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Biorxiv : the Preprint Server for Biology
|
March 3, 2023
FALCON systematically interrogates free fatty acid biology and identifies a novel mediator of lipotoxicity
Nicolas Wieder, Juliana Coraor Fried, Choah Kim, et al.
Cell Metabolism
|
April 19, 2023
FALCON systematically interrogates free fatty acid biology and identifies a novel mediator of lipotoxicity
Nicolas Wieder, Juliana Coraor Fried, Choah Kim, et al.
Medrxiv : the Preprint Server for Health Sciences
|
June 4, 2026
An ancestry-enriched HNF4A variant and GP2 reveal distinct mechanisms of type 2 diabetes in exome-wide study of 13,674 cases and 41,024 controls
Sam Hodgson, Vi Bui, Siqi Hu, et al.
Neuron
|
January 29, 2013
Rare complete knockouts in humans: population distribution and significant role in autism spectrum disorders
Elaine T Lim, Soumya Raychaudhuri, Stephan J Sanders, et al.
Nature Communications
|
January 24, 2018
Re-analysis of public genetic data reveals a rare X-chromosomal variant associated with type 2 diabetes
Sílvia Bonàs-Guarch, Marta Guindo-Martínez, Irene Miguel-Escalada, et al.
Nature Communications
|
June 1, 2018
Publisher Correction: Re-analysis of public genetic data reveals a rare X-chromosomal variant associated with type 2 diabetes
Sílvia Bonàs-Guarch, Marta Guindo-Martínez, Irene Miguel-Escalada, et al.
Nature Genetics
|
November 3, 2019
Loss of ZnT8 function protects against diabetes by enhanced insulin secretion
Om Prakash Dwivedi, Mikko Lehtovirta, Benoit Hastoy, et al.
American Journal of Human Genetics
|
June 5, 2018
Quantifying the Impact of Rare and Ultra-rare Coding Variation across the Phenotypic Spectrum
Andrea Ganna, F Kyle Satterstrom, Seyedeh M Zekavat, et al.
Science Translational Medicine
|
January 16, 2015
Integrated allelic, transcriptional, and phenomic dissection of the cardiac effects of titin truncations in health and disease
Angharad M Roberts, James S Ware, Daniel S Herman, et al.
Plos Genetics
|
August 1, 2014
Distribution and medical impact of loss-of-function variants in the Finnish founder population
Elaine T Lim, Peter Würtz, Aki S Havulinna, et al.
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Search research articles
Search
Showing results (71-80 of 101) with videos related to
Sort By:
Page
of 11
Biorxiv : the Preprint Server for Biology
|
March 3, 2023
FALCON systematically interrogates free fatty acid biology and identifies a novel mediator of lipotoxicity
Nicolas Wieder, Juliana Coraor Fried, Choah Kim, et al.
Cell Metabolism
|
April 19, 2023
FALCON systematically interrogates free fatty acid biology and identifies a novel mediator of lipotoxicity
Nicolas Wieder, Juliana Coraor Fried, Choah Kim, et al.
Medrxiv : the Preprint Server for Health Sciences
|
June 4, 2026
An ancestry-enriched HNF4A variant and GP2 reveal distinct mechanisms of type 2 diabetes in exome-wide study of 13,674 cases and 41,024 controls
Sam Hodgson, Vi Bui, Siqi Hu, et al.
Neuron
|
January 29, 2013
Rare complete knockouts in humans: population distribution and significant role in autism spectrum disorders
Elaine T Lim, Soumya Raychaudhuri, Stephan J Sanders, et al.
Nature Communications
|
January 24, 2018
Re-analysis of public genetic data reveals a rare X-chromosomal variant associated with type 2 diabetes
Sílvia Bonàs-Guarch, Marta Guindo-Martínez, Irene Miguel-Escalada, et al.
Nature Communications
|
June 1, 2018
Publisher Correction: Re-analysis of public genetic data reveals a rare X-chromosomal variant associated with type 2 diabetes
Sílvia Bonàs-Guarch, Marta Guindo-Martínez, Irene Miguel-Escalada, et al.
Nature Genetics
|
November 3, 2019
Loss of ZnT8 function protects against diabetes by enhanced insulin secretion
Om Prakash Dwivedi, Mikko Lehtovirta, Benoit Hastoy, et al.
American Journal of Human Genetics
|
June 5, 2018
Quantifying the Impact of Rare and Ultra-rare Coding Variation across the Phenotypic Spectrum
Andrea Ganna, F Kyle Satterstrom, Seyedeh M Zekavat, et al.
Science Translational Medicine
|
January 16, 2015
Integrated allelic, transcriptional, and phenomic dissection of the cardiac effects of titin truncations in health and disease
Angharad M Roberts, James S Ware, Daniel S Herman, et al.
Plos Genetics
|
August 1, 2014
Distribution and medical impact of loss-of-function variants in the Finnish founder population
Elaine T Lim, Peter Würtz, Aki S Havulinna, et al.
Page
of 11