Zobrazeno 1 - 10
of 506
pro vyhledávání: '"Doumatey A"'
Autor:
Brooke Szczesny, Meher Preethi Boorgula, Sameer Chavan, Monica Campbell, Randi K. Johnson, Kai Kammers, Emma E. Thompson, Madison S. Cox, Gautam Shankar, Corey Cox, Andréanne Morin, Wendy Lorizio, Michelle Daya, Samir N. P. Kelada, Terri H. Beaty, Ayo P. Doumatey, Alvaro A. Cruz, Harold Watson, Edward T. Naureckas, B. Louise Giles, Ganiyu A. Arinola, Olumide Sogaolu, Adegoke G. Falade, Nadia N. Hansel, Ivana V. Yang, Christopher O. Olopade, Charles N. Rotimi, R. Clive Landis, Camila A. Figueiredo, Matthew C. Altman, Eimear Kenny, Ingo Ruczinski, Andrew H. Liu, Carole Ober, Margaret A. Taub, Kathleen C. Barnes, Rasika A. Mathias
Publikováno v:
Nature Communications, Vol 15, Iss 1, Pp 1-12 (2024)
Abstract Asthma has striking disparities across ancestral groups, but the molecular underpinning of these differences is poorly understood and minimally studied. A goal of the Consortium on Asthma among African-ancestry Populations in the Americas (C
Externí odkaz:
https://doaj.org/article/db1254fb2cdc4e4c8565e2404e6adbdb
Autor:
Ayo P. Doumatey, Daniel Shriner, Jie Zhou, Lin Lei, Guanjie Chen, Omolara Oluwasola-Taiwo, Susan Nkem, Adela Ogundeji, Sally N. Adebamowo, Amy R. Bentley, Mateus H. Gouveia, Karlijn A. C. Meeks, Clement A. Adebamowo, Adebowale A. Adeyemo, Charles N. Rotimi
Publikováno v:
Genome Medicine, Vol 16, Iss 1, Pp 1-18 (2024)
Abstract Background Type 2 diabetes (T2D) has reached epidemic proportions globally, including in Africa. However, molecular studies to understand the pathophysiology of T2D remain scarce outside Europe and North America. The aims of this study are t
Externí odkaz:
https://doaj.org/article/4d020d773e6245dab0caa4b6f73e88be
Autor:
Karlijn A. C. Meeks, Amy R. Bentley, Themistocles L. Assimes, Nora Franceschini, Adebowale A. Adeyemo, Charles N. Rotimi, Ayo P. Doumatey
Publikováno v:
Genome Medicine, Vol 15, Iss 1, Pp 1-14 (2023)
Abstract Background In vitro and in vivo studies have shown that certain cytokines and hormones may play a role in the development and progression of type 2 diabetes (T2D). However, studies on their role in T2D in humans are scarce. We evaluated asso
Externí odkaz:
https://doaj.org/article/17086dc964274999bdc3791b8a9b648d
Autor:
Doumatey, Ayo P.1 (AUTHOR) doumateya@mail.nih.gov, Shriner, Daniel1 (AUTHOR), Zhou, Jie1 (AUTHOR), Lei, Lin1 (AUTHOR), Chen, Guanjie1 (AUTHOR), Oluwasola-Taiwo, Omolara2 (AUTHOR), Nkem, Susan3 (AUTHOR), Ogundeji, Adela3 (AUTHOR), Adebamowo, Sally N.4 (AUTHOR), Bentley, Amy R.1 (AUTHOR), Gouveia, Mateus H.1 (AUTHOR), Meeks, Karlijn A. C.1 (AUTHOR), Adebamowo, Clement A.4 (AUTHOR), Adeyemo, Adebowale A.1 (AUTHOR) adeyemoa@mail.nih.gov, Rotimi, Charles N.1 (AUTHOR)
Publikováno v:
Genome Medicine. 3/5/2024, Vol. 16 Issue 1, p1-18. 18p.
Autor:
Odessica Hughes, Amy R. Bentley, Charles E. Breeze, Francois Aguet, Xiaoguang Xu, Girish Nadkarni, Quan Sun, Bridget M. Lin, Thomas Gilliland, Mariah C. Meyer, Jiawen Du, Laura M. Raffield, Holly Kramer, Robert W. Morton, Mateus H. Gouveia, Elizabeth G. Atkinson, Adan Valladares-Salgado, Niels Wacher-Rodarte, Nicole D. Dueker, Xiuqing Guo, Yang Hai, Adebowale Adeyemo, Lyle G. Best, Jianwen Cai, Guanjie Chen, Michael Chong, Ayo Doumatey, James Eales, Mark O. Goodarzi, Eli Ipp, Marguerite Ryan Irvin, Minzhi Jiang, Alana C. Jones, Charles Kooperberg, Jose E. Krieger, Ethan M. Lange, Matthew B. Lanktree, James P. Lash, Paulo A. Lotufo, Ruth J.F. Loos, Vy Thi Ha My, Jesús Peralta-Romero, Lihong Qi, Leslie J. Raffel, Stephen S. Rich, Erik J. Rodriquez, Eduardo Tarazona-Santos, Kent D. Taylor, Jason G. Umans, Jia Wen, Bessie A. Young, Zhi Yu, Ying Zhang, Yii-Der Ida Chen, Tanja Rundek, Jerome I. Rotter, Miguel Cruz, Myriam Fornage, Maria Fernanda Lima-Costa, Alexandre C. Pereira, Guillaume Paré, Pradeep Natarajan, Shelley A. Cole, April P. Carson, Leslie A. Lange, Yun Li, Eliseo J. Perez-Stable, Ron Do, Fadi J. Charchar, Maciej Tomaszewski, Josyf C. Mychaleckyj, Charles Rotimi, Andrew P. Morris, Nora Franceschini
Publikováno v:
Cell Genomics, Vol 4, Iss 1, Pp 100468- (2024)
Summary: Chronic kidney disease is a leading cause of death and disability globally and impacts individuals of African ancestry (AFR) or with ancestry in the Americas (AMS) who are under-represented in genome-wide association studies (GWASs) of kidne
Externí odkaz:
https://doaj.org/article/975974e930614de28f7b1b95b70b9859
Autor:
Hughes, Odessica, Bentley, Amy R., Breeze, Charles E., Aguet, Francois, Xu, Xiaoguang, Nadkarni, Girish, Sun, Quan, Lin, Bridget M., Gilliland, Thomas, Meyer, Mariah C., Du, Jiawen, Raffield, Laura M., Kramer, Holly, Morton, Robert W., Gouveia, Mateus H., Atkinson, Elizabeth G., Valladares-Salgado, Adan, Wacher-Rodarte, Niels, Dueker, Nicole D., Guo, Xiuqing, Hai, Yang, Adeyemo, Adebowale, Best, Lyle G., Cai, Jianwen, Chen, Guanjie, Chong, Michael, Doumatey, Ayo, Eales, James, Goodarzi, Mark O., Ipp, Eli, Irvin, Marguerite Ryan, Jiang, Minzhi, Jones, Alana C., Kooperberg, Charles, Krieger, Jose E., Lange, Ethan M., Lanktree, Matthew B., Lash, James P., Lotufo, Paulo A., Loos, Ruth J.F., Ha My, Vy Thi, Peralta-Romero, Jesús, Qi, Lihong, Raffel, Leslie J., Rich, Stephen S., Rodriquez, Erik J., Tarazona-Santos, Eduardo, Taylor, Kent D., Umans, Jason G., Wen, Jia, Young, Bessie A., Yu, Zhi, Zhang, Ying, Ida Chen, Yii-Der, Rundek, Tanja, Rotter, Jerome I., Cruz, Miguel, Fornage, Myriam, Lima-Costa, Maria Fernanda, Pereira, Alexandre C., Paré, Guillaume, Natarajan, Pradeep, Cole, Shelley A., Carson, April P., Lange, Leslie A., Li, Yun, Perez-Stable, Eliseo J., Do, Ron, Charchar, Fadi J., Tomaszewski, Maciej, Mychaleckyj, Josyf C., Rotimi, Charles, Morris, Andrew P., Franceschini, Nora
Publikováno v:
In Cell Genomics 10 January 2024 4(1)
Autor:
Daniel Shriner, Amy R. Bentley, Mateus H. Gouveia, Elisabeth F. Heuston, Ayo P. Doumatey, Guanjie Chen, Jie Zhou, Adebowale Adeyemo, Charles N. Rotimi
Publikováno v:
HGG Advances, Vol 4, Iss 4, Pp 100235- (2023)
Summary: The vast majority of human populations and individuals have mixed ancestry. Consequently, adjustment for locus-specific ancestry is essential for genetic association studies. To empower association studies for all populations, it is necessar
Externí odkaz:
https://doaj.org/article/1614d4c036784e4f84fb1f27ae97ccf9
Autor:
Shriner, Daniel, Bentley, Amy R., Gouveia, Mateus H., Heuston, Elisabeth F., Doumatey, Ayo P., Chen, Guanjie, Zhou, Jie, Adeyemo, Adebowale, Rotimi, Charles N.
Publikováno v:
In Human Genetics and Genomics Advances 12 October 2023 4(4)
Autor:
Adeyemo Adebowale, Bentley Amy R, Meilleur Katherine G, Doumatey Ayo P, Chen Guanjie, Zhou Jie, Shriner Daniel, Huang Hanxia, Herbert Alan, Gerry Norman P, Christman Michael F, Rotimi Charles N
Publikováno v:
BMC Medical Genetics, Vol 13, Iss 1, p 88 (2012)
Abstract Background A recent, large genome-wide association study (GWAS) of European ancestry individuals has identified multiple genetic variants influencing serum lipids. Studies of the transferability of these associations to African Americans rem
Externí odkaz:
https://doaj.org/article/d88388c7b5c649dd87aac7d73d1f145f
Autor:
Gerry Norman P, Herbert Alan, Huang Hanxia, Zhou Jie, Chen Guanjie, Doumatey Ayo, Shriner Daniel, Charles Bashira A, Christman Michael F, Adeyemo Adebowale, Rotimi Charles N
Publikováno v:
BMC Medical Genomics, Vol 4, Iss 1, p 17 (2011)
Abstract Background Uric acid is the primary byproduct of purine metabolism. Hyperuricemia is associated with body mass index (BMI), sex, and multiple complex diseases including gout, hypertension (HTN), renal disease, and type 2 diabetes (T2D). Mult
Externí odkaz:
https://doaj.org/article/52a7cd1a9d36438f9e4cb6da3adcda93