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Eric Boerwinkle

Showing results (781-790 of 1,171) with videos related to

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JAMA Cardiology|February 1, 2023
Association of Rare Protein-Truncating DNA Variants in APOB or PCSK9 With Low-density Lipoprotein Cholesterol Level and Risk of Coronary Heart DiseaseJacqueline S Dron, Aniruddh P Patel, Yiyi Zhang, et al.
Nature Communications|September 12, 2022
Clonal hematopoiesis of indeterminate potential, DNA methylation, and risk for coronary artery diseaseM D Mesbah Uddin, Ngoc Quynh H Nguyen, Bing Yu, et al.
The Journal of Clinical Investigation|January 10, 2015
Global transcriptional disturbances underlie Cornelia de Lange syndrome and related phenotypesBo Yuan, Davut Pehlivan, Ender Karaca, et al.
Genome Medicine|September 24, 2017
Creating a data resource: what will it take to build a medical information commons?Patricia A Deverka, Mary A Majumder, Angela G Villanueva, et al.
Plos Genetics|April 18, 2013
Analysis of rare, exonic variation amongst subjects with autism spectrum disorders and population controlsLi Liu, Aniko Sabo, Benjamin M Neale, et al.
Journal of Hypertension|February 20, 2015
TET2 and CSMD1 genes affect SBP response to hydrochlorothiazide in never-treated essential hypertensivesMartina Chittani, Roberta Zaninello, Chiara Lanzani, et al.
Genome Medicine|November 2, 2016
MIPEP recessive variants cause a syndrome of left ventricular non-compaction, hypotonia, and infantile deathMohammad K Eldomery, Zeynep C Akdemir, F-Nora Vögtle, et al.
Hypertension (Dallas, Tex. : 1979)|October 4, 2022
Rare Variants in Genes Encoding Subunits of the Epithelial Na<sup>+</sup> Channel Are Associated With Blood Pressure and Kidney FunctionBrandon M Blobner, Annet Kirabo, Ossama B Kashlan, et al.
Blood|December 31, 2009
Duffy antigen receptor for chemokines (Darc) polymorphism regulates circulating concentrations of monocyte chemoattractant protein-1 and other inflammatory mediatorsRenate B Schnabel, Jens Baumert, Maja Barbalic, et al.
European Journal of Human Genetics : EJHG|May 1, 2018
Comprehensive genomic analysis of patients with disorders of cerebral cortical developmentWojciech Wiszniewski, Pawel Gawlinski, Tomasz Gambin, et al.
Pageof 118

Showing results (781-790 of 1,171) with videos related to

Sort By:
Pageof 118
JAMA Cardiology|February 1, 2023
Association of Rare Protein-Truncating DNA Variants in APOB or PCSK9 With Low-density Lipoprotein Cholesterol Level and Risk of Coronary Heart DiseaseJacqueline S Dron, Aniruddh P Patel, Yiyi Zhang, et al.
Nature Communications|September 12, 2022
Clonal hematopoiesis of indeterminate potential, DNA methylation, and risk for coronary artery diseaseM D Mesbah Uddin, Ngoc Quynh H Nguyen, Bing Yu, et al.
The Journal of Clinical Investigation|January 10, 2015
Global transcriptional disturbances underlie Cornelia de Lange syndrome and related phenotypesBo Yuan, Davut Pehlivan, Ender Karaca, et al.
Genome Medicine|September 24, 2017
Creating a data resource: what will it take to build a medical information commons?Patricia A Deverka, Mary A Majumder, Angela G Villanueva, et al.
Plos Genetics|April 18, 2013
Analysis of rare, exonic variation amongst subjects with autism spectrum disorders and population controlsLi Liu, Aniko Sabo, Benjamin M Neale, et al.
Journal of Hypertension|February 20, 2015
TET2 and CSMD1 genes affect SBP response to hydrochlorothiazide in never-treated essential hypertensivesMartina Chittani, Roberta Zaninello, Chiara Lanzani, et al.
Genome Medicine|November 2, 2016
MIPEP recessive variants cause a syndrome of left ventricular non-compaction, hypotonia, and infantile deathMohammad K Eldomery, Zeynep C Akdemir, F-Nora Vögtle, et al.
Hypertension (Dallas, Tex. : 1979)|October 4, 2022
Rare Variants in Genes Encoding Subunits of the Epithelial Na<sup>+</sup> Channel Are Associated With Blood Pressure and Kidney FunctionBrandon M Blobner, Annet Kirabo, Ossama B Kashlan, et al.
Blood|December 31, 2009
Duffy antigen receptor for chemokines (Darc) polymorphism regulates circulating concentrations of monocyte chemoattractant protein-1 and other inflammatory mediatorsRenate B Schnabel, Jens Baumert, Maja Barbalic, et al.
European Journal of Human Genetics : EJHG|May 1, 2018
Comprehensive genomic analysis of patients with disorders of cerebral cortical developmentWojciech Wiszniewski, Pawel Gawlinski, Tomasz Gambin, et al.
Pageof 118