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个人简介
While developing computational and statistical methods that can be broadly applied, his group has several primary medical genetics research foci. He has extensive research program in neuropsychiatric genetics – particularly in autism, schizophrenia and ADHD – and has led large-scale GWAS and exome sequencing efforts in this area. His lab serves as the analytic hub for the Psychiatric GWAS Consortium, and international consortium leading the largest collaborative GWAS studies in 5 major psychiatric disorders. He also has a longstanding effort in the mapping of genes for Crohn’s disease and ulcerative colitis where he helped found and lead an international effort that has identified more than 150 genetic risk factors and, in collaboration with Dr. Ramnik Xavier’s group, pursues the functional interpretation and clinical ramifications of these continued gene discovery efforts.
研究兴趣
论文共 971 篇作者统计合作学者相似作者
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Lea Urpa,Mitja I. Kurki,Elisa Rahikkala,Eija Hamalainen,Veikko Salomaa,Jaana Suvisaari,Riikka Keski-Filppula,Merja Rauhala, Satu Korpi-Heikkilae,Jonna Komulainen-Ebrahim,Heli Helander, Paeivi Vieira,
EUROPEAN JOURNAL OF HUMAN GENETICSno. 5 (2024): 1-8
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crossref(2024)
Bloodno. 23 (2024): 2425-2432
Nature Geneticsno. 2 (2024): 327-335
crossref(2024)
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biorxiv(2024)
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