Author: Hailiang Huang

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Preprints

Discovery Of The First Genome-Wide Significant Risk Loci For ADHD

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  • Site-wide: 624
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• Year to date:
  • Site-wide: 3,942
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  • Site-wide: 7,591

Common risk variants identified in autism spectrum disorder

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  • Site-wide: 1,025
  • In genetics: 35
• Year to date:
  • Site-wide: 1,835
• Since beginning of last month:
  • Site-wide: 2,763

Rewiring of the cellular and inter-cellular landscape of the human colon during ulcerative colitis

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  • Site-wide: 2,187
  • In genomics: 260
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  • Site-wide: None
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Association mapping of inflammatory bowel disease loci to single variant resolution

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  • Site-wide: 2,820
  • In genetics: 118
• Year to date:
  • Site-wide: 36,053
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  • Site-wide: 44,388

Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine

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  • Site-wide: 4,735
  • In genetics: 230
• Year to date:
  • Site-wide: 82,367
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  • Site-wide: 97,148

Exome sequencing identifies rare coding variants in 10 genes which confer substantial risk for schizophrenia

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  • Site-wide: 5,081
  • In genetic and genomic medicine: 12
• Year to date:
  • Site-wide: 1,100
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  • Site-wide: 1,396

Comparative genetic architectures of schizophrenia in East Asian and European populations

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  • Site-wide: 5,609
  • In genetics: 278
• Year to date:
  • Site-wide: 13,653
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Genome-wide maps of enhancer regulation connect risk variants to disease genes

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  • Site-wide: 5,999
  • In genetics: 302
• Year to date:
  • Site-wide: 2,140
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  • Site-wide: 2,457

A contribution of novel CNVs to schizophrenia from a genome-wide study of 41,321 subjects

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  • Site-wide: 7,923
  • In genetics: 399
• Year to date:
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Whole Genome Sequencing in Psychiatric Disorders: the WGSPD Consortium

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  • Site-wide: 8,671
  • In genomics: 1,006
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  • Site-wide: 42,481

Population-specific causal disease effect sizes in functionally important regions impacted by selection

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  • Site-wide: 8,675
  • In genetics: 441
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  • Site-wide: 18,551

Insights into the genetic epidemiology of Crohn's and rare diseases in the Ashkenazi Jewish population

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  • Site-wide: 9,881
  • In genetics: 499
• Year to date:
  • Site-wide: 73,346
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  • Site-wide: 86,821

Genomic dissection of bipolar disorder and schizophrenia including 28 subphenotypes

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  • Site-wide: 10,808
  • In genomics: 1,227
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  • Site-wide: 68,502
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  • Site-wide: 103,093

Integrative genetic and epigenetic analysis uncovers regulatory mechanisms of autoimmune disease

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  • Site-wide: 13,478
  • In genetics: 697
• Year to date:
  • Site-wide: 103,412
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  • Site-wide: 54,798

Bootstrat: Population Informed Bootstrapping for Rare Variant Tests

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  • Site-wide: 34,520
  • In genomics: 3,043
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  • Site-wide: 92,692
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  • Site-wide: 112,711

RICOPILI: Rapid Imputation for COnsortias PIpeLIne

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  • Site-wide: 35,310
  • In genetics: 1,765
• Year to date:
  • Site-wide: 110,692
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  • Site-wide: 117,726

The Cancer Epitope Trees of 23 Early Cervical Cancers in Chinese Women

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  • Site-wide: 49,740
  • In cancer biology: 1,378
• Year to date:
  • Site-wide: 111,787
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  • Site-wide: 91,215

Junction-skipping regulation in complex disease

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  • Site-wide: 67,624
  • In genetics: 3,205
• Year to date:
  • Site-wide: 98,172
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  • Site-wide: 109,651

Large-Scale Evaluation of the Positive and Negative Syndrome Scale (PANSS) Symptom Architecture in Schizophrenia

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  • Site-wide: 84,968
  • In psychiatry and clinical psychology: 260
• Year to date:
  • Site-wide: 11,726
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  • Site-wide: 13,068

Elucidating the Joint Genetic Architecture of Mood Disorder and Schizophrenia

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  • Site-wide: 89,964
  • In genetic and genomic medicine: 284
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  • Site-wide: 57,304
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  • Site-wide: 26,891

Improving Polygenic Prediction in Ancestrally Diverse Populations

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  • Site-wide: 92,190
  • In genetic and genomic medicine: 301
• Year to date:
  • Site-wide: 546
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  • Site-wide: None

Systematic comparative analysis of Mendelian randomization methods for inferring causal genes of complex phenotypes and the application to psychiatric diseases

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  • Site-wide: 122,516
  • In bioinformatics: 9,852
• Year to date:
  • Site-wide: 87,947
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  • Site-wide: 40,035