Author: Ayman H. Fanous

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Preprints

Genome wide meta-analysis identifies genomic relationships, novel loci, and pleiotropic mechanisms across eight psychiatric disorders.

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

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  • Site-wide: 4,117
  • In genetic and genomic medicine: 11
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  • Site-wide: 1,078

Ultra-rare genetic variation in the epilepsies: a whole-exome sequencing study of 17,606 individuals

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  • Site-wide: 6,907
  • In genetics: 338
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A contribution of novel CNVs to schizophrenia from a genome-wide study of 41,321 subjects

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  • In genetics: 405
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Genomic dissection of bipolar disorder and schizophrenia including 28 subphenotypes

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  • Site-wide: 11,324
  • In genomics: 1,258
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Genome-wide association study of suicide attempt in psychiatric disorders identifies association with major depression polygenic risk scores

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  • In genetics: 1,261
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QCAT: testing causality of variants using only summary association statistics

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Genome-wide Association Study of Clinical Features in the Schizophrenia Psychiatric Genomics Consortium: Confirmation of Polygenic Effect on Negative Symptoms

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Proof of concept: Molecular prediction of schizophrenia risk

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Contribution of rare copy number variants to bipolar disorder risk is limited to schizoaffective cases

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  • In genetics: 2,300
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FIQT: a simple, powerful method to accurately estimate effect sizes in genome scans

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  • In genetics: 2,646
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Dissecting the shared genetic architecture of suicide attempt, psychiatric disorders and known risk factors

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  • In genetic and genomic medicine: 182
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Investigation of convergent and divergent genetic influences underlying schizophrenia and alcohol use disorder

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  • Site-wide: 102,456
  • In genetic and genomic medicine: 396
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  • Site-wide: 55,951