthy Volunteers (2011) (80)
Allelic association analysis of the dopamine D2, D3, 5-HT2A, and GABA(A)gamma2 receptors and serotonin transporter genes with heroin abuse in Chinese subjects. (2002) (80)
Independent modulation of engagement and connectivity of the facial network during affect processing by CACNA1C and ANK3 risk genes for bipolar disorder. (2013) (79)
Linkage of Wolfram syndrome to chromosome 4p16.1 and evidence for heterogeneity. (1996) (79)
BrainSeq: Neurogenomics to Drive Novel Target Discovery for Neuropsychiatric Disorders (2015) (79)
Effects of the CACNA1C risk allele for bipolar disorder on cerebral gray matter volume in healthy individuals. (2009) (77)
Difference in susceptibility to activity-based anorexia in two inbred strains of mice (2007) (76)
Personality pathology among individuals with a lifetime history of anorexia nervosa. (2006) (75)
Sensorimotor Gating is Associated with CHRNA3 Polymorphisms in Schizophrenia and Healthy Volunteers (2010) (75)
Cytochrome P450IID6 genotype does not determine response to clozapine (1995) (75)
Predicting outcomes following cognitive behaviour therapy in child anxiety disorders: the influence of genetic, demographic and clinical information. (2013) (74)
Association study of CHRFAM7A copy number and 2bp deletion polymorphisms with schizophrenia and bipolar affective disorder (2006) (73)
Consensus paper of the WFSBP Task Force on Genetics: Genetics, epigenetics and gene expression markers of major depressive disorder and antidepressant response (2017) (73)
Lack of association between a polymorphism in the promoter region of the dopamine-2 receptor gene and clozapine response. (1998) (72)
-141 C del/ins polymorphism of the dopamine receptor 2 gene is associated with schizophrenia in a British population. (1999) (72)
Opposite Effects of Catechol-O-Methyltransferase Val158Met on Cortical Function in Healthy Subjects and Patients with Schizophrenia (2009) (72)
A study of chromosome 4p markers and dopamine D5 receptor gene in schizophrenia and bipolar disorder (1998) (72)
Brain-derived neurotrophic factor (BDNF) and set-shifting in currently ill and recovered anorexia nervosa (AN) patients (2008) (71)
Epilepsy-associated GRIN2A mutations reduce NMDA receptor trafficking and agonist potency – molecular profiling and functional rescue (2017) (70)
Sensorimotor Gating Depends on Polymorphisms of the Serotonin-2A Receptor and Catechol-O-Methyltransferase, but Not on Neuregulin-1 Arg38Gln Genotype: A Replication Study (2009) (70)
Behavioral, physiological, and molecular differences in response to dietary restriction in three inbred mouse strains. (2006) (67)
Neurocognitive deficits in first‐episode schizophrenic patients and their first‐degree relatives (2007) (67)
Analysis of clozapine response and polymorphisms of the dopamine D4 receptor gene (DRD4) in schizophrenic patients. (1995) (67)
Gene–environment interaction in anorexia nervosa: relevance of non-shared environment and the serotonin transporter gene (2011) (67)
The impact of the Val158Met catechol-O-methyltransferase genotype on neural correlates of sad facial affect processing in patients with bipolar disorder and their relatives (2010) (67)
A Common Variant in DRD3 Receptor Is Associated with Autism Spectrum Disorder (2009) (65)
5HT2a receptor T102C polymorphism and schizophrenia (1996) (65)
Identifying potential risk haplotypes for schizophrenia at the DTNBP1 locus in Han Chinese and Scottish populations (2005) (64)
An association study of the neuregulin 1 gene, bipolar affective disorder and psychosis (2009) (64)
Reaction time of the Continuous Performance Test is an endophenotypic marker for schizophrenia: A study of first-episode neuroleptic-naive schizophrenia, their non-psychotic first-degree relatives and healthy population controls (2007) (63)
Effect of disrupted-in-schizophrenia-1 on pre-frontal cortical function (2008) (63)
A linkage study of schizophrenia to markers within Xp11 near the MAOB gene (1997) (63)
Allelic association analysis of the 5-HT2C receptor gene in bipolar affective disorder (1996) (63)
Personality and psychopathological traits of males with an eating disorder (2004) (63)
Depression in Alzheimer's disease: The effect of serotonin receptor gene variation (2003) (63)
Genetic targeting of NRXN2 in mice unveils role in excitatory cortical synapse function and social behaviors (2015) (62)
The effects of neuregulin1 on brain function in controls and patients with schizophrenia and bipolar disorder (2008) (62)
Set shifting and central coherence as neurocognitive endophenotypes in eating disorders: A preliminary investigation in twins (2013) (62)
Eating disorders and obesity: two sides of the same coin? (2009) (62)
No association between (AAT)n repeats in the cannabinoid receptor gene (CNR1) and heroin abuse in a Chinese population (2000) (62)
Association of the dysbindin gene with bipolar affective disorder. (2006) (61)
Catechol-O-Methyltransferase (COMT) Val158Met Genotype is Associated with BOLD Response as a Function of Task Characteristic (2008) (59)
Association of DAO and G72(DAOA)/G30 genes with bipolar affective disorder (2008) (58)
Genome-Wide Association Analysis of Eating Disorder-Related Symptoms, Behaviors, and Personality Traits (2012) (57)
Failure to find linkage between a functional polymorphism in the dopamine D4 receptor gene and schizophrenia. (1994) (57)
Association analysis between dopamine receptor genes and bipolar affective disorder (1999) (57)
Volume increases in putamen associated with positive symptom reduction in previously drug-naive schizophrenia after 6 weeks antipsychotic treatment (2011) (57)
Linkage, association and mutational analysis of the dopamine D3 receptor gene in schizophrenia. (1996) (57)
Neurotrophic gene polymorphisms and response to psychological therapy (2012) (56)
A quantitative association study between schizotypal traits and COMT, PRODH and BDNF genes in a healthy Chinese population (2007) (56)
The impact of CACNA1C allelic variation on effective connectivity during emotional processing in bipolar disorder (2013) (56)
Expression-based drug screening of neural progenitor cells from individuals with schizophrenia (2018) (56)
Interspecies Trait Genetics Reveals Association of Adcy8 with Mouse Avoidance Behavior and a Human Mood Disorder (2009) (56)
A linkage study of schizophrenia with DNA markers from the long arm of chromosome 11 (1992) (55)
A large replication study and meta-analysis in European samples provides further support for association of AHI1 markers with schizophrenia. (2010) (55)
Two peptidase activities decrease in treated bipolar disorder not schizophrenic patients. (2004) (52)
Personality disorders and personality dimensions in anorexia nervosa. (2003) (52)
Association study of dysbindin gene with clinical and outcome measures in a representative cohort of Italian schizophrenic patients (2007) (52)
The serotonin transporter and clozapine response (2000) (52)
5-HT2A receptor and bipolar affective disorder: association studies in affected patients (1997) (52)
Assessment of white matter abnormalities in paranoid schizophrenia and bipolar mania patients (2011) (52)
Association of the 5-HT2c gene with susceptibility and minimum body mass index in anorexia nervosa (2003) (52)
Genetics of schizophrenia: A consensus paper of the WFSBP Task Force on Genetics (2017) (50)
Voxel based morphometric and diffusion tensor imaging analysis in male bipolar patients with first-episode mania (2012) (50)
Common schizophrenia alleles are enriched in mutation-intolerant genes and maintained by background selection (2016) (50)
Apolipoprotein E: Depressive illness, depressive symptoms, and Alzheimer's disease (1998) (49)
PACAP and PAC1 receptor in brain development and behavior (2013) (49)
Neuregulin-1 and the P300 waveform—A preliminary association study using a psychosis endophenotype (2008) (48)
The association of white matter volume in psychotic disorders with genotypic variation in NRG1, MOG and CNP: a voxel-based analysis in affected individuals and their unaffected relatives (2012) (48)
The Cognitive Impact of the ANK3 Risk Variant for Bipolar Disorder: Initial Evidence of Selectivity to Signal Detection during Sustained Attention (2011) (48)
Serum glutamine, set-shifting ability and anorexia nervosa (2010) (48)
Case-control and combined family trios analysis of three polymorphisms in the ghrelin gene in European patients with anorexia and bulimia nervosa. (2006) (47)
Nuclear Receptor Rev-Erb-α Circadian Gene Variants and Lithium Carbonate Prophylaxis in Bipolar Affective Disorder (2010) (47)
Meta-analysis of the human brain transcriptome identifies heterogeneity across human AD coexpression modules robust to sample collection and methodological approach (2019) (46)
Episodic memory performance predicted by the 2bp deletion in exon 6 of the "alpha 7-like" nicotinic receptor subunit gene. (2006) (46)
TCF4 (e2‐2; ITF2): A schizophrenia‐associated gene with pleiotropic effects on human disease (2013) (46)
Stargazin involvement with bipolar disorder and response to lithium treatment (2008) (46)
A Genome-wide Association Analysis of a Broad Psychosis Phenotype Identifies Three Loci for Further Investigation (2014) (46)
Convergent lines of evidence support CAMKK2 as a schizophrenia susceptibility gene (2014) (45)
Advanced paternal age increases the risk of schizophrenia and obsessive–compulsive disorder in a Chinese Han population (2012) (45)
Mutation screening of the Wolfram syndrome gene in psychiatric patients (2001) (45)
Genetic variation of the 5-HT2A receptor gene and bipolar affective disorder (1997) (45)
Genetic overlap between episodic memory deficits and schizophrenia: results from The Maudsley Twin Study (2010) (45)
Ohnologs are overrepresented in pathogenic copy number mutations (2013) (44)
Two novel variants in the DOPA decarboxylase gene: association with bipolar affective disorder (1999) (44)
StemBANCC: Governing Access to Material and Data in a Large Stem Cell Research Consortium (2015) (44)
Rare Variant Analysis of Human and Rodent Obesity Genes in Individuals with Severe Childhood Obesity (2017) (43)
Association analysis of polymorphisms in the DRD4 gene and heroin abuse in Chinese subjects. (2000) (43)
Childhood Eating and Weight in Eating Disorders: A Multi-Centre European Study of Affected Women and Their Unaffected Sisters (2007) (43)
Overlapping clusters of gray matter deficits in paranoid schizophrenia and psychotic bipolar mania with family history (2011) (43)
Is there an association between the COMT gene and P300 endophenotypes? (2006) (42)
Systematic screening of the 14-3-3 eta (eta) chain gene for polymorphic variants and case-control analysis in schizophrenia. (2000) (42)
Transmission disequilibrium analysis of HLA class II DRB1, DQA1, DQB1 and DPB1 polymorphisms in schizophrenia using family trios from a Han Chinese population (2001) (42)
Abnormalities in connectivity of white-matter tracts in patients with familial and non-familial schizophrenia (2010) (42)
Association analysis of the RGS4 gene in Han Chinese and Scottish populations with schizophrenia (2005) (42)
Case-control, haplotype relative risk and transmission disequilibrium analysis of a dopamine D2 receptor functional promoter polymorphism in schizophrenia (1998) (41)
Positional Pathway Screen of wnt Signaling Genes in Schizophrenia: Association with DKK4 (2008) (41)
A transmission disequilibrium and linkage analysis of D22S278 marker alleles in 574 families: further support for a susceptibility locus for schizophrenia at 22q12 (1998) (41)
Do COMT, BDNF and NRG1 polymorphisms influence P50 sensory gating in psychosis? (2010) (41)
Individual and family eating patterns during childhood and early adolescence: An analysis of associated eating disorder factors (2007) (41)
Genome-wide RNAseq study of the molecular mechanisms underlying microglia activation in response to pathological tau perturbation in the rTg4510 tau transgenic animal model (2018) (40)
Voxel-based morphometric analysis on the volume of gray matter in bipolar I disorder (2011) (39)
Failure to respond to treatment with typical antipsychotics is not associated with CYP2D6 ultrarapid hydroxylation. (1999) (39)
DNA methylation meta-analysis reveals cellular alterations in psychosis and markers of treatment-resistant schizophrenia (2021) (38)
Effect of COMT genotype on aggressive behaviour in a community cohort of schizophrenic patients (2011) (38)
Systematic screening of the LDL-PLA2 gene for polymorphic variants and case-control analysis in schizophrenia. (1997) (38)
Transcriptional Signatures of Tau and Amyloid Neuropathology (2020) (38)
Altered effect of dopamine transporter 3'UTR VNTR genotype on prefrontal and striatal function in schizophrenia. (2009) (38)
The –141C Ins/Del polymorphism of the dopamine D2 receptor gene is not associated with either migraine or Parkinson's disease (2001) (37)
Chromosome 22 markers demonstrate transmission disequilibrium with schizophrenia (1995) (37)
Protein kinase B (AKT1) genotype mediates sensitivity to cannabis-induced impairments in psychomotor control (2014) (37)
Pre-morbid Psychiatric Morbidity, Comorbidity and Personality in Patients with Anorexia Nervosa Compared to their Healthy Sisters (2002) (36)
A genome‐wide association study for quantitative traits in schizophrenia in China (2011) (36)
No association between a common single nucleotide polymorphism, rs4141463, in the MACROD2 gene and autism spectrum disorder (2011) (36)
NRXN1 deletions identified by array comparative genome hybridisation in a clinical case series – further understanding of the relevance of NRXN1 to neurodevelopmental disorders (2013) (36)
102T/C polymorphism of serotonin receptor type 2A gene is not associated with schizophrenia in either Chinese or British populations. (1999) (36)
Evidence for three genetic loci involved in both anorexia nervosa risk and variation of body mass index (2017) (36)
Pharmacogenetics for the Individualization of Psychiatric Treatment (2001) (36)
Identification of novel polymorphisms in the 5' flanking region of CYP1A2, characterization of interethnic variability, and investigation of their functional significance. (2000) (36)
Social and emotional processing as a behavioural endophenotype in eating disorders: a pilot investigation in twins. (2013) (36)
Analysis of CAG/CTG repeat size in chinese subjects with schizophrenia and bipolar affective disorder using the repeat expansion detection method (1998) (36)
Transmission disequilibrium analysis of a triplet repeat within the hKCa3 gene using family trios with schizophrenia. (1998) (36)
The dopamine D3 receptor gene: no association with bipolar affective disorder. (1993) (35)
Association analysis of polymorphisms in the mu opioid gene and heroin abuse in Chinese subjects (2000) (35)
Premorbid tobacco smoking is associated with later age at onset in schizophrenia (2010) (35)
Clozapine pharmacokinetics and pharmacodynamics studied with CYP1A2-null mice (2000) (35)
Novel polymorphisms in the somatostatin receptor 5 (SSTR5) gene associated with bipolar affective disorder (2002) (34)
Association analysis of the glycogen synthase kinase-3β gene in bipolar disorder (2006) (34)
Evidence for three genetic loci involved in both anorexia nervosa risk and variation of body mass index (2017) (34)
5HT2A receptor gene and bipolar affective disorder (1995) (34)
An epidemiological survey of alcohol use disorders in a Tibetan population (2008) (34)
Advances in multidisciplinary and cross-species approaches to examine the neurobiology of psychiatric disorders (2011) (34)
A systematic review and secondary data analysis of the interactions between the serotonin transporter 5-HTTLPR polymorphism and environmental and psychological factors in eating disorders. (2017) (33)
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)
Genetic variation in the 5-HT5A receptor gene in patients with bipolar disorder and major depression (2001) (32)
Associations of individual and family eating patterns during childhood and early adolescence: a multicentre European study of associated eating disorder factors (2008) (32)
Relevance of social and self-standards in eating disorders. (2012) (32)
No association between polymorphisms of methylenetetrahydrofolate reductase gene and schizophrenia in both Chinese and Scottish populations (2004) (32)
Steroid receptor coactivator-1 modulates the function of Pomc neurons and energy homeostasis (2019) (31)
The genetics of eating disorders. (2011) (31)
Evidence of association of KIBRA genotype with episodic memory in families of psychotic patients and controls. (2010) (31)
Risk factors, correlates, and markers in early-onset bulimia nervosa and EDNOS. (2011) (30)
Investigation of common, low-frequency and rare genome-wide variation in anorexia nervosa (2017) (30)
Chromosomal mapping of excessive physical activity in mice in response to a restricted feeding schedule (2010) (30)
Difficulties in replication of results (2000) (28)
Maternal Anxiety, Overprotection and Anxious Personality as Risk Factors for Eating Disorder: A Sister Pair Study (2013) (28)
Aberrant spontaneous neural activity and correlation with evoked-brain potentials in first-episode, treatment-naïve patients with deficit and non-deficit schizophrenia (2017) (28)
Quantitative promoter DNA methylation analysis of four candidate genes in anorexia nervosa: a pilot study. (2013) (28)
Replication of association of 3p21.1 with susceptibility to bipolar disorder but not major depression (2010) (28)
Investigation into the Presence of and Serological Response to XMRV in CFS Patients (2011) (28)
The development of the childhood retrospective perfectionism questionnaire (CHIRP) in an eating disorder sample. (2008) (27)
Loss of Trem2 in microglia leads to widespread disruption of cell coexpression networks in mouse brain (2018) (27)
The role of single nucleotide polymorphism of D2 dopamine receptor gene on major depressive disorder and response to antidepressant treatment (2012) (26)
Extensive brain structural network abnormality in first-episode treatment-naive patients with schizophrenia: morphometrical and covariation study (2014) (25)
Genome-Wide Association of Heroin Dependence in Han Chinese (2016) (25)
Is Neuregulin 1 Involved in Determining Cerebral Volumes in Schizophrenia? Preliminary Results Showing a Decrease in Superior Temporal Gyrus Volume (2012) (25)
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)
Effect of DISC1 on the P300 waveform in psychosis. (2013) (25)
Correlation and familial aggregation of dimensions of psychosis in affected sibling pairs from China (2001) (25)
A COMT gene haplotype associated with methamphetamine abuse (2011) (25)
Linkage disequilibrium analysis of the CHRNA7 gene and its partially duplicated region in schizophrenia (2007) (25)
Linkage studies of bipolar disorder with chromosome 18 markers. (1999) (24)
Differential effects of DAAO on regional activation and functional connectivity in schizophrenia, bipolar disorder and controls (2011) (24)
Factor Structures of the Neurocognitive Assessments and Familial Analysis in First-Episode Schizophrenia Patients, Their Relatives and Controls (2010) (24)
Interspecies comparisons of functional genetic variations and their implications in neuropsychiatry (2009) (24)
Normative data on a battery of neuropsychological tests in the Han Chinese population. (2011) (24)
Association of Neuregulin 1 rs3924999 genotype with antisaccades and smooth pursuit eye movements (2010) (23)
Establishing the characteristics of an effective pharmacogenetic test for clozapine-induced agranulocytosis (2014) (23)
Accuracy and sensitivity of DNA pooling with microsatellite repeats using capillary electrophoresis. (1999) (23)
High-throughput DNA methylation analysis in anorexia nervosa confirms TNXB hypermethylation (2018) (23)
Linkage studies in bipolar affective disorder with markers on chromosome 21. (1996) (23)
Gene-set analysis based on the pharmacological profiles of drugs to identify repurposing opportunities in schizophrenia (2016) (23)
Random or Stochastic Monoallelic Expressed Genes Are Enriched for Neurodevelopmental Disorder Candidate Genes (2013) (22)
The differential clinical and neurocognitive profiles of COMT SNP rs165599 genotypes in schizophrenia (2005) (22)
Low-frequency variation in TP53 has large effects on head circumference and intracranial volume (2018) (22)
Microduplications at the pseudoautosomal SHOX locus in autism spectrum disorders and related neurodevelopmental conditions (2016) (22)
Autosome search for schizophrenia susceptibility genes in multiply affected families (1999) (21)
No association of Disrupted‐in‐Schizophrenia‐1 variation with prefrontal function in patients with schizophrenia and bipolar disorder (2011) (21)
Mission: not impossible? Candidate gene studies in child psychiatric disorders (2000) (21)
[Molecular pharmacogenetic studies of drug responses to obsessive-compulsive disorder and six functional genes]. (2004) (20)
Do illness characteristics and familial risk differ between women with anorexia nervosa grouped on the basis of personality pathology? (2005) (20)
A dopamine D4 receptor exon 3 VNTR allele protecting against migraine without aura (2007) (20)
A GSTP1 functional variant associated with cocaine dependence in a Brazilian population. (2005) (19)
Translational Neuroscience of Schizophrenia: Seeking a Meeting of Minds Between Mouse and Man (2011) (19)
Regulatory characterisation of the schizophrenia-associated CACNA1C proximal promoter and the potential role for the transcription factor EZH2 in schizophrenia aetiology (2018) (19)
Effect of D‐amino acid oxidase activator (DAOA; G72) on brain function during verbal fluency (2012) (18)
Probing the Association between Early Evolutionary Markers and Schizophrenia (2017) (18)
123I-Iododexetimide Preferentially Binds to the Muscarinic Receptor Subtype M1 In Vivo (2015) (18)
Bipolar 1 disorder is not associated with the RGS4, PRODH, COMT and GRK3 genes. (2006) (18)
Replication Study and Meta-Analysis in European Samples Supports Association of the 3p21.1 Locus with Bipolar Disorder (2012) (18)
Perception of autonomy and connectedness prior to the onset of anorexia nervosa and bulimia nervosa. (2012) (17)
A new social-family model for eating disorders: A European multicentre project using a case–control design (2015) (17)
Sensorimotor gating and D2 receptor signalling: evidence from a molecular genetic approach. (2012) (17)
Mutation Screening and Association Analysis of the Parkin Gene in Parkinson’s Disease Patients from South-West China (2003) (17)
Analysis of microsatellite markers at the UCP2/UCP3 locus on chromosome 11q13 in anorexia nervosa (2002) (17)
Dissecting the many genetic faces of schizophrenia (2009) (17)
Association of the serotonin transporter gene, neuroticism and smoking behaviours (2008) (16)
Advances in the genetics of schizophrenia: toward a network and pathway view for drug discovery (2016) (16)
[Cases-Control association study and transmission disequilibrium test of T102C polymorphism in 5HT2A and Tourette syndrome]. (2001) (16)
A linkage study of schizophrenia with DNA markers from chromosome 8p21-p22 in 25 multiplex families (1996) (15)
No evidence for linkage between the X-chromosome marker DXS7 and schizophrenia. (1995) (15)
Genome‐wide association study of hoarding traits (2011) (15)
Interaction between effects of genes coding for dopamine and glutamate transmission on striatal and parahippocampal function (2013) (15)
Fronto-parietal white matter microstructural deficits are linked to performance IQ in a first-episode schizophrenia Han Chinese sample (2012) (15)
Debrisoquine 4-hydroxylase (CYP2D) locus and possible susceptibility to schizophrenia (1992) (15)
Clinical utility gene card for: 15q13.3 microdeletion syndrome (2014) (14)
Understanding the genetic predisposition to anorexia nervosa (1999) (14)
Failure to exclude a possible schizophrenia susceptibility locus on chromosome 13q14.1‐q32 in Southern African Bantu‐speaking families (1998) (14)
Correlation of miRNA expression with intensity of neuropathic pain in man (2019) (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)
Association analysis of STX1A gene variants in common forms of migraine (2012) (14)
PRODH gene is associated with executive function in schizophrenic families (2008) (14)
The dopamine D4 receptor in schizophrenia: an update (1996) (14)
Detection of metabolites in the white matter of frontal lobes and hippocampus with proton in first‐episode treatment‐naïve schizophrenia patients (2012) (14)
Novel brain expressed RNA identified at the MIR137 schizophrenia-associated locus (2017) (14)
Family-Based Analysis of Serotonin Transporter Gene Polymorphisms in Migraine With and Without Aura (2007) (14)
Factors of risk and maintenance for eating disorders: psychometric exploration of the cross-cultural questionnaire (CCQ) across five European countries. (2011) (13)
Clinical and Molecular Genetic Analysis of 19 Wolfram Syndrome Kindreds Demonstrating a Wide Spectrum of Mutations in WFS 1 (2007) (13)
Clinical utility gene card for: 16p13.11 microdeletion syndrome (2013) (13)
Linkage disequilibrium analysis of polymorphisms in the gene for myelin oligodendrocyte glycoprotein in Tourette's syndrome patients from a Chinese sample (2004) (13)
Associations between childhood maltreatment and inflammatory markers (2019) (13)
Animal Models — Disorders of Eating Behaviour and Body Composition (2001) (13)
Association study of POMC variants with body composition measures and nutrient choice. (2011) (12)
Functional neuroimaging and pharmacogenetic studies of clozapine's action at dopamine receptors. (1994) (12)
The impact of the Val 158 Met catechol-O-methyltransferase genotype on neural correlates of sad facial affect processing in patients with bipolar disorder and their relatives (2010) (12)
Dopamine D4 Receptors (1997) (12)
Author Correction: Expression-based drug screening of neural progenitor cells from individuals with schizophrenia (2018) (12)
Engineering in Genomics [variable number tandem repeats as agents of functional regulation in the genome] (2008) (12)
Cross‐species genetics converge to TLL2 for mouse avoidance behavior and human bipolar disorder (2013) (11)
FISH, flexible joints and panic: are anxiety disorders really expressions of instability in the human genome? (2002) (11)
The androgen receptor gene polyglycine repeat polymorphism is associated with memory performance in healthy Chinese individuals (2009) (11)
Pharmacogenetics in psychosis. (2003) (11)
Association study of the CACN1A4 (SCA6) triplet repeat and schizophrenia. (1999) (11)
Schizophrenia: the polygene princess and the pea (2008) (10)
Genetic underpinnings of sociability in the general population (2021) (10)
The Association between COMT, BDNF, and NRG1 and Premorbid Social Functioning in Patients with Psychosis, Their Relatives, and Controls (2012) (10)
No association between a promoter polymorphism in the noradrenaline transporter gene and anorexia nervosa. (2007) (10)
Publisher Correction: Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection (2019) (10)
Opening Pandora's box in the UK: a hypothetical pharmacogenetic test for clozapine. (2013) (10)
The DISC1 Ser704Cys polymorphism is associated with prefrontal function in healthy individuals (2008) (9)
The correlates of diagnostic instability in eating disorders: the role of psychopathology, environmental risk factors, personality and genes (2013) (9)
Susceptibility to bipolar affective disorders and unipolar depression is influenced by allelic variation of functional serotonin transporter expression (1996) (9)
A polymorphism in the promoter region of the dopamine D2 receptor gene (DRD2) and drug response: Association studies (1998) (9)
Affected sibling pair linkage analysis of qualitative and quantitative traits for schizophrenia on chromosome 22 in a Chinese population. (2001) (9)
CHRFAM7A copy number and 2-bp deletion polymorphisms and antisaccade performance. (2009) (8)
[Linkage analysis of susceptibility genes for familial schizophrenia on chromosome 1 in Chinese population]. (2002) (8)
Advances in the genetics of schizophrenia: will high-risk copy number variants be useful in clinical genetics or diagnostics? (2009) (8)
CNTF and psychiatric disorders (1996) (8)
Family-based association analysis of functional VNTR polymorphisms in the dopamine transporter gene in migraine with and without aura (2007) (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 functional MMP-9 microsatellite marker is not associated with episodic memory in humans. (2008) (8)
Failure to find linkage between schizophrenia and genetic markers on chromosome 21. (1993) (8)
Ill fitting genes: the biology of weight and shape control in relation to body composition and eating disorders (1997) (8)
The Spectrum of Eating Disorders in Humans (2001) (8)
Strong genetic evidence for a selective influence of GABAA receptors on a component of the bipolar disorder phenotype [Corrigendum] (2010) (7)
Altered Reward Reactivity as a Behavioural Endophenotype in Eating Disorders: A Pilot Investigation in Twins (2017) (7)
HLA-DQB1 6672G>C (rs113332494) is associated with clozapine-induced neutropenia and agranulocytosis in individuals of European ancestry (2021) (7)
Whole transcriptome in silico screening implicates cardiovascular and infectious disease in the mechanism of action underlying atypical antipsychotic side effects (2020) (6)
D4 polymorphisms in schizophrenic patients treated with clozapine (1995) (6)
Family-based linkage disequilibrium mapping using SNP marker haplotypes: application to a potential locus for schizophrenia at chromosome 22q11 (2000) (6)
DIDMOAD SYNDROME - CONFIRMATION OF LINKAGE TO CHROMOSOME-4P, EVIDENCE FOR LOCUS HETEROGENEITY AND A PATIENT WITH UNIPARENTAL ISODISOMY FOR CHROMOSOME-49 (1995) (6)
The genetics of cannabis involvement in humans: a genetic epidemiological perspective. (2006) (6)
Association analysis of GRK3 gene promoter variants in cocaine abuse (2007) (6)
Assessing 42 inflammatory markers in 321 control subjects and 887 major depressive disorder cases: BMI and other confounders and overall predictive ability for current depression (2018) (6)
Genetics of Schizophrenia — New Findings (1999) (5)
TractaViewer: a genome-wide tool for preliminary assessment of therapeutic target druggability (2019) (5)
BBGRE: brain and body genetic resource exchange (2013) (5)
High marker-density analyses of the α7-nicotinic cholinergic receptor subunit (CHRNA7) gene region on chromosome 15q13-q14 and 5′-rage cloning of fragments specific to CHRNA7 or its partial duplication (2000) (5)
Systematic search for major genes in schizophrenia: methodological issues and results from chromosome 12. (1995) (5)
Pharmacogenetics in Psychiatry Satellite Meeting at the American College of Neuropsychopharmacology, 2000 (2002) (5)
Identification and Potential Regulatory Properties of Evolutionary Conserved Regions (ECRs) at the Schizophrenia-Associated MIR137 Locus (2016) (5)
Interaction among genes influencing ethanol metabolism and sex is association with alcohol use disorders in a Tibet population (2010) (5)
Antipsychotic response prediction by genotype. (2000) (4)
Association between clozapine response and allelic variation in the 5-HT2A and 5-HT2C receptor genes (1996) (4)
No Association Between Bipolar Disorder Risk Polymorphisms in ANK3 and CACNA1C and Common Migraine (2011) (4)
Full-length transcript sequencing of human and mouse identifies widespread isoform diversity and alternative splicing in the cerebral cortex (2020) (4)
Gender-specific interactions between alcohol metabolism genes and severity of quantitative alcohol-related-traits in a Tibetan population (2011) (4)
No evidence of linkage disequilibrium between a CAG repeat in the SCA1 gene and schizophrenia in Caucasian and Chinese schizophrenic subjects. (1999) (4)
Effect of DISC 1 on the P 300 Waveform in Psychosis (2012) (4)
NRXN 1 deletions identified by array comparative genome hybridisation in a clinical case series – further understanding of the relevance of NRXN 1 to neurodevelopmental disorders (2013) (4)
No association between RFLPs at the porphobilinogen deaminase gene and schizophrenia (1992) (3)
SU38 A STUDY OF 42 INFLAMMATORY MARKERS IN 321 CONTROL SUBJECTS AND 887 MAJOR DEPRESSIVE DISORDER CASES: THE ROLE OF BMI AND OTHER CONFOUNDERS, AND THE PREDICTION OF CURRENT DEPRESSIVE EPISODE BY MACHINE LEARNING (2019) (3)
A Prospective Twin Registry in Southwestern China (TRiSC): Exploring the Effects of Genetic and Environmental Factors on Cognitive and Behavioral Development and Mental Health Wellbeing in Children and Adolescents (2009) (3)
Gene Environment and Developmental Issues in Eating Disorders (2006) (3)
Analysis of microsatellite markers at the UCP2/UCP3 locus on chromosome 11q13 in anorexia nervosa (2002) (3)
A transmission disequilibrium study on Catechol-O-Methyltransferase polymorphism in schizophrenia families (1996) (3)
A psychosocial risk factor model for female eating disorders: a European multicentre project (2014) (3)
5-HT2A gene promoter polymorphism and anorexia nervosa (1999) (3)
Corrigendum: Family-based linkage disequilibrium mapping using SNP marker haplotypes: Application to a potential locus for schizophrenia at chromosome 22q11 (Molecular Psychiatry (2000) 5 (77-84)) (2000) (3)
Association between the COMT gene and neurological abnormalities and poorer executive function in psychosis (2015) (2)
Analysis of the conserved Asp(114) residue of the dopamine D2 receptor in schizophrenic patient (1994) (2)
The Relationship of the Fat Controller to Eating Disorders (2000) (2)
Novel polymorphisms detected in the 5-HT3 receptor gene: Association studies with schizophrenia and clozapine response (1997) (2)
Gene X cannabis interaction: Case-only design analysis in a first-episode psychosis sample (2006) (2)
Correction: Investigation of common, low-frequency and rare genome-wide variation in anorexia nervosa (2017) (2)
Expression analysis of five schizophrenia candidate genes in post-mortem cerebellum samples using quantitative real time RT-PCR (2004) (2)
Major structural polymorphisms in the nicotinic acetylcholine receptor alpha-7 Subunit (CHRNA7) partial duplication on chromosome 15q13-q14. (2001) (2)
142 A linkage disequilibrium study of chromosome 4p16 and schizophrenia (1997) (2)
Co-segregation of schizophrenia and reifenstein syndrome (1993) (2)
Linkage studies of schizophrenia with markers of chromosome-11q (1991) (2)
DRD2 Ser311/Cys311 polymorphism in schizophrenia. (1994) (2)
Rare Variant Analysis of Human and Rodent Obesity Genes in Individuals with Severe Childhood Obesity (2017) (2)
Conference Report: Psychiatric Genomics Consortium Meeting: Pathways to Drugs, London, March 2017 (2018) (2)
Examination of the DRD2 (SER-CYS) variant in schizophrenia (1995) (2)
Neuroleptic sensitivity and enzyme deficiency in two schizophrenic brothers: A case report (1996) (2)
5 AN INTEGRATED GENETIC-EPIGENETIC ANALYSIS OF SCHIZOPHRENIA: EVIDENCE FOR CO-LOCALIZATION OF GENETIC ASSOCIATIONS AND DIFFERENTIAL DNA METHYLATION FROM A LARGE META-ANALYSIS OF WHOLE BLOOD DNA (2019) (2)
Individualisation of treatment: Genetic prediction of clozapine response (2000) (2)
235 Polymorphisms in the 5-HT2A receptor gene and promoter region associated with clozapine response (1997) (1)
15:00 BIOLOGICAL BASIS OF SENSITIVITY TO THE EFFECTS OF CANNABIS ON PSYCHOSIS: AKT1 AND DAT1 GENOTYPE MODULATES THE EFFECTS OF DELTA-9-TETRAHYDROCANNABINOL ON MIDBRAIN AND STRIATAL FUNCTION (2012) (1)
The Tower of Babel? An assessment of the development and state of genetic and SNP technologies. (2002) (1)
247 Apolipoprotein E and schizophrenia: Association with clinical response to clozapine (1997) (1)
EXPANDING THE ROLE OF COPY NUMBER VARIATION IN EPILEPSY PATHOLOGY (2012) (1)
Functional polymorphism of CYP2E1 gene and alcohol use disorders in a Tibetan population. (2008) (1)
Impulsivity in eating disorders and in their healthy sisters: Analysis of its relevance (2004) (1)
Association between brain structural endophenotypes of psychotic disorders and genotypic variation (2005) (1)
BDNF and COMT interaction in determining clinical presentation of first-episode psychosis: data from the PICOS-Veneto study (2011) (1)
A second novel polymorphism in the promotor region of the N-acetyltransferase gene (AA-NAT) is not associated with schizophrenia or bipolar affective disorder (1998) (1)
5HT 2a receptor T102C polymorphism and schizophrenia. (1996) (1)
Title Convergent lines of evidence support CAMKK 2 as a schizophrenia susceptibility gene (2014) (1)
Association study of INPP1, 5HTT, BDNF, AP-2B and GSK-3B gene variants and response to lithium prophylaxis in Bipolar Disorder (2004) (1)
Pharmacogenetics of Psychotropic Drugs: Clozapine response and genetic variation in neurotransmitter receptor targets (2002) (1)
SU102META-ANALYSIS OF CLOZAPINE-ASSOCIATED NEUTROPENIA AND AGRANULOCYTOSIS (2019) (1)
T50 Longitudinal Epigenetic Analysis Of Clozapine Use In Treatment-Resistant Schizophrenia: Data From The Crestar Consortium (2017) (1)
Hypermethylation in the ZBTB20 gene is associated with major depressive disorder (2014) (1)
Polymorphisms of COMT gene and cocaine abuse/dependence in a brazilian population study (2006) (1)
Short-term effects of antipsychotic treatment on cerebral function in drug-naive first-episode schzophrenia revealed by rFMRI (2010) (1)
Inheritance of a CAG/CTG repeat in the HKCA3 gene in families with bipolar affective disorder (1998) (1)
Large-scale analysis of DNA methylation identifies cellular alterations in blood from psychosis patients and molecular biomarkers of treatment-resistant schizophrenia (2020) (1)
SU116. Longitudinal Epigenetic Analysis of Clozapine Use in Treatment-Resistant Schizophrenia (2017) (1)
CNTF AND PSYCHIATRIC DISORDERS. AUTHORS' REPLY (1996) (1)
[A linkage analysis of quantitative trait loci for familial schizophrenia on chromosome 1]. (2002) (1)
Neurodegeneration and Diabetes: Nationwide Study of Wolfram (DIDMOAD) Syndrome (1996) (1)
Sudden impact? The human genome sequence and the pace of gene discovery in complex diseases (2001) (1)
Homozygosity at the DRD3 does not influence response to clozapine (1995) (1)
SU93 REPLICATION OF TWO INDEPENDENT LOCI IN HLA-DQB1 AND HLA-B CONTRIBUTING TO THE RISK OF CLOZAPINE-INDUCED AGRANULOCYTOSIS (2019) (1)
Linkage analysis of schizophrenia on chromosome 22 (1992) (1)
An integrated genetic-epigenetic analysis of schizophrenia: evidence for co-localization of genetic associations and differential DNA methylation (2016) (1)
The D3 receptor and improvement in positive symptoms of schizophrenia (2002) (1)
The alpha-7 nicotinic acetylcholine receptor subunit and schizophrenia: Beyond linkage evidence in a duplicated gene (2001) (1)
P0346 - Lifetime comorbidity of tobacco, alcohol and drug use in eating disorders: A European multicenter study (2008) (1)
P0347 - Individual and family eating patterns during childhood and early adolescence: A multicenter European study of associated eating disorder factors (2008) (1)
Dissecting the relationship between childhood abuse, personality traits and genetic markers in eating disorders using a discordant sister-pair design (2013) (1)
Low-frequency variation in TP53 has large effects on head circumference and intracranial volume (2019) (1)
Association of dysbindin with outcome measures in a cohort of Italian schizophrenic patients (2006) (0)
The dysbindin gene is associated with bipolar affective disorder (2005) (0)
THE IMPACT OF THE DUFFY-NULL GENOTYPE IN CLOZAPINE-ASSOCIATED NEUTROPENIA: A GENOME-WIDE ASSOCIATION STUDY IN INDIVIDUALS OF AFRICAN ANCESTRY (2019) (0)
Publisher Correction: Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection (2019) (0)
Educational achievement, cannabis use, and genotype in predicting psychosis (2006) (0)
Is there a link between schizophrenia and mutations at the fragile-X gene, FMR-1? (1993) (0)
The 5-HT 1C receptor gene and schizophrenia (1995) (0)
Investigation of an association between a CYP1A2 5 ' flanking SNP (T-3591G) and response to clozapine (2001) (0)
CYP2D6 gene dosage and typical antipsychotic intolerance, drug induced parkinsonism, and tardive dyskinesia (2005) (0)
Stable phenotypes : a developmental perspective (2004) (0)
ASSOCIATION BETWEEN COMT, BDNF AND LATERAL VENTRICULAR VOLUME IN SCHIZOPHRENIA AND BIPOLAR DISORDER (2008) (0)
Functional D4 polymorphism in schizophrenics treated with clozapine (1993) (0)
Effects of the DAT 3’UTR VNTR Genotype on Brain Function in Healthy Subjects and Patients with Schizophrenia (2009) (0)
Author response: DNA methylation meta-analysis reveals cellular alterations in psychosis and markers of treatment-resistant schizophrenia (2020) (0)
Association analysis between the DRD4 gene and anorexia nervosa. (2000) (0)
mp2010125x2 - 26 papges text file - supplement (2014) (0)
UK 10 K Consortium (2019) (0)
ReplicationStudyandMeta-AnalysisinEuropean SamplesSupportsAssociationofthe3p21.1Locuswith (2012) (0)
Can genes predict volumetric brain differences in schizophrenia (2006) (0)
S.18.02 Genetics of anorexia nervosa (2010) (0)
154 – Association between Neuregulin-1 and P300 wave deficits (an endophenotype for psychosis) (2008) (0)
Association of dysbindin gene with clinical and functioning outcome measures in a representative cohort of Italian schizophrenic patients (2007) (0)
NO ASSOCIATION BETWEEN COMT, BDNF AND NRG-1 POLYMORPHISMS AND P50 SENSORY GATING IN PSYCHOSIS (2010) (0)
Age at first birth in women is genetically associated with increased risk of schizophrenia (2018) (0)
Translating Genomewide Association Findings into New Therapeutics for Psychiatry 1 (2016) (0)
Identification and validation of biomarkers for Autism Spectrum Disorders: towards a shared understanding between academia, industry and regulatory authorities (2015) (0)
237 No association between a novel polymorphism in the 5-HT4 receptor gene and response to clozapine (1997) (0)
Analysis of serotonin transporter VNTR haplotypes in bipolar affective disorder (2006) (0)
Candidate transmission disequilibrium analysis for quantitative traits in tourette syndrome in a chinese family trio sample (2000) (0)
A meta-analysis of gene (5-HTT) × environment interactions in eating pathology using secondary data analyses (2016) (0)
Dopamine D3 receptor and improvement in positive symptoms of schizophrenia (2002) (0)
Genetic variation at three genetic loci involved in anorexia nervosa are associated with body weight regulation (2015) (0)
Does COMT promoter methylation regulate gene expression (2005) (0)
Title The differential clinical and neurocognitive profiles of COMTSNP rs 165599 genotypes in schizophrenia (2005) (0)
Interaction between childhood adversity and 5-HTTLPR polymorphism in psychosis (2006) (0)
Linkage map of schizophrenia 11q (1991) (0)
Replication of suggestive evidence linking the α7-nicotinic cholinergic receptor gene on chromosome 15gi3-q14 to schizophrenia in bantu and malay families (1998) (0)
Evaluating an association of RGS4 polymorphisms with schizophrenia: Mega-analysis of over 12,000 individuals from 11 international sites (2004) (0)
GENOMIC DISORDERS ANDDUPLICATION (2002) (0)
Genetic modulation of the acute psychological effects of cannabis in man (2011) (0)
P3-122 APOE-ε4 MODULATES LEVELS OF OMEGA-3 AND OMEGA-6 FATTYACIDS IN ALZHEIMER’S DISEASE DEMENTIA (2018) (0)
ASSOCIATION BETWEEN CANDIDATE GENES AND EEG ENDOPHENOTYPES FOR SCHIZOPHRENIA (2008) (0)
73 – Association between 2 bp deletion polymorphism in exon 6 of CHRFAM7A and the p300 endophenotype in schizophrenia (2008) (0)
An imaging genomics approach to endophenotype analysis of psychosis: Genetic analysis of verbal fluency, emotional face recognition and fractional anisotropy of white matter (2006) (0)
Association analysis between nACHR genes and schizophrenia patients with or without smoking (2006) (0)
Genetic mapping on chromosome 22 (1993) (0)
No evidence of association between a polymorphism in the COMT gene and clinical phenotypes of schizophrenia in China (2000) (0)
How Can Pharmacogenomics Biomarkers Be Translated into Patient Benefit (2015) (0)
Further evidence of transmission disequilibrium of the catechol-O-methyl transferase (COMT) gene in schizophrenia in a Chinese population (1998) (0)
D3 receptor polymorphisms and improvement in positive symptoms in schizophrenia (2002) (0)
Does puberty moderate the relationship between personality and eating disorders? (2015) (0)
Linkage disequilibrium mapping of chromosome 8, 13 and 22 linkage regions in schizophrenia using DNA pooling on Chinese and Scottish populations (1999) (0)
Genetic epidemiology 2: molecular genetics (2003) (0)
Genetic influences on brain physiology in schizophrenia (2005) (0)
DIFFERENTIAL EPISTATIC EFFECTS BETWEEN DAAO AND G72 IN HEALTHY CONTROLS AND PATIENTS WITH SCHIZOPHRENIA AND BIPOLAR DISORDER (2010) (0)
HLA-DQB1 6672 G>C is associated with the risk of clozapine-induced agranulocytosis in individuals of European ancestry (2020) (0)
No association between a variable number of tandem repeat (VNTR) in the 3 ' untranslated region of the dopamine transporter gene (DAT1) and bipolar affective disorder (1998) (0)
A first episode psychosis case-control genetic association study (2006) (0)
Duffy-null genotype in clozapine-associated neutropenia (2019) (0)
Analysis of candidate genes for prospectively assessed response to lithium in a collection of bipolar disorder patients from Sardinia (2006) (0)
Analysis of candidate genes for prospectively assessed response to lithium in a collection of bipolar disorder patients from Sardinia (2006) (0)
A combined population and family-based study of eight European populations demonstrates association between BDNF and eating disorders. (2003) (0)
234 Pharmacogenetic factors in treatment-resistant schizophrenia: The role of CYP2D6 variants (1997) (0)
Analysis of the NMDA receptor in schizophrenia (1997) (0)
No association between noradrenaline transporter gene and anorexia nervosa (2004) (0)
Open Access PRIMARY RESEARCH (2010) (0)
P0330 - Personality and psychopathological traits in spanish eating disorder males: A comparative study (2008) (0)
Evidence of genomic imprinting in families with Gilles de la Tourette syndrome in Chinese subjects (2001) (0)
withbipolar affective disorder (2011) (0)
Identification of variants in 15q13-qi4 predisposing to schizophrenia and bipolar affective disorder (2004) (0)
Linkage disequilibrium studies of D22S278 genotypes in 574 pedigrees (1996) (0)
Allelic association between a ser-9-gly polymorphism in the D3 receptor gene and schizophrenia (1996) (0)
Analyses of clozapine response and the 5-HT2 gene (1995) (0)
Linkage disequilibrium mapping of complex traits using SNP and microsatellite markers. (2000) (0)
Further evidence for association between polymorphisms in the 5-HT2A receptor gene and clozapine response (1998) (0)
Short-term effects of antipsychotic treatment on cerebral function in drug-naive first-episode schizophrenia revealed by rfMRI (2009) (0)
Transmission disequilibrium analysis of dopamine D3 and D4 receptors polymorphism (2004) (0)
Mapping complex disease phenotypes (2005) (0)
Does COMT polymorphism influence cognitive function in first episode psychosis (2006) (0)
University of Groningen Investigation of common , low-frequency and rare genome-wide variation in anorexia nervosa Kas (2017) (0)
PW01-153 - Effect Of Daao On Regional Brain Function In Healthy Individuals And Patients With Schizophrenia And Bipolar Disorder (2010) (0)
No association between polymorphisms of BDNF gene and schizophrenia in a Chinese population (2005) (0)
Primary researchSerum glutamine , set-shifting ability and anorexia nervosa (2015) (0)
Is there any association between polymorphisms of the dysbindin gene and lateral ventricular enlargement in psychosis (2011) (0)
176 – Stargazin involvement with bipolar disorder and response to lithium treatment (2008) (0)
Is dopa decarboxylase (DDC) a minor susceptibility gene for bipolar affective disorder (2000) (0)
Association study between genetic variants in the alpha- adrenergic receptor genes and bipolar affective disorder (1999) (0)
P01-89 - Preliminary Analysis of the Functional Consequences of the CACNA1C Gene Polymorphism on Emotional Processing in Bipolar Disorder (2010) (0)
Overview of the genetics of schizophrenia (2005) (0)
5-HT2A polymorphisms and mental disorders (1996) (0)
S-9-3 Pharmacological genetic association studies and clozapine response (1996) (0)
Family-based and case-control association analysis of dopamine D2, D4, serotonin 2A receptors, COMT and MAO-A genes with Gilles de la Tourette syndrome in Chinese subjects (2001) (0)
Association between psychoses and allelic variation in the 5-HT2C receptor gene (1996) (0)
Is serotonin involved in weight gain and metabolic syndromein psychosis (2006) (0)
Abstracts of the XXV World Congress of Psychiatric Genetics (WCPG)_ Oral Abstracts (2017) (0)
Brain structural endophenotypes of psychotic disorders and their association with genotypic variation (2004) (0)
Biomarkers of psychosis and their genetic basis (2011) (0)
Genetic mapping of 14 short tandem repeat polymorphisms on human chromosome 22 (1994) (0)
DISC1 affects prefrontal cortical function in healthy individuals (2008) (0)
Association of Neuregulin 1 rs3924999 with oculomotor endophenotypes for schizophrenia in healthy volunteers (2009) (0)
Is there a major gene for schizophrenia on chromosome 12? (1993) (0)
Title Abnormalities in connectivity of white-matter tracts in patientswith familial and non-familial schizophrenia (2011) (0)
Association between BDNF, NRG1 and DTNBP1 and outcome measures in an italian cohort of patients with schizophrenia (2005) (0)
Haplotype transmission disequilibrium in the alpha 7 nicotinic acetylcholine receptor subunit (CHRNA7) gene region in schizophrenia families. (2000) (0)
DOES THE DYSBINDIN GENE INFLUENCE HIPPOCAMPAL VOLUME IN PSYCHOSIS? (2010) (0)
Contribution of heritability to leanness and adiposity in inbred strains of mice (2004) (0)
RARE PATHOGENIC COPY NUMBER MUTATIONS IN MENTAL DISORDERS (2010) (0)
Polymorphisms in the 5-HTT gene and pituitary volume in first episode psychosis (2006) (0)
Catechol-O-Methyltransferase (comt) gene modulates the neural basis for the acute effects of cannabis on learning and psychosis (2009) (0)
Universitet Low-frequency variation in TP 53 has large effects on head circumference and intracranial (2019) (0)
Neurobiology of Disease The Schizophrenia Risk Allele C of the TCF 4 rs 9960767 Polymorphism Disrupts Sensorimotor Gating in Schizophrenia Spectrum and Healthy Volunteers (2011) (0)
mp2010125x1 - tables - supplement (2014) (0)
[Linkage disequilibrium analysis of chromosome 22 and schizophrenia in a Chinese population]. (2001) (0)
Characterization of mRNA isoform diversity in a transgenic model of tau pathology using targeted long‐read sequencing (2020) (0)
A meta-analysis of association between the Ser9Gly polymorphism in the DRD3 gene and schizophrenia (2004) (0)
Reelin as a candidate gene for schizophrenia (2003) (0)
Transcriptional signatures of progressive neuropathology in transgenic tau and amyloid mouse models (2019) (0)
Temperament in individuals at high risk for schizophrenia and the relationship with character to schizotypy multidimensionality (2005) (0)
Association between a 2030-G/A substitution in the human myo-inositol monophosphatase gene (IMPA) and bipolar disorder and schizophrenia (1999) (0)
Association study of the DOPA decarboxylase gene in bipolar affective disorder and schizophrenia (1999) (0)
AN EPIGENOME-WIDE ASSOCIATION STUDY OF CLOZAPINE USE IN TREATMENT-RESISTANT SCHIZOPHRENIA (2017) (0)
VKučinskas-2001-2016 (2016) (0)
A GTP1 function variant associated with cocaine abuse in the Brazilian population (2005) (0)
Association Between Monoamine Oxidase A Gene (CA)n Polymorphism and Risk for Schizophrenia in the Chinese Population (2004) (0)
Genetic variation in the 5-HT3 receptor gene: No association with schizophrenia or drug response (1998) (0)
ASSESSING TREM2 FUNCTION IN ALZHEIMER’S DISEASE WITH RNA-SEQ (2017) (0)
Linkage disequilibrium mapping of chromosome 22 in schizophrenia using DNA pooling on Chinese and Scottish populations (1998) (0)
244 An investigation of the GLUR6 receptor gene (GRIK2) in schizophrenia (1997) (0)
ASSESSING TREM2 RISK VARIANTS IN ALZHEIMER'S DISEASE WITH RNA-SEQ (2016) (0)
THE ROLE OF COMT GENE IN VULNERABILITY TO AFFECTIVE SYMPTOMS IN SCHIZOPHRENIA (2008) (0)
NAHR-mediated duplications and deletions of 16p13.11. (2013) (0)
Further suggestive evidence for linkage of schizophrenia to markers on chromosome 13 (1996) (0)
Selective serotonin reuptake inhibitors in anorexia nervosa (1997) (0)
Therapygenetics: predicting response to CBT in child anxiety from specific genetic markers (2012) (0)
are anxiety disorders really expressions are anxiety disorders really expressions of instability in the human genome? of instability in the human genome? (2002) (0)
Transmission disequilibrium analysis of the HLA region in schizophrenia in a chinese population (2000) (0)
Childhood Retrospective Personality Questionnaire (2019) (0)
Severity of Alcohol Dependence Questionnaire--Chinese Han Version (2015) (0)
The role of COMT functional and promoter polymorphisms in cocaine addiction : analysis of a large Brazilian case control sample (2006) (0)
The NMDAR1 receptor gene and schizophrenia (1998) (0)
Applying polygenic risk scoring for psychiatric disorders to a large family with bipolar disorder and major depressive disorder (2018) (0)
Sustained attention deficits in first-degree relatives of schizophrenic patients and drug naive first-onset schizophrenic patients: An endophenotypes for genetic susceptibility to schizophrenia (2005) (0)
Associations of six functional genes and obsessive-compulsive disorder with different onset age (2004) (0)
Transcriptional Signatures of Progressive Neuropathology in Transgenic Models of Tau and Amyloid Pathology (2019) (0)

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What Schools Are Affiliated With David Andrew Collier?

David Andrew Collier is affiliated with the following schools: