Zobrazeno 1 - 2
of 2
pro vyhledávání: '"F. S. P. Kury"'
Autor:
Martin I. Jones, Joseph D. Szustakowski, Giorgio Sirugo, Lukas Habegger, Adam J. Mansfield, Will Salerno, Joshua D. Backman, Athanasios Kousathanas, David J. Carey, Yi-Pin Lai, James F. Wilson, Alison M. Meynert, Anne E. Justice, Alexander H. Li, Jack A. Kosmicki, Anthony Marcketta, Sándor Szalma, Shane McCarthy, A. R. Shuldiner, A. Baras, Daniel J. Rader, Michael N. Cantor, Ashish Yadav, Manuel A. R. Ferreira, F. S. P. Kury, Konrad Rawlik, Loukas Moutsianas, Gonçalo R. Abecasis, Susan P. Walker, Xing Chen, Albert Tenesa, Paul Nioi, Adam E. Locke, Guillaume Butler-Laporte, E. N. Smith, Richard H Scott, Gundula Povysil, Joseph B. Leader, Lauren Gurski, Dorota Pasko, Marylyn D. Ritchie, A. Cordova-Palomera, Kyoko Watanabe, Colm O'Dushlaine, A. O'Neill, Tomoko Nakanishi, Erola Pairo-Castineira, Xiuwen Zheng, Emily Wong, Jeffrey G. Reid, Slavé Petrovski, Julie E. Horowitz, Anurag Verma, Justin W. Davis, Dylan Sun, Sahar Esmaeeli, Heiko Runz, Quanli Wang, John D. Overton, Shareef Khalid, Tooraj Mirshahi, Evan Maxwell, Mark J. Caulfield, Mark Lathrop, Olympe Chazara, Deepika Sharma, David Goldstein, Jonathan Marchini, Xiaodong Bai, Suganthi Balasubramanian, Krzysztof Kiryluk, Nilanjana Banerjee, Rouel Lanche, J. B. Richards, Hyun Min Kang, J. K. Baillie, Yunfeng Huang, Sean O'Keeffe, Erika Kvikstad, Margaret M. Parker, Joelle Mbatchou
Publikováno v:
American Journal of Human Genetics
2021, ' Pan-ancestry exome-wide association analyses of COVID-19 outcomes in 586,157 individuals ', American Journal of Human Genetics . https://doi.org/10.1016/j.ajhg.2021.05.017
2021, ' Pan-ancestry exome-wide association analyses of COVID-19 outcomes in 586,157 individuals ', American Journal of Human Genetics . https://doi.org/10.1016/j.ajhg.2021.05.017
Severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) causes coronavirus disease 2019 (COVID-19), a respiratory illness that can result in hospitalization or death. We used exome sequence data to investigate associations between rare genetic v
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::23e76c4cbfadf4bffed84b525d70957b
http://europepmc.org/articles/PMC8173480
http://europepmc.org/articles/PMC8173480
Common genetic variants identify targets for COVID-19 and individuals at high risk of severe disease
Autor:
J E, Horowitz, J A, Kosmicki, A, Damask, D, Sharma, G H L, Roberts, A E, Justice, N, Banerjee, M V, Coignet, A, Yadav, J B, Leader, A, Marcketta, D S, Park, R, Lanche, E, Maxwell, S C, Knight, X, Bai, H, Guturu, D, Sun, A, Baltzell, F S P, Kury, J D, Backman, A R, Girshick, C, O'Dushlaine, S R, McCurdy, R, Partha, A J, Mansfield, D A, Turissini, A H, Li, M, Zhang, J, Mbatchou, K, Watanabe, L, Gurski, S E, McCarthy, H M, Kang, L, Dobbyn, E, Stahl, A, Verma, G, Sirugo, M D, Ritchie, M, Jones, S, Balasubramanian, K, Siminovitch, W J, Salerno, A R, Shuldiner, D J, Rader, T, Mirshahi, A E, Locke, J, Marchini, J D, Overton, D J, Carey, L, Habegger, M N, Cantor, K A, Rand, E L, Hong, J G, Reid, C A, Ball, A, Baras, G R, Abecasis, M A, Ferreira
Publikováno v:
medRxiv
The need to identify and effectively treat COVID-19 cases at highest risk for severe disease remains critical. We identified five common genetic loci (two novel) that modulate both COVID-19 susceptibility and severity, implicating TMPRSS2, IFNAR2, CC
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::0280def6ca331ba9b219c4a4db248c7d
https://europepmc.org/articles/PMC7899471/
https://europepmc.org/articles/PMC7899471/
