Zobrazeno 1 - 10
of 6 781
pro vyhledávání: '"additive genetic effect"'
Autor:
Chen, Guanjie1 (AUTHOR), Shriner, Daniel1 (AUTHOR), Zhang, Jianhua2 (AUTHOR), Zhou, Jie1 (AUTHOR), Adikaram, Poorni3 (AUTHOR), Doumatey, Ayo P.1 (AUTHOR), Bentley, Amy R.1 (AUTHOR), Adeyemo, Adebowale1 (AUTHOR), Rotimi, Charles N.1 (AUTHOR) rotimic@mail.nih.gov
Publikováno v:
PLoS ONE. 6/3/2022, Vol. 17 Issue 6, p1-15. 15p.
Autor:
Guanjie Chen, Daniel Shriner, Jianhua Zhang, Jie Zhou, Poorni Adikaram, Ayo P. Doumatey, Amy R. Bentley, Adebowale Adeyemo, Charles N. Rotimi
Publikováno v:
PLoS ONE, Vol 17, Iss 6 (2022)
Impaired glucose tolerance is a major risk factor for type 2 diabetes (T2D) and several cardiometabolic disorders. To identify genetic loci underlying fasting glucose levels, we conducted an analysis of 9,232 individuals of European ancestry who at e
Externí odkaz:
https://doaj.org/article/cb8c189752934746ad6c3735f7a29d6e
Publikováno v:
In NeuroImage 1 April 2014 89:306-313
Autor:
Howard, Jeremy T.1, Haile-Mariam, Mekonnen2, Pryce, Jennie E.2,3, Maltecca, Christian1 christian_maltecca@ncsu.edu
Publikováno v:
BMC Genomics. 10/19/2015, Vol. 16, p1-13. 13p. 1 Diagram, 2 Charts, 2 Graphs.
Autor:
Guanjie Chen, Daniel Shriner, Jianhua Zhang, Jie Zhou, Poorni Adikaram, Ayo P. Doumatey, Amy R. Bentley, Adebowale Adeyemo, Charles N. Rotimi
Publikováno v:
PloS one. 17(6)
Impaired glucose tolerance is a major risk factor for type 2 diabetes (T2D) and several cardiometabolic disorders. To identify genetic loci underlying fasting glucose levels, we conducted an analysis of 9,232 individuals of European ancestry who at e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::23ef32a831dc6f3cfb624037b661bc37
https://pubmed.ncbi.nlm.nih.gov/35657990
https://pubmed.ncbi.nlm.nih.gov/35657990
Autor:
Ming Chen, Longjian Liu, Howard J. Eisen, Yuna Kim, Yong Long, Hong Jia, Ellie Kelepouris, Yichen Zhong
Publikováno v:
Arteriosclerosis, Thrombosis, and Vascular Biology. 38
Objective: Apolipoprotein L1 (APOL1), the major protein component of HDL, is identified having an association with renal disease in African Americans (AA). We assessed the hypothesis that the genetic variations in APOL1 (G1 and G2 alleles) are associ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5a30bed9a6f67a64f872b26521f3f725
https://doi.org/10.1161/atvb.38.suppl_1.469
https://doi.org/10.1161/atvb.38.suppl_1.469
Akademický článek
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Publikováno v:
NeuroImage. 89:306-313
Human memory is a highly heritable polygenic trait with complex inheritance patterns. To study the genetics of memory and memory-related diseases, hippocampal functioning has served as an intermediate phenotype. The importance of investigating gene-g
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f19fa2c3e75eb2b3146be4f85d27c8f6
https://doi.org/10.1016/j.neuroimage.2013.11.049
https://doi.org/10.1016/j.neuroimage.2013.11.049
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
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Autor:
Antónia Juliana Pais‐Costa, Eva J. P. Lievens, Stella Redón, Marta I. Sánchez, Roula Jabbour‐Zahab, Pauline Joncour, Nguyen Van Hoa, Gilbert Van Stappen, Thomas Lenormand
Publikováno v:
Evolution Letters, Vol 6, Iss 4, Pp 284-294 (2022)
Abstract The climate is currently warming fast, threatening biodiversity all over the globe. Populations often adapt rapidly to environmental change, but for climate warming very little evidence is available. Here, we investigate the pattern of adapt
Externí odkaz:
https://doaj.org/article/1d25788520234d4394dd007b65333e80