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Showing results (301-310 of 364) with videos related to

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Nature Communications|February 22, 2019
Association study in African-admixed populations across the Americas recapitulates asthma risk loci in non-African populationsMichelle Daya, Nicholas Rafaels, Tonya M Brunetti, et al.
Communications Biology|August 10, 2019
A genome-wide association study identifies genetic loci associated with specific lobar brain volumesSven J van der Lee, Maria J Knol, Ganesh Chauhan, et al.
Nature Communications|December 9, 2022
Whole genome sequencing identifies structural variants contributing to hematologic traits in the NHLBI TOPMed programMarsha M Wheeler, Adrienne M Stilp, Shuquan Rao, et al.
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.
Nature Communications|September 6, 2019
Author Correction: Association study in African-admixed populations across the Americas recapitulates asthma risk loci in non-African populationsMichelle Daya, Nicholas Rafaels, Tonya M Brunetti, 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.
Biorxiv : the Preprint Server for Biology|November 14, 2023
A statistical framework for powerful multi-trait rare variant analysis in large-scale whole-genome sequencing studiesXihao Li, Han Chen, Margaret Sunitha Selvaraj, 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.
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.
Pageof 37

Showing results (301-310 of 364) with videos related to

Sort By:
Pageof 37
Nature Communications|February 22, 2019
Association study in African-admixed populations across the Americas recapitulates asthma risk loci in non-African populationsMichelle Daya, Nicholas Rafaels, Tonya M Brunetti, et al.
Communications Biology|August 10, 2019
A genome-wide association study identifies genetic loci associated with specific lobar brain volumesSven J van der Lee, Maria J Knol, Ganesh Chauhan, et al.
Nature Communications|December 9, 2022
Whole genome sequencing identifies structural variants contributing to hematologic traits in the NHLBI TOPMed programMarsha M Wheeler, Adrienne M Stilp, Shuquan Rao, et al.
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.
Nature Communications|September 6, 2019
Author Correction: Association study in African-admixed populations across the Americas recapitulates asthma risk loci in non-African populationsMichelle Daya, Nicholas Rafaels, Tonya M Brunetti, 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.
Biorxiv : the Preprint Server for Biology|November 14, 2023
A statistical framework for powerful multi-trait rare variant analysis in large-scale whole-genome sequencing studiesXihao Li, Han Chen, Margaret Sunitha Selvaraj, 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.
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.
Pageof 37