Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Sarah D, Barns"'
Autor:
Tianyun Wang, Jessica Wright, Natalia Volfovsky, Simon Xuming Xu, Brian J. O'Roak, Christopher Fleisch, Leo Brueggeman, LeeAnne Green Snyder, Evan E. Eichler, Sarah D. Barns, Olena Marchenko, Wendy K. Chung, Shwetha C. Murali, Joseph U. Obiajulu, Xueya Zhou, Jacob B. Hall, William T. Harvey, Jacob J. Michaelson, Timothy S. Chang, Daniel H. Geschwind, Irina Astrovskaya, Pamela Feliciano, Bing Han, Andrew Nishida, Chang Shu, Taylor R. Thomas, Yufeng Shen, Tychele N. Turner
Despite the known heritable nature of autism spectrum disorder (ASD), studies have primarily identified risk genes with de novo variants (DNVs). To capture the full spectrum of ASD genetic risk, we performed a two-stage analysis of rare de novo and i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::57bbda70b96aededbabea20ebf74af08
https://doi.org/10.1101/2021.10.08.21264256
https://doi.org/10.1101/2021.10.08.21264256
Autor:
Xueya, Zhou, Pamela, Feliciano, Chang, Shu, Tianyun, Wang, Irina, Astrovskaya, Jacob B, Hall, Joseph U, Obiajulu, Jessica R, Wright, Shwetha C, Murali, Simon Xuming, Xu, Leo, Brueggeman, Taylor R, Thomas, Olena, Marchenko, Christopher, Fleisch, Sarah D, Barns, LeeAnne Green, Snyder, Bing, Han, Timothy S, Chang, Tychele N, Turner, William T, Harvey, Andrew, Nishida, Brian J, O'Roak, Daniel H, Geschwind, Jacob J, Michaelson, Natalia, Volfovsky, Evan E, Eichler, Yufeng, Shen, Zachary E, Warren
Publikováno v:
Nature genetics. 54(9)
To capture the full spectrum of genetic risk for autism, we performed a two-stage analysis of rare de novo and inherited coding variants in 42,607 autism cases, including 35,130 new cases recruited online by SPARK. We identified 60 genes with exome-w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::1081389b34b084f366c6d2fb73e39744
https://pubmed.ncbi.nlm.nih.gov/35982159
https://pubmed.ncbi.nlm.nih.gov/35982159
