Author: Shaun M. Purcell

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Preprints

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

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Genomewide association study identifies 30 loci associated with bipolar disorder

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  • Site-wide: 1,497
  • In genetics: 41
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Regulatory variants explain much more heritability than coding variants across 11 common diseases

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  • Site-wide: 2,938
  • In genetics: 92
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Ultra-rare disruptive and damaging mutations influence educational attainment in the general population

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  • Site-wide: 7,444
  • In genetics: 320
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Biological and clinical insights from genetics of insomnia symptoms

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  • In genomics: 798
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  • Site-wide: 12,908
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Gene Expression Elucidates Functional Impact of Polygenic Risk for Schizophrenia

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  • Site-wide: 9,262
  • In genomics: 927
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A contribution of novel CNVs to schizophrenia from a genome-wide study of 41,321 subjects

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  • Site-wide: 10,539
  • In genetics: 458
• Year to date:
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GWAS in 446,118 European adults identifies 78 genetic loci for self-reported habitual sleep duration supported by accelerometer-derived estimates

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  • Site-wide: 13,688
  • In genetics: 607
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Integrated Bayesian analysis of rare exonic variants to identify risk genes for schizophrenia and neurodevelopmental disorders

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  • In genomics: 1,416
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Genomic dissection of bipolar disorder and schizophrenia including 28 subphenotypes

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  • Site-wide: 14,513
  • In genomics: 1,444
• Year to date:
  • Site-wide: 114,563
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  • Site-wide: 100,105

Genome-wide association analyses of sleep disturbance traits identify new loci and highlight shared genetics with neuropsychiatric and metabolic traits

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  • Site-wide: 141,062
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  • Site-wide: 151,034

Gene expression imputation across multiple brain regions reveals schizophrenia risk throughout development.

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• Year to date:
  • Site-wide: 112,970
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  • Site-wide: 108,989

Rare loss-of-function variants in KMT2F are associated with schizophrenia and developmental disorders

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  • In genomics: 2,216
• Year to date:
  • Site-wide: 104,977
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  • Site-wide: 107,347

Integrative analysis of rare variants and pathway information shows convergent results between immune pathways, drug targets and epilepsy genes

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  • Site-wide: 35,288
  • In genomics: 2,952
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Genome-wide association analysis of excessive daytime sleepiness identifies 42 loci that suggest phenotypic subgroups

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  • Site-wide: 53,278
  • In genomics: 4,009
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Contribution of rare copy number variants to bipolar disorder risk is limited to schizoaffective cases

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  • Site-wide: 60,130
  • In genetics: 2,603
• Year to date:
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  • Site-wide: 142,288

Whole-Genome Association Analyses of Sleep-disordered Breathing Phenotypes in the NHLBI TOPMed Program

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  • Site-wide: 78,608

Characterization of single gene copy number variants in schizophrenia

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  • Site-wide: 69,703
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  • Site-wide: 152,002
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Epigenome-wide association analysis of daytime sleepiness in the Multi-Ethnic Study of Atherosclerosis reveals African-American specific associations

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  • Site-wide: 93,704
  • In genomics: 5,850
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  • Site-wide: 139,076
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mTADA: a framework for analyzing de novo mutations in multiple traits

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  • Site-wide: 95,722
  • In genomics: 5,915
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  • Site-wide: 150,960
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A group refactorization procedure for sleep electroencephalography

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  • Site-wide: 149,737
  • In bioinformatics: 11,394
• Year to date:
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  • Site-wide: 140,957