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pro vyhledávání: '"Broome, Jai"'
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Autor:
Mikhaylova, Anna V, McHugh, Caitlin P, Polfus, Linda M, Raffield, Laura M, Boorgula, Meher Preethi, Blackwell, Thomas W, Brody, Jennifer A, Broome, Jai, Chami, Nathalie, Chen, Ming-Huei, Conomos, Matthew P, Cox, Corey, Curran, Joanne E, Daya, Michelle, Ekunwe, Lynette, Glahn, David C, Heard-Costa, Nancy, Highland, Heather M, Hobbs, Brian D, Ilboudo, Yann, Jain, Deepti, Lange, Leslie A, Miller-Fleming, Tyne W, Min, Nancy, Moon, Jee-Young, Preuss, Michael H, Rosen, Jonathon, Ryan, Kathleen, Smith, Albert V, Sun, Quan, Surendran, Praveen, de Vries, Paul S, Walter, Klaudia, Wang, Zhe, Wheeler, Marsha, Yanek, Lisa R, Zhong, Xue, Abecasis, Goncalo R, Almasy, Laura, Barnes, Kathleen C, Beaty, Terri H, Becker, Lewis C, Blangero, John, Boerwinkle, Eric, Butterworth, Adam S, Chavan, Sameer, Cho, Michael H, Choquet, Hélène, Correa, Adolfo, Cox, Nancy, DeMeo, Dawn L, Faraday, Nauder, Fornage, Myriam, Gerszten, Robert E, Hou, Lifang, Johnson, Andrew D, Jorgenson, Eric, Kaplan, Robert, Kooperberg, Charles, Kundu, Kousik, Laurie, Cecelia A, Lettre, Guillaume, Lewis, Joshua P, Li, Bingshan, Li, Yun, Lloyd-Jones, Donald M, Loos, Ruth JF, Manichaikul, Ani, Meyers, Deborah A, Mitchell, Braxton D, Morrison, Alanna C, Ngo, Debby, Nickerson, Deborah A, Nongmaithem, Suraj, North, Kari E, O'Connell, Jeffrey R, Ortega, Victor E, Pankratz, Nathan, Perry, James A, Psaty, Bruce M, Rich, Stephen S, Soranzo, Nicole, Rotter, Jerome I, Silverman, Edwin K, Smith, Nicholas L, Tang, Hua, Tracy, Russell P, Thornton, Timothy A, Vasan, Ramachandran S, Zein, Joe, Mathias, Rasika A, NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium, Reiner, Alexander P, Auer, Paul L
Publikováno v:
American journal of human genetics, vol 108, iss 10
Many common and rare variants associated with hematologic traits have been discovered through imputation on large-scale reference panels. However, the majority of genome-wide association studies (GWASs) have been conducted in Europeans, and determini
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______325::1f3a94426432e7d8d437082d4c6c39d7
https://escholarship.org/uc/item/6432c6xx
https://escholarship.org/uc/item/6432c6xx
Autor:
Hu, Yao, Stilp, Adrienne M, McHugh, Caitlin P, Rao, Shuquan, Jain, Deepti, Zheng, Xiuwen, Lane, John, Méric de Bellefon, Sébastian, Raffield, Laura M, Chen, Ming-Huei, Yanek, Lisa R, Wheeler, Marsha, Yao, Yao, Ren, Chunyan, Broome, Jai, Moon, Jee-Young, de Vries, Paul S, Hobbs, Brian D, Sun, Quan, Surendran, Praveen, Brody, Jennifer A, Blackwell, Thomas W, Choquet, Hélène, Ryan, Kathleen, Duggirala, Ravindranath, Heard-Costa, Nancy, Wang, Zhe, Chami, Nathalie, Preuss, Michael H, Min, Nancy, Ekunwe, Lynette, Lange, Leslie A, Cushman, Mary, Faraday, Nauder, Curran, Joanne E, Almasy, Laura, Kundu, Kousik, Smith, Albert V, Gabriel, Stacey, Rotter, Jerome I, Fornage, Myriam, Lloyd-Jones, Donald M, Vasan, Ramachandran S, Smith, Nicholas L, North, Kari E, Boerwinkle, Eric, Becker, Lewis C, Lewis, Joshua P, Abecasis, Goncalo R, Hou, Lifang, O'Connell, Jeffrey R, Morrison, Alanna C, Beaty, Terri H, Kaplan, Robert, Correa, Adolfo, Blangero, John, Jorgenson, Eric, Psaty, Bruce M, Kooperberg, Charles, Walton, Russell T, Kleinstiver, Benjamin P, Tang, Hua, Loos, Ruth JF, Soranzo, Nicole, Butterworth, Adam S, Nickerson, Debbie, Rich, Stephen S, Mitchell, Braxton D, Johnson, Andrew D, Auer, Paul L, Li, Yun, Mathias, Rasika A, Lettre, Guillaume, Pankratz, Nathan, Laurie, Cathy C, Laurie, Cecelia A, Bauer, Daniel E, Conomos, Matthew P, Reiner, Alexander P, NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium
Publikováno v:
American journal of human genetics, vol 108, iss 5
Whole-genome sequencing (WGS), a powerful tool for detecting novel coding and non-coding disease-causing variants, has largely been applied to clinical diagnosis of inherited disorders. Here we leveraged WGS data in up to 62,653 ethnically diverse pa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______325::445eb02b1c412ec0c77798d591b7420a
https://escholarship.org/uc/item/24j6v92r
https://escholarship.org/uc/item/24j6v92r
Autor:
Mikhaylova, Anna V.1 (AUTHOR), McHugh, Caitlin P.1 (AUTHOR), Polfus, Linda M.1,2 (AUTHOR), Raffield, Laura M.3 (AUTHOR), Boorgula, Meher Preethi4 (AUTHOR), Blackwell, Thomas W.5 (AUTHOR), Brody, Jennifer A.6 (AUTHOR), Broome, Jai1 (AUTHOR), Chami, Nathalie7 (AUTHOR), Chen, Ming-Huei8,9 (AUTHOR), Conomos, Matthew P.1 (AUTHOR), Cox, Corey4 (AUTHOR), Curran, Joanne E.10 (AUTHOR), Daya, Michelle4 (AUTHOR), Ekunwe, Lynette11 (AUTHOR), Glahn, David C.12 (AUTHOR), Heard-Costa, Nancy9,13 (AUTHOR), Highland, Heather M.14 (AUTHOR), Hobbs, Brian D.15,16 (AUTHOR), Ilboudo, Yann17,18 (AUTHOR)
Publikováno v:
American Journal of Human Genetics. Oct2021, Vol. 108 Issue 10, p1836-1851. 16p.