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Jan Haas

Showing results (111-120 of 121) with videos related to

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Nature Communications|March 20, 2012
New insights into the Tyrolean Iceman's origin and phenotype as inferred by whole-genome sequencingAndreas Keller, Angela Graefen, Markus Ball, et al.
Nature Methods|September 6, 2011
Toward the blood-borne miRNome of human diseasesAndreas Keller, Petra Leidinger, Andrea Bauer, et al.
Medrxiv : the Preprint Server for Health Sciences|August 8, 2025
The contribution of <i>RBM20</i> truncating variants to human cardiomyopathyBrendan J Floyd, Joyce N Njoroge, Vikki A Krysov, et al.
JAMA Cardiology|April 8, 2026
RBM20 Truncating Variants and Human CardiomyopathyBrendan J Floyd, Joyce N Njoroge, Vikki A Krysov, et al.
European Heart Journal|July 16, 2013
A genome-wide association study identifies 6p21 as novel risk locus for dilated cardiomyopathyBenjamin Meder, Frank Rühle, Tanja Weis, et al.
European Heart Journal|August 29, 2014
Atlas of the clinical genetics of human dilated cardiomyopathyJan Haas, Karen S Frese, Barbara Peil, et al.
Research Square|February 6, 2026
Leveraging the shared and opposing genetic mechanisms in the heritable cardiomyopathiesDaria Kramarenko, Poeya Haydarlou, George Powell, et al.
Nature Genetics|November 21, 2024
Genome-wide association study reveals mechanisms underlying dilated cardiomyopathy and myocardial resilienceSean J Jurgens, Joel T Rämö, Daria R Kramarenko, et al.
Nature Genetics|December 5, 2024
Publisher Correction: Genome-wide association study reveals mechanisms underlying dilated cardiomyopathy and myocardial resilienceSean J Jurgens, Joel T Rämö, Daria R Kramarenko, 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 13

Showing results (111-120 of 121) with videos related to

Sort By:
Pageof 13
Nature Communications|March 20, 2012
New insights into the Tyrolean Iceman's origin and phenotype as inferred by whole-genome sequencingAndreas Keller, Angela Graefen, Markus Ball, et al.
Nature Methods|September 6, 2011
Toward the blood-borne miRNome of human diseasesAndreas Keller, Petra Leidinger, Andrea Bauer, et al.
Medrxiv : the Preprint Server for Health Sciences|August 8, 2025
The contribution of <i>RBM20</i> truncating variants to human cardiomyopathyBrendan J Floyd, Joyce N Njoroge, Vikki A Krysov, et al.
JAMA Cardiology|April 8, 2026
RBM20 Truncating Variants and Human CardiomyopathyBrendan J Floyd, Joyce N Njoroge, Vikki A Krysov, et al.
European Heart Journal|July 16, 2013
A genome-wide association study identifies 6p21 as novel risk locus for dilated cardiomyopathyBenjamin Meder, Frank Rühle, Tanja Weis, et al.
European Heart Journal|August 29, 2014
Atlas of the clinical genetics of human dilated cardiomyopathyJan Haas, Karen S Frese, Barbara Peil, et al.
Research Square|February 6, 2026
Leveraging the shared and opposing genetic mechanisms in the heritable cardiomyopathiesDaria Kramarenko, Poeya Haydarlou, George Powell, et al.
Nature Genetics|November 21, 2024
Genome-wide association study reveals mechanisms underlying dilated cardiomyopathy and myocardial resilienceSean J Jurgens, Joel T Rämö, Daria R Kramarenko, et al.
Nature Genetics|December 5, 2024
Publisher Correction: Genome-wide association study reveals mechanisms underlying dilated cardiomyopathy and myocardial resilienceSean J Jurgens, Joel T Rämö, Daria R Kramarenko, 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 13