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Quanli Wang

Showing results (51-60 of 67) with videos related to

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American Journal of Respiratory and Critical Care Medicine|January 19, 2017
An Exome Sequencing Study to Assess the Role of Rare Genetic Variation in Pulmonary FibrosisSlavé Petrovski, Jamie L Todd, Michael T Durheim, et al.
Nature|January 28, 2026
Population-scale sequencing resolves determinants of persistent EBV DNASherry S Nyeo, Erin M Cumming, Oliver S Burren, et al.
Nature Genetics|August 27, 2024
Genetic architecture of telomere length in 462,666 UK Biobank whole-genome sequencesOliver S Burren, Ryan S Dhindsa, Sri V V Deevi, et al.
Nature|October 4, 2023
Rare variant associations with plasma protein levels in the UK BiobankRyan S Dhindsa, Oliver S Burren, Benjamin B Sun, et al.
Communications Biology|March 24, 2021
Identification of a missense variant in SPDL1 associated with idiopathic pulmonary fibrosisRyan S Dhindsa, Johan Mattsson, Abhishek Nag, et al.
Nature Genetics|February 13, 2025
Comparative analysis of the Mexico City Prospective Study and the UK Biobank identifies ancestry-specific effects on clonal hematopoiesisSean Wen, Pablo Kuri-Morales, Fengyuan Hu, et al.
Cell Reports|March 8, 2025
Haploinsufficiency of ITSN1 is associated with a substantial increased risk of Parkinson's diseaseThomas P Spargo, Chloe F Sands, Isabella R Juan, et al.
Circulation. Genomic and Precision Medicine|October 30, 2020
Spontaneous Coronary Artery Dissection: Insights on Rare Genetic Variation From Genome SequencingKeren J Carss, Anna A Baranowska, Javier Armisen, et al.
Science Advances|November 16, 2022
Human genetics uncovers <i>MAP3K15</i> as an obesity-independent therapeutic target for diabetesAbhishek Nag, Ryan S Dhindsa, Jonathan Mitchell, et al.
Nature|February 4, 2026
Phenome-wide analysis of copy number variants in 470,727 UK Biobank genomesXueqing Zoe Zou, Fengyuan Hu, Haiyi Lou, et al.
Pageof 7

Showing results (51-60 of 67) with videos related to

Sort By:
Pageof 7
American Journal of Respiratory and Critical Care Medicine|January 19, 2017
An Exome Sequencing Study to Assess the Role of Rare Genetic Variation in Pulmonary FibrosisSlavé Petrovski, Jamie L Todd, Michael T Durheim, et al.
Nature|January 28, 2026
Population-scale sequencing resolves determinants of persistent EBV DNASherry S Nyeo, Erin M Cumming, Oliver S Burren, et al.
Nature Genetics|August 27, 2024
Genetic architecture of telomere length in 462,666 UK Biobank whole-genome sequencesOliver S Burren, Ryan S Dhindsa, Sri V V Deevi, et al.
Nature|October 4, 2023
Rare variant associations with plasma protein levels in the UK BiobankRyan S Dhindsa, Oliver S Burren, Benjamin B Sun, et al.
Communications Biology|March 24, 2021
Identification of a missense variant in SPDL1 associated with idiopathic pulmonary fibrosisRyan S Dhindsa, Johan Mattsson, Abhishek Nag, et al.
Nature Genetics|February 13, 2025
Comparative analysis of the Mexico City Prospective Study and the UK Biobank identifies ancestry-specific effects on clonal hematopoiesisSean Wen, Pablo Kuri-Morales, Fengyuan Hu, et al.
Cell Reports|March 8, 2025
Haploinsufficiency of ITSN1 is associated with a substantial increased risk of Parkinson's diseaseThomas P Spargo, Chloe F Sands, Isabella R Juan, et al.
Circulation. Genomic and Precision Medicine|October 30, 2020
Spontaneous Coronary Artery Dissection: Insights on Rare Genetic Variation From Genome SequencingKeren J Carss, Anna A Baranowska, Javier Armisen, et al.
Science Advances|November 16, 2022
Human genetics uncovers <i>MAP3K15</i> as an obesity-independent therapeutic target for diabetesAbhishek Nag, Ryan S Dhindsa, Jonathan Mitchell, et al.
Nature|February 4, 2026
Phenome-wide analysis of copy number variants in 470,727 UK Biobank genomesXueqing Zoe Zou, Fengyuan Hu, Haiyi Lou, et al.
Pageof 7