Patrick F Sullivan
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Computer Science
Patrick F Sullivan's Degrees
- PhD Computer Science Stanford University
- Masters Computer Science University of California, Berkeley
- Bachelors Computer Science University of California, Berkeley
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(Suggest an Edit or Addition)Patrick F Sullivan'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
- Biological Insights From 108 Schizophrenia-Associated Genetic Loci (2014) (6445)
- Common polygenic variation contributes to risk of schizophrenia and bipolar disorder (2009) (4437)
- Genetic epidemiology of major depression: review and meta-analysis. (2000) (2961)
- Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis (2013) (2439)
- Clonal hematopoiesis and blood-cancer risk inferred from blood DNA sequence. (2014) (2344)
- Schizophrenia as a complex trait: evidence from a meta-analysis of twin studies. (2003) (2095)
- 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)
- Genome-wide association study identifies five new schizophrenia loci (2011) (1680)
- Meta-analysis of the heritability of human traits based on fifty years of twin studies (2015) (1545)
- Rare chromosomal deletions and duplications increase risk of schizophrenia (2008) (1506)
- Rare chromosomal deletions and duplications increase risk of schizophrenia (2008) (1506)
- Genome-wide Association Analysis Identifies 14 New Risk Loci for Schizophrenia (2013) (1455)
- A polygenic burden of rare disruptive mutations in schizophrenia (2014) (1371)
- Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder (2018) (1248)
- Integrative approaches for large-scale transcriptome-wide association studies (2015) (1235)
- Genome-wide meta-analysis identifies new loci and functional pathways influencing Alzheimer’s disease risk (2019) (1232)
- Common genetic determinants of schizophrenia and bipolar disorder in Swedish families: a population-based study (2009) (1190)
- Identification of common genetic risk variants for autism spectrum disorder (2019) (1140)
- 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)
- Genome-wide meta-analyses identify multiple loci associated with smoking behavior (2010) (1107)
- Genetic architectures of psychiatric disorders: the emerging picture and its implications (2012) (1102)
- Genome-wide meta-analysis of depression identifies 102 independent variants and highlights the importance of the prefrontal brain regions (2018) (1090)
- Genome-wide association study identifies 30 Loci Associated with Bipolar Disorder (2017) (998)
- Genome-wide association study identifies 30 Loci Associated with Bipolar Disorder (2017) (998)
- A mega-analysis of genome-wide association studies for major depressive disorder (2013) (979)
- Large-scale genome-wide association analysis of bipolar disorder identifies a new susceptibility locus near ODZ4 (2011) (929)
- Gene Expression Elucidates Functional Impact of Polygenic Risk for Schizophrenia (2016) (831)
- 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)
- Genome-wide association meta-analysis in 269,867 individuals identifies new genetic and functional links to intelligence (2018) (705)
- Microduplications of 16p11.2 are Associated with Schizophrenia (2009) (685)
- Psychiatric genome-wide association study analyses implicate neuronal, immune and histone pathways (2015) (676)
- Estimating the proportion of variation in susceptibility to schizophrenia captured by common SNPs (2012) (599)
- Prevalence, heritability, and prospective risk factors for anorexia nervosa. (2006) (539)
- Evaluating the comparability of gene expression in blood and brain (2006) (518)
- Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes (2017) (517)
- Partitioning heritability of regulatory and cell-type-specific variants across 11 common diseases. (2014) (510)
- Discovery and statistical genotyping of copy-number variation from whole-exome sequencing depth. (2012) (496)
- The genetic epidemiology of smoking. (1999) (467)
- Integrative functional genomic analysis of human brain development and neuropsychiatric risks (2018) (464)
- A population-based twin study in women of smoking initiation and nicotine dependence (1999) (459)
- Genomewide association studies: history, rationale, and prospects for psychiatric disorders. (2009) (453)
- Unraveling the polygenic architecture of complex traits using blood eQTL metaanalysis (2018) (451)
- Meta-analysis of genome-wide association studies for neuroticism in 449,484 individuals identifies novel genetic loci and pathways (2018) (450)
- Psychiatric Genomics: An Update and an Agenda. (2018) (449)
- Genome-wide association study of major depressive disorder: new results, meta-analysis, and lessons learned (2010) (430)
- Genetic identification of brain cell types underlying schizophrenia (2017) (424)
- Genome-wide association analyses of risk tolerance and risky behaviors in over 1 million individuals identify hundreds of loci and shared genetic influences (2019) (421)
- The Genome Architecture of the Collaborative Cross Mouse Genetic Reference Population (2012) (416)
- The Swedish Twin Registry in the Third Millennium: An Update (2006) (413)
- Genomewide Association for Major Depressive Disorder: A possible role for the presynaptic protein Piccolo (2008) (410)
- Exome sequencing and the genetic basis of complex traits (2012) (409)
- Genome-wide analysis of insomnia in 1,331,010 individuals identifies new risk loci and functional pathways (2019) (396)
- A structural variation reference for medical and population genetics (2020) (394)
- Increased burden of ultra-rare protein-altering variants among 4,877 individuals with schizophrenia (2016) (381)
- Meta-analysis of genome-wide association studies for personality (2012) (369)
- Genome-wide association study of depression phenotypes in UK Biobank identifies variants in excitatory synaptic pathways (2018) (363)
- 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)
- Significant Locus and Metabolic Genetic Correlations Revealed in Genome-Wide Association Study of Anorexia Nervosa. (2017) (357)
- Eating disorders and antecedent anxiety disorders: a controlled study (1997) (354)
- Quantifying prion disease penetrance using large population control cohorts (2016) (352)
- No Support for Historical Candidate Gene or Candidate Gene-by-Interaction Hypotheses for Major Depression Across Multiple Large Samples. (2019) (345)
- Genome-wide association analysis identifies 30 new susceptibility loci for schizophrenia (2017) (341)
- Spurious Genetic Associations (2007) (335)
- Twin studies of eating disorders: a review. (2000) (332)
- Comparative genetic architectures of schizophrenia in East Asian and European populations (2018) (329)
- Transcriptome-wide association study of schizophrenia and chromatin activity yields mechanistic disease insights (2016) (327)
- Heritability and Genomics of Gene Expression in Peripheral Blood (2014) (325)
- Polygenic dissection of diagnosis and clinical dimensions of bipolar disorder and schizophrenia (2013) (325)
- Poor replication of candidate genes for major depressive disorder using genome-wide association data (2011) (317)
- Genome-wide association study identifies eight risk loci and implicates metabo-psychiatric origins for anorexia nervosa (2019) (314)
- New models of collaboration in genome-wide association studies: the Genetic Association Information Network (2007) (313)
- The PsychENCODE project (2015) (303)
- Genomewide association for schizophrenia in the CATIE study: results of stage 1 (2008) (301)
- The relation between eating disorders and components of perfectionism. (2003) (294)
- Evaluating Historical Candidate Genes for Schizophrenia (2015) (293)
- Latent class analysis of lifetime depressive symptoms in the national comorbidity survey. (1998) (287)
- All SNPs Are Not Created Equal: Genome-Wide Association Studies Reveal a Consistent Pattern of Enrichment among Functionally Annotated SNPs (2013) (284)
- Large-scale cis- and trans-eQTL analyses identify thousands of genetic loci and polygenic scores that regulate blood gene expression (2021) (284)
- A genome-wide association study of anorexia nervosa (2014) (284)
- Fine mapping of ZNF804A and genome-wide significant evidence for its involvement in schizophrenia and bipolar disorder (2011) (280)
- Medical and psychiatric morbidity in obese women with and without binge eating. (2002) (267)
- Genome-wide Association Studies in Ancestrally Diverse Populations: Opportunities, Methods, Pitfalls, and Recommendations (2019) (265)
- The Psychiatric GWAS Consortium: Big Science Comes to Psychiatry (2010) (256)
- Single nucleotide polymorphism genotyping: biochemistry, protocol, cost and throughput (2003) (255)
- Defining the Genetic, Genomic, Cellular, and Diagnostic Architectures of Psychiatric Disorders (2019) (250)
- Causes and recovery in anorexia nervosa: the patient's perspective. (2003) (248)
- Family history of schizophrenia and bipolar disorder as risk factors for autism. (2012) (247)
- A twin study of genetic and environmental influences on tobacco initiation, regular tobacco use and nicotine dependence (2004) (246)
- Copy number variation in schizophrenia in Sweden (2014) (245)
- Heritability of binge-eating and broadly defined bulimia nervosa (1998) (244)
- Genome-wide association study of over 40,000 bipolar disorder cases provides new insights into the underlying biology (2021) (240)
- Genome-wide association study in a Swedish population yields support for greater CNV and MHC involvement in schizophrenia compared with bipolar disorder (2012) (232)
- Discovery of the first genome-wide significant risk loci for ADHD (2017) (229)
- Chronic widespread pain and its comorbidities: a population-based study. (2006) (229)
- Fertility and reproduction in women with anorexia nervosa: a controlled study. (1999) (224)
- Polygenic Risk Score, Parental Socioeconomic Status, Family History of Psychiatric Disorders, and the Risk for Schizophrenia: A Danish Population-Based Study and Meta-analysis. (2015) (224)
- Methylome-wide association study of schizophrenia: identifying blood biomarker signatures of environmental insults. (2014) (221)
- Extremely low-coverage sequencing and imputation increases power for genome-wide association studies (2012) (217)
- Genome-wide association study of alcohol dependence. (2009) (216)
- A framework for interpreting genome-wide association studies of psychiatric disorders (2009) (213)
- Outcome of anorexia nervosa: eating attitudes, personality, and parental bonding. (2000) (210)
- zCall: a rare variant caller for array-based genotyping: Genetics and population analysis (2012) (209)
- A population-based twin study of functional somatic syndromes (2008) (206)
- Joint Analysis of Psychiatric Disorders Increases Accuracy of Risk Prediction for Schizophrenia, Bipolar Disorder, and Major Depressive Disorder (2015) (206)
- Genetic influences on schizophrenia and subcortical brain volumes: large-scale proof-of-concept and roadmap for future studies (2016) (198)
- Cross-disorder genomewide analysis of schizophrenia, bipolar disorder, and depression. (2010) (197)
- Common Disease Is More Complex Than Implied by the Core Gene Omnigenic Model (2018) (191)
- Analyses of Allele-Specific Gene Expression in Highly Divergent Mouse Crosses Identifies Pervasive Allelic Imbalance (2015) (187)
- Importance of genetic influences on chronic widespread pain. (2006) (184)
- Genome-wide Association for Major Depression Through Age at Onset Stratification: Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium☆ (2017) (183)
- Effect of polygenic risk scores on depression in childhood trauma (2014) (183)
- The contribution of rare variants to risk of schizophrenia in individuals with and without intellectual disability (2017) (182)
- Genome-wide association of major depression: description of samples for the GAIN Major Depressive Disorder Study: NTR and NESDA biobank projects (2008) (181)
- An empirical study of the classification of eating disorders. (2000) (179)
- The use of race variables in genetic studies of complex traits and the goal of reducing health disparities: a transdisciplinary perspective. (2005) (176)
- Gene expression in major depressive disorder (2016) (175)
- Meta-analysis of genome-wide association data of bipolar disorder and major depressive disorder (2011) (173)
- Susceptibility genes for nicotine dependence: a genome scan and followup in an independent sample suggest that regions on chromosomes 2, 4, 10, 16, 17 and 18 merit further study (1999) (172)
- Outcome of anorexia nervosa: a case-control study. (1998) (172)
- Heterogeneity of postpartum depression: a latent class analysis. (2015) (172)
- Genetic Identification of Cell Types Underlying Brain Complex Traits Yields Insights Into the Etiology of Parkinson’s Disease (2019) (171)
- Temperament in eating disorders. (1995) (171)
- Genetic and environmental contributions to obesity and binge eating. (2003) (171)
- Clinical phenotypes of perinatal depression and time of symptom onset: analysis of data from an international consortium. (2017) (169)
- Catechol o-methyltransferase, serotonin transporter, and tryptophan hydroxylase gene polymorphisms in bipolar disorder patients with and without comorbid panic disorder. (2002) (168)
- Recurrence risks for schizophrenia in a Swedish National Cohort (2006) (165)
- Functional gene group analysis identifies synaptic gene groups as risk factor for schizophrenia (2011) (165)
- Genetic risk profiles for depression and anxiety in adult and elderly cohorts (2010) (163)
- A genome-wide association study of Cloninger's temperament scales: Implications for the evolutionary genetics of personality (2010) (163)
- The Mouse Universal Genotyping Array: From Substrains to Subspecies (2015) (162)
- Genomewide pharmacogenomic study of metabolic side effects to antipsychotic drugs (2010) (160)
- Population structure, migration, and diversifying selection in the Netherlands (2013) (158)
- Genetic Studies of Major Depressive Disorder: Why Are There No Genome-wide Association Study Findings and What Can We Do About It? (2014) (156)
- The Genetics of Schizophrenia (2005) (156)
- False discoveries and models for gene discovery. (2003) (156)
- Genome-Wide Association Study Implicates Chromosome 9q21.31 as a Susceptibility Locus for Asthma in Mexican Children (2009) (154)
- Rare coding variants in ten genes confer substantial risk for schizophrenia (2022) (154)
- Genomewide Pharmacogenomic Analysis of Response to Treatment with Antipsychotics (2009) (150)
- A methylome-wide study of aging using massively parallel sequencing of the methyl-CpG-enriched genomic fraction from blood in over 700 subjects. (2014) (149)
- Patterns of remission, continuation and incidence of broadly defined eating disorders during early pregnancy in the Norwegian Mother and Child Cohort Study (MoBa) (2007) (149)
- Predictors of 1-year treatment outcome in bulimia nervosa. (1998) (148)
- A comprehensive family-based replication study of schizophrenia genes. (2013) (144)
- Deletion of TOP3β, a component of FMRP-containing mRNPs, contributes to neurodevelopmental disorders (2013) (144)
- Genomics of 1 million parent lifespans implicates novel pathways and common diseases and distinguishes survival chances (2018) (144)
- Identification of a high-risk haplotype for the dystrobrevin binding protein 1 (DTNBP1) gene in the Irish study of high-density schizophrenia families. (2003) (143)
- Predictors of the development of bulimia nervosa in women with anorexia nervosa. (1997) (143)
- The subtypes of major depression in a twin registry. (2002) (141)
- Clozapine-induced agranulocytosis is associated with rare HLA-DQB1 and HLA-B alleles (2014) (141)
- Genomes of the Mouse Collaborative Cross (2017) (141)
- Mendelian randomization integrating GWAS and eQTL data reveals genetic determinants of complex and clinical traits (2018) (139)
- Feeling Bad in More Ways than One: Comorbidity Patterns of Medically Unexplained and Psychiatric Conditions (2007) (138)
- Psychiatric and medical symptoms in binge eating in the absence of compensatory behaviors. (2004) (137)
- A Genetic Investigation of Sex Bias in the Prevalence of Attention-Deficit/Hyperactivity Disorder (2017) (136)
- Genome-wide association study of smoking initiation and current smoking. (2009) (136)
- Meta-analysis of genome-wide association studies with overlapping subjects. (2009) (135)
- The Antipsychotic Olanzapine Interacts with the Gut Microbiome to Cause Weight Gain in Mouse (2014) (134)
- seeQTL: a searchable database for human eQTLs (2011) (134)
- Gene expression imputation across multiple brain regions provides insights into schizophrenia risk (2019) (134)
- Premorbid predictors of chronic fatigue. (2006) (134)
- The relationship among three models of personality psychopathology: DSM-III-R personality disorder, TCI scores and DSQ defences (1999) (133)
- The role of exposure with response prevention in the cognitive-behavioural therapy for bulimia nervosa (1998) (133)
- Genome-wide association study of suicide attempts in mood disorder patients. (2010) (132)
- Sex differences in the human peripheral blood transcriptome (2014) (132)
- Evidence that duplications of 22q11.2 protect against schizophrenia (2013) (130)
- Borderline personality disorder in major depression: symptomatology, temperament, character, differential drug response, and 6-month outcome. (2003) (126)
- Genome-wide association study of post-traumatic stress disorder reexperiencing symptoms in >165,000 US veterans (2019) (126)
- CommonMind Consortium provides transcriptomic and epigenomic data for Schizophrenia and Bipolar Disorder (2019) (126)
- Temperament, Character, and Personality Disorder in Bulimia Nervosa (1995) (126)
- Exome Aggregation Consortium (2016) (125)
- Genomewide Association Study of Movement-Related Adverse Antipsychotic Effects (2010) (125)
- A Twin Study of Chronic Fatigue (2001) (124)
- Six months of treatment for depression: outcome and predictors of the course of illness. (2010) (122)
- A randomized controlled trial of motivational enhancement therapy (MET) for mild to moderate alcohol dependence. (2001) (121)
- Sequencing and de novo assembly of 150 genomes from Denmark as a population reference (2017) (118)
- Runs of Homozygosity Implicate Autozygosity as a Schizophrenia Risk Factor (2012) (117)
- Genome-Wide Pharmacogenomic Study of Neurocognition As an Indicator of Antipsychotic Treatment Response in Schizophrenia (2011) (115)
- The epidemiology and classification of bulimia nervosa (1998) (114)
- Translating genome-wide association findings into new therapeutics for psychiatry (2016) (113)
- Current Developments in the Genetics of Autism: From Phenome to Genome (2008) (113)
- Genomewide linkage study in the Irish affected sib pair study of alcohol dependence: evidence for a susceptibility region for symptoms of alcohol dependence on chromosome 4 (2006) (113)
- Birth outcomes in women with eating disorders in the Norwegian Mother and Child cohort study (MoBa). (2009) (112)
- Genetic case-control association studies in neuropsychiatry. (2001) (112)
- The genetic association between personality and major depression or bipolar disorder. A polygenic score analysis using genome-wide association data (2011) (111)
- Lifetime comorbidity of alcohol dependence in women with bulimia nervosa. (1997) (110)
- Evaluation of Analyses of Univariate Discrete Twin Data (2002) (107)
- Genetic correlation between amyotrophic lateral sclerosis and schizophrenia (2017) (107)
- Reproducible Genetic Risk Loci for Anxiety: Results From ∼200,000 Participants in the Million Veteran Program. (2020) (106)
- Evaluation of chromatin accessibility in prefrontal cortex of individuals with schizophrenia (2018) (106)
- The genomics of schizophrenia: update and implications. (2013) (106)
- Common risk variants identified in autism spectrum disorder (2017) (106)
- Recent advances in the neurobiology of schizophrenia. (2003) (105)
- Schizophrenia genetics: where next? (2011) (105)
- Hypothesis-driven candidate genes for schizophrenia compared to genome-wide association results (2011) (104)
- Expanding the ‘central dogma’: the regulatory role of nonprotein coding genes and implications for the genetic liability to schizophrenia (2005) (103)
- High density methylation QTL analysis in human blood via next-generation sequencing of the methylated genomic DNA fraction (2015) (101)
- LifeGene—a large prospective population-based study of global relevance (2010) (101)
- Landscape of Conditional eQTL in Dorsolateral Prefrontal Cortex and Co-localization with Schizophrenia GWAS (2018) (100)
- Specific glial functions contribute to schizophrenia susceptibility. (2014) (100)
- Adverse life events, psychiatric history, and biological predictors of postpartum depression in an ethnically diverse sample of postpartum women (2017) (100)
- Polygenic overlap between schizophrenia risk and antipsychotic response: a genomic medicine approach. (2016) (99)
- The Genetics of the Mood Disorder Spectrum: Genome-wide Association Analyses of More Than 185,000 Cases and 439,000 Controls (2018) (99)
- Childhood sexual abuse in women with bulimia. (1989) (98)
- Genome-wide association study of exercise behavior in Dutch and American adults. (2009) (97)
- No association between novelty seeking and the type 4 dopamine receptor gene (DRD4) in two New Zealand samples. (1998) (97)
- Questions about DISC1 as a genetic risk factor for schizophrenia (2013) (97)
- Genetic epidemiology of binging and vomiting (1998) (96)
- Environmental pollution is associated with increased risk of psychiatric disorders in the US and Denmark (2019) (96)
- Food cravers: characteristics of those who binge. (1998) (96)
- Genetic Differences in the Immediate Transcriptome Response to Stress Predict Risk-Related Brain Function and Psychiatric Disorders (2015) (95)
- Estimation of SNP heritability from dense genotype data. (2013) (94)
- MBD-seq as a cost-effective approach for methylome-wide association studies: demonstration in 1500 case--control samples. (2012) (92)
- Is Swedish snus associated with smoking initiation or smoking cessation? (2005) (92)
- Complement genes contribute sex-biased vulnerability in diverse illnesses (2020) (92)
- Patterns and predictors of remission, response and recovery in major depression treated with fluoxetine or nortriptyline. (2001) (91)
- Temperament, childhood environment and psychopathology as risk factors for avoidant and borderline personality disorders. (2003) (91)
- Uncovering the Genetic Architecture of Major Depression (2019) (91)
- Association study of 182 candidate genes in anorexia nervosa (2010) (91)
- The EPDS-Lifetime: assessment of lifetime prevalence and risk factors for perinatal depression in a large cohort of depressed women (2013) (90)
- Transcript expression-aware annotation improves rare variant interpretation (2020) (89)
- Genome-wide association studies: a primer (2009) (89)
- An Analysis of Two Genome-wide Association Meta-analyses Identifies a New Locus for Broad Depression Phenotype (2017) (89)
- Heritability of Perinatal Depression and Genetic Overlap With Nonperinatal Depression. (2015) (88)
- Characteristics of repeat users of a psychiatric emergency service. (1993) (88)
- Does Childhood Trauma Moderate Polygenic Risk for Depression? A Meta-analysis of 5765 Subjects From the Psychiatric Genomics Consortium (2017) (87)
- Genome-wide association study of antipsychotic induced QTc interval prolongation (2010) (87)
- Multivariate Phenotype Association Analysis by Marker‐Set Kernel Machine Regression (2012) (87)
- Converging Genetic and Functional Brain Imaging Evidence Links Neuronal Excitability to Working Memory, Psychiatric Disease, and Brain Activity (2014) (86)
- Association of ADH and ALDH genes with alcohol dependence in the Irish Affected Sib Pair Study of alcohol dependence (IASPSAD) sample. (2008) (86)
- Candidate genes for nicotine dependence via linkage, epistasis, and bioinformatics (2004) (86)
- Evaluating drug targets through human loss-of-function genetic variation (2019) (86)
- Haplotypes of four novel single nucleotide polymorphisms in the nicotinic acetylcholine receptor beta2-subunit (CHRNB2) gene show no association with smoking initiation or nicotine dependence. (2000) (86)
- NCAM1 and Neurocognition in Schizophrenia (2007) (86)
- Joint Contributions of Rare Copy Number Variants and Common SNPs to Risk for Schizophrenia. (2019) (85)
- Genomewide association for schizophrenia in the CATIE study: results of stage 1 (2009) (85)
- Obesity remodels activity and transcriptional state of a lateral hypothalamic brake on feeding (2019) (84)
- Latent class analysis of functional somatic symptoms in a population-based sample of twins. (2010) (84)
- Puzzling over schizophrenia: Schizophrenia as a pathway disease (2012) (84)
- Total cholesterol and suicidality in depression (1994) (84)
- GWA study data mining and independent replication identify cardiomyopathy-associated 5 (CMYA5) as a risk gene for schizophrenia (2011) (83)
- Predictors of rapid and sustained response to cognitive-behavioral therapy for bulimia nervosa. (1999) (83)
- CNV analysis in a large schizophrenia sample implicates deletions at 16p12.1 and SLC1A1 and duplications at 1p36.33 and CGNL1 (2013) (83)
- Genetic and Phenotypic Stability of Measures of Neuroticism Over 22 Years (2007) (82)
- Cigarettes and oral snuff use in Sweden: Prevalence and transitions. (2006) (82)
- Impact of Definition on Prevalence of Food Cravings in a Random Sample of Young Women (1997) (81)
- Studying gene and gene-environment effects of uncommon and common variants on continuous traits: a marker-set approach using gene-trait similarity regression. (2011) (81)
- Arginine Vasopressin Is Associated with Hypercortisolemia and Suicide Attempts in Depression (1997) (80)
- Obstetrical, pregnancy and socio-economic predictors for new-onset severe postpartum psychiatric disorders in primiparous women (2017) (80)
- Ultra-rare disruptive and damaging mutations influence educational attainment in the general population (2016) (79)
- Lifetime anxiety disorders in women with bulimia nervosa. (1996) (78)
- The epidemiology of chronic fatigue in the Swedish Twin Registry (2005) (78)
- Characterising the loss-of-function impact of 5’ untranslated region variants in 15,708 individuals (2019) (78)
- Association of the tryptophan hydroxylase gene with smoking initiation but not progression to nicotine dependence. (2001) (77)
- Genetic influences on eight psychiatric disorders based on family data of 4 408 646 full and half-siblings, and genetic data of 333 748 cases and controls (2018) (77)
- TAMAL: an integrated approach to choosing SNPs for genetic studies of human complex traits (2006) (77)
- Quantifying the Impact of Rare and Ultra-rare Coding Variation across the Phenotypic Spectrum. (2018) (76)
- Drug use in women with anorexia and bulimia nervosa (1992) (76)
- A Multi-Megabase Copy Number Gain Causes Maternal Transmission Ratio Distortion on Mouse Chromosome 2 (2015) (75)
- Flexible and robust co-regularized multi-domain graph clustering (2013) (75)
- Familial Clustering of Major Depression and Anxiety Disorders in Australian and Dutch Twins and Siblings (2005) (75)
- Lower birth weight indicates higher risk of autistic traits in discordant twin pairs (2011) (74)
- Non-coding variability at the APOE locus contributes to the Alzheimer’s risk (2019) (74)
- Integrated Bayesian analysis of rare exonic variants to identify risk genes for schizophrenia and neurodevelopmental disorders (2017) (73)
- The Genetic Structure of the Swedish Population (2011) (73)
- Extensions to the Modeling of Initiation and Progression: Applications to Substance Use and Abuse (2006) (72)
- Genome-wide gene-environment analyses of major depressive disorder and reported lifetime traumatic experiences in UK Biobank (2019) (72)
- Robust Hi-C Maps of Enhancer-Promoter Interactions Reveal the Function of Non-coding Genome in Neural Development and Diseases. (2020) (71)
- Latent class analysis of symptoms associated with chronic fatigue syndrome and fibromyalgia (2002) (70)
- Reciprocal Duplication of the Williams-Beuren Syndrome Deletion on Chromosome 7q11.23 Is Associated with Schizophrenia (2014) (70)
- Applying polygenic risk scores to postpartum depression (2014) (70)
- Chronic fatigue in a population sample: definitions and heterogeneity (2005) (69)
- A meta-analysis of gene expression quantitative trait loci in brain (2014) (69)
- The Relationship Between Polygenic Risk Scores and Cognition in Schizophrenia (2019) (69)
- The effect of LRRK2 loss-of-function variants in humans (2020) (69)
- Personality and dimensions of dietary restraint. (1998) (68)
- Initial manifestations of disordered eating behavior: dieting versus binging. (1997) (68)
- Simulating association studies: a data-based resampling method for candidate regions or whole genome scans (2007) (67)
- Genome-wide association studies in psychiatry: what have we learned? (2013) (67)
- Ethnic Stratification of the Association of RGS4 Variants with Antipsychotic Treatment Response in Schizophrenia (2008) (67)
- Modeling psychiatric disorders: from genomic findings to cellular phenotypes (2016) (67)
- Implication of a rare deletion at distal 16p11.2 in schizophrenia. (2013) (66)
- Contributions of common genetic variants to risk of schizophrenia among individuals of African and Latino ancestry (2019) (65)
- A genome scan of neuroticism in nicotine dependent smokers (2005) (63)
- HUGIn: Hi-C Unifying Genomic Interrogator (2017) (63)
- The genetics of anorexia nervosa. (2007) (63)
- A genome-wide association study of kynurenic acid in cerebrospinal fluid: implications for psychosis and cognitive impairment in bipolar disorder (2015) (62)
- Genetic effects influencing risk for major depressive disorder in China and Europe (2017) (62)
- Functional Architectures of Local and Distal Regulation of Gene Expression in Multiple Human Tissues. (2017) (61)
- A Comparison of Ten Polygenic Score Methods for Psychiatric Disorders Applied Across Multiple Cohorts (2020) (60)
- Allelic differences between Europeans and Chinese for CREB1 SNPs and their implications in gene expression regulation, hippocampal structure and function, and bipolar disorder susceptibility (2014) (60)
- Twin analyses of chronic fatigue in a Swedish national sample (2005) (60)
- Borderline Personality Disorder in Major Depression (1994) (60)
- Protein instability, haploinsufficiency, and cortical hyper-excitability underlie STXBP1 encephalopathy (2018) (60)
- Evidence of causal effect of major depression on alcohol dependence: Findings from the Psychiatric Genomics Consortium (2018) (59)
- Fifty Years of Twin Studies : A Meta-Analysis of the Heritability of Human Traits (2015) (59)
- The STAGE cohort: a prospective study of tobacco use among Swedish twins. (2008) (58)
- Attentional switching forms a genetic link between attention problems and autistic traits in adults (2012) (58)
- New data and an old puzzle: the negative association between schizophrenia and rheumatoid arthritis. (2015) (58)
- Typology of common psychiatric syndromes (1998) (58)
- Fine mapping of ZNF 804 A and genome-wide significant evidence for its involvement in schizophrenia and bipolar disorder (2011) (57)
- A Framework for Controlling False Discovery Rates and Minimizing the Amount of Genotyping in the Search for Disease Mutations (2004) (57)
- A dopamine transporter polymorphism is a risk factor for borderline personality disorder in depressed patients (2006) (57)
- A Single-Cell Model for Synaptic Transmission and Plasticity in Human iPSC-Derived Neurons. (2019) (57)
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- Temperament, childhood environment and psychopathology as risk factors for avoidant and borderline personality disorders (2003) (31)
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- Improved Ethical Guidance for the Return of Results from Psychiatric Genomics Research (2017) (24)
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- Interaction Testing and Polygenic Risk Scoring to Estimate the Association of Common Genetic Variants With Treatment Resistance in Schizophrenia (2022) (23)
- Psychosocial Factors Associated With Broadly Defined Bulimia Nervosa During Early Pregnancy: Findings from the Norwegian Mother and Child Cohort Study (2008) (23)
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- Disruption of the MicroRNA 137 Primary Transcript Results in Early Embryonic Lethality in Mice (2015) (22)
- Identifying bipolar disorder susceptibility loci in a densely affected pedigree (2013) (22)
- Transcriptome Atlases of Mouse Brain Reveals Differential Expression Across Brain Regions and Genetic Backgrounds (2012) (22)
- Sex-Dependent Shared and Nonshared Genetic Architecture Across Mood and Psychotic Disorders (2021) (21)
- Snus use and other correlates of smoking cessation in the Swedish Twin Registry (2007) (21)
- Modifiers and Subtype-Specific Analyses in Whole-Genome Association Studies: A Likelihood Framework (2011) (21)
- Examining the role of common and rare mitochondrial variants in schizophrenia (2018) (21)
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- No evidence for rare recessive and compound heterozygous disruptive variants in schizophrenia (2014) (21)
- Comparative Genomic Evidence for the Involvement of Schizophrenia Risk Genes in Antipsychotic Effects (2017) (20)
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- Classical Human Leukocyte Antigen Alleles and C4 Haplotypes Are Not Significantly Associated With Depression (2020) (20)
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- Genetics of disease: Associations with depression (2015) (15)
- No Effect of Genome-Wide Copy Number Variation on Measures of Intelligence in a New Zealand Birth Cohort (2013) (15)
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- 16 Genotype-environment interaction in transmission disequilibrium tests (2001) (15)
- Global similarity with local differences in linkage disequilibrium between the Dutch and HapMap–CEU populations (2009) (15)
- The dice are rolling for schizophrenia genetics (2008) (15)
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- The genomics of major psychiatric disorders in a large pedigree from Northern Sweden (2019) (14)
- Genome-wide association study of depression phenotypes in UK Biobank (n = 322,580) identifies the enrichment of variants in excitatory synaptic pathways (2017) (14)
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- Model-based gene selection shows engrailed 1 is associated with antipsychotic response (2008) (14)
- 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)
- Functional characterization of the PCLO p.Ser4814Ala variant associated with major depressive disorder reveals cellular but not behavioral differences (2015) (13)
- Erratum: Genome-wide common and rare variant analysis provides novel insights into clozapine-associated neutropenia (2017) (13)
- Characterization of Single Gene Copy Number Variants in Schizophrenia (2019) (13)
- Methylation age acceleration does not predict mortality in schizophrenia (2019) (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)
- Exploration of large, rare copy number variants associated with psychiatric and neurodevelopmental disorders in individuals with anorexia nervosa (2017) (13)
- A New Method for Detecting Associations with Rare Copy-Number Variants (2015) (13)
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- The public health utility of genome-wide association study results for smoking behavior (2010) (13)
- Transcriptome-wide association analysis of brain structures yields insights into pleiotropy with complex neuropsychiatric traits (2021) (12)
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- Evaluation of Chromatin Accessibility in Prefrontal Cortex of Schizophrenia Cases and Controls (2017) (12)
- Mania in the Swedish Twin Registry: criterion validity and prevalence. (2005) (12)
- Refining Attention-Deficit/Hyperactivity Disorder and Autism Spectrum Disorder Genetic Loci by Integrating Summary Data From Genome-wide Association, Gene Expression, and DNA Methylation Studies (2020) (11)
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- Test-statistic inflation in methylome-wide association studies (2020) (10)
- Heritability of binge-eating and bulimia nervosa (1998) (10)
- Addendum: Genome-wide association study of depression phenotypes in UK Biobank identifies variants in excitatory synaptic pathways (2018) (10)
- Lack of Support for the Genes by Early Environment Interaction Hypothesis in the Pathogenesis of Schizophrenia (2021) (10)
- Deep Sequencing of Three Loci Implicated in Large-Scale Genome-Wide Association Study Smoking Meta-Analyses. (2016) (10)
- A Powerful Test for SNP Effects on Multivariate Binary Outcomes Using Kernel Machine Regression (2018) (10)
- mTADA is a framework for identifying risk genes from de novo mutations in multiple traits (2020) (10)
- Genetic, Developmental and Personality Correlates of Self-Mutilation in Depressed Patients (2006) (10)
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- Assessment of gene expression in peripheral blood using RNAseq before and after weight restoration in anorexia nervosa (2013) (9)
- Genetic variation in 117 myelination-related genes in schizophrenia: Replication of association to lipid biosynthesis genes (2018) (9)
- Schizophrenia as a pathway disease (2014) (9)
- Leveraging Base Pair Mammalian Constraint to Understand Genetic Variation and Human Disease (2023) (9)
- Leveraging Base Pair Mammalian Constraint to Understand Genetic Variation and Human Disease (2023) (9)
- Analysis of epistasis in linked regions in the Irish study of high-density schizophrenia families. (2001) (9)
- Deep Sequencing of 71 Candidate Genes to Characterize Variation Associated with Alcohol Dependence (2017) (9)
- Genome-wide Association Study of Clinical Features in the Schizophrenia Psychiatric Genomics Consortium: Confirmation of Polygenic Effect on Negative Symptoms (2017) (9)
- Neuropsychological function in bulimia with comorbid borderline personality disorder and depression (2006) (8)
- Author Correction: Genome-wide meta-analysis identifies new loci and functional pathways influencing Alzheimer’s disease risk (2020) (8)
- Treatment-resistant psychotic symptoms and the 15q11.2 BP1–BP2 (Burnside-Butler) deletion syndrome: case report and review of the literature (2020) (8)
- IsoDOT Detects Differential RNA-Isoform Expression/Usage With Respect to a Categorical or Continuous Covariate With High Sensitivity and Specificity (2014) (8)
- Evolutionary constraint and innovation across hundreds of placental mammals (2023) (8)
- Cohort Profile: COVIDMENT: COVID-19 cohorts on mental health across six nations (2021) (8)
- Genotyping Accuracy for Whole-Genome Amplification of DNA from Buccal Epithelial Cells (2004) (8)
- Genotype-Based Ancestral Background Consistently Predicts Efficacy and Side Effects across Treatments in CATIE and STAR*D (2013) (8)
- Sex-Dependent Shared and Non-Shared Genetic Architecture Across Mood and Psychotic Disorders (2020) (8)
- Conditional GWAS analysis identifies putative disorder-specific SNPs for psychiatric disorders (2019) (8)
- Epistemic Injustice and Self-Injury: A Concept with Clinical Implications (2019) (7)
- HLA-DQB1 6672G>C (rs113332494) is associated with clozapine-induced neutropenia and agranulocytosis in individuals of European ancestry (2021) (7)
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- Genetics in eating disorders: extending the boundaries of research (2006) (6)
- Allelic differences between Europeans and Chinese for CREB1 SNPs and their implications in gene expression regulation, hippocampal structure and function, and bipolar disorder susceptibility (2014) (6)
- Increased risk of major depression by childhood abuse is not modified by CNR1 genotype (2013) (6)
- The Genomes Of The Collaborative Cross (2017) (6)
- Evaluating the Impact of Nonrandom Mating: Psychiatric Outcomes Among the Offspring of Pairs Diagnosed With Schizophrenia and Bipolar Disorder (2020) (6)
- Erratum: Patterns of remission, continuation and incidence of broadly defined eating disorders during early pregnancy in the Norwegian Mother and Child Cohort Study (MoBa) (Psychological Medicine (2007) 37 (1109-1118) DOI: 10.1017/S0033291707000724) (2012) (6)
- Treatment-resistant psychotic symptoms and early-onset dementia: A case report of the 3q29 deletion syndrome (2020) (6)
- Common-variant associations with fragile X syndrome (2017) (6)
- Genetic influences on eight psychiatric disorders based on family data of 4 408 646 full and half-siblings, and genetic data of 333 748 cases and controls – CORRIGENDUM (2018) (6)
- Salivary reactivity in women with bulimia nervosa across treatment (1996) (6)
- Effect of Mood and Food Cues on Information Processing in Women with Bulimia Nervosa and Controls (1997) (6)
- The Psychiatric Genomics Consortium: History, development, and the future (2020) (5)
- Haplotype-Based Pharmacogenetic Analysis for Longitudinal Quantitative Traits in the Presence of Dropout (2010) (5)
- Brain levels of the neurotoxic pyridinium metabolite HPP+ and extrapyramidal symptoms in haloperidol-treated mice. (2013) (5)
- PCM1 is necessary for focal ciliary integrity and is a candidate for severe schizophrenia (2020) (5)
- Response to Mitchell and Porteus (2010) (5)
- The epidemiology of psychiatric disorders in Africa: a scoping review. (2021) (5)
- Utilizing Twins as Controls for Non-Twin Case-Materials in Genome Wide Association Studies (2013) (5)
- Association test using Copy Number Profile Curves (CONCUR) enhances power in rare copy number variant analysis (2020) (5)
- The Genomics of Electroconvulsive Therapy International Consortium (GenECT-ic). (2019) (5)
- Large eQTL meta-analysis reveals differing patterns between cerebral cortical and cerebellar brain regions (2020) (5)
- Schizophrenia is characterized by age- and sex-specific effects on epigenetic aging (2019) (5)
- Eating Disorder Working Group of the PGC , Major Depressive Disorder Working Group of the PGC , Obsessive Compulsive Disorders and Tourette Syndrome Working Group of the PGC , Schizophrenia CLOZUK , Substance Use Disorder Working Group of the PGC (2018) (4)
- Pharmacotherapy and psychotherapy for major depression in a man with AIDS. (1993) (4)
- Publisher Correction: Gene expression imputation across multiple brain regions provides insights into schizophrenia risk (2019) (4)
- Gene expression changes following chronic antipsychotic exposure in single cells from mouse striatum (2022) (4)
- Chronicity and Sex Affect Genetic Risk Prediction in Schizophrenia (2020) (4)
- Functional consequences of genetic loci associated with intelligence in a meta-analysis of 87,740 individuals (2017) (4)
- Genome-wide annotation of gene regulatory elements linked to cell fitness (2021) (4)
- Reproducible Risk Loci and Psychiatric Comorbidities in Anxiety: Results from ~200,000 Million Veteran Program Participants (2019) (4)
- Mental health indicators in Sweden over a 12-month period during the COVID-19 pandemic – Baseline data of the Omtanke2020 Study (2021) (4)
- Fast eQTL Analysis for Twin Studies (2015) (4)
- The state of the science in psychiatric genomics (2021) (4)
- The effects of fluoxetine versus nortriptyline on body weight in depression. (2000) (4)
- Identifying tissues implicated in Anorexia Nervosa using Transcriptomic Imputation (2018) (3)
- Functional partitioning of local and distal gene expression regulation in multiple human tissues (2016) (3)
- Corrigendum: Analyses of allele-specific gene expression in highly divergent mouse crosses identifies pervasive allelic imbalance (2015) (3)
- Characterizing mood disorders in the AFFECT study: a large, longitudinal, and phenotypically rich genetic cohort in the US (2022) (3)
- Clinical phenotypes of peripartum depression and time of onset (2020) (3)
- Significant linkage on chromosome 14 for anxiety. (2006) (3)
- A phenome-wide association and Mendelian Randomisation study of polygenic risk for depression in UK Biobank (2020) (3)
- The Anorexia Nervosa Genetics Initiative: Overview and Methods (2017) (3)
- Two Cases of Body Dysmorphic Disorder in Women with Eating Disorders (1997) (3)
- Epigenetic age is accelerated in schizophrenia with age- and sex-specific effects and associated with polygenic disease risk (2019) (3)
- Building a schizophrenia genetic network: Transcription Factor 4 regulates genes involved in neuronal development and schizophrenia risk. (2018) (3)
- Schizophrenia: Hope on the Horizon (2015) (3)
- Author Correction: The mutational constraint spectrum quantified from variation in 141,456 humans (2021) (3)
- The functional and evolutionary impacts of human-specific deletions in conserved elements (2023) (3)
- Antipsychotic Behavioral Phenotypes in the Mouse Collaborative Cross Recombinant Inbred Inter-Crosses (RIX) (2019) (3)
- mBAT-combo: a more powerful test to detect gene-trait associations from GWAS data (2022) (2)
- A Munc18-1 mutant mimicking phosphorylation by Down Syndrome-related kinase Dyrk1a supports normal synaptic transmission and promotes recovery after intense activity (2020) (2)
- M93 A COMPREHENSIVE ANALYSIS OF NUCLEAR-ENCODED MITOCHONDRIAL GENES IN SCHIZOPHRENIA (2019) (2)
- Genetic variation in the Major Histocompatibility Complex and association with depression (2018) (2)
- Robust kernel association testing (RobKAT) (2020) (2)
- Gene expression imputation across multiple brain regions provides insights into schizophrenia risk (2019) (2)
- Gene expression imputation across multiple brain regions provides insights into schizophrenia risk (2019) (2)
- A genome-wide association study for educational attainment. (2008) (2)
- Genetic stratification of depression in UK Biobank suggests a subgroup linked to age of natural menopause (2019) (2)
- One CNV Discordance in NRXN1 Observed Upon Genome-wide Screening in 38 Pairs of Adult Healthy Monozygotic Twins (2016) (2)
- Association Between Polygenic Risk Scores and Outcome of ECT. (2022) (2)
- Robust Hi-C chromatin loop maps in human neurogenesis and brain tissues at high-resolution (2019) (2)
- Comparative genetic architectures of schizophrenia in East Asian and European populations (2019) (2)
- Conference Report: Psychiatric Genomics Consortium Meeting: Pathways to Drugs, London, March 2017 (2018) (2)
- Methylome-wide association study of early life stressors and adult mental health (2021) (2)
- Familial risk and heritability of intellectual disability: a population-based cohort study in Sweden. (2021) (2)
- Cardiovascular disease and subsequent risk of psychiatric disorders: a nationwide sibling-controlled study (2022) (2)
- Correction: Investigation of common, low-frequency and rare genome-wide variation in anorexia nervosa (2017) (2)
- Proof of concept: Molecular prediction of schizophrenia risk (2017) (2)
- Schizophrenia-associated somatic copy number variants from 12,834 cases reveal contribution to risk and recurrent, isoform-specific NRXN1 disruptions (2022) (2)
- INCREASED PREVALENCE OF RARE COPY NUMBER VARIANTS IN TREATMENT-RESISTANT PSYCHOSIS (2022) (2)
- SA35 PPD ACT, AN APP-BASED POSTPARTUM DEPRESSION GENETIC STUDY (2019) (2)
- Short-term improvement of mental health after a COVID-19 vaccination (2022) (2)
- Integrative analysis of rare variants and pathway information shows convergent results between immune pathways, drug targets and epilepsy genes (2018) (2)
- DeepGWAS: Enhance GWAS Signals for Neuropsychiatric Disorders via Deep Neural Network (2022) (1)
- Author Correction: Landscape of multi-nucleotide variants in 125,748 human exomes and 15,708 genomes (2021) (1)
- Editorial overview: Rare CNV disorders and neuropsychiatric phenotypes: opportunities, challenges, solutions. (2021) (1)
- or smoking cessation? Is Swedish snus associated with smoking initiation (2005) (1)
- Inference on phenotype‐specific effects of genes using multivariate kernel machine regression (2018) (1)
- SU93 REPLICATION OF TWO INDEPENDENT LOCI IN HLA-DQB1 AND HLA-B CONTRIBUTING TO THE RISK OF CLOZAPINE-INDUCED AGRANULOCYTOSIS (2019) (1)
- Ethical and Analytic Challenges With Genomic Sequencing of Relapsed Hematologic Malignancies Following Allogeneic Hematopoietic Stem-Cell Transplantation (2021) (1)
- Sex differences in the human peripheral blood transcriptome (2014) (1)
- M94 THE GENOMICS OF HIGHLY TREATMENT RESISTANT SCHIZOPHRENIA (2019) (1)
- Large-scale analysis of DNA methylation identifies cellular alterations in blood from psychosis patients and molecular biomarkers of treatment-resistant schizophrenia (2020) (1)
- SU62 A CHROMATIN CATALOG FOR THE INTERPRETATION OF GENETIC ASSOCIATIONS OF PSYCHIATRIC DISORDERS (2019) (1)
- Transcriptome-wide association study for postpartum depression implicates altered B-cell activation and insulin resistance (2022) (1)
- Genome-wide association study of patient and clinician rated global impression severity during antipsychotic treatment (2014) (1)
- Delusions, Hallucinations, and Cognitive Decline in Middle Age: A Case of Dementia, GIGYF2 Gene Mutation, and 22q11 Duplication (2022) (1)
- Analysis of 62 hybrid assembled human Y chromosomes exposes rapid structural changes and high rates of gene conversion (2017) (1)
- Genome-wide association for major depression through age at onset stratificationGenomic analysis of age at onset in depression (2016) (1)
- P0189 - Risk factors and associated features of childhood-, teenage-, and adult- onset depression (2008) (1)
- Evaluation of chromatin accessibility in prefrontal cortex of individuals with schizophrenia (2018) (1)
- Author Correction: Genome-wide association study of depression phenotypes in UK Biobank identifies variants in excitatory synaptic pathways (2018) (1)
- 55 LARGE META-ANALYSIS OF SCANDINAVIAN EXOME SEQUENCING STUDIES OF SCHIZOPHRENIA (2019) (1)
- 30 SCHIZOPHRENIA IS CHARACTERIZED BY AGE- AND SEX-SPECIFIC EFFECTS ON EPIGENETIC AGING (2019) (1)
- Unravelling the link between sleep and mental health during the COVID-19 pandemic (2022) (1)
- Transcript expression-aware annotation improves rare variant interpretation (2020) (1)
- Empirical Evaluation of the Genetic Similarity of Samples From Twin Registries in Australia and the Netherlands Using 359 STRP Markers (2006) (1)
- Author Correction: Increased burden of ultra-rare structural variants localizing to boundaries of topologically associated domains in schizophrenia (2022) (1)
- Genome-wide association mapping of loci for antipsychotic-induced extrapyramidal symptoms in mice (2011) (1)
- mTADA: a framework for analyzing de novo mutations in multiple traits (2018) (1)
- Correction: Genome-wide gene-environment analyses of major depressive disorder and reported lifetime traumatic experiences in UK Biobank (2020) (1)
- Hair Cortisol in Twins: Heritability and Genetic Overlap with Psychological Variables and Stress-System Genes (2017) (1)
- Non-random mating, parent-of-origin, and maternal–fetal incompatibility effects in schizophrenia (2013) (1)
- The longitudinal effects of stress and fear on psychiatric symptoms in mothers during the COVID-19 pandemic (2022) (1)
- Author Correction: Genome-wide meta-analysis identifies new loci and functional pathways influencing Alzheimer’s disease risk (2020) (1)
- The impact of educational attainment, intelligence and intellectual disability on schizophrenia: a Swedish population-based register and genetic study (2022) (1)
- F124. PPD ACT, an App-Based Postpartum Depression Genetic Study (2018) (1)
- SU102META-ANALYSIS OF CLOZAPINE-ASSOCIATED NEUTROPENIA AND AGRANULOCYTOSIS (2019) (1)
- Genome-wide association study for leisure-time exercise behavior (2008) (1)
- Self-induced abortion in a bulimic woman. (1994) (1)
- 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)
- Erratum: AKT1 and neurocognition in schizophrenia (Australian and New Zealand Journal of Psychiatry (2007) 41 (169-177)) (2009) (0)
- Genetic identification of brain cell types underlying schizophrenia (2018) (0)
- Author Correction: Increased burden of ultra-rare structural variants localizing to boundaries of topologically associated domains in schizophrenia (2022) (0)
- Meta-analysis of genome-wide association studies for neuroticism in 449,484 individuals identifies novel genetic loci and pathways (2018) (0)
- S87GENETIC DIFFERENTIAL DIAGNOSIS IN ULTRA TREATMENT RESISTANT SCHIZOPHRENIA (2019) (0)
- Roadmap for a precision-medicine initiative in the Nordic region (2019) (0)
- Dysregulation of Synaptic and Developmental Transcriptomic/Proteomic Profiles upon Depletion of MUNC18-1 (2022) (0)
- Correction: Genome-Wide Association Study Implicates Chromosome 9q21.31 as a Susceptibility Locus for Asthma in Mexican Children (2009) (0)
- Increased burden of ultra-rare structural variants localizing to boundaries of topologically associated domains in schizophrenia (2020) (0)
- Erratum: A genome-wide association study of anorexia nervosa suggests a risk locus implicated in dysregulated leptin signaling (2017) (0)
- Genome-wide association analyses identify 143 risk variants and putative regulatory mechanisms for type 2 diabetes (2018) (0)
- SA82 HLA-DQB1 6672G>C INFLUENCES THE RISK OF CLOZAPINE-INDUCED AGRANULOCYTOSIS IN INDIVIDUALS OF EUROPEAN ANCESTRY (2019) (0)
- Integrated Bayesian analysis of rare exonic variants to identify risk genes for schizophrenia and neurodevelopmental disorders (2017) (0)
- SA78 GAPS: GENOMIC AGGREGATION PROJECT IN SWEDEN (2019) (0)
- SA132THE RELATIONSHIP BETWEEN POLYGENIC RISK SCORES AND G IN PGC2 SCHIZOPHRENIA CASES (2019) (0)
- Author Correction: Genome-wide association study of depression phenotypes in UK Biobank identifies variants in excitatory synaptic pathways (2021) (0)
- 65 IDENTIFYING SUSCEPTIBILITY LOCI FOR TOURETTE'S SYNDROME IN A DENSELY AFFECTED PEDIGREE (2019) (0)
- Characterising the loss-of-function impact of 5’ untranslated region variants in 15,708 individuals (2020) (0)
- Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression (2018) (0)
- A structural variation reference for medical and population genetics (2020) (0)
- Leveraging base-pair mammalian constraint to understand genetic variation and human disease. (2023) (0)
- Leveraging base-pair mammalian constraint to understand genetic variation and human disease. (2023) (0)
- Rare tandem repeat expansions associate with genes involved in synaptic and neuronal signaling functions in schizophrenia (2022) (0)
- A Combined Cellomics and Proteomics Approach to Uncover Neuronal Pathways to Psychiatric Disorder (2019) (0)
- 53 IDENTIFICATION OF GENETIC RISK FACTORS FOR POSTPARTUM DEPRESSION (2019) (0)
- 43. CANNABIS, ALCOHOL AND SUBSTANCE ABUSE AND RISK OF SCHIZOPHRENIA AND BIPOLAR DISORDER IN A SWEDISH NATIONAL REGISTER STUDY (2022) (0)
- 59. SHARED GENETIC CONTRIBUTION TO MAJOR DEPRESSIVE DISORDER AND CARDIOVASCULAR DISEASE (2022) (0)
- Mania in the Swedish Twin Registry: Criterion Validity and Prevalence (2005) (0)
- Author's Response to Dr. Leo (2006) (0)
- Genes, environments, and developmental GEWIS: Methods for a multi-site study of early substance abuse (2013) (0)
- 57METHYLOMIC BIOMARKERS OF SCHIZOPHRENIA AND ANTIPSYCHOTIC MEDICATION EXPOSURE (2019) (0)
- Evaluating drug targets through human loss-of-function genetic variation (2020) (0)
- 50 FUNCTIONAL CONSEQUENCES OF GENETIC LOCI ASSOCIATED WITH IQ IN A META-ANALYSIS OF 87,740 INDIVIDUALS (2019) (0)
- Genome-wide association analyses identify 44 risk variants and refine the genetic architecture ofmajor depressive disorder (2018) (0)
- SA49 A QUANTITATIVE ANALYSIS OF DISCREPANCIES BETWEEN CANDIDATE GENE AND GENOME-WIDE STUDIES OF COMPLEX TRAITS AND RELATED ENDOPHENOTYPES (2019) (0)
- Refinement of schizophrenia GWAS loci using methylome-wide association data (2014) (0)
- A Munc18-1 mutant mimicking phosphorylation by Down Syndrome-related kinase Dyrk1a supports normal synaptic transmission and promotes recovery after intense activity (2020) (0)
- Barriers to genetic testing in clinical psychiatry and ways to overcome them: from clinicians’ attitudes to sociocultural differences between patients across the globe (2022) (0)
- Swedish large-scale schizophrenia study: Why do patients and healthy controls participate? (2021) (0)
- High density methylation QTL analysis in human blood via next-generation sequencing of the methylated genomic DNA fraction (2015) (0)
- The mutational constraint spectrum quantified from variation in 141,456 humans (2020) (0)
- Genome-wide meta-analysis identifies new loci and functional pathways influencing Alzheimer’s disease risk (2019) (0)
- R2d maps to a 9.3 Mb candidate interval. (2015) (0)
- Supplementary Material for: Modifiers and Subtype-Specific Analyses in Whole-Genome Association Studies: A Likelihood Framework (2017) (0)
- mTADA is a framework for identifying risk genes from de novo mutations in multiple traits (2020) (0)
- UNCOVERING THE GENETIC ARCHITECTURE OF MAJOR DEPRESSION AND ITS PHENOME-WIDE EFFECTS (2019) (0)
- A genome-wide association study of anorexia nervosa suggests a risk locus implicated in dysregulated leptin signaling (2017) (0)
- Whole exome sequencing in dense families suggests genetic pleiotropy amongst Mendelian and complex neuropsychiatric syndromes (2021) (0)
- contribution to risk and recurrent , isoform-specific NRXN 1 disruptions 2 (2021) (0)
- CommonMind Consortium provides transcriptomic and epigenomic data for Schizophrenia and Bipolar Disorder (2019) (0)
- Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder (2018) (0)
- Smoking Initiation and Persistence: First Results for Genome-Wide Association Analyses in Dutch Adults (2008) (0)
- Author Correction: The effect of LRRK2 loss-of-function variants in humans (2021) (0)
- Correction: Investigating rare pathogenic/likely pathogenic exonic variation in bipolar disorder (2021) (0)
- Identification of common genetic risk variants for autism spectrum disorder (2019) (0)
- Association Tests Using Copy Number Profile Curves (CONCUR) Enhances Power in Rare Copy Number Variant Analysis (2019) (0)
- SU39 GENOME WIDE ASSOCIATION STUDY OF TREATMENT RESPONSE TO COGNITIVE BEHAVIORAL THERAPY FOR DEPRESSION (2019) (0)
- T117. POLYGENIC RISK SCORES AND CONCORDANCE FOR SCHIZOPHRENIA AND BIPOLAR DISORDER IN SWEDISH MONOZYGOTIC AND DIZYGOTIC TWINS (2022) (0)
- Genome-wide association study of post-traumatic stress disorder reexperiencing symptoms in >165,000 US veterans (2019) (0)
- M8 Framework For The Return of Results To Psychiatric Genomics Research Participants: What Should Be Offered? (2017) (0)
- eQTLGen Consortium (2018). Genome-wide association analyses identify 143 risk variants and putative regulatory mechanisms for type 2 diabetes. (2018) (0)
- The association between family history and genomic burden with schizophrenia mortality: a Swedish population-based register and genetic sample study (2021) (0)
- Landscape of multi-nucleotide variants in 125,748 human exomes and 15,708 genomes (2020) (0)
- Genome-wide association study identifies eight risk loci and implicates metabo-psychiatric origins for anorexia nervosa (2019) (0)
- Author Correction: Characterising the loss-of-function impact of 5’ untranslated region variants in 15,708 individuals (2021) (0)
- Genetic variation in 117 myelination-related genes in schizophrenia: Replication of association to lipid biosynthesis genes (2018) (0)
- Genome-wide meta-analysis of depression identifies 102 independent variants and highlights the importance of the prefrontal brain regions (2019) (0)
- Applying polygenic risk scoring for psychiatric disorders to a large family with bipolar disorder and major depressive disorder (2018) (0)
- Author Correction: Evaluating drug targets through human loss-of-function genetic variation (2021) (0)
- W91. GENE-ENVIRONMENT INTERACTION AND BRAIN NETWORKS IN THE PATHOPHYSIOLOGY OF EXTERNALIZING BEHAVIORS AND SUBSTANCE USE RISK (2021) (0)
- Transcriptome-wide association study of schizophrenia and chromatin activity yields mechanistic disease insights (2018) (0)
- Genome-wide association meta-analysis in 269,867 individuals identifies new genetic and functional links to intelligence (2018) (0)
- Author Correction: Transcript expression-aware annotation improves rare variant interpretation (2021) (0)
- Genetic identification of cell types underlying brain complex traits yields insights into the etiology of Parkinson’s disease (2020) (0)
- Functional annotation of rare structural variation in the human brain (2020) (0)
- Genetic identification of cell types underlying brain complex traits yields insights into the etiology of Parkinson’s disease (2020) (0)
- MethylPCA: a toolkit to control for confounders in methylome-wide association studies (2013) (0)
- A Powerful Test for SNP Effects on Multivariate Binary Outcomes Using Kernel Machine Regression (2017) (0)
- The genetic basis of autonomic nervous system (2008) (0)
- The effect of LRRK2 loss-of-function variants in humans (2020) (0)
- Schizophrenia risk conferred by rare protein-truncating variants is conserved across diverse human populations (2023) (0)
- Transcriptional diversity in synaptic gene sets is sufficient to discriminate cortical neuronal identity (2022) (0)
- Erratum: Rates of depressive and anxiety disorders in a residential mother-infant unit for unsettled infants (Australian and New Zealand Journal of Psychiatry (2007) 41 (836-842)) (2009) (0)
- 39 TARGETED SEQUENCING OF GENES MOST LIKELY TO HARBOR RARE CAUSAL VARIANTS IN SCHIZOPHRENIA (2019) (0)
- M91 INCREASED SCHIZOPHRENIA FAMILY HISTORY BURDEN AND REDUCED PREMORBID IQ IN TREATMENT-RESISTANT SCHIZOPHRENIA: A SWEDISH NATIONAL REGISTER AND GENOMIC STUDY (2019) (0)
- TU71. SIGNIFICANT INCIDENCE OF RARE CHROMOSOMAL AND GENOMIC SEQUENCE VARIANTS IN HIGHLY TREATMENT-RESISTANT SCHIZOPHRENIA AND SCHIZOAFFECTIVE DISORDER (2021) (0)
- COGEDAP: A COmprehensive GEnomic Data Analysis Platform (2022) (0)
- Targeted Sequencing of Genes Most Likely to Harbor Rare Causal Variants in Schizophrenia (2020) (0)
- 47 TRYGGVE2: PREDICTING POOR OUTCOMES IN SCHIZOPHRENIA USING REGISTER GENOMICS IN SWEDEN (2019) (0)
- Investigating genetic overlap between antidepressant and lithium response and treatment resistance in major depressive disorder (2022) (0)
- A LARGE META-ANALYSIS ACROSS FOUR NORDIC COUNTRIES REVEALS SEVERAL SIGNIFICANT GENETIC ASSOCIATIONS FOR EARLY ONSET MAJOR DEPRESSIVE DISORDER (2022) (0)
- NEXT GENERATION GENOME-WIDE ASSOCIATION STUDY OF SCHIZOPHRENIA FROM SWEDEN (2022) (0)
- TH62. GENETICS OF SEVERE MENTAL DISORDERS IN EL HIERRO, AN ISOLATED CANARY ISLAND (2021) (0)
- THE GENETIC ARCHITECTURE OF MAJOR DEPRESSIVE DISORDER WITH SEVERE OUTCOME IN SCANDINAVIA (2022) (0)
- 82. INCREASED BURDEN OF RARE TANDEM REPEAT EXPANSIONS IN SCHIZOPHRENIA (2021) (0)
- ASSESSING THE UTILITY OF PHARMACOGENETIC TESTING IN A COHORT WITH TREATMENT-RESISTANT SCHIZOPHRENIA OR SCHIZOAFFECTIVE DISORDER (2022) (0)
- Publisher Correction: Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection (2019) (0)
- MULTI-PSYCH - A MULTIMODAL DATA PROJECT FOR DEPRESSION AND ANXIETY DISORDERS IN SWEDISH ROUTINE CLINICAL CARE (2022) (0)
- 40. BRAIN CELL TYPE SPECIFIC EQTLS AND SCHIZOPHRENIA (2022) (0)
- THE 4TH PSYCHIATRIC GENOMICS CONSORTIUM GRANT (2021-26): AIMS AND INTENTIONS (2021) (0)
- Massively parallel sequencing from prefrontal cortex reveals multiple novel small RNAs and microRNAs associated with schizophrenia (2011) (0)
- T50. THE CHALLENGES AND OPPORTUNITIES OF USING NATIONAL PATIENT REGISTERS FOR GENETICS RESEARCH: A DEPRESSION EXAMPLE (2022) (0)
- P508. Assessing Isoform Diversity in the Context of Psychiatric Disorders (2022) (0)
- M16 IDENTICAL BUT NOT THE SAME - WHOLE GENOME SEQUENCING OF MONOZYGOTIC TWINS DISCORDANT FOR PSYCHIATRIC ILLNESS (2019) (0)
- GWAS OF A QUANTITATIVE ANXIETY TRAIT IN THE MILLION VETERAN PROGRAM SAMPLE (2019) (0)
- TRYGGVE2: SECURE & PRECISE GENETIC ANALYSES IN THE NORDIC COUNTRIES AND BEYOND (2022) (0)
- 13 INTEGRATED ANALYSIS OF RARE VARIANTS AND SINGLE-CELL EXPRESSION DATA PROVIDES INSIGHTS INTO SCHIZOPHRENIA RISK (2019) (0)
- SA30VARIANCE COMPONENT TEST FOR CROSS-DISORDER PATHWAY ANALYSIS (2019) (0)
- How To Make A Million (Mdd Cases) (2019) (0)
- TU77. THE IMPACT OF EDUCATIONAL ATTAINMENT, INTELLIGENCE AND INTELLECTUAL DISABILITY ON SCHIZOPHRENIA: A SWEDISH POPULATION-BASED REGISTER AND GENETIC STUDY (2021) (0)
- 11. GENETIC EPIDEMIOLOGY AND POLYGENICITY OF PSYCHOTIC MAJOR DEPRESSIVE DISORDER (2022) (0)
- DIFFERENTIAL ISOFORM USAGE IN SCHIZOPHRENIA (2022) (0)
- S24. Characterizing the Association of Mobile Skin Conductance and Ambulatory Heart Rate on PTSD Symptom Clusters (2019) (0)
- TU31. GENETIC CONTRIBUTION TO MAJOR DEPRESSIVE DISORDER HETEROGENEITY- FAMILY DESIGNS USING SWEDISH NATIONAL REGISTERS (2021) (0)
- 893. Adverse Life Events, Psychiatric Comorbidity, and Biological Predictors of Postpartum Depression in an Ethnically Diverse Sample of Postpartum Women (2017) (0)
- The genetic base of insulin and glucose: A genome-wide analysis (2008) (0)
- SU33ANALYSIS OF WHOLE EXOME SEQUENCING OF 1000 BIPOLAR PATIENTS (2019) (0)
- Clustering of subjects on subsets of SNPs (2008) (0)
- Ultra-Rare Protein-Altering Variants Among 4,877 Swedish Individuals with Schizophrenia (2017) (0)
- IS GENETIC RISK FOR EARLY ONSET MAJOR DEPRESSIVE DISORDER ASSOCIATED WITH MORE SEVERE CLINICAL FEATURES THAN BROAD MAJOR DEPRESSIVE DISORDER? (2022) (0)
- Running Head : GWAS Meta-Analysis of Alzheimer ’ s Disease 1 Genetic meta-analysis identifies 9 novel loci and functional pathways for Alzheimer ’ s disease risk (2019) (0)
- Genome-wide meta-analysis identifies new loci and functional pathways influencing 1 Alzheimer ’ s disease risk 2 3 (2020) (0)
- Risk Overlap Between Clinical Disorders (2016) (0)
- The association of ADH gene cluster with alcohol dependence in the Irish affected Sib pair study (2006) (0)
- Identification of multiple genes associated with alcohol use and comorbid phenotypes on 4Q in the Irish Affected Sib-Pair Study of Alcohol dependence (2008) (0)
- Supplementary Information for Extremely low-coverage sequencing and imputation increases power for genome-wide association studies (2012) (0)
- Untapped resources for pharmacogenomic discovery in psychiatry. (2008) (0)
- The Robust Kernel Association Test. (2019) (0)
- 18 DIFFERENTIAL RESPONSE TO REPRODUCTIVE HORMONES CHARACTERIZES POSTPARTUM DEPRESSION ACROSS OMIC PLATFORMS (2019) (0)
- Can overlapping QTLs account for correlations between Eysenck and Cloninger personality dimensions (2005) (0)
- Fifty Years of Twin Studies On Psychiatric Traits Show That for the Majority of Traits Genetic Variation Is Mostly Additive (2017) (0)
- SU86GENETIC INFLUENCES ON EIGHT PSYCHIATRIC DISORDERS BASED ON FAMILY DATA OF 4,408,646 FULL AND HALF SIBLINGS, AND GENETIC DATA OF 333,748 CASES AND CONTROLS (2019) (0)
- SA72A HIGH-RESOLUTION MAP OF CHROMATIN INTERACTIONS IN ADULT AND FETAL CORTEX (2019) (0)
- POLYGENIC RISK AND BODY MASS INDEX IN THE SWEDEN SCHIZOPHRENIA STUDY (2022) (0)
- Transmission ratios in the progeny of R2d2 WSB/notWSB heterozygous F1 hybrid sires and dams. (2015) (0)
- EXOME SEQUENCING IN SCHIZOPHRENIA TO MAP DISEASE VARIANTS, GENES AND NETWORKS (2012) (0)
- Genome Wide Association analysis for Borderline Personality Disorder Characteristics (2008) (0)
- Cover Image, Volume 173A, Number 2, February 2017. (2017) (0)
- Original Research Reports Conditions Comorbid with Chronic Fatigue in a Population-Based Sample (2012) (0)
- Evaluation of genetic substructure in the Irish Study of High-Density Schizophrenia Families (2004) (0)
- Quantifying the impact of rare and ultra-rare coding variation across the phenotypic spectrum (2017) (0)
- Update On PGC Bipolar Disorder (2017) (0)
- GENETICS OF RESPONSE TO COGNITIVE BEHAVIOR THERAPY IN ADULTS WITH MAJOR DEPRESSION (2019) (0)
- Translating Genomewide Association Findings into New Therapeutics for Psychiatry 1 (2016) (0)
- S.18.02 Genetics of anorexia nervosa (2010) (0)
- Author response: DNA methylation meta-analysis reveals cellular alterations in psychosis and markers of treatment-resistant schizophrenia (2020) (0)
- Biovupsych : Electronic Medical Record-Based Identification of Dna Samples for Disorders Under-Represented n The'Pgc (2017) (0)
- SU28 THE GENOMICS OF BIPOLAR AND SCHIZOPHRENIC DISORDERS IN A LARGE PEDIGREE FROM A NORTHERN SWEDISH ISOLATE (2019) (0)
- QTLs for anxiety and depression using extreme discordant and concordant twins and sibs. (2004) (0)
- Genome-wide analysis of insomnia in 1,331,010 individuals identifies new risk loci and functional pathways (2019) (0)
- Addendum: Genome-wide association study of depression phenotypes in UK Biobank identifies variants in excitatory synaptic pathways (2018) (0)
- A rare deletion at distal 16 p 11 . 2 is implicated in schizophrenia (2013) (0)
- PHENOTYPIC AND GENETIC HETEROGENEITY OF POSTPARTUM DEPRESSION SUBTYPES (2022) (0)
- VKučinskas-2001-2016 (2016) (0)
- 268. Implications of twin studies of bulimia (1998) (0)
- GWAS meta-analysis (N=279,930) identifies new genes and functional links to general cognitive ability (2018) (0)
- Bibliography B IPOLAR D ISORDER (2011) (0)
- Building a schizophrenia genetic network: Evidence that Transcription Factor 4 regulates schizophrenia risk genes (2017) (0)
- Network Structure of Clinical Variables and a Schizophrenia Polygenic Risk Score in Treatment Resistant Psychosis (2021) (0)
- Addendum: The mutational constraint spectrum quantified from variation in 141,456 humans (2021) (0)
- Linkage mapping localizes R2d2 to a 900 kb region in Chr 2. (2015) (0)
- O36. Genetic Overlap and Causality Among Major Depressive Disorder, Alcohol Dependence, and Alcohol Consumption: Findings From the Psychiatric Genomics Consortium (2018) (0)
- SU36 ADVERSE LIFE EVENTS, PSYCHIATRIC COMORBIDITY, AND BIOLOGICAL PREDICTORS OF POSTPARTUM DEPRESSION IN AN ETHNICALLY DIVERSE SAMPLE OF POSTPARTUM WOMEN (2019) (0)
- The Science of The Psychiatric Genomics Consortium (Part 1) (2017) (0)
- Title : Functional consequences of genetic loci associated with intelligence in a 1 meta-analysis of 87 , 740 individuals 2 3 (2017) (0)
- SA45APPLYING GENETIC RISK SCORES TO AN ETHNICALLY DIVERSE SAMPLE OF POSTPARTUM WOMEN (2019) (0)
- F117EVALUATING THE IMPACT OF NON-RANDOM MATING: PSYCHIATRIC OUTCOMES AMONG THE OFFSPRING OF PAIRS DIAGNOSED WITH SCHIZOPHRENIA AND BIPOLAR DISORDER (2019) (0)
- Psychopharmacology and AIDS (1993) (0)
- Chronic fatigue with a gender-perspective in the Swedish twin registry (2006) (0)
- SU123PREDICTION OF MORTALITY USING DNA METHYLATION AGE IN SCHIZOPHRENIA (2019) (0)
- Psychiatric Genetics Before "Genetics". (2021) (0)
- Antipsychotic Trials in Schizophrenia: Genetic investigations in the CATIE sample (2010) (0)
- TH80. CLUSTERING OF SCHIZOPHRENIA CASES BASED ON COMMON GENETIC VARIANTS (2021) (0)
- Acute COVID-19 severity and 16-month mental morbidity trajectories in patient populations of six nations (2021) (0)
- Characterizing an inverse axis between orthogonal sources of genetic risk (2015) (0)
- Genome-wide study of CSF kynurenic acid in bipolar disorder implicates a molecular pathway underlying psychosis (2012) (0)
- Do depression and cardiovascular risk factors share a genetic basis (2008) (0)
- Mental health, gender, and care-seeking behavior during the COVID-19 pandemic in Sweden: An exploratory study (2023) (0)
- M33 TRYGGVE2: PREDICTING POOR OUTCOMES IN MAJOR DEPRESSION USING REGISTER GENOMICS IN SWEDEN (2019) (0)
- 41GENETIC RISK SCORES AND POSTPARTUM PSYCHIATRIC DISORDERS (2019) (0)
- IS BRAIN CELL TYPE THE KEY READOUT OF GWAS? (2022) (0)
- The Science of The Psychiatric Genomics Consortium (Part 2) (2017) (0)
- Prioritizing risk genes for neurodevelopmental disorders using pathway information (2018) (0)
- Association Between Autozygosity and Major Depression: Stratification Due to Religious Assortment (2013) (0)
- A Case-control and Co-twin Control Study of Personality as Risk for Chronic Fatigue and Chronic Widespread Pain in the Swedish Twin Registry - Session: Complex Disorders II and Immunology (2004) (0)
- S0033291718002039jra 1166..1173 (2019) (0)
- Genetic effects in fl uencing risk for major depressive disorder in China and Europe (2017) (0)
- The genetic basis of depression: The GAIN-MDD genome wide analysis among 3760 persons (2008) (0)
- T91LEVERAGING COMORBIDITIES TO DEFINE SCHIZOPHRENIA SUBTYPES (2019) (0)
- PGC3 AIM 6 - Large Scale Wgs of Multiply Affected Pedigrees (2017) (0)
- No xenotropic murine leukemia virus-related virus (XMRV) detected in Swedish monozygotic twins discordant for chronic fatigue (2011) (0)
- 1 Analysis of Shared Heritability in Common Disorders of the Brain 1 (2017) (0)
- University of Groningen Fine mapping of ZNF 804 A and genome-wide significant evidence for its involvement in schizophrenia and bipolar disorder (2017) (0)
- F50CREATING AN INTERNATIONAL CONSORTIUM TO INVESTIGATE GENETIC FINDINGS IN SEVERE DEPRESSION AND RESPONSE TO ECT (GENECT-IC) (2019) (0)
- Combined association analysis experiment for major depressive disorder (2011) (0)
- Elevated symptoms of depression and anxiety among family members and friends of critically ill COVID-19 patients - An observational study of five cohorts across four countries (2023) (0)
- A large copy number gain is present in strains with maternal TRD. (2015) (0)
- University of Groningen Investigation of common , low-frequency and rare genome-wide variation in anorexia nervosa Kas (2017) (0)
- Bayesian Integrated Analysis Of Multiple Types Of Rare Variants To Infer Risk Genes For Schizophrenia And Other Neurodevelopmental Disorders (2017) (0)
- The Genetics of Mdd In Sweden (2019) (0)
- Epilepsies, IMSGC consortium, IPDGC consortium, METASTROKE and Intracerebral Hemorrhage Studies of the International Stroke Genetics Consortium, Attention-Deficit Hyperactivity Disorder Working Group of the Psychiatric Genomics Consortium, Anorexia Nervosa Working Group of the Psychiatric Genomics C (2016) (0)
- GWAS of major depressive disorder (2011) (0)
- Correction: Common-variant associations with fragile X syndrome (2019) (0)
- HLA-DQB1 6672 G>C is associated with the risk of clozapine-induced agranulocytosis in individuals of European ancestry (2020) (0)
- Author Correction: A structural variation reference for medical and population genetics (2021) (0)
- Integrated analysis of environmental and genetic influences on cord blood DNA methylation in new-borns (2019) (0)
- TwinEQTL: Ultra Fast and Powerful Association Analysis for eQTL and GWAS in Twin Studies (2022) (0)
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What Schools Are Affiliated With Patrick F Sullivan?
Patrick F Sullivan is affiliated with the following schools:
