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G Drivas

Showing results (71-80 of 77) with videos related to

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JAMA Network Open|May 28, 2024
Progesterone for Neurodevelopment in Fetuses With Congenital Heart Defects: A Randomized Clinical TrialJ William Gaynor, Julie S Moldenhauer, Erin E Zullo, et al.
Blood|March 17, 2026
Clinical Spectrum of Hereditary Hemorrhagic Telangiectasia: Data from the Comprehensive HHT Outcomes Registry of the US (CHORUS)Hanny Al-Samkari, Cassi Friday, Raj S Kasthuri, et al.
Nature Medicine|January 12, 2021
Exome-wide evaluation of rare coding variants using electronic health records identifies new gene-phenotype associationsJoseph Park, Anastasia M Lucas, Xinyuan Zhang, et al.
Medrxiv : the Preprint Server for Health Sciences|August 6, 2025
The polygenic architecture of hidradenitis suppurativa reveals signaling mechanisms that implicate epithelial remodelingAtlas Khan, Poppy A Gould, Yiming Luo, et al.
European Journal of Human Genetics : EJHG|June 3, 2020
A second cohort of CHD3 patients expands the molecular mechanisms known to cause Snijders Blok-Campeau syndromeTheodore G Drivas, Dong Li, Divya Nair, et al.
Science (New York, N.Y.)|February 6, 2025
Kidney multiome-based genetic scorecard reveals convergent coding and regulatory variantsHongbo Liu, Amin Abedini, Eunji Ha, et al.
Science Advances|March 10, 2023
Mechanism of KMT5B haploinsufficiency in neurodevelopment in humans and miceSarah E Sheppard, Laura Bryant, Rochelle N Wickramasekara, et al.
Pageof 8

Showing results (71-80 of 77) with videos related to

Sort By:
Pageof 8
You have reached the last page of results.This site can display upto 77 results.
JAMA Network Open|May 28, 2024
Progesterone for Neurodevelopment in Fetuses With Congenital Heart Defects: A Randomized Clinical TrialJ William Gaynor, Julie S Moldenhauer, Erin E Zullo, et al.
Blood|March 17, 2026
Clinical Spectrum of Hereditary Hemorrhagic Telangiectasia: Data from the Comprehensive HHT Outcomes Registry of the US (CHORUS)Hanny Al-Samkari, Cassi Friday, Raj S Kasthuri, et al.
Nature Medicine|January 12, 2021
Exome-wide evaluation of rare coding variants using electronic health records identifies new gene-phenotype associationsJoseph Park, Anastasia M Lucas, Xinyuan Zhang, et al.
Medrxiv : the Preprint Server for Health Sciences|August 6, 2025
The polygenic architecture of hidradenitis suppurativa reveals signaling mechanisms that implicate epithelial remodelingAtlas Khan, Poppy A Gould, Yiming Luo, et al.
European Journal of Human Genetics : EJHG|June 3, 2020
A second cohort of CHD3 patients expands the molecular mechanisms known to cause Snijders Blok-Campeau syndromeTheodore G Drivas, Dong Li, Divya Nair, et al.
Science (New York, N.Y.)|February 6, 2025
Kidney multiome-based genetic scorecard reveals convergent coding and regulatory variantsHongbo Liu, Amin Abedini, Eunji Ha, et al.
Science Advances|March 10, 2023
Mechanism of KMT5B haploinsufficiency in neurodevelopment in humans and miceSarah E Sheppard, Laura Bryant, Rochelle N Wickramasekara, et al.
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