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Kenneth M Rice

Showing results (61-70 of 112) with videos related to

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European Heart Journal|October 18, 2011
Eight genetic loci associated with variation in lipoprotein-associated phospholipase A2 mass and activity and coronary heart disease: meta-analysis of genome-wide association studies from five community-based studiesHarald Grallert, Josée Dupuis, Joshua C Bis, et al.
Plos One|November 13, 2020
Genetic loci associated with prevalent and incident myocardial infarction and coronary heart disease in the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) ConsortiumJulie Hahn, Yi-Ping Fu, Michael R Brown, et al.
Nature Communications|September 30, 2022
Publisher Correction: Endophenotype effect sizes support variant pathogenicity in monogenic disease susceptibility genesJennifer L Halford, Valerie N Morrill, Seung Hoan Choi, et al.
American Journal of Human Genetics|January 15, 2019
Efficient Variant Set Mixed Model Association Tests for Continuous and Binary Traits in Large-Scale Whole-Genome Sequencing StudiesHan Chen, Jennifer E Huffman, Jennifer A Brody, et al.
Nature Communications|August 30, 2022
Endophenotype effect sizes support variant pathogenicity in monogenic disease susceptibility genesJennifer L Halford, Valerie N Morrill, Seung Hoan Choi, et al.
Plos Genetics|May 6, 2016
Discovery of Genetic Variation on Chromosome 5q22 Associated with Mortality in Heart FailureJ Gustav Smith, Janine F Felix, Alanna C Morrison, et al.
Plos Genetics|October 21, 2016
Rare Functional Variant in TM2D3 is Associated with Late-Onset Alzheimer's DiseaseJohanna Jakobsdottir, Sven J van der Lee, Joshua C Bis, et al.
American Journal of Human Genetics|August 4, 2016
Whole-Exome Sequencing Identifies Loci Associated with Blood Cell Traits and Reveals a Role for Alternative GFI1B Splice Variants in Human HematopoiesisLinda M Polfus, Rajiv K Khajuria, Ursula M Schick, et al.
American Journal of Human Genetics|September 3, 2016
Whole-Exome Sequencing Identifies Loci Associated with Blood Cell Traits and Reveals a Role for Alternative GFI1B Splice Variants in Human HematopoiesisLinda M Polfus, Rajiv K Khajuria, Ursula M Schick, et al.
Nature Genetics|July 15, 2009
Variants in ZFHX3 are associated with atrial fibrillation in individuals of European ancestryEmelia J Benjamin, Kenneth M Rice, Dan E Arking, et al.
Pageof 12

Showing results (61-70 of 112) with videos related to

Sort By:
Pageof 12
European Heart Journal|October 18, 2011
Eight genetic loci associated with variation in lipoprotein-associated phospholipase A2 mass and activity and coronary heart disease: meta-analysis of genome-wide association studies from five community-based studiesHarald Grallert, Josée Dupuis, Joshua C Bis, et al.
Plos One|November 13, 2020
Genetic loci associated with prevalent and incident myocardial infarction and coronary heart disease in the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) ConsortiumJulie Hahn, Yi-Ping Fu, Michael R Brown, et al.
Nature Communications|September 30, 2022
Publisher Correction: Endophenotype effect sizes support variant pathogenicity in monogenic disease susceptibility genesJennifer L Halford, Valerie N Morrill, Seung Hoan Choi, et al.
American Journal of Human Genetics|January 15, 2019
Efficient Variant Set Mixed Model Association Tests for Continuous and Binary Traits in Large-Scale Whole-Genome Sequencing StudiesHan Chen, Jennifer E Huffman, Jennifer A Brody, et al.
Nature Communications|August 30, 2022
Endophenotype effect sizes support variant pathogenicity in monogenic disease susceptibility genesJennifer L Halford, Valerie N Morrill, Seung Hoan Choi, et al.
Plos Genetics|May 6, 2016
Discovery of Genetic Variation on Chromosome 5q22 Associated with Mortality in Heart FailureJ Gustav Smith, Janine F Felix, Alanna C Morrison, et al.
Plos Genetics|October 21, 2016
Rare Functional Variant in TM2D3 is Associated with Late-Onset Alzheimer's DiseaseJohanna Jakobsdottir, Sven J van der Lee, Joshua C Bis, et al.
American Journal of Human Genetics|August 4, 2016
Whole-Exome Sequencing Identifies Loci Associated with Blood Cell Traits and Reveals a Role for Alternative GFI1B Splice Variants in Human HematopoiesisLinda M Polfus, Rajiv K Khajuria, Ursula M Schick, et al.
American Journal of Human Genetics|September 3, 2016
Whole-Exome Sequencing Identifies Loci Associated with Blood Cell Traits and Reveals a Role for Alternative GFI1B Splice Variants in Human HematopoiesisLinda M Polfus, Rajiv K Khajuria, Ursula M Schick, et al.
Nature Genetics|July 15, 2009
Variants in ZFHX3 are associated with atrial fibrillation in individuals of European ancestryEmelia J Benjamin, Kenneth M Rice, Dan E Arking, et al.
Pageof 12