Skip to main content

and
  1. Article

    Open Access

    Identification of potential genetic risk factors for bipolar disorder by whole-exome sequencing

    This study aims at assessing the burden of rare (minor allele frequency < 1%) predicted damaging variants in the whole exome of 92 bipolar I disorder (BD) patients and 1051 controls of French ancestry. Patient...

    Thomas Husson, Jean-Baptiste Duboc, Olivier Quenez in Translational Psychiatry (2018)

  2. Article

    Open Access

    Correction: Whole exome sequencing study identifies novel rare and common Alzheimer’s-Associated variants involved in immune response and transcriptional regulation

    A correction to this paper has been published and can be accessed via a link at the top of the paper.

    Joshua C. Bis, Xueqiu Jian, Brian W. Kunkle, Yuning Chen in Molecular Psychiatry (2020)

  3. Article

    Open Access

    Whole exome sequencing study identifies novel rare and common Alzheimer’s-Associated variants involved in immune response and transcriptional regulation

    The Alzheimer’s Disease Sequencing Project (ADSP) undertook whole exome sequencing in 5,740 late-onset Alzheimer disease (AD) cases and 5,096 cognitively normal controls primarily of European ancestry (EA), am...

    Joshua C. Bis, Xueqiu Jian, Brian W. Kunkle, Yuning Chen in Molecular Psychiatry (2020)