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Integrating de novo and inherited variants in 42,607 autism cases identifies mutations in new moderate-risk genes.
Zhou, Xueya; Feliciano, Pamela; Shu, Chang; Wang, Tianyun; Astrovskaya, Irina; Hall, Jacob B; Obiajulu, Joseph U; Wright, Jessica R; Murali, Shwetha C; Xu, Simon Xuming; Brueggeman, Leo; Thomas, Taylor R; Marchenko, Olena; Fleisch, Christopher; Barns, Sarah D; Snyder, LeeAnne Green; Han, Bing; Chang, Timothy S; Turner, Tychele N; Harvey, William T; Nishida, Andrew; O'Roak, Brian J; Geschwind, Daniel H; Michaelson, Jacob J; Volfovsky, Natalia; Eichler, Evan E; Shen, Yufeng; Chung, Wendy K.
Afiliación
  • Zhou X; Department of Pediatrics, Columbia University Medical Center, New York, NY, USA.
  • Feliciano P; Department of Systems Biology, Columbia University Medical Center, New York, NY, USA.
  • Shu C; Simons Foundation, New York, NY, USA.
  • Wang T; Department of Pediatrics, Columbia University Medical Center, New York, NY, USA.
  • Astrovskaya I; Department of Systems Biology, Columbia University Medical Center, New York, NY, USA.
  • Hall JB; Department of Genome Sciences, University of Washington School of Medicine, Seattle, WA, USA.
  • Obiajulu JU; Department of Medical Genetics, Center for Medical Genetics, School of Basic Medical Sciences, Peking University Health Science Center, Beijing, China.
  • Wright JR; Neuroscience Research Institute, Department of Neurobiology, School of Basic Medical Sciences, Peking University Health Science Center; Key Laboratory for Neuroscience, Ministry of Education of China & National Health Commission of China, Beijing, China.
  • Murali SC; Simons Foundation, New York, NY, USA.
  • Xu SX; Simons Foundation, New York, NY, USA.
  • Brueggeman L; Department of Pediatrics, Columbia University Medical Center, New York, NY, USA.
  • Thomas TR; Department of Systems Biology, Columbia University Medical Center, New York, NY, USA.
  • Marchenko O; Simons Foundation, New York, NY, USA.
  • Fleisch C; Department of Genome Sciences, University of Washington School of Medicine, Seattle, WA, USA.
  • Barns SD; Howard Hughes Medical Institute, University of Washington, Seattle, WA, USA.
  • Snyder LG; Simons Foundation, New York, NY, USA.
  • Han B; Department of Psychiatry, University of Iowa Carver College of Medicine, Iowa City, IA, USA.
  • Chang TS; Department of Psychiatry, University of Iowa Carver College of Medicine, Iowa City, IA, USA.
  • Turner TN; Simons Foundation, New York, NY, USA.
  • Harvey WT; Simons Foundation, New York, NY, USA.
  • Nishida A; Simons Foundation, New York, NY, USA.
  • O'Roak BJ; Simons Foundation, New York, NY, USA.
  • Geschwind DH; Simons Foundation, New York, NY, USA.
  • Michaelson JJ; Department of Genetics, Washington University, St. Louis, MO, USA.
  • Volfovsky N; Department of Genome Sciences, University of Washington School of Medicine, Seattle, WA, USA.
  • Eichler EE; Department of Molecular & Medical Genetics, Oregon Health & Science University, Portland, OR, USA.
  • Shen Y; Department of Molecular & Medical Genetics, Oregon Health & Science University, Portland, OR, USA.
  • Chung WK; Program in Neurogenetics, Department of Neurology, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, CA, USA.
Nat Genet ; 54(9): 1305-1319, 2022 09.
Article en En | MEDLINE | ID: mdl-35982159
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Trastorno Autístico / Trastorno del Espectro Autista Tipo de estudio: Etiology_studies / Prognostic_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: Nat Genet Asunto de la revista: GENETICA MEDICA Año: 2022 Tipo del documento: Article País de afiliación: Estados Unidos
Texto completo
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Buscar en Google

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Trastorno Autístico / Trastorno del Espectro Autista Tipo de estudio: Etiology_studies / Prognostic_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: Nat Genet Asunto de la revista: GENETICA MEDICA Año: 2022 Tipo del documento: Article País de afiliación: Estados Unidos