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Conference Papers

Ito K; McDonough B; Gorham JM; DeParma SR; Adler EE; Mohiuddin SM; Fatkin D; Seidman JG; Seidman CE, 2014, 'A lamin A/C Synonymous Mutation Creates a Novel Splice Site and Causes Progressive Atrioventricular Conduction Defect', in CIRCULATION, LIPPINCOTT WILLIAMS & WILKINS, http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000209790204220&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a

Fatkin D, 2014, 'EVOLUTION OF THE GENETICS REVOLUTION IN FAMILIAL CARDIOMYOPATHIES', in INTERNAL MEDICINE JOURNAL, WILEY-BLACKWELL, pp. 16 - 16, http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000335884600064&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a

Yu Z-Y; Tan J-C; McMahon AC; Lismaa SF; Xiao X-H; Kesteven SH; Reichelt ME; Mohl MC; Dai Y; Sketchley AE; Yanq LL; Gong H; Smith NJ; Fatkin D; Allen D; Head SI; Graham RM; Feneley MP, 2013, 'Critical Role of RhoA/ROCK Signaling in Cardiac Contractility', in CIRCULATION, LIPPINCOTT WILLIAMS & WILKINS, Dallas, TX, presented at Scientific Sessions and Resuscitation Science Symposium of the American-Heart-Association, Dallas, TX, 16 November 2013 - 17 November 2013, http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000332162903138&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a

Nikolova-Krstevski V; Wagner S; Friedrich O; Fatkin D, 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, Las Vegas, NV, presented at Scientific Sessions of the American-Heart-Association on Basic Cardiovascular Sciences, Las Vegas, NV, 22 July 2013 - 25 July 2013, http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000332063200041&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a

Tong J; Vidal C; Li W; Yeo L; Fatkin D; Duque G, 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, National Harbor, MD, pp. S78 - S78, presented at Annual Scientific Meeting on the American-Geriatrics-Society, National Harbor, MD, 11 May 2011 - 14 May 2011, http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000289524600227&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a

Riveron JTG; Ghosh TK; Pope M; Eason J; BuLock F; Thomborough C; Kirk EP; Fatkin D; Feneley MP; Harvey RP; Armour JAL; Brook JD, 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, Warwick, RI, pp. S76 - S76, presented at British Human Genetics Conference, Warwick, RI, 06 September 2010 - 08 September 2010, http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000283762600155&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a

Duque G; Li WJ; Yeo L; Fatkin D, 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, http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000264611900029&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a

Granados-Riveron J; Pope M; Eason J; BuLock F; Cox J; Thomborough C; Kirk EP; Fatkin D; Feneley MP; Harvey RP; Armour J; Brook J, 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, Univ York, York, ENGLAND, 15 September 2008 - 17 September 2008, http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000259436400186&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a

Cannon L; Marcinlec T; Mearns B; Graham RM; Fatkin D, 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, New Orleans, LA, pp. S423 - S423, presented at 81st Annual Scientific Session of the American-Heart-Association, New Orleans, LA, 08 November 2008 - 12 November 2008, http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000262104500695&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a

Otway RT; Vandenberg JI; Guo G; Fatkin D, 2007, 'Interaction between a KCNQ1 mutation and cell stretch in familial atrial fibrillation', in BIOPHYSICAL JOURNAL, BIOPHYSICAL SOCIETY, Baltimore, MD, pp. 463A - 463A, presented at 51st Annual Meeting of the Biophysical-Society, Baltimore, MD, 03 March 2007 - 07 March 2007, http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000243972403011&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a

Semsarian C; McConnell BK; Fatkin D; Mudd JO; Olson EN; Moskowitz I; Schoen FJ; Giewat M; Seidman CE; Seidman JG, 2000, 'Cyclosporin A and minoxidil exacerbate cardiac hypertrophy in hypertrophic cardiomyopathy via a calcium-mediated pathway', in CIRCULATION, LIPPINCOTT WILLIAMS & WILKINS, pp. 98 - 98, http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000090072300463&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a

Sasaki T; Fatkin D; Macrae C; Wolff MR; Vidaillet HJ; Darras BT; De Girolami U; Seidman JG; Seidman CE, 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, http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000090072301368&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a

Levy H; Schonberger J; Somkiat S; Fatkin D; MacRae E; Halpin C; Eavey R; Philbin E; Seidman JG; Seidman C, 2000, 'Dilated cardiomyopathy and sensorineural hearing loss: A heritable syndrome that maps to 6q23-24', in PEDIATRIC RESEARCH, INT PEDIATRIC RESEARCH FOUNDATION, INC, pp. 46A - 46A, http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000086155300270&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a

Fatkin D; McConnell BK; Jones K; Healey MJ; Mudd JO; Conner DA; Schoen FJ; Schoen J; Seidman JG; Seidman CE, 1999, 'Evaluation of cardiac structure and function in two moose models of familial hypertrophic cardiomyopathy', in CIRCULATION, LIPPINCOTT WILLIAMS & WILKINS, pp. 494 - 494, http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000083417102599&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a

Berul CI; Fatkin D; McConnell BK; Maguire CT; Gehrmann J; Rakhit A; Jones K; Seidman JG; Seidman CE, 1999, 'Electrophysiological characterization of familial hypertrophic cardiomyopathy mice with mutant myosin binding protein C gene', in CIRCULATION, LIPPINCOTT WILLIAMS & WILKINS, pp. 207 - 207, http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000083417101071&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a

Schoenberger J; Levy H; Gruenig E; Ronald E; Sangwatanaroj S; Fatkin D; Staeckler H; Halpin C; Philbin EF; Katus HA; Seidman JG; Seidman CE, 1999, 'Dilated cardiomyopathy and sensorineurinal hearing loss: A heritable syndrome, that maps to 6q23-24', in CIRCULATION, LIPPINCOTT WILLIAMS & WILKINS, pp. 618 - 619, http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000083417103257&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a29b250adbe88d1

Bruneau BG; Bao ZZ; Fatkin D; Georgakopoulos D; Mudd JO; Conner DA; Schoen FJ; de Bold A; Cepko CL; Seidman JG; Seidman E, 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, http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000083417101821&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a

Gruver EJ; Fatkin D; Dodds GA; Kisslo J; Maron BJ; Seidman JG; Seidman CE, 1999, 'Familial hypertrophic cardiomyopathy and atrial fibrillation caused by Arg663His beta-cardiac myosin heavy chain mutation', in AMERICAN JOURNAL OF CARDIOLOGY, EXCERPTA MEDICA INC, BADEN BADEN, GERMANY, pp. 13H - 18H, presented at Symposium on From Increased Energy Metabolism to Cardiac Hypertrophy and Failure - Mediators and Molecular Mechanisms, BADEN BADEN, GERMANY, 25 September 1998 - 27 September 1998, http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000081307900005&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a

McConnell BK; Jones K; Fatkin D; Arroyo LH; Lee RT; Aristizabal O; Turnbull DH; Georgakopoulos D; Kass DA, 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, http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000076594403305&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a

Healey MJ; Fatkin D; Arroyo LH; Lee RT; Maguire CT; Bevilacqua ML; Berul CI; Seidman JG; Seidman CE, 1998, 'Exercise and beta-blocker therapy in alpha-myosin heavy chain mutant mice with hypertrophic cardiomyopathy', in CIRCULATION, LIPPINCOTT WILLIAMS & WILKINS, pp. 70 - 70, http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000076594400401&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a

Benson DW; Strauss AW; Sharkey A; Fatkin D; Schott JJ; Sangwatanaroj S; Pease WE; Basson CT; Seidman JG; Seidman CE, 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, http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:A1997YC88000076&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a

Fatkin D; Aristizabal O; Srinivasan S; Christe ME; Seidman JG; Seidman CE; Turnbull DH, 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, http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:A1997YC88004110&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a

Fatkin D; Christe ME; Aristizabal O; Schoen FJ; Turnbull DH; Seidman CE; Seidman JG, 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, http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:A1997YC88003167&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a


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