![[höher]](/style/images/multi_up.png)
Eine Ebene höherGruppiert nach: Dokumententyp |
Veröffentlichungsdatum
Anzahl der Publikationen: 3
2018
Macri, Vincenzo; Brody, Jennifer A.; Arking, Dan E.; Hucker, William J.; Yin, Xiaoyan; Lin, Honghuang; Mills, Robert W.; Sinner, Moritz F.; Lubitz, Steven A.; Liu, Ching-Ti; Morrison, Alanna C.; Alonso, Alvaro; Li, Ning; Fedorov, Vadim V.; Janssen, Paul M.; Bis, Joshua C.; Heckbert, Susan R.; Dolmatova, Elena V.; Lumley, Thomas; Sitlani, Colleen M.; Cupples, L. Adrienne; Pulit, Sara L.; Newton-Cheh, Christopher; Barnard, John; Smith, Jonathan D.; Wagoner, David R. van; Chung, Mina K.; Vlahakes, Gus J.; O'Donnell, Christopher J.; Rotter, Jerome I.; Margulies, Kenneth B.; Morley, Michael P.; Cappola, Thomas P.; Benjamin, Emelia J.; Muzny, Donna; Gibbs, Richard A.; Jackson, Rebecca D.; Magnani, Jared W.; Herndon, Caroline N.; Rich, Stephen S.; Psaty, Bruce M.; Milan, David J.; Börwinkle, Eric; Mohler, Peter J.; Sotoodehnia, Nona und Ellinor, Patrick T.
(2018):
Common Coding Variants in SCN10A Are Associated With the Nav1.8 Late Current and Cardiac Conduction.
In: Circulation-Genomic and Precision Medicine, Bd. 11, Nr. 5, e001663
2017
Tucker, Nathan R.; Dolmatova, Elena V.; Lin, Honghuang; Cooper, Rebecca R.; Ye, Jiangchuan; Hucker, William J.; Jameson, Heather S.; Parsons, Victoria A.; Weng, Lu-Chen; Mills, Robert W.; Sinner, Moritz F.; Imakäv, Maxim; Leyton-Mange, Jordan; Vlahakes, Gus; Benjamin, Emelia J.; Lunetta, Kathryn L.; Lubitz, Steven A.; Mirny, Leonid; Milan, David J. und Ellinor, Patrick T.
(2017):
Diminished PRRX1 Expression Is Associated With Increased Risk of Atrial Fibrillation and Shortening of the Cardiac Action Potential.
In: Circulation-Cardiovascular Genetics, Bd. 10, Nr. 5, e001902
Tucker, Nathan R.; McLellan, Micheal A.; Hu, Dongjian; Ye, Jiangchuan; Parsons, Victoria A.; Mills, Robert W.; Clauss, Sebastian; Dolmatova, Elena; Shea, Marisa A.; Milan, David J.; Scott, Nandita S.; Lindsay, Mark; Lubitz, Steven A.; Domian, Ibrahim J.; Stone, James R.; Lin, Honghuang und Ellinor, Patrick T.
(2017):
Novel Mutation in FLNC (Filamin C) Causes Familial Restrictive Cardiomyopathy.
In: Circulation-Cardiovascular Genetics, Bd. 10, Nr. 6, e001780