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Thomas Meitinger

Showing results (391-400 of 508) with videos related to

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European Heart Journal|September 1, 2018
A comprehensive evaluation of the genetic architecture of sudden cardiac arrestForam N Ashar, Rebecca N Mitchell, Christine M Albert, et al.
Brain : a Journal of Neurology|February 12, 2025
Combined genomics and proteomics unveils elusive variants and vast aetiologic heterogeneity in dystoniaMichael Zech, Ivana Dzinovic, Matej Skorvanek, et al.
Wellcome Open Research|June 7, 2021
Variants associated with <i>HHIP</i> expression have sex-differential effects on lung functionKatherine A Fawcett, Ma'en Obeidat, Carl Melbourne, et al.
Nature Genetics|February 23, 2010
Common variants in KCNN3 are associated with lone atrial fibrillationPatrick T Ellinor, Kathryn L Lunetta, Nicole L Glazer, et al.
JAMA|July 9, 2009
Genetic variants associated with cardiac structure and function: a meta-analysis and replication of genome-wide association dataRamachandran S Vasan, Nicole L Glazer, Janine F Felix, et al.
Nature Genetics|May 6, 2008
Common variants near MC4R are associated with fat mass, weight and risk of obesityRuth J F Loos, Cecilia M Lindgren, Shengxu Li, et al.
Nature Genetics|January 26, 2021
Shared genetic pathways contribute to risk of hypertrophic and dilated cardiomyopathies with opposite directions of effectRafik Tadros, Catherine Francis, Xiao Xu, 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.
Science Advances|July 8, 2016
Novel multiple sclerosis susceptibility loci implicated in epigenetic regulationTill F M Andlauer, Dorothea Buck, Gisela Antony, et al.
The New England Journal of Medicine|November 13, 2014
Inactivating mutations in NPC1L1 and protection from coronary heart disease, Nathan O Stitziel, Hong-Hee Won, et al.
Pageof 51

Showing results (391-400 of 508) with videos related to

Sort By:
Pageof 51
European Heart Journal|September 1, 2018
A comprehensive evaluation of the genetic architecture of sudden cardiac arrestForam N Ashar, Rebecca N Mitchell, Christine M Albert, et al.
Brain : a Journal of Neurology|February 12, 2025
Combined genomics and proteomics unveils elusive variants and vast aetiologic heterogeneity in dystoniaMichael Zech, Ivana Dzinovic, Matej Skorvanek, et al.
Wellcome Open Research|June 7, 2021
Variants associated with <i>HHIP</i> expression have sex-differential effects on lung functionKatherine A Fawcett, Ma'en Obeidat, Carl Melbourne, et al.
Nature Genetics|February 23, 2010
Common variants in KCNN3 are associated with lone atrial fibrillationPatrick T Ellinor, Kathryn L Lunetta, Nicole L Glazer, et al.
JAMA|July 9, 2009
Genetic variants associated with cardiac structure and function: a meta-analysis and replication of genome-wide association dataRamachandran S Vasan, Nicole L Glazer, Janine F Felix, et al.
Nature Genetics|May 6, 2008
Common variants near MC4R are associated with fat mass, weight and risk of obesityRuth J F Loos, Cecilia M Lindgren, Shengxu Li, et al.
Nature Genetics|January 26, 2021
Shared genetic pathways contribute to risk of hypertrophic and dilated cardiomyopathies with opposite directions of effectRafik Tadros, Catherine Francis, Xiao Xu, 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.
Science Advances|July 8, 2016
Novel multiple sclerosis susceptibility loci implicated in epigenetic regulationTill F M Andlauer, Dorothea Buck, Gisela Antony, et al.
The New England Journal of Medicine|November 13, 2014
Inactivating mutations in NPC1L1 and protection from coronary heart disease, Nathan O Stitziel, Hong-Hee Won, et al.
Pageof 51