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Common genetic variants, acting additively, are a major source of risk for autism

Molecular autism, 2012-10, Vol.3 (1), p.9-9, Article 9

2012

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Transcriptome alterations are enriched for synapse-associated genes in the striatum of subjects with obsessive-compulsive disorder

Translational psychiatry, 2021-03, Vol.11 (1), p.171-171, Article 171

2021

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DAWN: a framework to identify autism genes and subnetworks using gene expression and genetics

Molecular autism, 2014-03, Vol.5 (1), p.22-22, Article 22

2014

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Gene Expression Deconvolution Implicates Cell-Type-Specific Gene Expression and Co-Expression in Autism

Biological psychiatry (1969), 2020-05, Vol.87 (9), p.S60-S61

2020

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A selective inference approach for false discovery rate control using multiomics covariates yields insights into disease risk

Proceedings of the National Academy of Sciences - PNAS, 2020-06, Vol.117 (26), p.15028-15035

2020

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A UNIFIED STATISTICAL FRAMEWORK FOR SINGLE CELL AND BULK RNA SEQUENCING DATA

The annals of applied statistics, 2018-03, Vol.12 (1), p.609-632

2018

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T20. POLYGENIC RISK FOR SCHIZOPHRENIA IS ASSOCIATED WITH HIPPOCAMPAL VOLUME IN TYPICALLY DEVELOPING YOUTH

Schizophrenia bulletin, 2019-04, Vol.45 (Supplement_2), p.S211-S211

2019

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H‐MAGMA, inheriting a shaky statistical foundation, yields excess false positives

Annals of human genetics, 2021-05, Vol.85 (3-4), p.97-100

2021

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O11.1. MULTIPLE GENOMIC MEASURES OF SCHIZOPHRENIA RISK ARE RELATED TO CORTICAL THICKNESS IN TYPICALLY DEVELOPING YOUTH AND YOUNG ADULTS

Schizophrenia bulletin, 2020-05, Vol.46 (Supplement_1), p.S27-S27

2020

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O11.1. MULTIPLE GENOMIC MEASURES OF SCHIZOPHRENIA RISK ARE RELATED TO CORTICAL THICKNESS IN TYPICALLY DEVELOPING YOUTH AND YOUNG ADULTS

Schizophrenia bulletin, 2020-05, Vol.46 (Suppl 1), p.S27-S27

2020

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Genetics in psychiatry: common variant association studies

Molecular autism, 2010-03, Vol.1 (1), p.6-6

2010

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TESTING HIGH-DIMENSIONAL COVARIANCE MATRICES, WITH APPLICATION TO DETECTING SCHIZOPHRENIA RISK GENES

The annals of applied statistics, 2017-09, Vol.11 (3), p.1810-1831

2017

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Functional connectome fingerprinting accuracy in youths and adults is similar when examined on the same day and 1.5‐years apart

Human brain mapping, 2020-10, Vol.41 (15), p.4187-4199

2020

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43 SCHIZOPHRENIA POLYGENIC RISK IS ASSOCIATED WITH BRAIN MATURATION IN TYPICALLY DEVELOPING YOUTH

European neuropsychopharmacology, 2019-10, Vol.29, p.S83-S83

2019

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Intelligence, Genes, and Success: Scientists Respond to the Bell Curve

1, 1997

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Using a CRISPR/Cas9-Based Epigenetic Editing Tool to Study the Cell-Type-Specific Effects of the DNA Methylation Alterations Observed in the Auditory Cortex Subjects With Schizophrenia

Biological psychiatry (1969), 2020-05, Vol.87 (9), p.S61

2020

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Heritable Variation, With Little or No Maternal Effect, Accounts for Recurrence Risk to Autism Spectrum Disorder in Sweden

Biological psychiatry (1969), 2018-04, Vol.83 (7), p.589-597

2018

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T63GENETIC AND ENVIRONMENTAL FACTORS AND RISK OF OBSESSIVE-COMPULSIVE DISORDER

European neuropsychopharmacology, 2019-10, Vol.29, p.S249-S249

2019

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T63. CROSS-DISORDER ANALYSIS OF AUTISM AND ADHD USING RARE VARIANTS: INSIGHTS FROM DANISH IPSYCH EXOMES

European neuropsychopharmacology, 2023-10, Vol.75, p.S195-S196

2023

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F52. Age-Associated Functional Network Organization in Psychosis

Biological psychiatry (1969), 2018-05, Vol.83 (9), p.S258-S258

2018

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ANALYSIS OF RARE CODING AND COMMON VARIANTS IN AUTISM AND COMORBID SUBGROUPS

European neuropsychopharmacology, 2022-10, Vol.63, p.e19-e20

2022

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Spatiotemporal and genetic regulation of A-to-I editing throughout human brain development

Cell reports (Cambridge), 2022-11, Vol.41 (5), p.111585-111585, Article 111585

2022

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5.45 RECURRENT AND LARGE COPY NUMBER VARIATION IN OCD RISK: RESULTS FROM THE EGOS STUDY

Journal of the American Academy of Child and Adolescent Psychiatry, 2019-10, Vol.58 (10), p.S260-S260

2019

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The genetic architecture of obsessive-compulsive disorder: alleles across the frequency spectrum contribute liability to OCD

The American journal of psychiatry, 2021-11, Vol.179 (3), p.216-225

2021

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47. GENE DISCOVERY FROM EXOME SEQUENCING IN AUTISM AND COMPARISON TO DEVELOPMENTAL DELAY AND SCHIZOPHRENIA

European neuropsychopharmacology, 2021-10, Vol.51, p.e65-e66

2021

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Common genetic variants, acting additively, are a major source of risk for autism

Transcriptome alterations are enriched for synapse-associated genes in the striatum of subjects with obsessive-compulsive disorder

DAWN: a framework to identify autism genes and subnetworks using gene expression and genetics

Gene Expression Deconvolution Implicates Cell-Type-Specific Gene Expression and Co-Expression in Autism

A selective inference approach for false discovery rate control using multiomics covariates yields insights into disease risk

A UNIFIED STATISTICAL FRAMEWORK FOR SINGLE CELL AND BULK RNA SEQUENCING DATA

T20. POLYGENIC RISK FOR SCHIZOPHRENIA IS ASSOCIATED WITH HIPPOCAMPAL VOLUME IN TYPICALLY DEVELOPING YOUTH

H‐MAGMA, inheriting a shaky statistical foundation, yields excess false positives

O11.1. MULTIPLE GENOMIC MEASURES OF SCHIZOPHRENIA RISK ARE RELATED TO CORTICAL THICKNESS IN TYPICALLY DEVELOPING YOUTH AND YOUNG ADULTS

O11.1. MULTIPLE GENOMIC MEASURES OF SCHIZOPHRENIA RISK ARE RELATED TO CORTICAL THICKNESS IN TYPICALLY DEVELOPING YOUTH AND YOUNG ADULTS

Genetics in psychiatry: common variant association studies

TESTING HIGH-DIMENSIONAL COVARIANCE MATRICES, WITH APPLICATION TO DETECTING SCHIZOPHRENIA RISK GENES

Functional connectome fingerprinting accuracy in youths and adults is similar when examined on the same day and 1.5‐years apart

43 SCHIZOPHRENIA POLYGENIC RISK IS ASSOCIATED WITH BRAIN MATURATION IN TYPICALLY DEVELOPING YOUTH

Intelligence, Genes, and Success: Scientists Respond to the Bell Curve

Using a CRISPR/Cas9-Based Epigenetic Editing Tool to Study the Cell-Type-Specific Effects of the DNA Methylation Alterations Observed in the Auditory Cortex Subjects With Schizophrenia

Heritable Variation, With Little or No Maternal Effect, Accounts for Recurrence Risk to Autism Spectrum Disorder in Sweden

T63GENETIC AND ENVIRONMENTAL FACTORS AND RISK OF OBSESSIVE-COMPULSIVE DISORDER

T63. CROSS-DISORDER ANALYSIS OF AUTISM AND ADHD USING RARE VARIANTS: INSIGHTS FROM DANISH IPSYCH EXOMES

F52. Age-Associated Functional Network Organization in Psychosis

ANALYSIS OF RARE CODING AND COMMON VARIANTS IN AUTISM AND COMORBID SUBGROUPS

Spatiotemporal and genetic regulation of A-to-I editing throughout human brain development

5.45 RECURRENT AND LARGE COPY NUMBER VARIATION IN OCD RISK: RESULTS FROM THE EGOS STUDY

The genetic architecture of obsessive-compulsive disorder: alleles across the frequency spectrum contribute liability to OCD

47. GENE DISCOVERY FROM EXOME SEQUENCING IN AUTISM AND COMPARISON TO DEVELOPMENTAL DELAY AND SCHIZOPHRENIA

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