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1 Ergebnisse
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Rare coding variants in RCN3 are associated with blood pres..:
He, Karen Y
;
Kelly, Tanika N
;
Wang, Heming
...
qt3ks8m14f. , 2022
Link:
https://escholarship.org/uc/item/3ks8m14f
RT Journal T1
Rare coding variants in RCN3 are associated with blood pressure
UL https://suche.suub.uni-bremen.de/peid=base-ftcdlib:oai:escholarship.org:ark:_13030_qt3ks8m14f&Exemplar=1&LAN=DE A1 He, Karen Y A1 Kelly, Tanika N A1 Wang, Heming A1 Liang, Jingjing A1 Zhu, Luke A1 Cade, Brian E A1 Assimes, Themistocles L A1 Becker, Lewis C A1 Beitelshees, Amber L A1 Bielak, Lawrence F A1 Bress, Adam P A1 Brody, Jennifer A A1 Chang, Yen-Pei Christy A1 Chang, Yi-Cheng A1 de Vries, Paul S A1 Duggirala, Ravindranath A1 Fox, Ervin R A1 Franceschini, Nora A1 Furniss, Anna L A1 Gao, Yan A1 Guo, Xiuqing A1 Haessler, Jeffrey A1 Hung, Yi-Jen A1 Hwang, Shih-Jen A1 Irvin, Marguerite Ryan A1 Kalyani, Rita R A1 Liu, Ching-Ti A1 Liu, Chunyu A1 Martin, Lisa Warsinger A1 Montasser, May E A1 Muntner, Paul M A1 Mwasongwe, Stanford A1 Naseri, Take A1 Palmas, Walter A1 Reupena, Muagututi'a Sefuiva A1 Rice, Kenneth M A1 Sheu, Wayne H-H A1 Shimbo, Daichi A1 Smith, Jennifer A A1 Snively, Beverly M A1 Yanek, Lisa R A1 Zhao, Wei A1 Blangero, John A1 Boerwinkle, Eric A1 Chen, Yii-Der Ida A1 Correa, Adolfo A1 Cupples, L Adrienne A1 Curran, Joanne E A1 Fornage, Myriam A1 He, Jiang A1 Hou, Lifang A1 Kaplan, Robert C A1 Kardia, Sharon LR A1 Kenny, Eimear E A1 Kooperberg, Charles A1 Lloyd-Jones, Donald A1 Loos, Ruth JF A1 Mathias, Rasika A A1 McGarvey, Stephen T A1 Mitchell, Braxton D A1 North, Kari E A1 Peyser, Patricia A A1 Psaty, Bruce M A1 Raffield, Laura M A1 Rao, DC A1 Redline, Susan A1 Reiner, Alex P A1 Rich, Stephen S A1 Rotter, Jerome I A1 Taylor, Kent D A1 Tracy, Russell A1 Vasan, Ramachandran S A1 Morrison, Alanna C A1 Levy, Daniel A1 Chakravarti, Aravinda A1 Arnett, Donna K A1 Zhu, Xiaofeng PB eScholarship, University of California YR 2022 K1 Biological Sciences K1 Genetics K1 Cardiovascular K1 Human Genome K1 Clinical Research K1 Aetiology K1 2.1 Biological and endogenous factors K1 Good Health and Well Being K1 Blood Pressure K1 Genetic Linkage K1 Genetic Predisposition to Disease K1 Genome-Wide Association Study K1 Humans K1 Polymorphism K1 Single Nucleotide K1 Precision Medicine K1 Whole Genome Sequencing K1 Rare variant analysis K1 Samoan Obesity K1 Lifestyle and Genetic Adaptations Study (OLaGA) Group K1 NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium K1 Information and Computing Sciences K1 Medical and Health Sciences K1 Bioinformatics K1 Biomedical and clinical sciences JF qt3ks8m14f LK http://dx.doi.org/https://escholarship.org/uc/item/3ks8m14f DO https://escholarship.org/uc/item/3ks8m14f SF ELIB - SuUB Bremen
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