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Kent D Taylor

Showing results (401-410 of 515) with videos related to

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Nature Genetics|September 13, 2016
Meta-analysis identifies common and rare variants influencing blood pressure and overlapping with metabolic trait lociChunyu Liu, Aldi T Kraja, Jennifer A Smith, et al.
Nature Genetics|January 8, 2013
Genome-wide association analyses identify multiple loci associated with central corneal thickness and keratoconusYi Lu, Veronique Vitart, Kathryn P Burdon, et al.
Journal of Medical Genetics|September 3, 2016
Meta-analysis of genome-wide association studies of HDL cholesterol response to statinsIris Postmus, Helen R Warren, Stella Trompet, et al.
Science Advances|May 1, 2023
The genetic determinants of recurrent somatic mutations in 43,693 blood genomesJoshua S Weinstock, Cecelia A Laurie, Jai G Broome, et al.
Communications Biology|July 28, 2022
Whole genome sequence association analysis of fasting glucose and fasting insulin levels in diverse cohorts from the NHLBI TOPMed programDaniel DiCorpo, Sheila M Gaynor, Emily M Russell, et al.
Blood|February 6, 2024
A genetic association study of circulating coagulation factor VIII and von Willebrand factor levelsPaul S de Vries, Paula Reventun, Michael R Brown, et al.
Nature Genetics|September 28, 2023
Multi-ancestry genome-wide study identifies effector genes and druggable pathways for coronary artery calcificationMaryam Kavousi, Maxime M Bos, Hanna J Barnes, et al.
American Journal of Human Genetics|June 28, 2016
Large-Scale Exome-wide Association Analysis Identifies Loci for White Blood Cell Traits and Pleiotropy with Immune-Mediated DiseasesSalman M Tajuddin, Ursula M Schick, John D Eicher, et al.
Circulation. Genomic and Precision Medicine|May 12, 2018
Common and Rare Coding Genetic Variation Underlying the Electrocardiographic PR IntervalHonghuang Lin, Jessica van Setten, Albert V Smith, et al.
Nature Human Behaviour|August 4, 2022
Rare genetic variants explain missing heritability in smokingSeon-Kyeong Jang, Luke Evans, Allison Fialkowski, et al.
Pageof 52

Showing results (401-410 of 515) with videos related to

Sort By:
Pageof 52
Nature Genetics|September 13, 2016
Meta-analysis identifies common and rare variants influencing blood pressure and overlapping with metabolic trait lociChunyu Liu, Aldi T Kraja, Jennifer A Smith, et al.
Nature Genetics|January 8, 2013
Genome-wide association analyses identify multiple loci associated with central corneal thickness and keratoconusYi Lu, Veronique Vitart, Kathryn P Burdon, et al.
Journal of Medical Genetics|September 3, 2016
Meta-analysis of genome-wide association studies of HDL cholesterol response to statinsIris Postmus, Helen R Warren, Stella Trompet, et al.
Science Advances|May 1, 2023
The genetic determinants of recurrent somatic mutations in 43,693 blood genomesJoshua S Weinstock, Cecelia A Laurie, Jai G Broome, et al.
Communications Biology|July 28, 2022
Whole genome sequence association analysis of fasting glucose and fasting insulin levels in diverse cohorts from the NHLBI TOPMed programDaniel DiCorpo, Sheila M Gaynor, Emily M Russell, et al.
Blood|February 6, 2024
A genetic association study of circulating coagulation factor VIII and von Willebrand factor levelsPaul S de Vries, Paula Reventun, Michael R Brown, et al.
Nature Genetics|September 28, 2023
Multi-ancestry genome-wide study identifies effector genes and druggable pathways for coronary artery calcificationMaryam Kavousi, Maxime M Bos, Hanna J Barnes, et al.
American Journal of Human Genetics|June 28, 2016
Large-Scale Exome-wide Association Analysis Identifies Loci for White Blood Cell Traits and Pleiotropy with Immune-Mediated DiseasesSalman M Tajuddin, Ursula M Schick, John D Eicher, et al.
Circulation. Genomic and Precision Medicine|May 12, 2018
Common and Rare Coding Genetic Variation Underlying the Electrocardiographic PR IntervalHonghuang Lin, Jessica van Setten, Albert V Smith, et al.
Nature Human Behaviour|August 4, 2022
Rare genetic variants explain missing heritability in smokingSeon-Kyeong Jang, Luke Evans, Allison Fialkowski, et al.
Pageof 52