Fatkin D - Search Results

1

Genome sequencing as a first-line genetic test in familial dilated cardiomyopathy.

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. Minoche AE, et al. Among authors: fatkin d. Genet Med. 2019 Mar;21(3):650-662. doi: 10.1038/s41436-018-0084-7. Epub 2018 Jul 2. Genet Med. 2019. PMID: 29961767 Free PMC article.

2

Reduced penetrance, variable expressivity, and genetic heterogeneity of familial atrial septal defects.

Benson DW, Sharkey A, Fatkin D, Lang P, Basson CT, McDonough B, Strauss AW, Seidman JG, Seidman CE. Benson DW, et al. Among authors: fatkin d. Circulation. 1998 May 26;97(20):2043-8. doi: 10.1161/01.cir.97.20.2043. Circulation. 1998. PMID: 9610535

3

Neonatal cardiomyopathy in mice homozygous for the Arg403Gln mutation in the alpha cardiac myosin heavy chain gene.

Fatkin D, Christe ME, Aristizabal O, McConnell BK, Srinivasan S, Schoen FJ, Seidman CE, Turnbull DH, Seidman JG. Fatkin D, et al. J Clin Invest. 1999 Jan;103(1):147-53. doi: 10.1172/JCI4631. J Clin Invest. 1999. PMID: 9884344 Free PMC article.

4

Familial dilated cardiomyopathy locus maps to chromosome 2q31.

Siu BL, Niimura H, Osborne JA, Fatkin D, MacRae C, Solomon S, Benson DW, Seidman JG, Seidman CE. Siu BL, et al. Among authors: fatkin d. Circulation. 1999 Mar 2;99(8):1022-6. doi: 10.1161/01.cir.99.8.1022. Circulation. 1999. PMID: 10051295

5

Electrophysiologic characteristics of accessory atrioventricular connections in an inherited form of Wolff-Parkinson-White syndrome.

Mehdirad AA, Fatkin D, DiMarco JP, MacRae CA, Wase A, Seidman JG, Seidman CE, Benson DW. Mehdirad AA, et al. Among authors: fatkin d. J Cardiovasc Electrophysiol. 1999 May;10(5):629-35. doi: 10.1111/j.1540-8167.1999.tb00239.x. J Cardiovasc Electrophysiol. 1999. PMID: 10355918

6

Dilated cardiomyopathy in homozygous myosin-binding protein-C mutant mice.

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. McConnell BK, et al. Among authors: fatkin d. J Clin Invest. 1999 Nov;104(9):1235-44. doi: 10.1172/JCI7377. J Clin Invest. 1999. PMID: 10545522 Free PMC article.

7

Missense mutations in the rod domain of the lamin A/C gene as causes of dilated cardiomyopathy and conduction-system disease.

Fatkin D, MacRae C, Sasaki T, Wolff MR, Porcu M, Frenneaux M, Atherton J, Vidaillet HJ Jr, Spudich S, De Girolami U, Seidman JG, Seidman C, Muntoni F, Müehle G, Johnson W, McDonough B. Fatkin D, et al. N Engl J Med. 1999 Dec 2;341(23):1715-24. doi: 10.1056/NEJM199912023412302. N Engl J Med. 1999. PMID: 10580070 Free article.

8

Familial hypertrophic cardiomyopathy and atrial fibrillation caused by Arg663His beta-cardiac myosin heavy chain mutation.

Gruver EJ, Fatkin D, Dodds GA, Kisslo J, Maron BJ, Seidman JG, Seidman CE. Gruver EJ, et al. Among authors: fatkin d. Am J Cardiol. 1999 Jun 17;83(12A):13H-18H. doi: 10.1016/s0002-9149(99)00251-9. Am J Cardiol. 1999. PMID: 10750581

9

Dilated cardiomyopathy and sensorineural hearing loss: a heritable syndrome that maps to 6q23-24.

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. Schönberger J, et al. Among authors: fatkin d. Circulation. 2000 Apr 18;101(15):1812-8. doi: 10.1161/01.cir.101.15.1812. Circulation. 2000. PMID: 10769282

10

An abnormal Ca(2+) response in mutant sarcomere protein-mediated familial hypertrophic cardiomyopathy.

Fatkin D, McConnell BK, Mudd JO, Semsarian C, Moskowitz IG, Schoen FJ, Giewat M, Seidman CE, Seidman JG. Fatkin D, et al. J Clin Invest. 2000 Dec;106(11):1351-9. doi: 10.1172/JCI11093. J Clin Invest. 2000. PMID: 11104788 Free PMC article.

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