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Barbara McKnight

Showing results (131-140 of 174) with videos related to

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HGG Advances|December 26, 2022
Whole-exome sequence analysis of anthropometric traits illustrates challenges in identifying effects of rare genetic variantsKristin L Young, Virginia Fisher, Xuan Deng, et al.
Blood|August 18, 2019
Genomic and transcriptomic association studies identify 16 novel susceptibility loci for venous thromboembolismSara Lindström, Lu Wang, Erin N Smith, et al.
Human Molecular Genetics|January 12, 2013
A genome-wide association study of early menopause and the combined impact of identified variantsJohn R B Perry, Tanguy Corre, Tõnu Esko, et al.
Plos One|May 11, 2019
Mendelian randomization evaluation of causal effects of fibrinogen on incident coronary heart diseaseCavin K Ward-Caviness, Paul S de Vries, Kerri L Wiggins, et al.
Circulation|April 20, 2011
Genetic predictors of fibrin D-dimer levels in healthy adultsNicholas L Smith, Jennifer E Huffman, David P Strachan, et al.
European Heart Journal|September 1, 2018
A comprehensive evaluation of the genetic architecture of sudden cardiac arrestForam N Ashar, Rebecca N Mitchell, Christine M Albert, et al.
Blood|June 25, 2015
Rare and low-frequency variants and their association with plasma levels of fibrinogen, FVII, FVIII, and vWFJennifer E Huffman, Paul S de Vries, Alanna C Morrison, et al.
Circulation|December 28, 2018
Genome-Wide Association Transethnic Meta-Analyses Identifies Novel Associations Regulating Coagulation Factor VIII and von Willebrand Factor Plasma LevelsMaria Sabater-Lleal, Jennifer E Huffman, Paul S de Vries, et al.
Circulation|April 12, 2019
Biomarkers of Dietary Omega-6 Fatty Acids and Incident Cardiovascular Disease and MortalityMatti Marklund, Jason H Y Wu, Fumiaki Imamura, et al.
Plos One|January 21, 2017
Comparison of HapMap and 1000 Genomes Reference Panels in a Large-Scale Genome-Wide Association StudyPaul S de Vries, Maria Sabater-Lleal, Daniel I Chasman, et al.
Pageof 18

Showing results (131-140 of 174) with videos related to

Sort By:
Pageof 18
HGG Advances|December 26, 2022
Whole-exome sequence analysis of anthropometric traits illustrates challenges in identifying effects of rare genetic variantsKristin L Young, Virginia Fisher, Xuan Deng, et al.
Blood|August 18, 2019
Genomic and transcriptomic association studies identify 16 novel susceptibility loci for venous thromboembolismSara Lindström, Lu Wang, Erin N Smith, et al.
Human Molecular Genetics|January 12, 2013
A genome-wide association study of early menopause and the combined impact of identified variantsJohn R B Perry, Tanguy Corre, Tõnu Esko, et al.
Plos One|May 11, 2019
Mendelian randomization evaluation of causal effects of fibrinogen on incident coronary heart diseaseCavin K Ward-Caviness, Paul S de Vries, Kerri L Wiggins, et al.
Circulation|April 20, 2011
Genetic predictors of fibrin D-dimer levels in healthy adultsNicholas L Smith, Jennifer E Huffman, David P Strachan, et al.
European Heart Journal|September 1, 2018
A comprehensive evaluation of the genetic architecture of sudden cardiac arrestForam N Ashar, Rebecca N Mitchell, Christine M Albert, et al.
Blood|June 25, 2015
Rare and low-frequency variants and their association with plasma levels of fibrinogen, FVII, FVIII, and vWFJennifer E Huffman, Paul S de Vries, Alanna C Morrison, et al.
Circulation|December 28, 2018
Genome-Wide Association Transethnic Meta-Analyses Identifies Novel Associations Regulating Coagulation Factor VIII and von Willebrand Factor Plasma LevelsMaria Sabater-Lleal, Jennifer E Huffman, Paul S de Vries, et al.
Circulation|April 12, 2019
Biomarkers of Dietary Omega-6 Fatty Acids and Incident Cardiovascular Disease and MortalityMatti Marklund, Jason H Y Wu, Fumiaki Imamura, et al.
Plos One|January 21, 2017
Comparison of HapMap and 1000 Genomes Reference Panels in a Large-Scale Genome-Wide Association StudyPaul S de Vries, Maria Sabater-Lleal, Daniel I Chasman, et al.
Pageof 18