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Genetic identification of brain cell types underlying schizophrenia

Nature genetics, 2018-06, Vol.50 (6), p.825-833

2018

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The contribution of rare variants to risk of schizophrenia in individuals with and without intellectual disability

Nature genetics, 2017-08, Vol.49 (8), p.1167-1173

2017

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Genome-wide association study identifies 30 loci associated with bipolar disorder

Nature genetics, 2019-05, Vol.51 (5), p.793-803

2019

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Analyses of allele-specific gene expression in highly divergent mouse crosses identifies pervasive allelic imbalance

Nature genetics, 2015-04, Vol.47 (4), p.353-360

2015

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Genome-wide association study identifies eight risk loci and implicates metabo-psychiatric origins for anorexia nervosa

Nature genetics, 2019-08, Vol.51 (8), p.1207-1214

2019

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Microduplications of 16p11.2 are associated with schizophrenia

Nature genetics, 2009-11, Vol.41 (11), p.1223-1227

2009

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Widespread adenine N6-methylation of active genes in fungi

Nature genetics, 2017-06, Vol.49 (6), p.964-968

2017

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Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression

Nature genetics, 2018-05, Vol.50 (5), p.668-681

2018

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Large-scale genome-wide association analysis of bipolar disorder identifies a new susceptibility locus near ODZ4

Nature genetics, 2011-10, Vol.43 (10), p.977-983

2011

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Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder

Nature genetics, 2019-01, Vol.51 (1), p.63-75

2019

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Genome-wide association study of more than 40,000 bipolar disorder cases provides new insights into the underlying biology

Nature genetics, 2021-06, Vol.53 (6), p.817-829

2021

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Identification of common genetic risk variants for autism spectrum disorder

Nature genetics, 2019-03, Vol.51 (3), p.431-444

2019

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The NCI Genomic Data Commons

Nature genetics, 2021-03, Vol.53 (3), p.257-262

2021

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LD Score regression distinguishes confounding from polygenicity in genome-wide association studies

Nature genetics, 2015-03, Vol.47 (3), p.291-295

2015

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Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects

Nature genetics, 2017-01, Vol.49 (1), p.27-35

2017

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Genetic identification of cell types underlying brain complex traits yields insights into the etiology of Parkinson's disease

Nature genetics, 2020-05, Vol.52 (5), p.482-493

2020

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Dominant and recessive deafness caused by mutations of a novel gene, TMC1 , required for cochlear hair-cell function

Nature genetics, 2002-03, Vol.30 (3), p.277-284

2002

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Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs

Nature genetics, 2013-09, Vol.45 (9), p.984-994

2013

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Genome-wide meta-analyses identify multiple loci associated with smoking behavior

Nature genetics, 2010-05, Vol.42 (5), p.441-447

2010

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Inferring compound heterozygosity from large-scale exome sequencing data

Nature genetics, 2024-01, Vol.56 (1), p.152-161

2024

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Author Correction: The NCI Genomic Data Commons

Nature genetics, 2021-06, Vol.53 (6), p.935-935

2021

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Erratum: Corrigendum: Analyses of allele-specific gene expression in highly divergent mouse crosses identifies pervasive allelic imbalance

Nature genetics, 2015-05, Vol.47 (6), p.690-690

2015

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Genetic identification of brain cell types underlying schizophrenia

The contribution of rare variants to risk of schizophrenia in individuals with and without intellectual disability

Genome-wide association study identifies 30 loci associated with bipolar disorder

Analyses of allele-specific gene expression in highly divergent mouse crosses identifies pervasive allelic imbalance

Genome-wide association study identifies eight risk loci and implicates metabo-psychiatric origins for anorexia nervosa

Microduplications of 16p11.2 are associated with schizophrenia

Triplication of a 21q22 region contributes to B cell transformation through HMGN1 overexpression and loss of histone H3 Lys27 trimethylation

Widespread adenine N6-methylation of active genes in fungi

Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression

Large-scale genome-wide association analysis of bipolar disorder identifies a new susceptibility locus near ODZ4

Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder

Genome-wide association study of more than 40,000 bipolar disorder cases provides new insights into the underlying biology

Identification of common genetic risk variants for autism spectrum disorder

The NCI Genomic Data Commons

LD Score regression distinguishes confounding from polygenicity in genome-wide association studies

Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects

Genetic identification of cell types underlying brain complex traits yields insights into the etiology of Parkinson's disease

Dominant and recessive deafness caused by mutations of a novel gene, TMC1 , required for cochlear hair-cell function

Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs

Gene expression imputation across multiple brain regions provides insights into schizophrenia risk

Publisher Correction: Gene expression imputation across multiple brain regions provides insights into schizophrenia risk

Genome-wide meta-analyses identify multiple loci associated with smoking behavior

Inferring compound heterozygosity from large-scale exome sequencing data

Author Correction: The NCI Genomic Data Commons

Erratum: Corrigendum: Analyses of allele-specific gene expression in highly divergent mouse crosses identifies pervasive allelic imbalance

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