Select Publications
Conference Papers
2022, 'Influence of sex on cardiovascular outcomes in RBM20 variant carriers', in EUROPEAN HEART JOURNAL, OXFORD UNIV PRESS, pp. 1744 - 1744, https://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000894947900919&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a29b250adbe88d1
,2022, 'Natural history of MYH7-related dilated cardiomyopathy', in EUROPEAN HEART JOURNAL, OXFORD UNIV PRESS, pp. 1745 - 1745, https://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000894947900920&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a29b250adbe88d1
,2014, 'A lamin A/C Synonymous Mutation Creates a Novel Splice Site and Causes Progressive Atrioventricular Conduction Defect', in CIRCULATION, LIPPINCOTT WILLIAMS & WILKINS, https://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000209790204220&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a29b250adbe88d1
,2014, 'EVOLUTION OF THE GENETICS REVOLUTION IN FAMILIAL CARDIOMYOPATHIES', in INTERNAL MEDICINE JOURNAL, WILEY-BLACKWELL, pp. 16 - 16, https://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000335884600064&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a29b250adbe88d1
,2013, 'Critical Role of RhoA/ROCK Signaling in Cardiac Contractility', in CIRCULATION, LIPPINCOTT WILLIAMS & WILKINS, TX, Dallas, presented at Scientific Sessions and Resuscitation Science Symposium of the American-Heart-Association, TX, Dallas, 16 November 2013 - 17 November 2013, https://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000332162903138&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a29b250adbe88d1
,2013, 'Transient Receptor Potential Channel 6 (TRPC6) Is An Important Mediator Of Mechanical Stretch Responses In The Atrial Endocardial Endothelium', in CIRCULATION RESEARCH, LIPPINCOTT WILLIAMS & WILKINS, NV, Las Vegas, presented at Scientific Sessions of the American-Heart-Association on Basic Cardiovascular Sciences, NV, Las Vegas, 22 July 2013 - 25 July 2013, https://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000332063200041&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a29b250adbe88d1
,2011, 'Lamin A/C Deficiency is Associated with Fat Infiltration of Muscle and Bone: A Proposed Model of Sarco-Osteopenia.', in JOURNAL OF THE AMERICAN GERIATRICS SOCIETY, WILEY-BLACKWELL, MD, National Harbor, pp. S78 - S78, presented at Annual Scientific Meeting on the American-Geriatrics-Society, MD, National Harbor, 11 May 2011 - 14 May 2011, https://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000289524600227&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a29b250adbe88d1
,2010, 'alpha,-cardiac myosin heavy chain (MYH6) mutations affecting myofibril formation are associated with congenital heart defects', in JOURNAL OF MEDICAL GENETICS, B M J PUBLISHING GROUP, RI, Warwick, pp. S76 - S76, presented at British Human Genetics Conference, RI, Warwick, 06 September 2010 - 08 September 2010, https://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000283762600155&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a29b250adbe88d1
,2009, 'Exercise has a Deleterious Effect on Bone Quality in Lamin A/C-Deficient Mice', in Journal of the American Geriatrics Society, Blackwell Publishing Inc, Malden, MA, pp. S11 - S11, presented at American Geriatrics Society (AGS) 2009 Annual Scientific Meeting, Chicago, Illinois, USA, 29 April 2009 - 03 May 2009
,2008, 'alpha-cardiac myosin heavy chain (MYH6) mutations are associated with congenital heart defects', in Journal of Medical Genetics, B M J Publishing Group, London, England, pp. S86 - S86, presented at Journal of Medical Genetics
,2008, 'Left Ventricular Hypertrophy Is Resistant to Inhibition of Expression of the R403Q Alpha-Myosin Heavy Chain Cardiac Hypertrophy-Inducing Mutant Protein', in Circulation, Lippincott Williams & Wilkins, Philadelphia, PA, USA, pp. S423 - S423
,2007, 'Interaction between a KCNQ1 mutation and cell stretch in familial atrial fibrillation', in BIOPHYSICAL JOURNAL, BIOPHYSICAL SOCIETY, MD, Baltimore, pp. 463A - 463A, presented at 51st Annual Meeting of the Biophysical-Society, MD, Baltimore, 03 March 2007 - 07 March 2007, https://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000243972403011&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a29b250adbe88d1
,2000, 'Cyclosporin A and minoxidil exacerbate cardiac hypertrophy in hypertrophic cardiomyopathy via a calcium-mediated pathway', in CIRCULATION, LIPPINCOTT WILLIAMS & WILKINS, pp. 98 - 98, https://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000090072300463&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a29b250adbe88d1
,2000, 'Dilated cardiomyopathy, Emery-Dreifuss muscular dystrophy and partial lipodystrophy: Structure function relationships in lamin A/C', in CIRCULATION, LIPPINCOTT WILLIAMS & WILKINS, pp. 280 - 280, https://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000090072301368&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a29b250adbe88d1
,2000, 'Dilated cardiomyopathy and sensorineural hearing loss: A heritable syndrome that maps to 6q23-24', in PEDIATRIC RESEARCH, NATURE PUBLISHING GROUP, pp. 46A - 46A, https://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000086155300270&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a29b250adbe88d1
,1999, 'Dilated cardiomyopathy and sensorineurinal hearing loss: A heritable syndrome, that maps to 6q23-24', in CIRCULATION, LIPPINCOTT WILLIAMS & WILKINS, pp. 618 - 619, https://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000083417103257&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a29b250adbe88d1
,1999, 'Disruption of the ventricle-specific homeobox gene lrx4 in mice leads to cardiac dysfunction and hypertrophy', in CIRCULATION, LIPPINCOTT WILLIAMS & WILKINS, pp. 347 - 348, https://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000083417101821&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a29b250adbe88d1
,1999, 'Electrophysiological characterization of familial hypertrophic cardiomyopathy mice with mutant myosin binding protein C gene', in CIRCULATION, LIPPINCOTT WILLIAMS & WILKINS, pp. 207 - 207, https://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000083417101071&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a29b250adbe88d1
,1999, 'Evaluation of cardiac structure and function in two moose models of familial hypertrophic cardiomyopathy', in CIRCULATION, LIPPINCOTT WILLIAMS & WILKINS, pp. 494 - 494, https://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000083417102599&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a29b250adbe88d1
,1998, 'Exercise and beta-blocker therapy in alpha-myosin heavy chain mutant mice with hypertrophic cardiomyopathy', in CIRCULATION, LIPPINCOTT WILLIAMS & WILKINS, pp. 70 - 70, https://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000076594400401&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a29b250adbe88d1
,1998, 'Mice with a mutant myosin binding protein C gene provide a model for familial hypertrophic cardiomyopathy.', in CIRCULATION, LIPPINCOTT WILLIAMS & WILKINS, pp. 625 - 625, https://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000076594403305&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a29b250adbe88d1
,1998, 'Familial hypertrophic cardiomyopathy and atrial fibrillation caused by Arg663His beta-cardiac myosin heavy chain mutation', in AMERICAN JOURNAL OF CARDIOLOGY, EXCERPTA MEDICA INC-ELSEVIER SCIENCE INC, GERMANY, BADEN BADEN, pp. 13H - 18H, presented at Symposium on From Increased Energy Metabolism to Cardiac Hypertrophy and Failure - Mediators and Molecular Mechanisms, GERMANY, BADEN BADEN, 25 September 1998 - 27 September 1998, https://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000081307900005&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a29b250adbe88d1
,1997, 'A familial atrial septal defect gene maps to chromosome 5p: Evidence for reduced gene penetrance, variable expressivity and genetic heterogeneity', in CIRCULATION, AMER HEART ASSOC, pp. 76 - 76, https://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:A1997YC88000076&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a29b250adbe88d1
,1997, 'Characterization of cardiac structure and function in the homozygous alpha-myosin heavy chain (Arg403Gln) mutant mouse', in CIRCULATION, AMER HEART ASSOC, pp. 3186 - 3186, https://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:A1997YC88003167&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a29b250adbe88d1
,1997, 'Noninvasive in vivo assessment of cardiac function in the neonatal murine heart using high frequency (50 MHz) ultrasound backscatter microscopy', in CIRCULATION, AMER HEART ASSOC, pp. 4144 - 4144, https://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:A1997YC88004110&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a29b250adbe88d1
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