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Eric Boerwinkle

Showing results (791-800 of 1,171) with videos related to

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Plos One|April 28, 2012
Evaluation of the metabochip genotyping array in African Americans and implications for fine mapping of GWAS-identified loci: the PAGE studySteven Buyske, Ying Wu, Cara L Carty, et al.
The American Journal of Clinical Nutrition|February 4, 2012
Measuring alcohol consumption for genomic meta-analyses of alcohol intake: opportunities and challengesArpana Agrawal, Neal D Freedman, Yu-Ching Cheng, et al.
American Journal of Human Genetics|June 19, 2012
Genetic associations for activated partial thromboplastin time and prothrombin time, their gene expression profiles, and risk of coronary artery diseaseWeihong Tang, Christine Schwienbacher, Lorna M Lopez, et al.
Circulation. Cardiovascular Genetics|June 22, 2014
Sequencing of SCN5A identifies rare and common variants associated with cardiac conduction: Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) ConsortiumJared W Magnani, Jennifer A Brody, Bram P Prins, et al.
Medrxiv : the Preprint Server for Health Sciences|November 22, 2024
Gene-Excessive Sleepiness Interactions Suggest Treatment Targets for Obstructive Sleep Apnea SubtypePavithra Nagarajan, Nuzulul Kurniansyah, Jiwon Lee, et al.
American Journal of Respiratory and Critical Care Medicine|July 13, 2022
Targeted Genome Sequencing Identifies Multiple Rare Variants in Caveolin-1 Associated with Obstructive Sleep ApneaJingjing Liang, Heming Wang, Brian E Cade, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|May 18, 2021
Plasma amyloid β levels are driven by genetic variants near APOE, BACE1, APP, PSEN2: A genome-wide association study in over 12,000 non-demented participantsVincent Damotte, Sven J van der Lee, Vincent Chouraki, et al.
Human Molecular Genetics|May 13, 2022
Whole-exome sequencing of 14 389 individuals from the ESP and CHARGE consortia identifies novel rare variation associated with hemostatic factorsNathan Pankratz, Peng Wei, Jennifer A Brody, et al.
Pharmacogenomics|November 21, 2014
Genome-wide association study identifies CAMKID variants involved in blood pressure response to losartan: the SOPHIA studyFrancesca Frau, Roberta Zaninello, Erika Salvi, et al.
European Journal of Epidemiology|October 25, 2017
Trends in the incidence of dementia: design and methods in the Alzheimer Cohorts ConsortiumLori B Chibnik, Frank J Wolters, Kristoffer Bäckman, et al.
Pageof 118

Showing results (791-800 of 1,171) with videos related to

Sort By:
Pageof 118
Plos One|April 28, 2012
Evaluation of the metabochip genotyping array in African Americans and implications for fine mapping of GWAS-identified loci: the PAGE studySteven Buyske, Ying Wu, Cara L Carty, et al.
The American Journal of Clinical Nutrition|February 4, 2012
Measuring alcohol consumption for genomic meta-analyses of alcohol intake: opportunities and challengesArpana Agrawal, Neal D Freedman, Yu-Ching Cheng, et al.
American Journal of Human Genetics|June 19, 2012
Genetic associations for activated partial thromboplastin time and prothrombin time, their gene expression profiles, and risk of coronary artery diseaseWeihong Tang, Christine Schwienbacher, Lorna M Lopez, et al.
Circulation. Cardiovascular Genetics|June 22, 2014
Sequencing of SCN5A identifies rare and common variants associated with cardiac conduction: Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) ConsortiumJared W Magnani, Jennifer A Brody, Bram P Prins, et al.
Medrxiv : the Preprint Server for Health Sciences|November 22, 2024
Gene-Excessive Sleepiness Interactions Suggest Treatment Targets for Obstructive Sleep Apnea SubtypePavithra Nagarajan, Nuzulul Kurniansyah, Jiwon Lee, et al.
American Journal of Respiratory and Critical Care Medicine|July 13, 2022
Targeted Genome Sequencing Identifies Multiple Rare Variants in Caveolin-1 Associated with Obstructive Sleep ApneaJingjing Liang, Heming Wang, Brian E Cade, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|May 18, 2021
Plasma amyloid β levels are driven by genetic variants near APOE, BACE1, APP, PSEN2: A genome-wide association study in over 12,000 non-demented participantsVincent Damotte, Sven J van der Lee, Vincent Chouraki, et al.
Human Molecular Genetics|May 13, 2022
Whole-exome sequencing of 14 389 individuals from the ESP and CHARGE consortia identifies novel rare variation associated with hemostatic factorsNathan Pankratz, Peng Wei, Jennifer A Brody, et al.
Pharmacogenomics|November 21, 2014
Genome-wide association study identifies CAMKID variants involved in blood pressure response to losartan: the SOPHIA studyFrancesca Frau, Roberta Zaninello, Erika Salvi, et al.
European Journal of Epidemiology|October 25, 2017
Trends in the incidence of dementia: design and methods in the Alzheimer Cohorts ConsortiumLori B Chibnik, Frank J Wolters, Kristoffer Bäckman, et al.
Pageof 118