Zobrazeno 1 - 10
of 32
pro vyhledávání: '"Jiangchuan Ye"'
Publikováno v:
Child and Adolescent Psychiatry and Mental Health, Vol 17, Iss 1, Pp 1-29 (2023)
Abstract Background The coronavirus disease (COVID‐19) and universal mitigation strategies have fundamentally affected peoples’ lives worldwide, particularly during the first two years of the pandemic. Reductions in physical activity (PA) and inc
Externí odkaz:
https://doaj.org/article/b4853ce1b2834086beabb7b32e131f3c
Autor:
Xinchen Wang, Nathan R Tucker, Gizem Rizki, Robert Mills, Peter HL Krijger, Elzo de Wit, Vidya Subramanian, Eric Bartell, Xinh-Xinh Nguyen, Jiangchuan Ye, Jordan Leyton-Mange, Elena V Dolmatova, Pim van der Harst, Wouter de Laat, Patrick T Ellinor, Christopher Newton-Cheh, David J Milan, Manolis Kellis, Laurie A Boyer
Publikováno v:
eLife, Vol 5 (2016)
Genetic variants identified by genome-wide association studies explain only a modest proportion of heritability, suggesting that meaningful associations lie 'hidden' below current thresholds. Here, we integrate information from association studies wi
Externí odkaz:
https://doaj.org/article/221d678fc5c0450a9661a32b5b9356f4
Autor:
Lin, Amy Erica, Bapat, Aneesh C., Ling Xiao, Niroula, Abhishek, Jiangchuan Ye, Wong, Waihay J., Agrawal, Mridul, Farady, Christopher J., Boettcher, Andreas, Hergott, Christopher B., McConkey, Marie, Flores-Bringas, Patricio, Shkolnik, Veronica, Bick, Alexander G., Milan, David, Natarajan, Pradeep, Libby, Peter, Ellinor, Patrick T., Ebert, Benjamin L.
Publikováno v:
Circulation; 4/30/2024, Vol. 149 Issue 18, p1419-1434, 16p
Autor:
Mark Chaffin, Irinna Papangeli, Bridget Simonson, Amer-Denis Akkad, Matthew C. Hill, Alessandro Arduini, Stephen J. Fleming, Michelle Melanson, Sikander Hayat, Maria Kost-Alimova, Ondine Atwa, Jiangchuan Ye, Kenneth C. Bedi, Matthias Nahrendorf, Virendar K. Kaushik, Christian M. Stegmann, Kenneth B. Margulies, Nathan R. Tucker, Patrick T. Ellinor
Publikováno v:
Nature. 608:174-180
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3953303da37730099f0ab2b5ff9e6a36
https://doi.org/10.1038/s41586-022-04817-8
https://doi.org/10.1038/s41586-022-04817-8
Autor:
Jameson, Heather S., Hanley, Alan, Hill, Matthew C., Ling Xiao, Jiangchuan Ye, Bapat, Aneesh, Ronzier, Elsa, Hall, Amelia Weber, Hucker, William J., Clauss, Sebastian, Barazza, Miranda, Silber, Elizabeth, Mina, Julie A., Tucker, Nathan R., Mills, Robert W., Jin-Tang Dong, Milan, David J., Ellinor, Patrick T.
Publikováno v:
Circulation Research; 8/4/2023, Vol. 133 Issue 4, p313-329, 17p
Autor:
Mark, Chaffin, Irinna, Papangeli, Bridget, Simonson, Amer-Denis, Akkad, Matthew C, Hill, Alessandro, Arduini, Stephen J, Fleming, Michelle, Melanson, Sikander, Hayat, Maria, Kost-Alimova, Ondine, Atwa, Jiangchuan, Ye, Kenneth C, Bedi, Matthias, Nahrendorf, Virendar K, Kaushik, Christian M, Stegmann, Kenneth B, Margulies, Nathan R, Tucker, Patrick T, Ellinor
Publikováno v:
Nature. 608(7921)
Heart failure encompasses a heterogeneous set of clinical features that converge on impaired cardiac contractile function
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::f97f4a16987cefc7247f8f3be3b4547b
https://pubmed.ncbi.nlm.nih.gov/35732739
https://pubmed.ncbi.nlm.nih.gov/35732739
Autor:
Lu-Chen Weng, Sebastian Clauss, Patrick T. Ellinor, Steven A. Lubitz, Nathan R. Tucker, Jiangchuan Ye
Publikováno v:
The American Journal of Human Genetics. 99:1281-1291
The most significantly associated genetic locus for atrial fibrillation (AF) is in chromosomal region 4q25, where four independent association signals have been identified. Although model-system studies suggest that altered PITX2c expression might un
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::32a567488432a7339c2a306ca40359ee
https://doi.org/10.1016/j.ajhg.2016.10.001
https://doi.org/10.1016/j.ajhg.2016.10.001
Autor:
Elena Dolmatova, Moritz F. Sinner, Steven A. Lubitz, Maxim Imakaev, Jiangchuan Ye, Emelia J. Benjamin, Victoria A. Parsons, Nathan R. Tucker, Honghuang Lin, Kathryn L. Lunetta, Jordan Leyton-Mange, Rebecca R. Cooper, Leonid A. Mirny, Patrick T. Ellinor, William J. Hucker, Gus J. Vlahakes, Lu-Chen Weng, Heather Jameson, David J. Milan, Robert W. Mills
Publikováno v:
PMC
Background— Atrial fibrillation (AF) affects over 33 million individuals worldwide. Genome-wide association studies have identified at least 30 AF loci, but the mechanisms through which individual variants lead to altered disease risk have remained
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1abd9ff20272a245d63f6735176fcc44
https://hdl.handle.net/1721.1/124839
https://hdl.handle.net/1721.1/124839
Autor:
Nathan R, Tucker, Elena V, Dolmatova, Honghuang, Lin, Rebecca R, Cooper, Jiangchuan, Ye, William J, Hucker, Heather S, Jameson, Victoria A, Parsons, Lu-Chen, Weng, Robert W, Mills, Moritz F, Sinner, Maxim, Imakaev, Jordan, Leyton-Mange, Gus, Vlahakes, Emelia J, Benjamin, Kathryn L, Lunetta, Steven A, Lubitz, Leonid, Mirny, David J, Milan, Patrick T, Ellinor
Publikováno v:
Circulation. Cardiovascular genetics. 10(5)
Atrial fibrillation (AF) affects over 33 million individuals worldwide. Genome-wide association studies have identified at least 30 AF loci, but the mechanisms through which individual variants lead to altered disease risk have remained unclear for t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::33ee3d85471e884aec52a04f95d665dd
https://pubmed.ncbi.nlm.nih.gov/28974515
https://pubmed.ncbi.nlm.nih.gov/28974515
Autor:
Marisa A. Shea, Honghuang Lin, Jiangchuan Ye, James R. Stone, Nandita S. Scott, Patrick T. Ellinor, Victoria A. Parsons, Micheal A. McLellan, Steven A. Lubitz, Robert W. Mills, Elena Dolmatova, Sebastian Clauss, Nathan R. Tucker, Ibrahim J. Domian, Mark E. Lindsay, David J. Milan, Dongjian Hu
Publikováno v:
Circulation. Cardiovascular genetics. 10(6)
Background— Restrictive cardiomyopathy (RCM) is a rare cardiomyopathy characterized by impaired diastolic ventricular function resulting in a poor clinical prognosis. Rarely, heritable forms of RCM have been reported, and mutations underlying RCM h
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::abbc4e9ace505884cd7def8c29be88da
https://pubmed.ncbi.nlm.nih.gov/29650770
https://pubmed.ncbi.nlm.nih.gov/29650770