Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Snively, Beverly"'
Autor:
He, Karen Y, Kelly, Tanika N, Wang, Heming, Liang, Jingjing, Zhu, Luke, Cade, Brian E, Assimes, Themistocles L, Becker, Lewis C, Beitelshees, Amber L, Bielak, Lawrence F, Bress, Adam P, Brody, Jennifer A, Chang, Yen-Pei Christy, Chang, Yi-Cheng, de Vries, Paul S, Duggirala, Ravindranath, Fox, Ervin R, Franceschini, Nora, Furniss, Anna L, Gao, Yan, Guo, Xiuqing, Haessler, Jeffrey, Hung, Yi-Jen, Hwang, Shih-Jen, Irvin, Marguerite Ryan, Kalyani, Rita R, Liu, Ching-Ti, Liu, Chunyu, Martin, Lisa Warsinger, Montasser, May E, Muntner, Paul M, Mwasongwe, Stanford, Naseri, Take, Palmas, Walter, Reupena, Muagututi'a Sefuiva, Rice, Kenneth M, Sheu, Wayne H-H, Shimbo, Daichi, Smith, Jennifer A, Snively, Beverly M, Yanek, Lisa R, Zhao, Wei, Blangero, John, Boerwinkle, Eric, Chen, Yii-Der Ida, Correa, Adolfo, Cupples, L Adrienne, Curran, Joanne E, Fornage, Myriam, He, Jiang, Hou, Lifang, Kaplan, Robert C, Kardia, Sharon LR, Kenny, Eimear E, Kooperberg, Charles, Lloyd-Jones, Donald, Loos, Ruth JF, Mathias, Rasika A, McGarvey, Stephen T, Mitchell, Braxton D, North, Kari E, Peyser, Patricia A, Psaty, Bruce M, Raffield, Laura M, Rao, DC, Redline, Susan, Reiner, Alex P, Rich, Stephen S, Rotter, Jerome I, Taylor, Kent D, Tracy, Russell, Vasan, Ramachandran S, Samoan Obesity, Lifestyle and Genetic Adaptations Study (OLaGA) Group, NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium, Morrison, Alanna C, Levy, Daniel, Chakravarti, Aravinda, Arnett, Donna K, Zhu, Xiaofeng
Publikováno v:
BMC genomics, vol 23, iss 1
BackgroundWhile large genome-wide association studies have identified nearly one thousand loci associated with variation in blood pressure, rare variant identification is still a challenge. In family-based cohorts, genome-wide linkage scans have been
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______325::285b8c9f208e149812416c0d306deb7d
https://escholarship.org/uc/item/3ks8m14f
https://escholarship.org/uc/item/3ks8m14f
Autor:
He, Karen Y, Li, Xiaoyin, Kelly, Tanika N, Liang, Jingjing, Cade, Brian E, Assimes, Themistocles L, Becker, Lewis C, Beitelshees, Amber L, Bress, Adam P, Chang, Yen-Pei Christy, Chen, Yii-Der Ida, de Vries, Paul S, Fox, Ervin R, Franceschini, Nora, Furniss, Anna, Gao, Yan, Guo, Xiuqing, Haessler, Jeffrey, Hwang, Shih-Jen, Irvin, Marguerite Ryan, Kalyani, Rita R, Liu, Ching-Ti, Liu, Chunyu, Martin, Lisa Warsinger, Montasser, May E, Muntner, Paul M, Mwasongwe, Stanford, Palmas, Walter, Reiner, Alex P, Shimbo, Daichi, Smith, Jennifer A, Snively, Beverly M, Yanek, Lisa R, Boerwinkle, Eric, Correa, Adolfo, Cupples, L Adrienne, He, Jiang, Kardia, Sharon LR, Kooperberg, Charles, Mathias, Rasika A, Mitchell, Braxton D, Psaty, Bruce M, Vasan, Ramachandran S, Rao, DC, Rich, Stephen S, Rotter, Jerome I, Wilson, James G, NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium, TOPMed Blood Pressure Working Group, Chakravarti, Aravinda, Morrison, Alanna C, Levy, Daniel, Arnett, Donna K, Redline, Susan, Zhu, Xiaofeng
Publikováno v:
Human genetics, vol 138, iss 2
In this study, we investigated low-frequency and rare variants associated with blood pressure (BP) by focusing on a linkage region on chromosome 16p13. We used whole genome sequencing (WGS) data obtained through the NHLBI Trans-Omics for Precision Me
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______325::32365db53ec317f89e796f03c9dfc782
https://escholarship.org/uc/item/2g02g3gs
https://escholarship.org/uc/item/2g02g3gs
Autor:
McLaren, Christine E., Garner, Chad P., Constantine, Clare C., McLachlan, Stela, Vulpe, Chris D., Snively, Beverly M., Gordeuk, Victor R., Nickerson, Debbie A., Cook, James D., Leiendecker-Foster, Catherine, Beckman, Kenneth B., Eckfeldt, John H., Barcellos, Lisa F., Murray, Joseph A., Adams, Paul C., Acton, Ronald T., Killeen, Anthony A., McLaren, Gordon D.
Publikováno v:
McLaren, Christine E.; Garner, Chad P.; Constantine, Clare C.; McLachlan, Stela; Vulpe, Chris D.; Snively, Beverly M.; et al.(2011). Genome-Wide Association Study Identifies Genetic Loci Associated with Iron Deficiency. PLoS ONE, 6(3). UC Irvine: Retrieved from: http://www.escholarship.org/uc/item/7rp664d2
The existence of multiple inherited disorders of iron metabolism in man, rodents and other vertebrates suggests genetic contributions to iron deficiency. To identify new genomic locations associated with iron deficiency, a genome-wide association stu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______325::77a195bb05f5860350430b5bb336970e
http://www.escholarship.org/uc/item/7rp664d2
http://www.escholarship.org/uc/item/7rp664d2