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Showing results (401-410 of 590) with videos related to

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BMC Genomics|February 20, 2022
Rare coding variants in RCN3 are associated with blood pressureKaren Y He, Tanika N Kelly, Heming Wang, et al.
Biology of Sex Differences|May 4, 2017
Does the sex of one's co-twin affect height and BMI in adulthood? A study of dizygotic adult twins from 31 cohortsLeonie H Bogl, Aline Jelenkovic, Eero Vuoksimaa, et al.
American Journal of Respiratory and Critical Care Medicine|July 28, 2012
Genome-wide association studies identify CHRNA5/3 and HTR4 in the development of airflow obstructionJemma B Wilk, Nick R G Shrine, Laura R Loehr, et al.
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|March 29, 2012
Common breast cancer susceptibility variants in LSP1 and RAD51L1 are associated with mammographic density measures that predict breast cancer riskCeline M Vachon, Christopher G Scott, Peter A Fasching, et al.
Plos Genetics|December 24, 2019
Use of >100,000 NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium whole genome sequences improves imputation quality and detection of rare variant associations in admixed African and Hispanic/Latino populationsMadeline H Kowalski, Huijun Qian, Ziyi Hou, et al.
American Journal of Human Genetics|April 22, 2021
Whole-genome sequencing association analysis of quantitative red blood cell phenotypes: The NHLBI TOPMed programYao Hu, Adrienne M Stilp, Caitlin P McHugh, et al.
Research Square|May 18, 2026
Rare coding variant architecture and gene discovery from 130,000 sequenced cases of atrial fibrillationSean Jurgens, Nobuyuki Enzan, Ian Dinsmore, et al.
Biorxiv : the Preprint Server for Biology|February 7, 2023
Structural variation across 138,134 samples in the TOPMed consortiumGoo Jun, Adam C English, Ginger A Metcalf, et al.
Nature Computational Science|February 7, 2025
A statistical framework for multi-trait rare variant analysis in large-scale whole-genome sequencing studiesXihao Li, Han Chen, Margaret Sunitha Selvaraj, et al.
Nature Genetics|December 17, 2009
Genome-wide association study identifies five loci associated with lung functionEmmanouela Repapi, Ian Sayers, Louise V Wain, et al.
Pageof 59

Showing results (401-410 of 590) with videos related to

Sort By:
Pageof 59
BMC Genomics|February 20, 2022
Rare coding variants in RCN3 are associated with blood pressureKaren Y He, Tanika N Kelly, Heming Wang, et al.
Biology of Sex Differences|May 4, 2017
Does the sex of one's co-twin affect height and BMI in adulthood? A study of dizygotic adult twins from 31 cohortsLeonie H Bogl, Aline Jelenkovic, Eero Vuoksimaa, et al.
American Journal of Respiratory and Critical Care Medicine|July 28, 2012
Genome-wide association studies identify CHRNA5/3 and HTR4 in the development of airflow obstructionJemma B Wilk, Nick R G Shrine, Laura R Loehr, et al.
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|March 29, 2012
Common breast cancer susceptibility variants in LSP1 and RAD51L1 are associated with mammographic density measures that predict breast cancer riskCeline M Vachon, Christopher G Scott, Peter A Fasching, et al.
Plos Genetics|December 24, 2019
Use of >100,000 NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium whole genome sequences improves imputation quality and detection of rare variant associations in admixed African and Hispanic/Latino populationsMadeline H Kowalski, Huijun Qian, Ziyi Hou, et al.
American Journal of Human Genetics|April 22, 2021
Whole-genome sequencing association analysis of quantitative red blood cell phenotypes: The NHLBI TOPMed programYao Hu, Adrienne M Stilp, Caitlin P McHugh, et al.
Research Square|May 18, 2026
Rare coding variant architecture and gene discovery from 130,000 sequenced cases of atrial fibrillationSean Jurgens, Nobuyuki Enzan, Ian Dinsmore, et al.
Biorxiv : the Preprint Server for Biology|February 7, 2023
Structural variation across 138,134 samples in the TOPMed consortiumGoo Jun, Adam C English, Ginger A Metcalf, et al.
Nature Computational Science|February 7, 2025
A statistical framework for multi-trait rare variant analysis in large-scale whole-genome sequencing studiesXihao Li, Han Chen, Margaret Sunitha Selvaraj, et al.
Nature Genetics|December 17, 2009
Genome-wide association study identifies five loci associated with lung functionEmmanouela Repapi, Ian Sayers, Louise V Wain, et al.
Pageof 59