Author: James A. Knowles

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

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

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Deconvolution of Transcriptional Networks Identifies TCF4 as a Master Regulator in Schizophrenia

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Genomic dissection of bipolar disorder and schizophrenia including 28 subphenotypes

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Assessing the measurement transfer function of single-cell RNA sequencing

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Polygenic selection underlies evolution of human brain structure and behavioral traits

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Rare copy number variants in NRXN1 and CNTN6 increase risk for Tourette syndrome

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Examination of the Shared Genetic Basis of Anorexia Nervosa and Obsessive-Compulsive Disorder

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Evolutionary and functional data power search for obsessive-compulsive disorder genes

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Gene expression in patient-derived neural progenitors implicates WNT5A signaling in the etiology of schizophrenia

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

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Genetic variation in the Major Histocompatibility Complex and association with depression

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Concordance Of Genetic Variation That Increases Risk For Tourette Syndrome And That Influences Its Underlying Neurocircuitry

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Transcriptional Profiling of Primate Central Nucleus of the Amygdala Neurons to Understand the Molecular Underpinnings of Early Life Anxious Temperament

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A CTGF-YAP regulatory pathway is essential for angiogenesis and barriergenesis in the retina

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