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Eric Boerwinkle

Showing results (941-950 of 1,171) with videos related to

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Human Molecular Genetics|September 23, 2021
Whole genome sequence analysis of platelet traits in the NHLBI Trans-Omics for Precision Medicine (TOPMed) initiativeAmarise Little, Yao Hu, Quan Sun, et al.
Nature Genetics|August 26, 2020
Dynamic incorporation of multiple in silico functional annotations empowers rare variant association analysis of large whole-genome sequencing studies at scaleXihao Li, Zilin Li, Hufeng Zhou, et al.
Human Molecular Genetics|January 15, 2013
Genetic variation associated with circulating monocyte count in the eMERGE NetworkDavid R Crosslin, Andrew McDavid, Noah Weston, 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.
Nature Genetics|February 23, 2010
Common variants in KCNN3 are associated with lone atrial fibrillationPatrick T Ellinor, Kathryn L Lunetta, Nicole L Glazer, et al.
Nature Communications|January 29, 2021
Genome-wide meta-analysis of muscle weakness identifies 15 susceptibility loci in older men and womenGaran Jones, Katerina Trajanoska, Adam J Santanasto, et al.
American Journal of Epidemiology|June 4, 2019
The Consortium of Metabolomics Studies (COMETS): Metabolomics in 47 Prospective Cohort StudiesBing Yu, Krista A Zanetti, Marinella Temprosa, et al.
Medrxiv : the Preprint Server for Health Sciences|May 3, 2024
Genomic and phenotypic correlates of mosaic loss of chromosome Y in bloodYasminka A Jakubek, Xiaolong Ma, Adrienne M Stilp, et al.
Nature Communications|May 21, 2026
Co-occurring clonal hematopoiesis exhibits strong selection and high leukemia riskKara M Barnao, Aubrey K Hubbard, Irenaeus C C Chan, et al.
Journal of the American Heart Association|February 14, 2025
Unveiling the Genetic Landscape of Coronary Artery Disease Through Common and Rare Structural VariantsKruthika R Iyer, Shoa L Clarke, Rodrigo Guarischi-Sousa, et al.
Pageof 118

Showing results (941-950 of 1,171) with videos related to

Sort By:
Pageof 118
Human Molecular Genetics|September 23, 2021
Whole genome sequence analysis of platelet traits in the NHLBI Trans-Omics for Precision Medicine (TOPMed) initiativeAmarise Little, Yao Hu, Quan Sun, et al.
Nature Genetics|August 26, 2020
Dynamic incorporation of multiple in silico functional annotations empowers rare variant association analysis of large whole-genome sequencing studies at scaleXihao Li, Zilin Li, Hufeng Zhou, et al.
Human Molecular Genetics|January 15, 2013
Genetic variation associated with circulating monocyte count in the eMERGE NetworkDavid R Crosslin, Andrew McDavid, Noah Weston, 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.
Nature Genetics|February 23, 2010
Common variants in KCNN3 are associated with lone atrial fibrillationPatrick T Ellinor, Kathryn L Lunetta, Nicole L Glazer, et al.
Nature Communications|January 29, 2021
Genome-wide meta-analysis of muscle weakness identifies 15 susceptibility loci in older men and womenGaran Jones, Katerina Trajanoska, Adam J Santanasto, et al.
American Journal of Epidemiology|June 4, 2019
The Consortium of Metabolomics Studies (COMETS): Metabolomics in 47 Prospective Cohort StudiesBing Yu, Krista A Zanetti, Marinella Temprosa, et al.
Medrxiv : the Preprint Server for Health Sciences|May 3, 2024
Genomic and phenotypic correlates of mosaic loss of chromosome Y in bloodYasminka A Jakubek, Xiaolong Ma, Adrienne M Stilp, et al.
Nature Communications|May 21, 2026
Co-occurring clonal hematopoiesis exhibits strong selection and high leukemia riskKara M Barnao, Aubrey K Hubbard, Irenaeus C C Chan, et al.
Journal of the American Heart Association|February 14, 2025
Unveiling the Genetic Landscape of Coronary Artery Disease Through Common and Rare Structural VariantsKruthika R Iyer, Shoa L Clarke, Rodrigo Guarischi-Sousa, et al.
Pageof 118