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Showing results (31-40 of 70) with videos related to

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Nature Communications|June 30, 2016
The genetic regulatory signature of type 2 diabetes in human skeletal muscleLaura J Scott, Michael R Erdos, Jeroen R Huyghe, et al.
Nature Genetics|January 15, 2008
Common variants in the GDF5-UQCC region are associated with variation in human heightSerena Sanna, Anne U Jackson, Ramaiah Nagaraja, et al.
Nature Communications|July 7, 2017
A defect in myoblast fusion underlies Carey-Fineman-Ziter syndromeSilvio Alessandro Di Gioia, Samantha Connors, Norisada Matsunami, et al.
Science (New York, N.Y.)|April 28, 2007
A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variantsLaura J Scott, Karen L Mohlke, Lori L Bonnycastle, et al.
Genetics in Medicine Open|July 15, 2025
Systematic phenotype and genotype characterization of Moebius syndromeBryn D Webb, Julie A Jurgens, Narisu Narisu, et al.
Plos Genetics|August 10, 2012
The metabochip, a custom genotyping array for genetic studies of metabolic, cardiovascular, and anthropometric traitsBenjamin F Voight, Hyun Min Kang, Jun Ding, et al.
Diabetes|December 4, 2013
Impact of type 2 diabetes susceptibility variants on quantitative glycemic traits reveals mechanistic heterogeneityAntigone S Dimas, Vasiliki Lagou, Adam Barker, et al.
Nature Genetics|June 29, 2023
Noncoding variants alter GATA2 expression in rhombomere 4 motor neurons and cause dominant hereditary congenital facial paresisAlan P Tenney, Silvio Alessandro Di Gioia, Bryn D Webb, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 28, 2017
Evaluating the contribution of rare variants to type 2 diabetes and related traits using pedigreesGoo Jun, Alisa Manning, Marcio Almeida, et al.
Nature Genetics|April 1, 2008
Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetesEleftheria Zeggini, Laura J Scott, Richa Saxena, et al.
Pageof 7

Showing results (31-40 of 70) with videos related to

Sort By:
Pageof 7
Nature Communications|June 30, 2016
The genetic regulatory signature of type 2 diabetes in human skeletal muscleLaura J Scott, Michael R Erdos, Jeroen R Huyghe, et al.
Nature Genetics|January 15, 2008
Common variants in the GDF5-UQCC region are associated with variation in human heightSerena Sanna, Anne U Jackson, Ramaiah Nagaraja, et al.
Nature Communications|July 7, 2017
A defect in myoblast fusion underlies Carey-Fineman-Ziter syndromeSilvio Alessandro Di Gioia, Samantha Connors, Norisada Matsunami, et al.
Science (New York, N.Y.)|April 28, 2007
A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variantsLaura J Scott, Karen L Mohlke, Lori L Bonnycastle, et al.
Genetics in Medicine Open|July 15, 2025
Systematic phenotype and genotype characterization of Moebius syndromeBryn D Webb, Julie A Jurgens, Narisu Narisu, et al.
Plos Genetics|August 10, 2012
The metabochip, a custom genotyping array for genetic studies of metabolic, cardiovascular, and anthropometric traitsBenjamin F Voight, Hyun Min Kang, Jun Ding, et al.
Diabetes|December 4, 2013
Impact of type 2 diabetes susceptibility variants on quantitative glycemic traits reveals mechanistic heterogeneityAntigone S Dimas, Vasiliki Lagou, Adam Barker, et al.
Nature Genetics|June 29, 2023
Noncoding variants alter GATA2 expression in rhombomere 4 motor neurons and cause dominant hereditary congenital facial paresisAlan P Tenney, Silvio Alessandro Di Gioia, Bryn D Webb, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 28, 2017
Evaluating the contribution of rare variants to type 2 diabetes and related traits using pedigreesGoo Jun, Alisa Manning, Marcio Almeida, et al.
Nature Genetics|April 1, 2008
Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetesEleftheria Zeggini, Laura J Scott, Richa Saxena, et al.
Pageof 7