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Jason Flannick

Showing results (61-70 of 101) with videos related to

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Nature Genetics|August 29, 2024
Rare coding variant analysis for human diseases across biobanks and ancestriesSean J Jurgens, Xin Wang, Seung Hoan Choi, et al.
American Journal of Human Genetics|December 25, 2012
Rare, low-frequency, and common variants in the protein-coding sequence of biological candidate genes from GWASs contribute to risk of rheumatoid arthritisDorothée Diogo, Fina Kurreeman, Eli A Stahl, et al.
American Journal of Human Genetics|September 11, 2012
Burden of rare sarcomere gene variants in the Framingham and Jackson Heart Study cohortsAlexander G Bick, Jason Flannick, Kaoru Ito, et al.
The Journal of Clinical Investigation|September 15, 2022
Haploinsufficiency of CYP8B1 associates with increased insulin sensitivity in humansShiqi Zhong, Raphael Chèvre, David Castaño Mayan, et al.
Nature Genetics|January 24, 2025
Integrative proteogenomic analysis identifies COL6A3-derived endotrophin as a mediator of the effect of obesity on coronary artery diseaseSatoshi Yoshiji, Tianyuan Lu, Guillaume Butler-Laporte, et al.
Nature Genetics|October 8, 2013
Assessing the phenotypic effects in the general population of rare variants in genes for a dominant Mendelian form of diabetesJason Flannick, Nicola L Beer, Alexander G Bick, et al.
Biorxiv : the Preprint Server for Biology|June 22, 2026
PanKbase Integrated Single-Cell Map: A Comprehensive Atlas of Human Pancreatic IsletsHa T H Vu, Han Sun, Parul Kudtarkar, et al.
Nature Communications|October 19, 2017
Integrating evolutionary and regulatory information with a multispecies approach implicates genes and pathways in obsessive-compulsive disorderHyun Ji Noh, Ruqi Tang, Jason Flannick, et al.
The New England Journal of Medicine|November 27, 2014
Age-related clonal hematopoiesis associated with adverse outcomesSiddhartha Jaiswal, Pierre Fontanillas, Jason Flannick, et al.
Plos Genetics|April 18, 2013
Analysis of rare, exonic variation amongst subjects with autism spectrum disorders and population controlsLi Liu, Aniko Sabo, Benjamin M Neale, et al.
Pageof 11

Showing results (61-70 of 101) with videos related to

Sort By:
Pageof 11
Nature Genetics|August 29, 2024
Rare coding variant analysis for human diseases across biobanks and ancestriesSean J Jurgens, Xin Wang, Seung Hoan Choi, et al.
American Journal of Human Genetics|December 25, 2012
Rare, low-frequency, and common variants in the protein-coding sequence of biological candidate genes from GWASs contribute to risk of rheumatoid arthritisDorothée Diogo, Fina Kurreeman, Eli A Stahl, et al.
American Journal of Human Genetics|September 11, 2012
Burden of rare sarcomere gene variants in the Framingham and Jackson Heart Study cohortsAlexander G Bick, Jason Flannick, Kaoru Ito, et al.
The Journal of Clinical Investigation|September 15, 2022
Haploinsufficiency of CYP8B1 associates with increased insulin sensitivity in humansShiqi Zhong, Raphael Chèvre, David Castaño Mayan, et al.
Nature Genetics|January 24, 2025
Integrative proteogenomic analysis identifies COL6A3-derived endotrophin as a mediator of the effect of obesity on coronary artery diseaseSatoshi Yoshiji, Tianyuan Lu, Guillaume Butler-Laporte, et al.
Nature Genetics|October 8, 2013
Assessing the phenotypic effects in the general population of rare variants in genes for a dominant Mendelian form of diabetesJason Flannick, Nicola L Beer, Alexander G Bick, et al.
Biorxiv : the Preprint Server for Biology|June 22, 2026
PanKbase Integrated Single-Cell Map: A Comprehensive Atlas of Human Pancreatic IsletsHa T H Vu, Han Sun, Parul Kudtarkar, et al.
Nature Communications|October 19, 2017
Integrating evolutionary and regulatory information with a multispecies approach implicates genes and pathways in obsessive-compulsive disorderHyun Ji Noh, Ruqi Tang, Jason Flannick, et al.
The New England Journal of Medicine|November 27, 2014
Age-related clonal hematopoiesis associated with adverse outcomesSiddhartha Jaiswal, Pierre Fontanillas, Jason Flannick, et al.
Plos Genetics|April 18, 2013
Analysis of rare, exonic variation amongst subjects with autism spectrum disorders and population controlsLi Liu, Aniko Sabo, Benjamin M Neale, et al.
Pageof 11