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Nature Communications
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March 20, 2012
New insights into the Tyrolean Iceman's origin and phenotype as inferred by whole-genome sequencing
Andreas Keller, Angela Graefen, Markus Ball, et al.
Nature Methods
|
September 6, 2011
Toward the blood-borne miRNome of human diseases
Andreas 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 cardiomyopathy
Brendan J Floyd, Joyce N Njoroge, Vikki A Krysov, et al.
JAMA Cardiology
|
April 8, 2026
RBM20 Truncating Variants and Human Cardiomyopathy
Brendan 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 cardiomyopathy
Benjamin Meder, Frank Rühle, Tanja Weis, et al.
European Heart Journal
|
August 29, 2014
Atlas of the clinical genetics of human dilated cardiomyopathy
Jan Haas, Karen S Frese, Barbara Peil, et al.
Research Square
|
February 6, 2026
Leveraging the shared and opposing genetic mechanisms in the heritable cardiomyopathies
Daria Kramarenko, Poeya Haydarlou, George Powell, et al.
Nature Genetics
|
November 21, 2024
Genome-wide association study reveals mechanisms underlying dilated cardiomyopathy and myocardial resilience
Sean 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 resilience
Sean 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 22q11.23
Sophie Garnier, Magdalena Harakalova, Stefan Weiss, et al.
Page
of 13
Search research articles
Search
Showing results (111-120 of 121) with videos related to
Sort By:
Page
of 13
Nature Communications
|
March 20, 2012
New insights into the Tyrolean Iceman's origin and phenotype as inferred by whole-genome sequencing
Andreas Keller, Angela Graefen, Markus Ball, et al.
Nature Methods
|
September 6, 2011
Toward the blood-borne miRNome of human diseases
Andreas 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 cardiomyopathy
Brendan J Floyd, Joyce N Njoroge, Vikki A Krysov, et al.
JAMA Cardiology
|
April 8, 2026
RBM20 Truncating Variants and Human Cardiomyopathy
Brendan 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 cardiomyopathy
Benjamin Meder, Frank Rühle, Tanja Weis, et al.
European Heart Journal
|
August 29, 2014
Atlas of the clinical genetics of human dilated cardiomyopathy
Jan Haas, Karen S Frese, Barbara Peil, et al.
Research Square
|
February 6, 2026
Leveraging the shared and opposing genetic mechanisms in the heritable cardiomyopathies
Daria Kramarenko, Poeya Haydarlou, George Powell, et al.
Nature Genetics
|
November 21, 2024
Genome-wide association study reveals mechanisms underlying dilated cardiomyopathy and myocardial resilience
Sean 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 resilience
Sean 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 22q11.23
Sophie Garnier, Magdalena Harakalova, Stefan Weiss, et al.
Page
of 13