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Jason Flannick

Showing results (21-30 of 101) with videos related to

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Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 12, 2025
Common and rare genetic variants explain distinct diagnostic variance in pediatric attention deficit hyperactivity disorderAnne B Arnett, Ryan Koesterer, Paulina Gonzalez Tovar, et al.
Nature Communications|September 14, 2024
Genome-wide discovery and integrative genomic characterization of insulin resistance loci using serum triglycerides to HDL-cholesterol ratio as a proxyNatalie DeForest, Yuqi Wang, Zhiyi Zhu, et al.
Diabetes|December 1, 2016
Functional Investigations of HNF1A Identify Rare Variants as Risk Factors for Type 2 Diabetes in the General PopulationLaeya Abdoli Najmi, Ingvild Aukrust, Jason Flannick, et al.
Diabetes|January 24, 2025
An Alternatively Translated Isoform of PPARG Suggests AF-1 Domain Inhibition as an Insulin Sensitization TargetXiaomi Du, Karen Mendez-Lara, Siqi Hu, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|August 11, 2020
The Musculoskeletal Knowledge Portal: Making Omics Data Useful to the Broader Scientific CommunityDouglas P Kiel, John P Kemp, Fernando Rivadeneira, et al.
Plos Genetics|April 24, 2015
The power of gene-based rare variant methods to detect disease-associated variation and test hypotheses about complex diseaseLoukas Moutsianas, Vineeta Agarwala, Christian Fuchsberger, et al.
Human Molecular Genetics|October 18, 2022
Ancestry-specific high-risk gene variant profiling unmasks diabetes-associated genesJianhua Zhang, Weiping Chen, Guanjie Chen, et al.
Nature Genetics|October 25, 2022
A combined polygenic score of 21,293 rare and 22 common variants improves diabetes diagnosis based on hemoglobin A1C levelsPeter Dornbos, Ryan Koesterer, Andrew Ruttenburg, et al.
Reproductive Biomedicine Online|August 24, 2010
A universal carrier test for the long tail of Mendelian diseaseBalaji S Srinivasan, Eric A Evans, Jason Flannick, et al.
Kidney International|December 20, 2021
A glomerular transcriptomic landscape of apolipoprotein L1 in Black patients with focal segmental glomerulosclerosisMichelle T McNulty, Damian Fermin, Felix Eichinger, et al.
Pageof 11

Showing results (21-30 of 101) with videos related to

Sort By:
Pageof 11
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 12, 2025
Common and rare genetic variants explain distinct diagnostic variance in pediatric attention deficit hyperactivity disorderAnne B Arnett, Ryan Koesterer, Paulina Gonzalez Tovar, et al.
Nature Communications|September 14, 2024
Genome-wide discovery and integrative genomic characterization of insulin resistance loci using serum triglycerides to HDL-cholesterol ratio as a proxyNatalie DeForest, Yuqi Wang, Zhiyi Zhu, et al.
Diabetes|December 1, 2016
Functional Investigations of HNF1A Identify Rare Variants as Risk Factors for Type 2 Diabetes in the General PopulationLaeya Abdoli Najmi, Ingvild Aukrust, Jason Flannick, et al.
Diabetes|January 24, 2025
An Alternatively Translated Isoform of PPARG Suggests AF-1 Domain Inhibition as an Insulin Sensitization TargetXiaomi Du, Karen Mendez-Lara, Siqi Hu, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|August 11, 2020
The Musculoskeletal Knowledge Portal: Making Omics Data Useful to the Broader Scientific CommunityDouglas P Kiel, John P Kemp, Fernando Rivadeneira, et al.
Plos Genetics|April 24, 2015
The power of gene-based rare variant methods to detect disease-associated variation and test hypotheses about complex diseaseLoukas Moutsianas, Vineeta Agarwala, Christian Fuchsberger, et al.
Human Molecular Genetics|October 18, 2022
Ancestry-specific high-risk gene variant profiling unmasks diabetes-associated genesJianhua Zhang, Weiping Chen, Guanjie Chen, et al.
Nature Genetics|October 25, 2022
A combined polygenic score of 21,293 rare and 22 common variants improves diabetes diagnosis based on hemoglobin A1C levelsPeter Dornbos, Ryan Koesterer, Andrew Ruttenburg, et al.
Reproductive Biomedicine Online|August 24, 2010
A universal carrier test for the long tail of Mendelian diseaseBalaji S Srinivasan, Eric A Evans, Jason Flannick, et al.
Kidney International|December 20, 2021
A glomerular transcriptomic landscape of apolipoprotein L1 in Black patients with focal segmental glomerulosclerosisMichelle T McNulty, Damian Fermin, Felix Eichinger, et al.
Pageof 11