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Benjamin A Salisbury

Showing results (11-20 of 29) with videos related to

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Heart Rhythm|July 5, 2006
Allelic dropout in long QT syndrome genetic testing: a possible mechanism underlying false-negative resultsDavid J Tester, Lisa B Cronk, Janet L Carr, et al.
JMIR Mhealth and Uhealth|October 4, 2022
Retention, Fasting Patterns, and Weight Loss With an Intermittent Fasting App: Large-Scale, 52-Week Observational StudyLuisa Torres, Joy L Lee, Seho Park, et al.
Circulation. Cardiovascular Genetics|September 6, 2012
Phylogenetic and physicochemical analyses enhance the classification of rare nonsynonymous single nucleotide variants in type 1 and 2 long-QT syndromeJohn R Giudicessi, Jamie D Kapplinger, David J Tester, et al.
Circulation. Cardiovascular Genetics|December 25, 2009
Pharmacogenetic predictors of statin-mediated low-density lipoprotein cholesterol reduction and dose responseDeepak Voora, Svati H Shah, Carol R Reed, et al.
Circulation|October 21, 2009
Genetic testing for long-QT syndrome: distinguishing pathogenic mutations from benign variantsSuraj Kapa, David J Tester, Benjamin A Salisbury, et al.
Heart Rhythm|April 21, 2010
Epidemiologic, molecular, and functional evidence suggest A572D-SCN5A should not be considered an independent LQT3-susceptibility mutationDavid J Tester, Carmen Valdivia, Carole Harris-Kerr, et al.
Journal of Cardiovascular Translational Research|April 10, 2015
Enhancing the Predictive Power of Mutations in the C-Terminus of the KCNQ1-Encoded Kv7.1 Voltage-Gated Potassium ChannelJamie D Kapplinger, Andrew S Tseng, Benjamin A Salisbury, et al.
Heart Rhythm|September 1, 2009
Spectrum and prevalence of mutations from the first 2,500 consecutive unrelated patients referred for the FAMILION long QT syndrome genetic testJamie D Kapplinger, David J Tester, Benjamin A Salisbury, et al.
Journal of Cardiovascular Electrophysiology|October 13, 2009
Expression of a common LQT1 mutation in five apparently unrelated families in a regional inherited arrhythmia clinicChristopher Gray, Lorne J Gula, George J Klein, et al.
Plos One|July 7, 2015
The Use of Non-Variant Sites to Improve the Clinical Assessment of Whole-Genome Sequence DataAlberto Ferrarini, Luciano Xumerle, Francesca Griggio, et al.
Pageof 3

Showing results (11-20 of 29) with videos related to

Sort By:
Pageof 3
Heart Rhythm|July 5, 2006
Allelic dropout in long QT syndrome genetic testing: a possible mechanism underlying false-negative resultsDavid J Tester, Lisa B Cronk, Janet L Carr, et al.
JMIR Mhealth and Uhealth|October 4, 2022
Retention, Fasting Patterns, and Weight Loss With an Intermittent Fasting App: Large-Scale, 52-Week Observational StudyLuisa Torres, Joy L Lee, Seho Park, et al.
Circulation. Cardiovascular Genetics|September 6, 2012
Phylogenetic and physicochemical analyses enhance the classification of rare nonsynonymous single nucleotide variants in type 1 and 2 long-QT syndromeJohn R Giudicessi, Jamie D Kapplinger, David J Tester, et al.
Circulation. Cardiovascular Genetics|December 25, 2009
Pharmacogenetic predictors of statin-mediated low-density lipoprotein cholesterol reduction and dose responseDeepak Voora, Svati H Shah, Carol R Reed, et al.
Circulation|October 21, 2009
Genetic testing for long-QT syndrome: distinguishing pathogenic mutations from benign variantsSuraj Kapa, David J Tester, Benjamin A Salisbury, et al.
Heart Rhythm|April 21, 2010
Epidemiologic, molecular, and functional evidence suggest A572D-SCN5A should not be considered an independent LQT3-susceptibility mutationDavid J Tester, Carmen Valdivia, Carole Harris-Kerr, et al.
Journal of Cardiovascular Translational Research|April 10, 2015
Enhancing the Predictive Power of Mutations in the C-Terminus of the KCNQ1-Encoded Kv7.1 Voltage-Gated Potassium ChannelJamie D Kapplinger, Andrew S Tseng, Benjamin A Salisbury, et al.
Heart Rhythm|September 1, 2009
Spectrum and prevalence of mutations from the first 2,500 consecutive unrelated patients referred for the FAMILION long QT syndrome genetic testJamie D Kapplinger, David J Tester, Benjamin A Salisbury, et al.
Journal of Cardiovascular Electrophysiology|October 13, 2009
Expression of a common LQT1 mutation in five apparently unrelated families in a regional inherited arrhythmia clinicChristopher Gray, Lorne J Gula, George J Klein, et al.
Plos One|July 7, 2015
The Use of Non-Variant Sites to Improve the Clinical Assessment of Whole-Genome Sequence DataAlberto Ferrarini, Luciano Xumerle, Francesca Griggio, et al.
Pageof 3