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Blood
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July 5, 2011
Prospective evaluation of a pharmacogenetics-guided warfarin loading and maintenance dose regimen for initiation of therapy
Inna Y Gong, Rommel G Tirona, Ute I Schwarz, et al.
Medrxiv : the Preprint Server for Health Sciences
|
June 29, 2026
Prevalence and Clinical Impact of Pathogenic Variants in Cardiomyopathy Genes Among Individuals with Cardiac Conduction Disorders
Temidayo A Abe, Favour E Markson, Quinn S Wells, et al.
Journal of Biomedical Informatics
|
December 14, 2020
A retrospective approach to evaluating potential adverse outcomes associated with delay of procedures for cardiovascular and cancer-related diagnoses in the context of COVID-19
Neil S Zheng, Jeremy L Warner, Travis J Osterman, et al.
American Journal of Human Genetics
|
December 2, 2022
Genomic Medicine Year in Review: 2022
Teri A Manolio, Jahnavi Narula, Carol J Bult, et al.
Circulation
|
August 10, 2011
Striking In vivo phenotype of a disease-associated human SCN5A mutation producing minimal changes in vitro
Hiroshi Watanabe, Tao Yang, Dina Myers Stroud, et al.
Nature Reviews. Cardiology
|
September 1, 2025
Creating an atlas of variant effects to resolve variants of uncertain significance and guide cardiovascular medicine
Andrew M Glazer, Daniel R Tabet, Victoria N Parikh, et al.
Nature Communications
|
October 13, 2016
KCNE1 induces fenestration in the Kv7.1/KCNE1 channel complex that allows for highly specific pharmacological targeting
Eva Wrobel, Ina Rothenberg, Christoph Krisp, et al.
Annals of Internal Medicine
|
November 23, 2006
Pharmacogenomics: challenges and opportunities
Dan M Roden, Russ B Altman, Neal L Benowitz, et al.
International Journal of Radiation Oncology, Biology, Physics
|
October 25, 2025
Clonal Hematopoiesis of Indeterminate Potential After Radiation Therapy
Shelby A Crants, Sydney S Olson, Yajing Li, et al.
The Journal of Clinical Investigation
|
May 3, 2008
The E1784K mutation in SCN5A is associated with mixed clinical phenotype of type 3 long QT syndrome
Naomasa Makita, Elijah Behr, Wataru Shimizu, et al.
Page
of 60
Search research articles
Search
Showing results (381-390 of 593) with videos related to
Sort By:
Page
of 60
Blood
|
July 5, 2011
Prospective evaluation of a pharmacogenetics-guided warfarin loading and maintenance dose regimen for initiation of therapy
Inna Y Gong, Rommel G Tirona, Ute I Schwarz, et al.
Medrxiv : the Preprint Server for Health Sciences
|
June 29, 2026
Prevalence and Clinical Impact of Pathogenic Variants in Cardiomyopathy Genes Among Individuals with Cardiac Conduction Disorders
Temidayo A Abe, Favour E Markson, Quinn S Wells, et al.
Journal of Biomedical Informatics
|
December 14, 2020
A retrospective approach to evaluating potential adverse outcomes associated with delay of procedures for cardiovascular and cancer-related diagnoses in the context of COVID-19
Neil S Zheng, Jeremy L Warner, Travis J Osterman, et al.
American Journal of Human Genetics
|
December 2, 2022
Genomic Medicine Year in Review: 2022
Teri A Manolio, Jahnavi Narula, Carol J Bult, et al.
Circulation
|
August 10, 2011
Striking In vivo phenotype of a disease-associated human SCN5A mutation producing minimal changes in vitro
Hiroshi Watanabe, Tao Yang, Dina Myers Stroud, et al.
Nature Reviews. Cardiology
|
September 1, 2025
Creating an atlas of variant effects to resolve variants of uncertain significance and guide cardiovascular medicine
Andrew M Glazer, Daniel R Tabet, Victoria N Parikh, et al.
Nature Communications
|
October 13, 2016
KCNE1 induces fenestration in the Kv7.1/KCNE1 channel complex that allows for highly specific pharmacological targeting
Eva Wrobel, Ina Rothenberg, Christoph Krisp, et al.
Annals of Internal Medicine
|
November 23, 2006
Pharmacogenomics: challenges and opportunities
Dan M Roden, Russ B Altman, Neal L Benowitz, et al.
International Journal of Radiation Oncology, Biology, Physics
|
October 25, 2025
Clonal Hematopoiesis of Indeterminate Potential After Radiation Therapy
Shelby A Crants, Sydney S Olson, Yajing Li, et al.
The Journal of Clinical Investigation
|
May 3, 2008
The E1784K mutation in SCN5A is associated with mixed clinical phenotype of type 3 long QT syndrome
Naomasa Makita, Elijah Behr, Wataru Shimizu, et al.
Page
of 60