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  1. Article

    Publisher Correction: Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes

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

    Rainer Malik, Ganesh Chauhan, Matthew Traylor… in Nature Genetics (2019)

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  2. Article

    Open Access

    Integrated analysis of human genetic association study and mouse transcriptome suggests LBH and SHF genes as novel susceptible genes for amyloid-β accumulation in Alzheimer’s disease

    Alzheimer’s disease (AD) is a common neurological disease that causes dementia in humans. Although the reports of associated pathological genes have been increasing, the molecular mechanism leading to the accu...

    Yumi Yamaguchi-Kabata, Takashi Morihara, Tomoyuki Ohara… in Human Genetics (2018)

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  3. No Access

    Article

    Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes

    Stroke has multiple etiologies, but the underlying genes and pathways are largely unknown. We conducted a multiancestry genome-wide-association meta-analysis in 521,612 individuals (67,162 cases and 454,450 co...

    Rainer Malik, Ganesh Chauhan, Matthew Traylor… in Nature Genetics (2018)

  4. No Access

    Article

    A nonsynonymous SNP in PRKCH (protein kinase C η) increases the risk of cerebral infarction

    Cerebral infarction is the most common type of stroke and often causes long-term disability. To investigate the genetic contribution to cerebral infarction, we conducted a case-control study using 52,608 gene-...

    Michiaki Kubo, Jun Hata, Toshiharu Ninomiya, Koichi Matsuda… in Nature Genetics (2007)