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Jason Flannick

Showing results (91-100 of 101) with videos related to

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Biorxiv : the Preprint Server for Biology|April 17, 2026
The Common Fund Data Ecosystem (CFDE)Julie A Jurgens, Andreas Bueckle, Jeet Vora, et al.
Plos Genetics|January 28, 2015
Identification and functional characterization of G6PC2 coding variants influencing glycemic traits define an effector transcript at the G6PC2-ABCB11 locusAnubha Mahajan, Xueling Sim, Hui Jin Ng, et al.
American Journal of Human Genetics|February 11, 2014
Whole-exome sequencing identifies rare and low-frequency coding variants associated with LDL cholesterolLeslie A Lange, Youna Hu, He Zhang, et al.
Nature Communications|June 10, 2021
Determinants of penetrance and variable expressivity in monogenic metabolic conditions across 77,184 exomesJulia K Goodrich, Moriel Singer-Berk, Rachel Son, et al.
Nature|May 24, 2019
Exome sequencing of 20,791 cases of type 2 diabetes and 24,440 controlsJason Flannick, Josep M Mercader, Christian Fuchsberger, et al.
Nature Genetics|November 10, 2015
Genetic fine mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility lociKyle J Gaulton, Teresa Ferreira, Yeji Lee, et al.
Nature Genetics|April 11, 2018
Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetesAnubha Mahajan, Jennifer Wessel, Sara M Willems, et al.
Diabetes|March 26, 2017
A Low-Frequency Inactivating <i>AKT2</i> Variant Enriched in the Finnish Population Is Associated With Fasting Insulin Levels and Type 2 Diabetes RiskAlisa Manning, Heather M Highland, Jessica Gasser, et al.
Nature|July 12, 2016
The genetic architecture of type 2 diabetesChristian Fuchsberger, Jason Flannick, Tanya M Teslovich, et al.
Scientific Data|December 20, 2017
Sequence data and association statistics from 12,940 type 2 diabetes cases and controlsJason Flannick, Christian Fuchsberger, Anubha Mahajan, et al.
Pageof 11

Showing results (91-100 of 101) with videos related to

Sort By:
Pageof 11
Biorxiv : the Preprint Server for Biology|April 17, 2026
The Common Fund Data Ecosystem (CFDE)Julie A Jurgens, Andreas Bueckle, Jeet Vora, et al.
Plos Genetics|January 28, 2015
Identification and functional characterization of G6PC2 coding variants influencing glycemic traits define an effector transcript at the G6PC2-ABCB11 locusAnubha Mahajan, Xueling Sim, Hui Jin Ng, et al.
American Journal of Human Genetics|February 11, 2014
Whole-exome sequencing identifies rare and low-frequency coding variants associated with LDL cholesterolLeslie A Lange, Youna Hu, He Zhang, et al.
Nature Communications|June 10, 2021
Determinants of penetrance and variable expressivity in monogenic metabolic conditions across 77,184 exomesJulia K Goodrich, Moriel Singer-Berk, Rachel Son, et al.
Nature|May 24, 2019
Exome sequencing of 20,791 cases of type 2 diabetes and 24,440 controlsJason Flannick, Josep M Mercader, Christian Fuchsberger, et al.
Nature Genetics|November 10, 2015
Genetic fine mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility lociKyle J Gaulton, Teresa Ferreira, Yeji Lee, et al.
Nature Genetics|April 11, 2018
Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetesAnubha Mahajan, Jennifer Wessel, Sara M Willems, et al.
Diabetes|March 26, 2017
A Low-Frequency Inactivating <i>AKT2</i> Variant Enriched in the Finnish Population Is Associated With Fasting Insulin Levels and Type 2 Diabetes RiskAlisa Manning, Heather M Highland, Jessica Gasser, et al.
Nature|July 12, 2016
The genetic architecture of type 2 diabetesChristian Fuchsberger, Jason Flannick, Tanya M Teslovich, et al.
Scientific Data|December 20, 2017
Sequence data and association statistics from 12,940 type 2 diabetes cases and controlsJason Flannick, Christian Fuchsberger, Anubha Mahajan, et al.
Pageof 11