Literature DB >> 21787999

HRS/EHRA expert consensus statement on the state of genetic testing for the channelopathies and cardiomyopathies this document was developed as a partnership between the Heart Rhythm Society (HRS) and the European Heart Rhythm Association (EHRA).

Michael J Ackerman1, Silvia G Priori, Stephan Willems, Charles Berul, Ramon Brugada, Hugh Calkins, A John Camm, Patrick T Ellinor, Michael Gollob, Robert Hamilton, Ray E Hershberger, Daniel P Judge, Hervè Le Marec, William J McKenna, Eric Schulze-Bahr, Chris Semsarian, Jeffrey A Towbin, Hugh Watkins, Arthur Wilde, Christian Wolpert, Douglas P Zipes.   

Abstract

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Year:  2011        PMID: 21787999     DOI: 10.1016/j.hrthm.2011.05.020

Source DB:  PubMed          Journal:  Heart Rhythm        ISSN: 1547-5271            Impact factor:   6.343


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  279 in total

Review 1.  Clinical interpretation of genetic variants in arrhythmogenic right ventricular cardiomyopathy.

Authors:  Mireia Alcalde; Oscar Campuzano; Georgia Sarquella-Brugada; Elena Arbelo; Catarina Allegue; Sara Partemi; Anna Iglesias; Antonio Oliva; Josep Brugada; Ramon Brugada
Journal:  Clin Res Cardiol       Date:  2014-11-15       Impact factor: 5.460

2.  A connexin40 mutation associated with a malignant variant of progressive familial heart block type I.

Authors:  Naomasa Makita; Akiko Seki; Naokata Sumitomo; Halina Chkourko; Shigetomo Fukuhara; Hiroshi Watanabe; Wataru Shimizu; Connie R Bezzina; Can Hasdemir; Hideo Mugishima; Takeru Makiyama; Alban Baruteau; Estelle Baron; Minoru Horie; Nobuhisa Hagiwara; Arthur A M Wilde; Vincent Probst; Hervé Le Marec; Dan M Roden; Naoki Mochizuki; Jean-Jacques Schott; Mario Delmar
Journal:  Circ Arrhythm Electrophysiol       Date:  2012-01-13

3.  Cardiac channel molecular autopsy: insights from 173 consecutive cases of autopsy-negative sudden unexplained death referred for postmortem genetic testing.

Authors:  David J Tester; Argelia Medeiros-Domingo; Melissa L Will; Carla M Haglund; Michael J Ackerman
Journal:  Mayo Clin Proc       Date:  2012-06       Impact factor: 7.616

Review 4.  The molecular autopsy: should the evaluation continue after the funeral?

Authors:  David J Tester; Michael J Ackerman
Journal:  Pediatr Cardiol       Date:  2012-02-04       Impact factor: 1.655

5.  Hypertrophic cardiomyopathy and planned in vitro fertilization. Genetic testing and clinical evaluation.

Authors:  J Zhu Hu; J Xiang Li; K Hong; J Xin Hu; P Brugada; X Shu Cheng
Journal:  Herz       Date:  2012-06       Impact factor: 1.443

Review 6.  Early repolarization syndrome: A cause of sudden cardiac death.

Authors:  Abdi Ali; Nida Butt; Azeem S Sheikh
Journal:  World J Cardiol       Date:  2015-08-26

7.  Novel Mutation in FLNC (Filamin C) Causes Familial Restrictive Cardiomyopathy.

Authors:  Nathan R Tucker; Micheal A McLellan; Dongjian Hu; Jiangchuan Ye; Victoria A Parsons; Robert W Mills; Sebastian Clauss; Elena Dolmatova; Marisa A Shea; David J Milan; Nandita S Scott; Mark Lindsay; Steven A Lubitz; Ibrahim J Domian; James R Stone; Honghuang Lin; Patrick T Ellinor
Journal:  Circ Cardiovasc Genet       Date:  2017-12

8.  Toward Personalized Medicine: Does Genetic Diagnosis of Pediatric Cardiomyopathy Influence Patient Management?

Authors:  Teresa M Lee; Stephanie M Ware
Journal:  Prog Pediatr Cardiol       Date:  2015-07-01

9.  Beyond Gene Panels: Whole Exome Sequencing for Diagnosis of Congenital Heart Disease.

Authors:  Sharon L Paige; Priyanka Saha; James R Priest
Journal:  Circ Genom Precis Med       Date:  2018-03

10.  Temporal relationship of conduction system disease and ventricular dysfunction in LMNA cardiomyopathy.

Authors:  Chad Brodt; Jill D Siegfried; Mark Hofmeyer; Jose Martel; Evadnie Rampersaud; Duanxiang Li; Ana Morales; Ray E Hershberger
Journal:  J Card Fail       Date:  2013-04       Impact factor: 5.712

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