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Jason Flannick

Showing results (81-90 of 101) with videos related to

Pageof 11
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Nature|April 13, 2012
Patterns and rates of exonic de novo mutations in autism spectrum disordersBenjamin M Neale, Yan Kou, Li Liu, et al.
Cell Metabolism|March 24, 2023
The Type 2 Diabetes Knowledge Portal: An open access genetic resource dedicated to type 2 diabetes and related traitsMaria C Costanzo, Marcin von Grotthuss, Jeffrey Massung, et al.
Nature Communications|January 29, 2016
Genome-wide association studies in the Japanese population identify seven novel loci for type 2 diabetesMinako Imamura, Atsushi Takahashi, Toshimasa Yamauchi, et al.
JAMA|June 11, 2014
Association of a low-frequency variant in HNF1A with type 2 diabetes in a Latino population, Karol Estrada, Ingvild Aukrust, et al.
Diabetologia|May 6, 2023
The power of TOPMed imputation for the discovery of Latino-enriched rare variants associated with type 2 diabetesAlicia Huerta-Chagoya, Philip Schroeder, Ravi Mandla, et al.
Nature|August 19, 2016
Analysis of protein-coding genetic variation in 60,706 humansMonkol Lek, Konrad J Karczewski, Eric V Minikel, et al.
Nature Genetics|March 4, 2014
Loss-of-function mutations in SLC30A8 protect against type 2 diabetesJason Flannick, Gudmar Thorleifsson, Nicola L Beer, et al.
Nature Communications|June 15, 2018
Genetic inactivation of ANGPTL4 improves glucose homeostasis and is associated with reduced risk of diabetesViktoria Gusarova, Colm O'Dushlaine, Tanya M Teslovich, et al.
Diabetes|August 26, 2017
A Loss-of-Function Splice Acceptor Variant in <i>IGF2</i> Is Protective for Type 2 DiabetesJosep M Mercader, Rachel G Liao, Avery D Bell, et al.
Nature Genetics|December 6, 2022
Discovery and systematic characterization of risk variants and genes for coronary artery disease in over a million participantsKrishna G Aragam, Tao Jiang, Anuj Goel, et al.
Pageof 11

Showing results (81-90 of 101) with videos related to

Sort By:
Pageof 11
Nature|April 13, 2012
Patterns and rates of exonic de novo mutations in autism spectrum disordersBenjamin M Neale, Yan Kou, Li Liu, et al.
Cell Metabolism|March 24, 2023
The Type 2 Diabetes Knowledge Portal: An open access genetic resource dedicated to type 2 diabetes and related traitsMaria C Costanzo, Marcin von Grotthuss, Jeffrey Massung, et al.
Nature Communications|January 29, 2016
Genome-wide association studies in the Japanese population identify seven novel loci for type 2 diabetesMinako Imamura, Atsushi Takahashi, Toshimasa Yamauchi, et al.
JAMA|June 11, 2014
Association of a low-frequency variant in HNF1A with type 2 diabetes in a Latino population, Karol Estrada, Ingvild Aukrust, et al.
Diabetologia|May 6, 2023
The power of TOPMed imputation for the discovery of Latino-enriched rare variants associated with type 2 diabetesAlicia Huerta-Chagoya, Philip Schroeder, Ravi Mandla, et al.
Nature|August 19, 2016
Analysis of protein-coding genetic variation in 60,706 humansMonkol Lek, Konrad J Karczewski, Eric V Minikel, et al.
Nature Genetics|March 4, 2014
Loss-of-function mutations in SLC30A8 protect against type 2 diabetesJason Flannick, Gudmar Thorleifsson, Nicola L Beer, et al.
Nature Communications|June 15, 2018
Genetic inactivation of ANGPTL4 improves glucose homeostasis and is associated with reduced risk of diabetesViktoria Gusarova, Colm O'Dushlaine, Tanya M Teslovich, et al.
Diabetes|August 26, 2017
A Loss-of-Function Splice Acceptor Variant in <i>IGF2</i> Is Protective for Type 2 DiabetesJosep M Mercader, Rachel G Liao, Avery D Bell, et al.
Nature Genetics|December 6, 2022
Discovery and systematic characterization of risk variants and genes for coronary artery disease in over a million participantsKrishna G Aragam, Tao Jiang, Anuj Goel, et al.
Pageof 11