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Phenome-wide association study of the major histocompatibility complex region in the Korean population identifies novel association signals.
Kim, Chanwoo; Kim, Young Jin; Choi, Wanson; Jang, Hye-Mi; Hwang, Mi Yeong; Jung, Sunwoo; Lim, Hyunjoon; Hong, Sang Bin; Yoon, Kyungheon; Kim, Bong-Jo; Park, Hyun-Young; Han, Buhm.
Afiliação
  • Kim C; Department of Electrical and Computer Engineering, Seoul National University, Seoul 08826, Republic of Korea.
  • Kim YJ; Paul G. Allen School of Computer Science and Engineering, University of Washington, Seattle, WA 98195, USA.
  • Choi W; Division of Genome Science, Department of Precision Medicine, National Institute of Health, Cheongju-si, Chungcheongbuk-do 28159,, Republic of Korea.
  • Jang HM; Department of Biomedical Sciences, BK21 Plus Biomedical Science Project, Seoul National University College of Medicine, Seoul 03080, Republic of Korea.
  • Hwang MY; Division of Genome Science, Department of Precision Medicine, National Institute of Health, Cheongju-si, Chungcheongbuk-do 28159,, Republic of Korea.
  • Jung S; Division of Genome Science, Department of Precision Medicine, National Institute of Health, Cheongju-si, Chungcheongbuk-do 28159,, Republic of Korea.
  • Lim H; Interdisciplinary Program in Bioengineering, Seoul National University, Seoul 08826, Republic of Korea.
  • Hong SB; Interdisciplinary Program in Bioengineering, Seoul National University, Seoul 08826, Republic of Korea.
  • Yoon K; Department of Neurology, Seoul National University College of Medicine, Seoul 03080, Republic of Korea.
  • Kim BJ; Division of Genome Science, Department of Precision Medicine, National Institute of Health, Cheongju-si, Chungcheongbuk-do 28159,, Republic of Korea.
  • Park HY; Division of Genome Science, Department of Precision Medicine, National Institute of Health, Cheongju-si, Chungcheongbuk-do 28159,, Republic of Korea.
  • Han B; Department of Precision Medicine, National Institute of Health, Cheongju-si, Chungcheongbuk-do 28159, Republic of Korea.
Hum Mol Genet ; 31(15): 2655-2667, 2022 08 17.
Article em En | MEDLINE | ID: mdl-35043955
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Polimorfismo de Nucleotídeo Único / Estudo de Associação Genômica Ampla Tipo de estudo: Risk_factors_studies Limite: Humans Idioma: En Revista: Hum Mol Genet Assunto da revista: BIOLOGIA MOLECULAR / GENETICA MEDICA Ano de publicação: 2022 Tipo de documento: Article
Texto completo
Adicionar na Minha BVS
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Polimorfismo de Nucleotídeo Único / Estudo de Associação Genômica Ampla Tipo de estudo: Risk_factors_studies Limite: Humans Idioma: En Revista: Hum Mol Genet Assunto da revista: BIOLOGIA MOLECULAR / GENETICA MEDICA Ano de publicação: 2022 Tipo de documento: Article