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Dan M Roden

Showing results (351-360 of 593) with videos related to

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Circulation. Arrhythmia and Electrophysiology|October 8, 2009
Biophysical properties of 9 KCNQ1 mutations associated with long-QT syndromeTao Yang, Seo-Kyung Chung, Wei Zhang, et al.
Circulation. Cardiovascular Genetics|July 18, 2013
Whole exome sequencing identifies a causal RBM20 mutation in a large pedigree with familial dilated cardiomyopathyQuinn S Wells, Jason R Becker, Yan R Su, et al.
Blood|June 7, 2008
A genome-wide scan for common genetic variants with a large influence on warfarin maintenance doseGregory M Cooper, Julie A Johnson, Taimour Y Langaee, et al.
American Journal of Human Genetics|December 5, 2025
Genomic medicine year in review: 2025Teri A Manolio, Alauna Rupert, Jahnavi Narula, et al.
The Journal of Clinical Investigation|August 26, 2006
Casq2 deletion causes sarcoplasmic reticulum volume increase, premature Ca2+ release, and catecholaminergic polymorphic ventricular tachycardiaBjörn C Knollmann, Nagesh Chopra, Thinn Hlaing, et al.
Pharmacogenomics|December 19, 2014
Genotype and risk of major bleeding during warfarin treatmentVivian K Kawai, Andrew Cunningham, Susan I Vear, et al.
JAMA Network Open|January 22, 2024
Antipsychotics and the QTc Interval During Delirium in the Intensive Care Unit: A Secondary Analysis of a Randomized Clinical TrialJoanna L Stollings, Christina S Boncyk, Caroline I Birdrow, et al.
Genome Medicine|May 30, 2024
High-throughput functional mapping of variants in an arrhythmia gene, KCNE1, reveals novel biologyAyesha Muhammad, Maria E Calandranis, Bian Li, et al.
Circulation. Cardiovascular Genetics|March 16, 2016
Merging Electronic Health Record Data and Genomics for Cardiovascular Research: A Science Advisory From the American Heart AssociationJennifer L Hall, John J Ryan, Bruce E Bray, et al.
American Journal of Human Genetics|December 8, 2023
Genomic medicine year in review: 2023Teri A Manolio, Jahnavi Narula, Carol J Bult, et al.
Pageof 60

Showing results (351-360 of 593) with videos related to

Sort By:
Pageof 60
Circulation. Arrhythmia and Electrophysiology|October 8, 2009
Biophysical properties of 9 KCNQ1 mutations associated with long-QT syndromeTao Yang, Seo-Kyung Chung, Wei Zhang, et al.
Circulation. Cardiovascular Genetics|July 18, 2013
Whole exome sequencing identifies a causal RBM20 mutation in a large pedigree with familial dilated cardiomyopathyQuinn S Wells, Jason R Becker, Yan R Su, et al.
Blood|June 7, 2008
A genome-wide scan for common genetic variants with a large influence on warfarin maintenance doseGregory M Cooper, Julie A Johnson, Taimour Y Langaee, et al.
American Journal of Human Genetics|December 5, 2025
Genomic medicine year in review: 2025Teri A Manolio, Alauna Rupert, Jahnavi Narula, et al.
The Journal of Clinical Investigation|August 26, 2006
Casq2 deletion causes sarcoplasmic reticulum volume increase, premature Ca2+ release, and catecholaminergic polymorphic ventricular tachycardiaBjörn C Knollmann, Nagesh Chopra, Thinn Hlaing, et al.
Pharmacogenomics|December 19, 2014
Genotype and risk of major bleeding during warfarin treatmentVivian K Kawai, Andrew Cunningham, Susan I Vear, et al.
JAMA Network Open|January 22, 2024
Antipsychotics and the QTc Interval During Delirium in the Intensive Care Unit: A Secondary Analysis of a Randomized Clinical TrialJoanna L Stollings, Christina S Boncyk, Caroline I Birdrow, et al.
Genome Medicine|May 30, 2024
High-throughput functional mapping of variants in an arrhythmia gene, KCNE1, reveals novel biologyAyesha Muhammad, Maria E Calandranis, Bian Li, et al.
Circulation. Cardiovascular Genetics|March 16, 2016
Merging Electronic Health Record Data and Genomics for Cardiovascular Research: A Science Advisory From the American Heart AssociationJennifer L Hall, John J Ryan, Bruce E Bray, et al.
American Journal of Human Genetics|December 8, 2023
Genomic medicine year in review: 2023Teri A Manolio, Jahnavi Narula, Carol J Bult, et al.
Pageof 60