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Gillian M Belbin

Showing results (11-20 of 33) with videos related to

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BMC Genetics|July 4, 2019
Genome-wide analysis indicates association between heterozygote advantage and healthy aging in humansKe Xu, Roman Kosoy, Khader Shameer, et al.
Clinical Gastroenterology and Hepatology : the Official Clinical Practice Journal of the American Gastroenterological Association|January 7, 2023
Association of HSD17B13 and PNPLA3 With Liver Enzymes and Fibrosis in Hispanic/Latino Individuals of Diverse Genetic AncestriesStephanie M Rutledge, Emily R Soper, Ning Ma, et al.
JCO Precision Oncology|December 7, 2020
Lynch Syndrome-Associated Variants and Cancer Rates in an Ancestrally Diverse BiobankRachel E Rosenblum, Celina Ang, Sabrina A Suckiel, et al.
The Pharmacogenomics Journal|November 10, 2020
Rapid response to the alpha-1 adrenergic agent phenylephrine in the perioperative period is impacted by genomics and ancestryStephane Wenric, Janina M Jeff, Thomas Joseph, et al.
American Journal of Human Genetics|October 22, 2021
Leveraging health systems data to characterize a large effect variant conferring risk for liver disease in Puerto RicansGillian M Belbin, Stephanie Rutledge, Tetyana Dodatko, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|June 19, 2023
Life is pain: Fibromyalgia as a nexus of multiple liability distributionsArden Moscati, Annika B Faucon, Cayetana Arnaiz-Yépez, et al.
Journal of Hepatology|March 8, 2020
A common variant in PNPLA3 is associated with age at diagnosis of NAFLD in patients from a multi-ethnic biobankRyan W Walker, Gillian M Belbin, Elena P Sorokin, et al.
Genome Medicine|January 2, 2020
Exome sequencing reveals a high prevalence of BRCA1 and BRCA2 founder variants in a diverse population-based biobankNoura S Abul-Husn, Emily R Soper, Jacqueline A Odgis, et al.
Frontiers in Genetics|August 21, 2023
Admixture mapping of peripheral artery disease in a Dominican population reveals a putative risk locus on 2q35Sinead Cullina, Genevieve L Wojcik, Ruhollah Shemirani, et al.
Medrxiv : the Preprint Server for Health Sciences|April 10, 2023
Admixture Mapping of Peripheral Artery Disease in a Dominican Population Reveals a Novel Risk Locus on 2q35Sinead Cullina, Genevieve L Wojcik, Ruhollah Shemirani, et al.
Pageof 4

Showing results (11-20 of 33) with videos related to

Sort By:
Pageof 4
BMC Genetics|July 4, 2019
Genome-wide analysis indicates association between heterozygote advantage and healthy aging in humansKe Xu, Roman Kosoy, Khader Shameer, et al.
Clinical Gastroenterology and Hepatology : the Official Clinical Practice Journal of the American Gastroenterological Association|January 7, 2023
Association of HSD17B13 and PNPLA3 With Liver Enzymes and Fibrosis in Hispanic/Latino Individuals of Diverse Genetic AncestriesStephanie M Rutledge, Emily R Soper, Ning Ma, et al.
JCO Precision Oncology|December 7, 2020
Lynch Syndrome-Associated Variants and Cancer Rates in an Ancestrally Diverse BiobankRachel E Rosenblum, Celina Ang, Sabrina A Suckiel, et al.
The Pharmacogenomics Journal|November 10, 2020
Rapid response to the alpha-1 adrenergic agent phenylephrine in the perioperative period is impacted by genomics and ancestryStephane Wenric, Janina M Jeff, Thomas Joseph, et al.
American Journal of Human Genetics|October 22, 2021
Leveraging health systems data to characterize a large effect variant conferring risk for liver disease in Puerto RicansGillian M Belbin, Stephanie Rutledge, Tetyana Dodatko, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|June 19, 2023
Life is pain: Fibromyalgia as a nexus of multiple liability distributionsArden Moscati, Annika B Faucon, Cayetana Arnaiz-Yépez, et al.
Journal of Hepatology|March 8, 2020
A common variant in PNPLA3 is associated with age at diagnosis of NAFLD in patients from a multi-ethnic biobankRyan W Walker, Gillian M Belbin, Elena P Sorokin, et al.
Genome Medicine|January 2, 2020
Exome sequencing reveals a high prevalence of BRCA1 and BRCA2 founder variants in a diverse population-based biobankNoura S Abul-Husn, Emily R Soper, Jacqueline A Odgis, et al.
Frontiers in Genetics|August 21, 2023
Admixture mapping of peripheral artery disease in a Dominican population reveals a putative risk locus on 2q35Sinead Cullina, Genevieve L Wojcik, Ruhollah Shemirani, et al.
Medrxiv : the Preprint Server for Health Sciences|April 10, 2023
Admixture Mapping of Peripheral Artery Disease in a Dominican Population Reveals a Novel Risk Locus on 2q35Sinead Cullina, Genevieve L Wojcik, Ruhollah Shemirani, et al.
Pageof 4