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Diane Fatkin, M.D., M.B.,B.S.

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Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Faculty can login to make corrections and additions.
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  1. Yengo L, Vedantam S, Marouli E, Sidorenko J, Bartell E, Sakaue S, Graff M, Eliasen AU, Jiang Y, Raghavan S, Miao J, Arias JD, Graham SE, Mukamel RE, Spracklen CN, Yin X, Chen SH, Ferreira T, Highland HH, Ji Y, Karaderi T, Lin K, Lüll K, Malden DE, Medina-Gomez C, Machado M, Moore A, Rüeger S, Sim X, Vrieze S, Ahluwalia TS, Akiyama M, Allison MA, Alvarez M, Andersen MK, Ani A, Appadurai V, Arbeeva L, Bhaskar S, Bielak LF, Bollepalli S, Bonnycastle LL, Bork-Jensen J, Bradfield JP, Bradford Y, Braund PS, Brody JA, Burgdorf KS, Cade BE, Cai H, Cai Q, Campbell A, Cañadas-Garre M, Catamo E, Chai JF, Chai X, Chang LC, Chang YC, Chen CH, Chesi A, Choi SH, Chung RH, Cocca M, Concas MP, Couture C, Cuellar-Partida G, Danning R, Daw EW, Degenhard F, Delgado GE, Delitala A, Demirkan A, Deng X, Devineni P, Dietl A, Dimitriou M, Dimitrov L, Dorajoo R, Ekici AB, Engmann JE, Fairhurst-Hunter Z, Farmaki AE, Faul JD, Fernandez-Lopez JC, Forer L, Francescatto M, Freitag-Wolf S, Fuchsberger C, Galesloot TE, Gao Y, Gao Z, Geller F, Giannakopoulou O, Giulianini F, Gjesing AP, Goel A, Gordon SD, Gorski M, Grove J, Guo X, Gustafsson S, Haessler J, Hansen TF, Havulinna AS, Haworth SJ, He J, Heard-Costa N, Hebbar P, Hindy G, Ho YA, Hofer E, Holliday E, Horn K, Hornsby WE, Hottenga JJ, Huang H, Huang J, Huerta-Chagoya A, Huffman JE, Hung YJ, Huo S, Hwang MY, Iha H, Ikeda DD, Isono M, Jackson AU, Jäger S, Jansen IE, Johansson I, Jonas JB, Jonsson A, Jørgensen T, Kalafati IP, Kanai M, Kanoni S, Kårhus LL, Kasturiratne A, Katsuya T, Kawaguchi T, Kember RL, Kentistou KA, Kim HN, Kim YJ, Kleber ME, Knol MJ, Kurbasic A, Lauzon M, Le P, Lea R, Lee JY, Leonard HL, Li SA, Li X, Li X, Liang J, Lin H, Lin SY, Liu J, Liu X, Lo KS, Long J, Lores-Motta L, Luan J, Lyssenko V, Lyytikäinen LP, Mahajan A, Mamakou V, Mangino M, Manichaikul A, Marten J, Mattheisen M, Mavarani L, McDaid AF, Meidtner K, Melendez TL, Mercader JM, Milaneschi Y, Miller JE, Millwood IY, Mishra PP, Mitchell RE, Møllehave LT, Morgan A, Mucha S, Munz M, Nakatochi M, Nelson CP, Nethander M, Nho CW, Nielsen AA, Nolte IM, Nongmaithem SS, Noordam R, Ntalla I, Nutile T, Pandit A, Christofidou P, Pärna K, Pauper M, Petersen ERB, Petersen LV, Pitkänen N, Polašek O, Poveda A, Preuss MH, Pyarajan S, Raffield LM, Rakugi H, Ramirez J, Rasheed A, Raven D, Rayner NW, Riveros C, Rohde R, Ruggiero D, Ruotsalainen SE, Ryan KA, Sabater-Lleal M, Saxena R, Scholz M, Sendamarai A, Shen B, Shi J, Shin JH, Sidore C, Sitlani CM, Slieker RC, Smit RAJ, Smith AV, Smith JA, Smyth LJ, Southam L, Steinthorsdottir V, Sun L, Takeuchi F, Tallapragada DSP, Taylor KD, Tayo BO, Tcheandjieu C, Terzikhan N, Tesolin P, Teumer A, Theusch E, Thompson DJ, Thorleifsson G, Timmers PRHJ, Trompet S, Turman C, Vaccargiu S, van der Laan SW, van der Most PJ, van Klinken JB, van Setten J, Verma SS, Verweij N, Veturi Y, Wang CA, Wang C, Wang L, Wang Z, Warren HR, Bin Wei W, Wickremasinghe AR, Wielscher M, Wiggins KL, Winsvold BS, Wong A, Wu Y, Wuttke M, Xia R, Xie T, Yamamoto K, Yang J, Yao J, Young H, Yousri NA, Yu L, Zeng L, Zhang W, Zhang X, Zhao JH, Zhao W, Zhou W, Zimmermann ME, Zoledziewska M, Adair LS, Adams HHH, Aguilar-Salinas CA, Al-Mulla F, Arnett DK, Asselbergs FW, Åsvold BO, Attia J, Banas B, Bandinelli S, Bennett DA, Bergler T, Bharadwaj D, Biino G, Bisgaard H, Boerwinkle E, Böger CA, Bønnelykke K, Boomsma DI, Børglum AD, Borja JB, Bouchard C, Bowden DW, Brandslund I, Brumpton B, et al. A saturated map of common genetic variants associated with human height. Nature. 2022 10; 610(7933):704-712. PMID: 36224396; PMCID: PMC9605867.
    Citations: 3     Fields:    Translation:Humans
  2. La Gerche A, Wasfy MM, Brosnan MJ, Claessen G, Fatkin D, Heidbuchel H, Baggish AL, Kovacic JC. The Athlete's Heart-Challenges and Controversies: JACC Focus Seminar 4/4. J Am Coll Cardiol. 2022 10 04; 80(14):1346-1362. PMID: 36075838.
    Citations:    Fields:    Translation:Humans
  3. Paul C, Peters S, Perrin M, Fatkin D, Amerena J. Non-ischaemic dilated cardiomyopathy: recognising the genetic links. Intern Med J. 2022 Aug 31. PMID: 36043846.
    Citations:    Fields:    
  4. de Frutos F, Ochoa JP, Navarro-Peñalver M, Baas A, Bjerre JV, Zorio E, Méndez I, Lorca R, Verdonschot JAJ, García-Granja PE, Bilinska Z, Fatkin D, Fuentes-Cañamero ME, García-Pinilla JM, García-Álvarez MI, Girolami F, Barriales-Villa R, Díez-López C, Lopes LR, Wahbi K, García-Álvarez A, Rodríguez-Sánchez I, Rekondo-Olaetxea J, Rodríguez-Palomares JF, Gallego-Delgado M, Meder B, Kubanek M, Hansen FG, Restrepo-Córdoba MA, Palomino-Doza J, Ruiz-Guerrero L, Sarquella-Brugada G, Perez-Perez AJ, Bermúdez-Jiménez FJ, Ripoll-Vera T, Rasmussen TB, Jansen M, Sabater-Molina M, Elliot PM, Garcia-Pavia P. Natural History of MYH7-Related Dilated Cardiomyopathy. J Am Coll Cardiol. 2022 10 11; 80(15):1447-1461. PMID: 36007715.
    Citations:    Fields:    Translation:Humans
  5. Santiago CF, Huttner IG, Fatkin D. Titin-related Cardiomyopathy: Is it a Distinct Disease? Curr Cardiol Rep. 2022 09; 24(9):1069-1075. PMID: 35759169.
    Citations:    Fields:    Translation:Humans
  6. Tarr I, Hesselson S, Iismaa SE, Rath E, Monger S, Troup M, Mishra K, Wong CMY, Hsu PC, Junday K, Humphreys DT, Adlam D, Webb TR, Baranowska-Clarke AA, Hamby SE, Carss KJ, Samani NJ, Bax M, McGrath-Cadell L, Kovacic JC, Dunwoodie SL, Fatkin D, Muller DWM, Graham RM, Giannoulatou E. Exploring the Genetic Architecture of Spontaneous Coronary Artery Dissection Using Whole-Genome Sequencing. Circ Genom Precis Med. 2022 08; 15(4):e003527. PMID: 35583931; PMCID: PMC9388555.
    Citations: 1     Fields:    Translation:Humans
  7. Fatkin D, Cox CD, Martinac B. Fishing for Links Between Omega-3 Fatty Acids and Atrial Fibrillation. Circulation. 2022 04 05; 145(14):1037-1039. PMID: 35377743.
    Citations:    Fields:    Translation:Humans
  8. Cannatà A, Merlo M, Dal Ferro M, Barbati G, Manca P, Paldino A, Graw S, Gigli M, Stolfo D, Johnson R, Roy D, Tharratt K, Bromage DI, Jirikowic J, Abbate A, Goodwin A, Rao K, Marawan A, Carr-White G, Robert L, Parikh V, Ashley E, McDonagh T, Lakdawala NK, Fatkin D, Taylor MRG, Mestroni L, Sinagra G. Association of Titin Variations With Late-Onset Dilated Cardiomyopathy. JAMA Cardiol. 2022 04 01; 7(4):371-377. PMID: 35138330; PMCID: PMC8829739.
    Citations:    Fields:    Translation:Humans
  9. De Bosscher R, Dausin C, Janssens K, Bogaert J, Elliott A, Ghekiere O, Van De Heyning CM, Sanders P, Kalman J, Fatkin D, Herbots L, Willems R, Heidbuchel H, La Gerche A, Claessen G. Rationale and design of the PROspective ATHletic Heart (Pro@Heart) study: long-term assessment of the determinants of cardiac remodelling and its clinical consequences in endurance athletes. BMJ Open Sport Exerc Med. 2022; 8(1):e001309. PMID: 35368514; PMCID: PMC8935177.
    Citations: 2     
  10. Peters S, James PA, Fatkin D, Zentner D. Pregnancy Outcomes in Females With Dilated Cardiomyopathy-Associated Rare Genetic Variants. Circ Genom Precis Med. 2022 04; 15(2):e003540. PMID: 35113650.
    Citations:    Fields:    Translation:Humans
  11. Peters S, Thompson BA, Perrin M, James P, Zentner D, Kalman JM, Vandenberg JI, Fatkin D. Arrhythmic Phenotypes Are a Defining Feature of Dilated Cardiomyopathy-Associated SCN5A Variants: A Systematic Review. Circ Genom Precis Med. 2022 02; 15(1):e003432. PMID: 34949099.
    Citations: 1     Fields:    Translation:Humans
  12. Gigli M, Stolfo D, Graw SL, Merlo M, Gregorio C, Nee Chen S, Dal Ferro M, PaldinoMD A, De Angelis G, Brun F, Jirikowic J, Salcedo EE, Turja S, Fatkin D, Johnson R, van Tintelen JP, Te Riele ASJM, Wilde AAM, Lakdawala NK, Picard K, Miani D, Muser D, Maria Severini G, Calkins H, James CA, Murray B, Tichnell C, Parikh VN, Ashley EA, Reuter C, Song J, Judge DP, McKenna WJ, Taylor MRG, Sinagra G, Mestroni L. Phenotypic Expression, Natural History, and Risk Stratification of Cardiomyopathy Caused by Filamin C Truncating Variants. Circulation. 2021 11 16; 144(20):1600-1611. PMID: 34587765; PMCID: PMC8595845.
    Citations: 3     Fields:    Translation:HumansCells
  13. Li JV, Ng CA, Cheng D, Zhou Z, Yao M, Guo Y, Yu ZY, Ramaswamy Y, Ju LA, Kuchel PW, Feneley MP, Fatkin D, Cox CD. Modified N-linked glycosylation status predicts trafficking defective human Piezo1 channel mutations. Commun Biol. 2021 09 06; 4(1):1038. PMID: 34489534; PMCID: PMC8421374.
    Citations: 5     Translation:HumansCells
  14. Patel PN, Ito K, Willcox JAL, Haghighi A, Jang MY, Gorham JM, DePalma SR, Lam L, McDonough B, Johnson R, Lakdawala NK, Roberts A, Barton PJR, Cook SA, Fatkin D, Seidman CE, Seidman JG. Contribution of Noncanonical Splice Variants to TTN Truncating Variant Cardiomyopathy. Circ Genom Precis Med. 2021 10; 14(5):e003389. PMID: 34461741; PMCID: PMC8788938.
    Citations: 1     Fields:    Translation:HumansCellsCTClinical Trials
  15. Lacaze P, Sebra R, Riaz M, Ingles J, Tiller J, Thompson BA, James PA, Fatkin D, Semsarian C, Reid CM, Tonkin AM, Winship I, Schadt E, McNeil JJ. Genetic variants associated with inherited cardiovascular disorders among 13,131 asymptomatic older adults of European descent. NPJ Genom Med. 2021 Jun 16; 6(1):51. PMID: 34135346; PMCID: PMC8209162.
    Citations: 5     
  16. Giudicessi JR, Ackerman MJ, Fatkin D, Kovacic JC. Precision Medicine Approaches to Cardiac Arrhythmias: JACC Focus Seminar 4/5. J Am Coll Cardiol. 2021 05 25; 77(20):2573-2591. PMID: 34016268.
    Citations: 3     Fields:    Translation:Humans
  17. Fatkin D, Calkins H, Elliott P, James CA, Peters S, Kovacic JC. Contemporary and Future Approaches to Precision Medicine in Inherited Cardiomyopathies: JACC Focus Seminar 3/5. J Am Coll Cardiol. 2021 05 25; 77(20):2551-2572. PMID: 34016267.
    Citations: 2     Fields:    Translation:Humans
  18. Pineda S, Nikolova-Krstevski V, Leimena C, Atkinson AJ, Altekoester AK, Cox CD, Jacoby A, Huttner IG, Ju YK, Soka M, Ohanian M, Trivedi G, Kalvakuri S, Birker K, Johnson R, Molenaar P, Kuchar D, Allen DG, van Helden DF, Harvey RP, Hill AP, Bodmer R, Vogler G, Dobrzynski H, Ocorr K, Fatkin D. Conserved Role of the Large Conductance Calcium-Activated Potassium Channel, KCa1.1, in Sinus Node Function and Arrhythmia Risk. Circ Genom Precis Med. 2021 04; 14(2):e003144. PMID: 33629867; PMCID: PMC8058291.
    Citations: 4     Fields:    Translation:HumansAnimals
  19. Yu ZY, Gong H, Wu J, Dai Y, Kesteven SH, Fatkin D, Martinac B, Graham RM, Feneley MP. Cardiac Gq Receptors and Calcineurin Activation Are Not Required for the Hypertrophic Response to Mechanical Left Ventricular Pressure Overload. Front Cell Dev Biol. 2021; 9:639509. PMID: 33659256; PMCID: PMC7917224.
    Citations: 1     
  20. Taliun D, Harris DN, Kessler MD, Carlson J, Szpiech ZA, Torres R, Taliun SAG, Corvelo A, Gogarten SM, Kang HM, Pitsillides AN, LeFaive J, Lee SB, Tian X, Browning BL, Das S, Emde AK, Clarke WE, Loesch DP, Shetty AC, Blackwell TW, Smith AV, Wong Q, Liu X, Conomos MP, Bobo DM, Aguet F, Albert C, Alonso A, Ardlie KG, Arking DE, Aslibekyan S, Auer PL, Barnard J, Barr RG, Barwick L, Becker LC, Beer RL, Benjamin EJ, Bielak LF, Blangero J, Boehnke M, Bowden DW, Brody JA, Burchard EG, Cade BE, Casella JF, Chalazan B, Chasman DI, Chen YI, Cho MH, Choi SH, Chung MK, Clish CB, Correa A, Curran JE, Custer B, Darbar D, Daya M, de Andrade M, DeMeo DL, Dutcher SK, Ellinor PT, Emery LS, Eng C, Fatkin D, Fingerlin T, Forer L, Fornage M, Franceschini N, Fuchsberger C, Fullerton SM, Germer S, Gladwin MT, Gottlieb DJ, Guo X, Hall ME, He J, Heard-Costa NL, Heckbert SR, Irvin MR, Johnsen JM, Johnson AD, Kaplan R, Kardia SLR, Kelly T, Kelly S, Kenny EE, Kiel DP, Klemmer R, Konkle BA, Kooperberg C, Köttgen A, Lange LA, Lasky-Su J, Levy D, Lin X, Lin KH, Liu C, Loos RJF, Garman L, Gerszten R, Lubitz SA, Lunetta KL, Mak ACY, Manichaikul A, Manning AK, Mathias RA, McManus DD, McGarvey ST, Meigs JB, Meyers DA, Mikulla JL, Minear MA, Mitchell BD, Mohanty S, Montasser ME, Montgomery C, Morrison AC, Murabito JM, Natale A, Natarajan P, Nelson SC, North KE, O'Connell JR, Palmer ND, Pankratz N, Peloso GM, Peyser PA, Pleiness J, Post WS, Psaty BM, Rao DC, Redline S, Reiner AP, Roden D, Rotter JI, Ruczinski I, Sarnowski C, Schoenherr S, Schwartz DA, Seo JS, Seshadri S, Sheehan VA, Sheu WH, Shoemaker MB, Smith NL, Smith JA, Sotoodehnia N, Stilp AM, Tang W, Taylor KD, Telen M, Thornton TA, Tracy RP, Van Den Berg DJ, Vasan RS, Viaud-Martinez KA, Vrieze S, Weeks DE, Weir BS, Weiss ST, Weng LC, Willer CJ, Zhang Y, Zhao X, Arnett DK, Ashley-Koch AE, Barnes KC, Boerwinkle E, Gabriel S, Gibbs R, Rice KM, Rich SS, Silverman EK, Qasba P, Gan W, Papanicolaou GJ, Nickerson DA, Browning SR, Zody MC, Zöllner S, Wilson JG, Cupples LA, Laurie CC, Jaquish CE, Hernandez RD, O'Connor TD, Abecasis GR. Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program. Nature. 2021 02; 590(7845):290-299. PMID: 33568819; PMCID: PMC7875770.
    Citations: 249     Fields:    Translation:Humans
  21. Santiago CF, Huttner IG, Fatkin D. Mechanisms of TTNtv-Related Dilated Cardiomyopathy: Insights from Zebrafish Models. J Cardiovasc Dev Dis. 2021 Jan 25; 8(2). PMID: 33504111; PMCID: PMC7912658.
    Citations: 3     
  22. Peters S, Johnson R, Zentner D, James P, Kalman JM, Fatkin D. Long-Term Efficacy and Safety of Sodium Channel Antagonists in Patients With p.R222Q SCN5A-Related Arrhythmic Dilated Cardiomyopathy. JACC Clin Electrophysiol. 2021 01; 7(1):126-128. PMID: 33478705.
    Citations:    Fields:    Translation:Humans
  23. Carss KJ, Baranowska AA, Armisen J, Webb TR, Hamby SE, Premawardhana D, Al-Hussaini A, Wood A, Wang Q, Deevi SVV, Vitsios D, Lewis SH, Kotecha D, Bouatia-Naji N, Hesselson S, Iismaa SE, Tarr I, McGrath-Cadell L, Muller DW, Dunwoodie SL, Fatkin D, Graham RM, Giannoulatou E, Samani NJ, Petrovski S, Haefliger C, Adlam D. Spontaneous Coronary Artery Dissection: Insights on Rare Genetic Variation From Genome Sequencing. Circ Genom Precis Med. 2020 12; 13(6):e003030. PMID: 33125268; PMCID: PMC7748045.
    Citations: 9     Fields:    Translation:Humans
  24. Akhtar MM, Lorenzini M, Cicerchia M, Ochoa JP, Hey TM, Sabater Molina M, Restrepo-Cordoba MA, Dal Ferro M, Stolfo D, Johnson R, Larrañaga-Moreira JM, Robles-Mezcua A, Rodriguez-Palomares JF, Casas G, Peña-Peña ML, Lopes LR, Gallego-Delgado M, Franaszczyk M, Laucey G, Rangel-Sousa D, Basurte M, Palomino-Doza J, Villacorta E, Bilinska Z, Limeres Freire J, Garcia Pinilla JM, Barriales-Villa R, Fatkin D, Sinagra G, Garcia-Pavia P, Gimeno JR, Mogensen J, Monserrat L, Elliott PM. Clinical Phenotypes and Prognosis of Dilated Cardiomyopathy Caused by Truncating Variants in the TTN Gene. Circ Heart Fail. 2020 10; 13(10):e006832. PMID: 32964742.
    Citations: 15     Fields:    Translation:Humans
  25. Wong GR, Nalliah CJ, Lee G, Voskoboinik A, Prabhu S, Parameswaran R, Sugumar H, Anderson RD, Ling LH, McLellan A, Johnson R, Sanders P, Kistler PM, Fatkin D, Kalman JM. Genetic Susceptibility to Atrial Fibrillation Is Associated With Atrial Electrical Remodeling and Adverse Post-Ablation Outcome. JACC Clin Electrophysiol. 2020 11; 6(12):1509-1521. PMID: 33213811.
    Citations: 1     Fields:    Translation:Humans
  26. Guo Y, Merten AL, Schöler U, Yu ZY, Cvetkovska J, Fatkin D, Feneley MP, Martinac B, Friedrich O. In vitro cell stretching technology (IsoStretcher) as an approach to unravel Piezo1-mediated cardiac mechanotransduction. Prog Biophys Mol Biol. 2021 01; 159:22-33. PMID: 32763257.
    Citations: 5     Fields:    Translation:HumansAnimalsCells
  27. Iismaa SE, Hesselson S, McGrath-Cadell L, Muller DW, Fatkin D, Giannoulatou E, Kovacic J, Graham RM. Spontaneous Coronary Artery Dissection and Fibromuscular Dysplasia: Vasculopathies With a Predilection for Women. Heart Lung Circ. 2021 Jan; 30(1):27-35. PMID: 32713767; PMCID: PMC7710561.
    Citations: 2     Fields:    Translation:Humans
  28. Ntalla I, Weng LC, Cartwright JH, Hall AW, Sveinbjornsson G, Tucker NR, Choi SH, Chaffin MD, Roselli C, Barnes MR, Mifsud B, Warren HR, Hayward C, Marten J, Cranley JJ, Concas MP, Gasparini P, Boutin T, Kolcic I, Polasek O, Rudan I, Araujo NM, Lima-Costa MF, Ribeiro ALP, Souza RP, Tarazona-Santos E, Giedraitis V, Ingelsson E, Mahajan A, Morris AP, Del Greco M F, Foco L, Gögele M, Hicks AA, Cook JP, Lind L, Lindgren CM, Sundström J, Nelson CP, Riaz MB, Samani NJ, Sinagra G, Ulivi S, Kähönen M, Mishra PP, Mononen N, Nikus K, Caulfield MJ, Dominiczak A, Padmanabhan S, Montasser ME, O'Connell JR, Ryan K, Shuldiner AR, Aeschbacher S, Conen D, Risch L, Thériault S, Hutri-Kähönen N, Lehtimäki T, Lyytikäinen LP, Raitakari OT, Barnes CLK, Campbell H, Joshi PK, Wilson JF, Isaacs A, Kors JA, van Duijn CM, Huang PL, Gudnason V, Harris TB, Launer LJ, Smith AV, Bottinger EP, Loos RJF, Nadkarni GN, Preuss MH, Correa A, Mei H, Wilson J, Meitinger T, Müller-Nurasyid M, Peters A, Waldenberger M, Mangino M, Spector TD, Rienstra M, van de Vegte YJ, van der Harst P, Verweij N, Kääb S, Schramm K, Sinner MF, Strauch K, Cutler MJ, Fatkin D, London B, Olesen M, Roden DM, Benjamin Shoemaker M, Gustav Smith J, Biggs ML, Bis JC, Brody JA, Psaty BM, Rice K, Sotoodehnia N, De Grandi A, Fuchsberger C, Pattaro C, Pramstaller PP, Ford I, Wouter Jukema J, Macfarlane PW, Trompet S, Dörr M, Felix SB, Völker U, Weiss S, Havulinna AS, Jula A, Sääksjärvi K, Salomaa V, Guo X, Heckbert SR, Lin HJ, Rotter JI, Taylor KD, Yao J, de Mutsert R, Maan AC, Mook-Kanamori DO, Noordam R, Cucca F, Ding J, Lakatta EG, Qian Y, Tarasov KV, Levy D, Lin H, Newton-Cheh CH, Lunetta KL, Murray AD, Porteous DJ, Smith BH, Stricker BH, Uitterlinden A, van den Berg ME, Haessler J, Jackson RD, Kooperberg C, Peters U, Reiner AP, Whitsel EA, Alonso A, Arking DE, Boerwinkle E, Ehret GB, Soliman EZ, Avery CL, Gogarten SM, Kerr KF, Laurie CC, Seyerle AA, Stilp A, Assa S, Abdullah Said M, Yldau van der Ende M, Lambiase PD, Orini M, Ramirez J, Van Duijvenboden S, Arnar DO, Gudbjartsson DF, Holm H, Sulem P, Thorleifsson G, Thorolfsdottir RB, Thorsteinsdottir U, Benjamin EJ, Tinker A, Stefansson K, Ellinor PT, Jamshidi Y, Lubitz SA, Munroe PB. Multi-ancestry GWAS of the electrocardiographic PR interval identifies 202 loci underlying cardiac conduction. Nat Commun. 2020 05 21; 11(1):2542. PMID: 32439900; PMCID: PMC7242331.
    Citations: 12     Fields:    Translation:Humans
  29. Gray B, Semsarian C, Fatkin D, Ingles J, Atherton JJ, Davis AM, Sanders P, Pachter N, Skinner JR, Stiles MK. Patients With Genetic Heart Disease and COVID-19: A Cardiac Society of Australia and New Zealand (CSANZ) Consensus Statement. Heart Lung Circ. 2020 Jul; 29(7):e85-e87. PMID: 32418874; PMCID: PMC7192105.
    Citations: 3     Fields:    Translation:HumansCellsPHPublic Health
  30. Fatkin D, Johnson R. Variants of Uncertain Significance and "Missing Pathogenicity". J Am Heart Assoc. 2020 02 04; 9(3):e015588. PMID: 32009523; PMCID: PMC7033868.
    Citations: 6     Fields:    Translation:Humans
  31. Gladding PA, Legget M, Fatkin D, Larsen P, Doughty R. Polygenic Risk Scores in Coronary Artery Disease and Atrial Fibrillation. Heart Lung Circ. 2020 Apr; 29(4):634-640. PMID: 31974023.
    Citations: 10     Fields:    Translation:Humans
  32. Bart NK, Thomas L, Korczyk D, Atherton JJ, Stewart GJ, Fatkin D. Amyloid Cardiomyopathy. Heart Lung Circ. 2020 Apr; 29(4):575-583. PMID: 32001152.
    Citations: 6     Fields:    Translation:Humans
  33. Peters S, Johnson R, Birch S, Zentner D, Hershberger RE, Fatkin D. Familial Dilated Cardiomyopathy. Heart Lung Circ. 2020 Apr; 29(4):566-574. PMID: 31974027.
    Citations: 7     Fields:    Translation:Humans
  34. Fatkin D, Huttner IG, Kovacic JC, Seidman JG, Seidman CE. Precision Medicine in the Management of Dilated Cardiomyopathy: JACC State-of-the-Art Review. J Am Coll Cardiol. 2019 12 10; 74(23):2921-2938. PMID: 31806137.
    Citations: 21     Fields:    Translation:Humans
  35. Fatkin D, Huttner IG, Johnson R. Genetics of atrial cardiomyopathy. Curr Opin Cardiol. 2019 05; 34(3):275-281. PMID: 30672791.
    Citations: 3     Fields:    Translation:Humans
  36. Adlam D, Olson TM, Combaret N, Kovacic JC, Iismaa SE, Al-Hussaini A, O'Byrne MM, Bouajila S, Georges A, Mishra K, Braund PS, d'Escamard V, Huang S, Margaritis M, Nelson CP, de Andrade M, Kadian-Dodov D, Welch CA, Mazurkiewicz S, Jeunemaitre X, Wong CMY, Giannoulatou E, Sweeting M, Muller D, Wood A, McGrath-Cadell L, Fatkin D, Dunwoodie SL, Harvey R, Holloway C, Empana JP, Jouven X, Olin JW, Gulati R, Tweet MS, Hayes SN, Samani NJ, Graham RM, Motreff P, Bouatia-Naji N. Association of the PHACTR1/EDN1 Genetic Locus With Spontaneous Coronary Artery Dissection. J Am Coll Cardiol. 2019 01 08; 73(1):58-66. PMID: 30621952.
    Citations: 43     Fields:    Translation:Humans
  37. Peters S, Kumar S, Elliott P, Kalman JM, Fatkin D. Arrhythmic Genotypes in Familial Dilated Cardiomyopathy: Implications for Genetic Testing and Clinical Management. Heart Lung Circ. 2019 Jan; 28(1):31-38. PMID: 30482687.
    Citations: 26     Fields:    Translation:HumansPHPublic Health
  38. Minoche AE, Horvat C, Johnson R, Gayevskiy V, Morton SU, Drew AP, Woo K, Statham AL, Lundie B, Bagnall RD, Ingles J, Semsarian C, Seidman JG, Seidman CE, Dinger ME, Cowley MJ, Fatkin D. Response to Brodehl et al. Genet Med. 2019 05; 21(5):1248-1249. PMID: 30262924.
    Citations:    Fields:    Translation:HumansCells
  39. Zhang H, Dvornikov AV, Huttner IG, Ma X, Santiago CF, Fatkin D, Xu X. A Langendorff-like system to quantify cardiac pump function in adult zebrafish. Dis Model Mech. 2018 09 10; 11(9). PMID: 30012855; PMCID: PMC6177000.
    Citations: 11     Fields:    Translation:Animals
  40. Fatkin D. ETV1: A New Player in Atrial Remodeling. Circ Res. 2018 08 17; 123(5):515-517. PMID: 30355145.
    Citations: 1     Fields:    Translation:Humans
  41. Huttner IG, Wang LW, Santiago CF, Horvat C, Johnson R, Cheng D, von Frieling-Salewsky M, Hillcoat K, Bemand TJ, Trivedi G, Braet F, Hesselson D, Alford K, Hayward CS, Seidman JG, Seidman CE, Feneley MP, Linke WA, Fatkin D. A-Band Titin Truncation in Zebrafish Causes Dilated Cardiomyopathy and Hemodynamic Stress Intolerance. Circ Genom Precis Med. 2018 08; 11(8):e002135. PMID: 30354343.
    Citations: 11     Fields:    Translation:HumansAnimalsCells
  42. Bagnall RD, Ingles J, Dinger ME, Cowley MJ, Ross SB, Minoche AE, Lal S, Turner C, Colley A, Rajagopalan S, Berman Y, Ronan A, Fatkin D, Semsarian C. Whole Genome Sequencing Improves Outcomes of Genetic Testing in Patients With Hypertrophic Cardiomyopathy. J Am Coll Cardiol. 2018 07 24; 72(4):419-429. PMID: 30025578.
    Citations: 46     Fields:    Translation:Humans
  43. Minoche AE, Horvat C, Johnson R, Gayevskiy V, Morton SU, Drew AP, Woo K, Statham AL, Lundie B, Bagnall RD, Ingles J, Semsarian C, Seidman JG, Seidman CE, Dinger ME, Cowley MJ, Fatkin D. Genome sequencing as a first-line genetic test in familial dilated cardiomyopathy. Genet Med. 2019 03; 21(3):650-662. PMID: 29961767; PMCID: PMC7271716.
    Citations: 19     Fields:    Translation:HumansCells
  44. Horvat C, Johnson R, Lam L, Munro J, Mazzarotto F, Roberts AM, Herman DS, Parfenov M, Haghighi A, McDonough B, DePalma SR, Keogh AM, Macdonald PS, Hayward CS, Roberts A, Barton PJR, Felkin LE, Giannoulatou E, Cook SA, Seidman JG, Seidman CE, Fatkin D. A gene-centric strategy for identifying disease-causing rare variants in dilated cardiomyopathy. Genet Med. 2019 01; 21(1):133-143. PMID: 29892087; PMCID: PMC7336363.
    Citations: 7     Fields:    Translation:Humans
  45. Roselli C, Chaffin MD, Weng LC, Aeschbacher S, Ahlberg G, Albert CM, Almgren P, Alonso A, Anderson CD, Aragam KG, Arking DE, Barnard J, Bartz TM, Benjamin EJ, Bihlmeyer NA, Bis JC, Bloom HL, Boerwinkle E, Bottinger EB, Brody JA, Calkins H, Campbell A, Cappola TP, Carlquist J, Chasman DI, Chen LY, Chen YI, Choi EK, Choi SH, Christophersen IE, Chung MK, Cole JW, Conen D, Cook J, Crijns HJ, Cutler MJ, Damrauer SM, Daniels BR, Darbar D, Delgado G, Denny JC, Dichgans M, Dörr M, Dudink EA, Dudley SC, Esa N, Esko T, Eskola M, Fatkin D, Felix SB, Ford I, Franco OH, Geelhoed B, Grewal RP, Gudnason V, Guo X, Gupta N, Gustafsson S, Gutmann R, Hamsten A, Harris TB, Hayward C, Heckbert SR, Hernesniemi J, Hocking LJ, Hofman A, Horimoto ARVR, Huang J, Huang PL, Huffman J, Ingelsson E, Ipek EG, Ito K, Jimenez-Conde J, Johnson R, Jukema JW, Kääb S, Kähönen M, Kamatani Y, Kane JP, Kastrati A, Kathiresan S, Katschnig-Winter P, Kavousi M, Kessler T, Kietselaer BL, Kirchhof P, Kleber ME, Knight S, Krieger JE, Kubo M, Launer LJ, Laurikka J, Lehtimäki T, Leineweber K, Lemaitre RN, Li M, Lim HE, Lin HJ, Lin H, Lind L, Lindgren CM, Lokki ML, London B, Loos RJF, Low SK, Lu Y, Lyytikäinen LP, Macfarlane PW, Magnusson PK, Mahajan A, Malik R, Mansur AJ, Marcus GM, Margolin L, Margulies KB, März W, McManus DD, Melander O, Mohanty S, Montgomery JA, Morley MP, Morris AP, Müller-Nurasyid M, Natale A, Nazarian S, Neumann B, Newton-Cheh C, Niemeijer MN, Nikus K, Nilsson P, Noordam R, Oellers H, Olesen MS, Orho-Melander M, Padmanabhan S, Pak HN, Paré G, Pedersen NL, Pera J, Pereira A, Porteous D, Psaty BM, Pulit SL, Pullinger CR, Rader DJ, Refsgaard L, Ribasés M, Ridker PM, Rienstra M, Risch L, Roden DM, Rosand J, Rosenberg MA, Rost N, Rotter JI, Saba S, Sandhu RK, Schnabel RB, Schramm K, Schunkert H, Schurman C, Scott SA, Seppälä I, Shaffer C, Shah S, Shalaby AA, Shim J, Shoemaker MB, Siland JE, Sinisalo J, Sinner MF, Slowik A, Smith AV, Smith BH, Smith JG, Smith JD, Smith NL, Soliman EZ, Sotoodehnia N, Stricker BH, Sun A, Sun H, Svendsen JH, Tanaka T, Tanriverdi K, Taylor KD, Teder-Laving M, Teumer A, Thériault S, Trompet S, Tucker NR, Tveit A, Uitterlinden AG, Van Der Harst P, Van Gelder IC, Van Wagoner DR, Verweij N, Vlachopoulou E, Völker U, Wang B, Weeke PE, Weijs B, Weiss R, Weiss S, Wells QS, Wiggins KL, Wong JA, Woo D, Worrall BB, Yang PS, Yao J, Yoneda ZT, Zeller T, Zeng L, Lubitz SA, Lunetta KL, Ellinor PT. Multi-ethnic genome-wide association study for atrial fibrillation. Nat Genet. 2018 06 11; 50(9):1225-1233. PMID: 29892015; PMCID: PMC6136836.
    Citations: 207     Fields:    Translation:HumansCells
  46. Fatkin D, Cox CD, Huttner IG, Martinac B. Is There a Role for Genes in Exercise-Induced Atrial Cardiomyopathy? Heart Lung Circ. 2018 Sep; 27(9):1093-1098. PMID: 29706494.
    Citations: 2     Fields:    Translation:Humans
  47. Fatkin D. Left Ventricular Diastolic Dysfunction in Hutchinson-Gilford Progeria Syndrome. JAMA Cardiol. 2018 04 01; 3(4):334-335. PMID: 29466548.
    Citations:    Fields:    Translation:Humans
  48. Wang LW, Kesteven SH, Huttner IG, Feneley MP, Fatkin D. High-Frequency Echocardiography - Transformative Clinical and Research Applications in Humans, Mice, and Zebrafish. Circ J. 2018 02 23; 82(3):620-628. PMID: 29415914.
    Citations: 8     Fields:    Translation:HumansAnimals
  49. Nikolova-Krstevski V, Wagner S, Yu ZY, Cox CD, Cvetkovska J, Hill AP, Huttner IG, Benson V, Werdich AA, MacRae C, Feneley MP, Friedrich O, Martinac B, Fatkin D. Endocardial TRPC-6 Channels Act as Atrial Mechanosensors and Load-Dependent Modulators of Endocardial/Myocardial Cross-Talk. JACC Basic Transl Sci. 2017 Oct; 2(5):575-590. PMID: 30062171; PMCID: PMC6058914.
    Citations: 9     
  50. Ito K, Patel PN, Gorham JM, McDonough B, DePalma SR, Adler EE, Lam L, MacRae CA, Mohiuddin SM, Fatkin D, Seidman CE, Seidman JG. Identification of pathogenic gene mutations in LMNA and MYBPC3 that alter RNA splicing. Proc Natl Acad Sci U S A. 2017 07 18; 114(29):7689-7694. PMID: 28679633; PMCID: PMC5528995.
    Citations: 28     Fields:    Translation:HumansCells
  51. Friedrich O, Schneidereit D, Nikolaev YA, Nikolova-Krstevski V, Schürmann S, Wirth-Hücking A, Merten AL, Fatkin D, Martinac B. Adding dimension to cellular mechanotransduction: Advances in biomedical engineering of multiaxial cell-stretch systems and their application to cardiovascular biomechanics and mechano-signaling. Prog Biophys Mol Biol. 2017 11; 130(Pt B):170-191. PMID: 28647645.
    Citations: 7     Fields:    Translation:HumansAnimalsCells
  52. Fatkin D, Johnson R, McGaughran J, Weintraub RG, Atherton JJ. Position Statement on the Diagnosis and Management of Familial Dilated Cardiomyopathy. Heart Lung Circ. 2017 Nov; 26(11):1127-1132. PMID: 28655534.
    Citations: 2     Fields:    Translation:Humans
  53. Fatkin D, Santiago CF, Huttner IG, Lubitz SA, Ellinor PT. Genetics of Atrial Fibrillation: State of the Art in 2017. Heart Lung Circ. 2017 Sep; 26(9):894-901. PMID: 28601532.
    Citations: 28     Fields:    Translation:Humans
  54. Fatkin D, Huttner IG. Titin-truncating mutations in dilated cardiomyopathy: the long and short of it. Curr Opin Cardiol. 2017 May; 32(3):232-238. PMID: 28151760.
    Citations: 8     Fields:    
  55. Fatkin D, Johnson R. Are Double Mutations Double Trouble? Circ Cardiovasc Genet. 2017 04; 10(2). PMID: 28420667.
    Citations: 2     Fields:    Translation:Humans
  56. Furtado MB, Wilmanns JC, Chandran A, Perera J, Hon O, Biben C, Willow TJ, Nim HT, Kaur G, Simonds S, Wu Q, Willians D, Salimova E, Plachta N, Denegre JM, Murray SA, Fatkin D, Cowley M, Pearson JT, Kaye D, Ramialison M, Harvey RP, Rosenthal NA, Costa MW. Point mutations in murine Nkx2-5 phenocopy human congenital heart disease and induce pathogenic Wnt signaling. JCI Insight. 2017 03 23; 2(6):e88271. PMID: 28352650; PMCID: PMC5358496.
    Citations: 15     Fields:    Translation:HumansAnimalsCells
  57. Wang LW, Huttner IG, Santiago CF, Kesteven SH, Yu ZY, Feneley MP, Fatkin D. Standardized echocardiographic assessment of cardiac function in normal adult zebrafish and heart disease models. Dis Model Mech. 2017 01 01; 10(1):63-76. PMID: 28067629; PMCID: PMC5278526.
    Citations: 31     Fields:    Translation:AnimalsCells
  58. Wang LW, Huttner IG, Santiago CF, Fatkin D. Bradycardia in Zebrafish Heart Failure: A True Physiological Response or Anesthetic-Induced Red Herring? Zebrafish. 2016 12; 13(6):475-476. PMID: 27676282.
    Citations: 1     Fields:    Translation:Animals
  59. Christensen AH, Chatelain FC, Huttner IG, Olesen MS, Soka M, Feliciangeli S, Horvat C, Santiago CF, Vandenberg JI, Schmitt N, Olesen SP, Lesage F, Fatkin D. The two-pore domain potassium channel, TWIK-1, has a role in the regulation of heart rate and atrial size. J Mol Cell Cardiol. 2016 08; 97:24-35. PMID: 27103460.
    Citations: 13     Fields:    Translation:HumansAnimals
  60. Iyngkaran P, Thomas MC, Johnson R, French J, Ilton M, McDonald P, Hare DL, Fatkin D. Contextualizing Genetics for Regional Heart Failure Care. Curr Cardiol Rev. 2016; 12(3):231-42. PMID: 27280306; PMCID: PMC5011192.
    Citations: 6     Fields:    Translation:Humans
  61. Cannon L, Yu ZY, Marciniec T, Waardenberg AJ, Iismaa SE, Nikolova-Krstevski V, Neist E, Ohanian M, Qiu MR, Rainer S, Harvey RP, Feneley MP, Graham RM, Fatkin D. Irreversible triggers for hypertrophic cardiomyopathy are established in the early postnatal period. J Am Coll Cardiol. 2015 Feb 17; 65(6):560-9. PMID: 25677315.
    Citations: 14     Fields:    Translation:AnimalsCells
  62. Wang LW, Grygiel JJ, O'Neill JH, Fatkin D, Feneley MP. Snowflakes in the heart: an ultrasonic marker of severe hypercoagulability. Lancet. 2015 Jan 17; 385(9964):302. PMID: 25706710.
    Citations:    Fields:    Translation:HumansCells
  63. Roberts AM, Ware JS, Herman DS, Schafer S, Baksi J, Bick AG, Buchan RJ, Walsh R, John S, Wilkinson S, Mazzarotto F, Felkin LE, Gong S, MacArthur JA, Cunningham F, Flannick J, Gabriel SB, Altshuler DM, Macdonald PS, Heinig M, Keogh AM, Hayward CS, Banner NR, Pennell DJ, O'Regan DP, San TR, de Marvao A, Dawes TJ, Gulati A, Birks EJ, Yacoub MH, Radke M, Gotthardt M, Wilson JG, O'Donnell CJ, Prasad SK, Barton PJ, Fatkin D, Hubner N, Seidman JG, Seidman CE, Cook SA. Integrated allelic, transcriptional, and phenomic dissection of the cardiac effects of titin truncations in health and disease. Sci Transl Med. 2015 Jan 14; 7(270):270ra6. PMID: 25589632; PMCID: PMC4560092.
    Citations: 160     Fields:    Translation:HumansCells
  64. Yu ZY, Tan JC, McMahon AC, Iismaa SE, Xiao XH, Kesteven SH, Reichelt ME, Mohl MC, Smith NJ, Fatkin D, Allen D, Head SI, Graham RM, Feneley MP. RhoA/ROCK signaling and pleiotropic a1A-adrenergic receptor regulation of cardiac contractility. PLoS One. 2014; 9(6):e99024. PMID: 24919197; PMCID: PMC4053326.
    Citations: 8     Fields:    Translation:AnimalsCells
  65. Fatkin D, Seidman CE, Seidman JG. Genetics and disease of ventricular muscle. Cold Spring Harb Perspect Med. 2014 Jan 01; 4(1):a021063. PMID: 24384818.
    Citations: 23     Fields:    Translation:HumansAnimals
  66. Liang B, Soka M, Christensen AH, Olesen MS, Larsen AP, Knop FK, Wang F, Nielsen JB, Andersen MN, Humphreys D, Mann SA, Huttner IG, Vandenberg JI, Svendsen JH, Haunsø S, Preiss T, Seebohm G, Olesen SP, Schmitt N, Fatkin D. Genetic variation in the two-pore domain potassium channel, TASK-1, may contribute to an atrial substrate for arrhythmogenesis. J Mol Cell Cardiol. 2014 Feb; 67:69-76. PMID: 24374141.
    Citations: 25     Fields:    Translation:HumansAnimalsCells
  67. Ballouz S, Liu JY, Oti M, Gaeta B, Fatkin D, Bahlo M, Wouters MA. Candidate disease gene prediction using Gentrepid: application to a genome-wide association study on coronary artery disease. Mol Genet Genomic Med. 2014 Jan; 2(1):44-57. PMID: 24498628.
    Citations: 8     Fields:    
  68. Priori SG, Wilde AA, Horie M, Cho Y, Behr ER, Berul C, Blom N, Brugada J, Chiang CE, Huikuri H, Kannankeril P, Krahn A, Leenhardt A, Moss A, Schwartz PJ, Shimizu W, Tomaselli G, Tracy C, Ackerman M, Belhassen B, Estes NA, Fatkin D, Kalman J, Kaufman E, Kirchhof P, Schulze-Bahr E, Wolpert C, Vohra J, Refaat M, Etheridge SP, Campbell RM, Martin ET, Quek SC. Executive summary: HRS/EHRA/APHRS expert consensus statement on the diagnosis and management of patients with inherited primary arrhythmia syndromes. Europace. 2013 Oct; 15(10):1389-406. PMID: 23994779.
    Citations: 154     Fields:    Translation:Humans
  69. Ballouz S, Liu JY, George RA, Bains N, Liu A, Oti M, Gaeta B, Fatkin D, Wouters MA. Gentrepid V2.0: a web server for candidate disease gene prediction. BMC Bioinformatics. 2013 Aug 16; 14:249. PMID: 23947436.
    Citations: 3     Fields:    Translation:Humans
  70. Christensen AH, Fatkin D. Efficacy of carvedilol in pediatric heart failure. Future Cardiol. 2013 Jul; 9(4):475-8. PMID: 23834688.
    Citations:    Fields:    Translation:Humans
  71. Huttner IG, Trivedi G, Jacoby A, Mann SA, Vandenberg JI, Fatkin D. A transgenic zebrafish model of a human cardiac sodium channel mutation exhibits bradycardia, conduction-system abnormalities and early death. J Mol Cell Cardiol. 2013 Aug; 61:123-32. PMID: 23791817.
    Citations: 23     Fields:    Translation:HumansAnimalsCells
  72. Costa MW, Guo G, Wolstein O, Vale M, Castro ML, Wang L, Otway R, Riek P, Cochrane N, Furtado M, Semsarian C, Weintraub RG, Yeoh T, Hayward C, Keogh A, Macdonald P, Feneley M, Graham RM, Seidman JG, Seidman CE, Rosenthal N, Fatkin D, Harvey RP. Functional characterization of a novel mutation in NKX2-5 associated with congenital heart disease and adult-onset cardiomyopathy. Circ Cardiovasc Genet. 2013 Jun; 6(3):238-47. PMID: 23661673.
    Citations: 32     Fields:    Translation:HumansAnimalsCells
  73. Ohanian M, Humphreys DT, Anderson E, Preiss T, Fatkin D. A heterozygous variant in the human cardiac miR-133 gene, MIR133A2, alters miRNA duplex processing and strand abundance. BMC Genet. 2013 Mar 06; 14:18. PMID: 23497314.
    Citations: 24     Fields:    Translation:HumansAnimals
  74. Fatkin D, Nikolova-Krstevski V. Atrial cardiomyopathy an orphan disease or common disorder? Circ Cardiovasc Genet. 2013 Feb; 6(1):5-6. PMID: 23424254.
    Citations:    Fields:    Translation:Humans
  75. Ohanian M, Otway R, Fatkin D. Heuristic methods for finding pathogenic variants in gene coding sequences. J Am Heart Assoc. 2012 Oct; 1(5):e002642. PMID: 23316295.
    Citations: 5     Fields:    Translation:Humans
  76. Mann SA, Castro ML, Ohanian M, Guo G, Zodgekar P, Sheu A, Stockhammer K, Thompson T, Playford D, Subbiah R, Kuchar D, Aggarwal A, Vandenberg JI, Fatkin D. R222Q SCN5A mutation is associated with reversible ventricular ectopy and dilated cardiomyopathy. J Am Coll Cardiol. 2012 Oct 16; 60(16):1566-73. PMID: 22999724.
    Citations: 49     Fields:    Translation:HumansAnimalsCells
  77. Fatkin D. Familial dilated cardiomyopathy: Current challenges and future directions. Glob Cardiol Sci Pract. 2012; 2012(1):8. PMID: 25610839; PMCID: PMC4239822.
    Citations: 7     
  78. Vidal C, Bermeo S, Fatkin D, Duque G. Role of the nuclear envelope in the pathogenesis of age-related bone loss and osteoporosis. Bonekey Rep. 2012; 1:62. PMID: 23951459.
    Citations: 8     
  79. Zhang BT, Whitehead NP, Gervasio OL, Reardon TF, Vale M, Fatkin D, Dietrich A, Yeung EW, Allen DG. Pathways of Ca²? entry and cytoskeletal damage following eccentric contractions in mouse skeletal muscle. J Appl Physiol (1985). 2012 Jun; 112(12):2077-86. PMID: 22461447.
    Citations: 25     Fields:    Translation:AnimalsCells
  80. Mann SA, Otway R, Guo G, Soka M, Karlsdotter L, Trivedi G, Ohanian M, Zodgekar P, Smith RA, Wouters MA, Subbiah R, Walker B, Kuchar D, Sanders P, Griffiths L, Vandenberg JI, Fatkin D. Epistatic effects of potassium channel variation on cardiac repolarization and atrial fibrillation risk. J Am Coll Cardiol. 2012 Mar 13; 59(11):1017-25. PMID: 22402074.
    Citations: 31     Fields:    Translation:Humans
  81. Humphreys DT, Hynes CJ, Patel HR, Wei GH, Cannon L, Fatkin D, Suter CM, Clancy JL, Preiss T. Complexity of murine cardiomyocyte miRNA biogenesis, sequence variant expression and function. PLoS One. 2012; 7(2):e30933. PMID: 22319597.
    Citations: 41     Fields:    Translation:AnimalsCells
  82. Ballouz S, Liu JY, Oti M, Gaeta B, Fatkin D, Bahlo M, Wouters MA. Analysis of genome-wide association study data using the protein knowledge base. BMC Genet. 2011 Nov 13; 12:98. PMID: 22077927.
    Citations: 6     Fields:    Translation:Humans
  83. Ingles J, Zodgekar PR, Yeates L, Macciocca I, Semsarian C, Fatkin D. Guidelines for genetic testing of inherited cardiac disorders. Heart Lung Circ. 2011 Nov; 20(11):681-7. PMID: 22000298.
    Citations: 17     Fields:    Translation:Humans
  84. Granados-Riveron JT, Pope M, Bu'lock FA, Thornborough C, Eason J, Setchfield K, Ketley A, Kirk EP, Fatkin D, Feneley MP, Harvey RP, Brook JD. Combined mutation screening of NKX2-5, GATA4, and TBX5 in congenital heart disease: multiple heterozygosity and novel mutations. Congenit Heart Dis. 2012 Mar-Apr; 7(2):151-9. PMID: 22011241.
    Citations: 32     Fields:    Translation:Humans
  85. Tong J, Li W, Vidal C, Yeo LS, Fatkin D, Duque G. Lamin A/C deficiency is associated with fat infiltration of muscle and bone. Mech Ageing Dev. 2011 Nov-Dec; 132(11-12):552-9. PMID: 21982926.
    Citations: 19     Fields:    Translation:HumansAnimalsCells
  86. Fatkin D. Guidelines for the diagnosis and management of familial dilated cardiomyopathy. Heart Lung Circ. 2011 Nov; 20(11):691-3. PMID: 21885340.
    Citations: 21     Fields:    Translation:Humans
  87. Yeoh T, Hayward C, Benson V, Sheu A, Richmond Z, Feneley MP, Keogh AM, Macdonald P, Fatkin D. A randomised, placebo-controlled trial of carvedilol in early familial dilated cardiomyopathy. Heart Lung Circ. 2011 Sep; 20(9):566-73. PMID: 21763198.
    Citations: 3     Fields:    Translation:Humans
  88. Qian L, Wythe JD, Liu J, Cartry J, Vogler G, Mohapatra B, Otway RT, Huang Y, King IN, Maillet M, Zheng Y, Crawley T, Taghli-Lamallem O, Semsarian C, Dunwoodie S, Winlaw D, Harvey RP, Fatkin D, Towbin JA, Molkentin JD, Srivastava D, Ocorr K, Bruneau BG, Bodmer R. Tinman/Nkx2-5 acts via miR-1 and upstream of Cdc42 to regulate heart function across species. J Cell Biol. 2011 Jun 27; 193(7):1181-96. PMID: 21690310.
    Citations: 37     Fields:    Translation:HumansAnimalsCells
  89. Moradi Marjaneh M, Kirk EP, Posch MG, Ozcelik C, Berger F, Hetzer R, Otway R, Butler TL, Blue GM, Griffiths LR, Fatkin D, Martinson JJ, Winlaw DS, Feneley MP, Harvey RP. Investigation of association between PFO complicated by cryptogenic stroke and a common variant of the cardiac transcription factor GATA4. PLoS One. 2011; 6(6):e20711. PMID: 21673957.
    Citations: 1     Fields:    Translation:Humans
  90. Fatkin D, Yeoh T, Hayward CS, Benson V, Sheu A, Richmond Z, Feneley MP, Keogh AM, Macdonald PS. Evaluation of left ventricular enlargement as a marker of early disease in familial dilated cardiomyopathy. Circ Cardiovasc Genet. 2011 Aug 01; 4(4):342-8. PMID: 21636824.
    Citations: 9     Fields:    Translation:Humans
  91. Duque G, Li W, Yeo LS, Vidal C, Fatkin D. Attenuated anabolic response to exercise in lamin A/C haploinsufficient mice. Bone. 2011 Sep; 49(3):412-8. PMID: 21575749.
    Citations: 5     Fields:    Translation:AnimalsCells
  92. Mohl MC, Iismaa SE, Xiao XH, Friedrich O, Wagner S, Nikolova-Krstevski V, Wu J, Yu ZY, Feneley M, Fatkin D, Allen DG, Graham RM. Regulation of murine cardiac contractility by activation of a(1A)-adrenergic receptor-operated Ca(2+) entry. Cardiovasc Res. 2011 Jul 15; 91(2):310-9. PMID: 21546445.
    Citations: 24     Fields:    Translation:HumansAnimalsCells
  93. Li W, Yeo LS, Vidal C, McCorquodale T, Herrmann M, Fatkin D, Duque G. Decreased bone formation and osteopenia in lamin a/c-deficient mice. PLoS One. 2011 Apr 25; 6(4):e19313. PMID: 21547077.
    Citations: 35     Fields:    Translation:Animals
  94. Lopes Floro K, Artap ST, Preis JI, Fatkin D, Chapman G, Furtado MB, Harvey RP, Hamada H, Sparrow DB, Dunwoodie SL. Loss of Cited2 causes congenital heart disease by perturbing left-right patterning of the body axis. Hum Mol Genet. 2011 Mar 15; 20(6):1097-110. PMID: 21224256.
    Citations: 25     Fields:    Translation:HumansAnimalsCells
  95. Nikolova-Krstevski V, Leimena C, Xiao XH, Kesteven S, Tan JC, Yeo LS, Yu ZY, Zhang Q, Carlton A, Head S, Shanahan C, Feneley MP, Fatkin D. Nesprin-1 and actin contribute to nuclear and cytoskeletal defects in lamin A/C-deficient cardiomyopathy. J Mol Cell Cardiol. 2011 Mar; 50(3):479-86. PMID: 21156181.
    Citations: 20     Fields:    Translation:AnimalsCells
  96. Granados-Riveron JT, Ghosh TK, Pope M, Bu'Lock F, Thornborough C, Eason J, Kirk EP, Fatkin D, Feneley MP, Harvey RP, Armour JA, David Brook J. Alpha-cardiac myosin heavy chain (MYH6) mutations affecting myofibril formation are associated with congenital heart defects. Hum Mol Genet. 2010 Oct 15; 19(20):4007-16. PMID: 20656787.
    Citations: 54     Fields:    Translation:HumansAnimalsCells
  97. Lai D, Liu X, Forrai A, Wolstein O, Michalicek J, Ahmed I, Garratt AN, Birchmeier C, Zhou M, Hartley L, Robb L, Feneley MP, Fatkin D, Harvey RP. Neuregulin 1 sustains the gene regulatory network in both trabecular and nontrabecular myocardium. Circ Res. 2010 Sep 17; 107(6):715-27. PMID: 20651287.
    Citations: 47     Fields:    Translation:AnimalsCells
  98. Fatkin D, Otway R, Richmond Z. Genetics of dilated cardiomyopathy. Heart Fail Clin. 2010 Apr; 6(2):129-40. PMID: 20347783.
    Citations: 27     Fields:    Translation:Humans
  99. Chandar S, Yeo LS, Leimena C, Tan JC, Xiao XH, Nikolova-Krstevski V, Yasuoka Y, Gardiner-Garden M, Wu J, Kesteven S, Karlsdotter L, Natarajan S, Carlton A, Rainer S, Feneley MP, Fatkin D. Effects of mechanical stress and carvedilol in lamin A/C-deficient dilated cardiomyopathy. Circ Res. 2010 Feb 19; 106(3):573-82. PMID: 20019332.
    Citations: 28     Fields:    Translation:Animals
  100. Carballo S, Robinson P, Otway R, Fatkin D, Jongbloed JD, de Jonge N, Blair E, van Tintelen JP, Redwood C, Watkins H. Identification and functional characterization of cardiac troponin I as a novel disease gene in autosomal dominant dilated cardiomyopathy. Circ Res. 2009 Aug 14; 105(4):375-82. PMID: 19590045.
    Citations: 42     Fields:    Translation:Humans
  101. Teber ET, Liu JY, Ballouz S, Fatkin D, Wouters MA. Comparison of automated candidate gene prediction systems using genes implicated in type 2 diabetes by genome-wide association studies. BMC Bioinformatics. 2009 Jan 30; 10 Suppl 1:S69. PMID: 19208173.
    Citations: 11     Fields:    Translation:Humans
  102. Sparrow DB, Guillén-Navarro E, Fatkin D, Dunwoodie SL. Mutation of Hairy-and-Enhancer-of-Split-7 in humans causes spondylocostal dysostosis. Hum Mol Genet. 2008 Dec 01; 17(23):3761-6. PMID: 18775957.
    Citations: 49     Fields:    Translation:HumansAnimalsCells
  103. Palmer BM, Wang Y, Teekakirikul P, Hinson JT, Fatkin D, Strouse S, Vanburen P, Seidman CE, Seidman JG, Maughan DW. Myofilament mechanical performance is enhanced by R403Q myosin in mouse myocardium independent of sex. Am J Physiol Heart Circ Physiol. 2008 Apr; 294(4):H1939-47. PMID: 18281382.
    Citations: 31     Fields:    Translation:AnimalsCells
  104. Otway R, Vandenberg JI, Fatkin D. Atrial fibrillation--a new cardiac channelopathy. Heart Lung Circ. 2007 Oct; 16(5):356-60. PMID: 17768091.
    Citations: 3     Fields:    Translation:Humans
  105. Fatkin D, Otway R, Vandenberg JI. Genes and atrial fibrillation: a new look at an old problem. Circulation. 2007 Aug 14; 116(7):782-92. PMID: 17698744.
    Citations: 31     Fields:    Translation:Humans
  106. Kirk EP, Sunde M, Costa MW, Rankin SA, Wolstein O, Castro ML, Butler TL, Hyun C, Guo G, Otway R, Mackay JP, Waddell LB, Cole AD, Hayward C, Keogh A, Macdonald P, Griffiths L, Fatkin D, Sholler GF, Zorn AM, Feneley MP, Winlaw DS, Harvey RP. Mutations in cardiac T-box factor gene TBX20 are associated with diverse cardiac pathologies, including defects of septation and valvulogenesis and cardiomyopathy. Am J Hum Genet. 2007 Aug; 81(2):280-91. PMID: 17668378; PMCID: PMC1950799.
    Citations: 132     Fields:    Translation:Humans
  107. Otway R, Vandenberg JI, Guo G, Varghese A, Castro ML, Liu J, Zhao J, Bursill JA, Wyse KR, Crotty H, Baddeley O, Walker B, Kuchar D, Thorburn C, Fatkin D. Stretch-sensitive KCNQ1 mutation A link between genetic and environmental factors in the pathogenesis of atrial fibrillation? J Am Coll Cardiol. 2007 Feb 06; 49(5):578-86. PMID: 17276182.
    Citations: 59     Fields:    Translation:Humans
  108. Fatkin D. Guidelines for the diagnosis and management of familial dilated cardiomyopathy. Heart Lung Circ. 2007 Feb; 16(1):19-21. PMID: 17188933.
    Citations: 11     Fields:    Translation:Humans
  109. George RA, Liu JY, Feng LL, Bryson-Richardson RJ, Fatkin D, Wouters MA. Analysis of protein sequence and interaction data for candidate disease gene prediction. Nucleic Acids Res. 2006; 34(19):e130. PMID: 17020920; PMCID: PMC1636487.
    Citations: 63     Fields:    Translation:HumansCells
  110. Sparrow DB, Chapman G, Wouters MA, Whittock NV, Ellard S, Fatkin D, Turnpenny PD, Kusumi K, Sillence D, Dunwoodie SL. Mutation of the LUNATIC FRINGE gene in humans causes spondylocostal dysostosis with a severe vertebral phenotype. Am J Hum Genet. 2006 Jan; 78(1):28-37. PMID: 16385447; PMCID: PMC1380221.
    Citations: 72     Fields:    Translation:HumansCells
  111. Stennard FA, Costa MW, Lai D, Biben C, Furtado MB, Solloway MJ, McCulley DJ, Leimena C, Preis JI, Dunwoodie SL, Elliott DE, Prall OW, Black BL, Fatkin D, Harvey RP. Murine T-box transcription factor Tbx20 acts as a repressor during heart development, and is essential for adult heart integrity, function and adaptation. Development. 2005 May; 132(10):2451-62. PMID: 15843414.
    Citations: 90     Fields:    Translation:Animals
  112. Nikolova V, Leimena C, McMahon AC, Tan JC, Chandar S, Jogia D, Kesteven SH, Michalicek J, Otway R, Verheyen F, Rainer S, Stewart CL, Martin D, Feneley MP, Fatkin D. Defects in nuclear structure and function promote dilated cardiomyopathy in lamin A/C-deficient mice. J Clin Invest. 2004 Feb; 113(3):357-69. PMID: 14755333; PMCID: PMC324538.
    Citations: 166     Fields:    Translation:AnimalsCells
  113. Elliott DA, Kirk EP, Yeoh T, Chandar S, McKenzie F, Taylor P, Grossfeld P, Fatkin D, Jones O, Hayes P, Feneley M, Harvey RP. Cardiac homeobox gene NKX2-5 mutations and congenital heart disease: associations with atrial septal defect and hypoplastic left heart syndrome. J Am Coll Cardiol. 2003 Jun 04; 41(11):2072-6. PMID: 12798584.
    Citations: 93     Fields:    Translation:Humans
  114. Fatkin D, Graham RM. Molecular mechanisms of inherited cardiomyopathies. Physiol Rev. 2002 Oct; 82(4):945-80. PMID: 12270949.
    Citations: 86     Fields:    Translation:HumansAnimals
  115. Semsarian C, Healey MJ, Fatkin D, Giewat M, Duffy C, Seidman CE, Seidman JG. A polymorphic modifier gene alters the hypertrophic response in a murine model of familial hypertrophic cardiomyopathy. J Mol Cell Cardiol. 2001 Nov; 33(11):2055-60. PMID: 11708849.
    Citations: 21     Fields:    Translation:HumansAnimalsCells
  116. McConnell BK, Fatkin D, Semsarian C, Jones KA, Georgakopoulos D, Maguire CT, Healey MJ, Mudd JO, Moskowitz IP, Conner DA, Giewat M, Wakimoto H, Berul CI, Schoen FJ, Kass DA, Seidman CE, Seidman JG. Comparison of two murine models of familial hypertrophic cardiomyopathy. Circ Res. 2001 Mar 02; 88(4):383-9. PMID: 11230104.
    Citations: 48     Fields:    Translation:AnimalsCells
  117. Bruneau BG, Bao ZZ, Fatkin D, Xavier-Neto J, Georgakopoulos D, Maguire CT, Berul CI, Kass DA, Kuroski-de Bold ML, de Bold AJ, Conner DA, Rosenthal N, Cepko CL, Seidman CE, Seidman JG. Cardiomyopathy in Irx4-deficient mice is preceded by abnormal ventricular gene expression. Mol Cell Biol. 2001 Mar; 21(5):1730-6. PMID: 11238910; PMCID: PMC86719.
    Citations: 49     Fields:    Translation:AnimalsCells
  118. Fatkin D, Graham RM. Prognostic value of left ventricular hypertrophy in hypertrophic cardiomyopathy. N Engl J Med. 2001 Jan 04; 344(1):63-5. PMID: 11187116.
    Citations: 1     Fields:    Translation:Humans
  119. Fatkin D, McConnell BK, Mudd JO, Semsarian C, Moskowitz IG, Schoen FJ, Giewat M, Seidman CE, Seidman JG. An abnormal Ca(2+) response in mutant sarcomere protein-mediated familial hypertrophic cardiomyopathy. J Clin Invest. 2000 Dec; 106(11):1351-9. PMID: 11104788; PMCID: PMC381468.
    Citations: 87     Fields:    Translation:AnimalsCells
  120. Schönberger J, Levy H, Grünig E, Sangwatanaroj S, Fatkin D, MacRae C, Stäcker H, Halpin C, Eavey R, Philbin EF, Katus H, Seidman JG, Seidman CE. Dilated cardiomyopathy and sensorineural hearing loss: a heritable syndrome that maps to 6q23-24. Circulation. 2000 Apr 18; 101(15):1812-8. PMID: 10769282.
    Citations: 21     Fields:    Translation:HumansCells
  121. Fatkin D, MacRae C, Sasaki T, Wolff MR, Porcu M, Frenneaux M, Atherton J, Vidaillet HJ, Spudich S, De Girolami U, Seidman JG, Seidman C, Muntoni F, Müehle G, Johnson W, McDonough B. Missense mutations in the rod domain of the lamin A/C gene as causes of dilated cardiomyopathy and conduction-system disease. N Engl J Med. 1999 Dec 02; 341(23):1715-24. PMID: 10580070.
    Citations: 349     Fields:    Translation:HumansCells
  122. McConnell BK, Jones KA, Fatkin D, Arroyo LH, Lee RT, Aristizabal O, Turnbull DH, Georgakopoulos D, Kass D, Bond M, Niimura H, Schoen FJ, Conner D, Fischman DA, Seidman CE, Seidman JG, Fischman DH. Dilated cardiomyopathy in homozygous myosin-binding protein-C mutant mice. J Clin Invest. 1999 Nov; 104(9):1235-44. PMID: 10545522; PMCID: PMC409819.
    Citations: 97     Fields:    Translation:AnimalsCells
  123. Gruver EJ, Fatkin D, Dodds GA, Kisslo J, Maron BJ, Seidman JG, Seidman CE. Familial hypertrophic cardiomyopathy and atrial fibrillation caused by Arg663His beta-cardiac myosin heavy chain mutation. Am J Cardiol. 1999 Jun 17; 83(12A):13H-18H. PMID: 10750581.
    Citations: 22     Fields:    Translation:HumansCells
  124. Mehdirad AA, Fatkin D, DiMarco JP, MacRae CA, Wase A, Seidman JG, Seidman CE, Benson DW. Electrophysiologic characteristics of accessory atrioventricular connections in an inherited form of Wolff-Parkinson-White syndrome. J Cardiovasc Electrophysiol. 1999 May; 10(5):629-35. PMID: 10355918.
    Citations: 8     Fields:    Translation:HumansCells
  125. Siu BL, Niimura H, Osborne JA, Fatkin D, MacRae C, Solomon S, Benson DW, Seidman JG, Seidman CE. Familial dilated cardiomyopathy locus maps to chromosome 2q31. Circulation. 1999 Mar 02; 99(8):1022-6. PMID: 10051295.
    Citations: 32     Fields:    Translation:HumansCells
  126. Fatkin D, Christe ME, Aristizabal O, McConnell BK, Srinivasan S, Schoen FJ, Seidman CE, Turnbull DH, Seidman JG. Neonatal cardiomyopathy in mice homozygous for the Arg403Gln mutation in the alpha cardiac myosin heavy chain gene. J Clin Invest. 1999 Jan; 103(1):147-53. PMID: 9884344; PMCID: PMC407864.
    Citations: 30     Fields:    Translation:HumansAnimals
  127. Benson DW, Sharkey A, Fatkin D, Lang P, Basson CT, McDonough B, Strauss AW, Seidman JG, Seidman CE. Reduced penetrance, variable expressivity, and genetic heterogeneity of familial atrial septal defects. Circulation. 1998 May 26; 97(20):2043-8. PMID: 9610535.
    Citations: 22     Fields:    Translation:HumansCells
  128. Fatkin D, Roy P, Sindone A, Feneley M. Rapid onset and dissipation of left atrial spontaneous echo contrast during percutaneous balloon mitral valvotomy. Am Heart J. 1998 Apr; 135(4):609-13. PMID: 9539475.
    Citations: 1     Fields:    Translation:Humans
  129. Fatkin D, Loupas T, Low J, Feneley M. Inhibition of red cell aggregation prevents spontaneous echocardiographic contrast formation in human blood. Circulation. 1997 Aug 05; 96(3):889-96. PMID: 9264497.
    Citations: 7     Fields:    Translation:HumansCells
  130. Fatkin D, Feneley MP. Qualitative or quantitative assessment of spontaneous echo contrast? J Am Coll Cardiol. 1997 Jan; 29(1):222-4. PMID: 8996320.
    Citations: 2     Fields:    Translation:Humans
  131. Fatkin D, Loupas T, Feneley MP. Direct effects of DC cardioversion on blood echogenicity: an in vitro study. Ultrasound Med Biol. 1997; 23(1):135-42. PMID: 9080626.
    Citations:    Fields:    Translation:HumansCells
  132. Fatkin D, Feneley MP. Patterns of Doppler-measured blood flow velocity in the normal and fibrillating human left atrial appendage. Am Heart J. 1996 Nov; 132(5):995-1003. PMID: 8892774.
    Citations: 3     Fields:    Translation:Humans
  133. Fatkin D, Feneley M. Stratification of thromboembolic risk of atrial fibrillation by transthoracic echocardiography and transesophageal echocardiography: the relative role of left atrial appendage function, mitral valve disease, and spontaneous echocardiographic contrast. Prog Cardiovasc Dis. 1996 Jul-Aug; 39(1):57-68. PMID: 8693096.
    Citations: 4     Fields:    Translation:Humans
  134. Fatkin D, Scalia G, Jacobs N, Burstow D, Leung D, Walsh W, Feneley M. Accuracy of biplane transesophageal echocardiography in detecting left atrial thrombus. Am J Cardiol. 1996 Feb 01; 77(4):321-3. PMID: 8607421.
    Citations: 7     Fields:    Translation:HumansCTClinical Trials
  135. Fatkin D, Loupas T, Jacobs N, Feneley MP. Quantification of blood echogenicity: evaluation of a semiquantitative method of grading spontaneous echo contrast. Ultrasound Med Biol. 1995; 21(9):1191-8. PMID: 8849833.
    Citations: 14     Fields:    Translation:Humans
  136. Fatkin D, Kelly R, Feneley MP. Left atrial appendage blood velocity and thromboembolic risk in patients with atrial fibrillation. J Am Coll Cardiol. 1994 Nov 01; 24(5):1429-30. PMID: 7930271.
    Citations: 4     Fields:    Translation:Humans
  137. Fatkin D, Carroll G, Kuchar D, Feneley MP. Thromboembolic complications after pharmacologic cardioversion of atrial fibrillation. Aust N Z J Med. 1994 Oct; 24(5):584-5. PMID: 7848172.
    Citations: 1     Fields:    Translation:Humans
  138. Black IW, Fatkin D, Sagar KB, Khandheria BK, Leung DY, Galloway JM, Feneley MP, Walsh WF, Grimm RA, Stollberger C, et al. Exclusion of atrial thrombus by transesophageal echocardiography does not preclude embolism after cardioversion of atrial fibrillation. A multicenter study. Circulation. 1994 Jun; 89(6):2509-13. PMID: 8205657.
    Citations: 35     Fields:    Translation:HumansCTClinical Trials
  139. Fatkin D, Herbert E, Feneley MP. Hematologic correlates of spontaneous echo contrast in patients with atrial fibrillation and implications for thromboembolic risk. Am J Cardiol. 1994 Apr 01; 73(9):672-6. PMID: 8166064.
    Citations: 14     Fields:    Translation:Humans
  140. Fatkin D, Kelly RP, Feneley MP. Relations between left atrial appendage blood flow velocity, spontaneous echocardiographic contrast and thromboembolic risk in vivo. J Am Coll Cardiol. 1994 Mar 15; 23(4):961-9. PMID: 8106703.
    Citations: 145     Fields:    Translation:Humans
  141. Fatkin D, Kuchar DL, Thorburn CW, Feneley MP. Transesophageal echocardiography before and during direct current cardioversion of atrial fibrillation: evidence for "atrial stunning" as a mechanism of thromboembolic complications. J Am Coll Cardiol. 1994 Feb; 23(2):307-16. PMID: 8294679.
    Citations: 51     Fields:    Translation:Humans
  142. Fatkin D, Roy P, Morgan JJ, Feneley MP. Percutaneous balloon mitral valvotomy with the Inoue single-balloon catheter: commissural morphology as a determinant of outcome. J Am Coll Cardiol. 1993 Feb; 21(2):390-7. PMID: 8426003.
    Citations: 19     Fields:    Translation:Humans
  143. Fatkin D, Hickie J, Thorburn C, Kuchar D. Arrhythmogenic right ventricular dysplasia. Aust N Z J Med. 1991 Aug; 21(4):451-3. PMID: 1953536.
    Citations:    Fields:    Translation:Humans
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Funded by the NIH National Center for Advancing Translational Sciences through its Clinical and Translational Science Awards Program, grant number UL1TR002541.