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The impact of rare protein coding genetic variation on adult cognitive function.
Chen, Chia-Yen; Tian, Ruoyu; Ge, Tian; Lam, Max; Sanchez-Andrade, Gabriela; Singh, Tarjinder; Urpa, Lea; Liu, Jimmy Z; Sanderson, Mark; Rowley, Christine; Ironfield, Holly; Fang, Terry; Daly, Mark; Palotie, Aarno; Tsai, Ellen A; Huang, Hailiang; Hurles, Matthew E; Gerety, Sebastian S; Lencz, Todd; Runz, Heiko.
Afiliação
  • Chen CY; Research and Development, Biogen Inc, Cambridge, MA, USA. chiayenc@gmail.com.
  • Tian R; Research and Development, Biogen Inc, Cambridge, MA, USA.
  • Ge T; Dewpoint Therapeutics, Boston, MA, USA.
  • Lam M; Psychiatric and Neurodevelopmental Genetics Unit, Center for Genomic Medicine, Massachusetts General Hospital, Boston, MA, USA.
  • Sanchez-Andrade G; Department of Psychiatry, Massachusetts General Hospital, Harvard Medical School, Boston, MA, USA.
  • Singh T; Stanley Center for Psychiatric Research, Broad Institute of MIT and Harvard, Cambridge, MA, USA.
  • Urpa L; Stanley Center for Psychiatric Research, Broad Institute of MIT and Harvard, Cambridge, MA, USA.
  • Liu JZ; Division of Psychiatry Research, The Zucker Hillside Hospital, Northwell Health, Glen Oaks, NY, USA.
  • Sanderson M; Institute of Behavioral Science, Feinstein Institutes for Medical Research, Manhasset, NY, USA.
  • Rowley C; Wellcome Sanger Institute, Cambridge, UK.
  • Ironfield H; Stanley Center for Psychiatric Research, Broad Institute of MIT and Harvard, Cambridge, MA, USA.
  • Fang T; Analytic and Translational Genetics Unit, Massachusetts General Hospital, Boston, MA, USA.
  • Daly M; Wellcome Sanger Institute, Cambridge, UK.
  • Palotie A; Wellcome Sanger Institute, Cambridge, UK.
  • Tsai EA; Wellcome Sanger Institute, Cambridge, UK.
  • Huang H; Research and Development, Biogen Inc, Cambridge, MA, USA.
  • Runz H; Stanley Center for Psychiatric Research, Broad Institute of MIT and Harvard, Cambridge, MA, USA.
Nat Genet ; 55(6): 927-938, 2023 06.
Article em En | MEDLINE | ID: mdl-37231097
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Variação Genética / Transtornos do Neurodesenvolvimento Limite: Adult / Animals / Humans Idioma: En Revista: Nat Genet Assunto da revista: GENETICA MEDICA Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Estados Unidos
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: Variação Genética / Transtornos do Neurodesenvolvimento Limite: Adult / Animals / Humans Idioma: En Revista: Nat Genet Assunto da revista: GENETICA MEDICA Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Estados Unidos