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Thomas Meitinger

Showing results (381-390 of 508) with videos related to

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European Journal of Human Genetics : EJHG|January 26, 2019
Genome-wide association meta-analysis of 30,000 samples identifies seven novel loci for quantitative ECG traitsJessica van Setten, Niek Verweij, Hamdi Mbarek, et al.
Human Molecular Genetics|March 12, 2013
Meta-analysis of genome-wide association studies in five cohorts reveals common variants in RBFOX1, a regulator of tissue-specific splicing, associated with refractive errorDwight Stambolian, Robert Wojciechowski, Konrad Oexle, et al.
Nature Communications|June 29, 2021
A multi-ethnic epigenome-wide association study of leukocyte DNA methylation and blood lipidsMin-A Jhun, Michael Mendelson, Rory Wilson, et al.
Nature Genetics|August 31, 2010
Genome-wide association study of migraine implicates a common susceptibility variant on 8q22.1Verneri Anttila, Hreinn Stefansson, Mikko Kallela, et al.
Scientific Reports|November 9, 2016
Gene-gene Interaction Analyses for Atrial FibrillationHonghuang Lin, Martina Mueller-Nurasyid, Albert V Smith, et al.
Nature Communications|October 30, 2014
Novel loci affecting iron homeostasis and their effects in individuals at risk for hemochromatosisBeben Benyamin, Tonu Esko, Janina S Ried, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 11, 2020
Defining the genotypic and phenotypic spectrum of X-linked MSL3-related disorderTheresa Brunet, Kirsty McWalter, Katharina Mayerhanser, et al.
Plos One|May 11, 2019
Mendelian randomization evaluation of causal effects of fibrinogen on incident coronary heart diseaseCavin K Ward-Caviness, Paul S de Vries, Kerri L Wiggins, et al.
Nature Genetics|January 12, 2010
Genome-wide association study of PR intervalArne Pfeufer, Charlotte van Noord, Kristin D Marciante, et al.
European Heart Journal|March 7, 2021
Genome-wide association analysis in dilated cardiomyopathy reveals two new players in systolic heart failure on chromosomes 3p25.1 and 22q11.23Sophie Garnier, Magdalena Harakalova, Stefan Weiss, et al.
Pageof 51

Showing results (381-390 of 508) with videos related to

Sort By:
Pageof 51
European Journal of Human Genetics : EJHG|January 26, 2019
Genome-wide association meta-analysis of 30,000 samples identifies seven novel loci for quantitative ECG traitsJessica van Setten, Niek Verweij, Hamdi Mbarek, et al.
Human Molecular Genetics|March 12, 2013
Meta-analysis of genome-wide association studies in five cohorts reveals common variants in RBFOX1, a regulator of tissue-specific splicing, associated with refractive errorDwight Stambolian, Robert Wojciechowski, Konrad Oexle, et al.
Nature Communications|June 29, 2021
A multi-ethnic epigenome-wide association study of leukocyte DNA methylation and blood lipidsMin-A Jhun, Michael Mendelson, Rory Wilson, et al.
Nature Genetics|August 31, 2010
Genome-wide association study of migraine implicates a common susceptibility variant on 8q22.1Verneri Anttila, Hreinn Stefansson, Mikko Kallela, et al.
Scientific Reports|November 9, 2016
Gene-gene Interaction Analyses for Atrial FibrillationHonghuang Lin, Martina Mueller-Nurasyid, Albert V Smith, et al.
Nature Communications|October 30, 2014
Novel loci affecting iron homeostasis and their effects in individuals at risk for hemochromatosisBeben Benyamin, Tonu Esko, Janina S Ried, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 11, 2020
Defining the genotypic and phenotypic spectrum of X-linked MSL3-related disorderTheresa Brunet, Kirsty McWalter, Katharina Mayerhanser, et al.
Plos One|May 11, 2019
Mendelian randomization evaluation of causal effects of fibrinogen on incident coronary heart diseaseCavin K Ward-Caviness, Paul S de Vries, Kerri L Wiggins, et al.
Nature Genetics|January 12, 2010
Genome-wide association study of PR intervalArne Pfeufer, Charlotte van Noord, Kristin D Marciante, et al.
European Heart Journal|March 7, 2021
Genome-wide association analysis in dilated cardiomyopathy reveals two new players in systolic heart failure on chromosomes 3p25.1 and 22q11.23Sophie Garnier, Magdalena Harakalova, Stefan Weiss, et al.
Pageof 51