Basson CT - Search Results

1

A gene defect that causes conduction system disease and dilated cardiomyopathy maps to chromosome 1p1-1q1.

Kass S, MacRae C, Graber HL, Sparks EA, McNamara D, Boudoulas H, Basson CT, Baker PB 3rd, Cody RJ, Fishman MC, et al. Kass S, et al. Among authors: basson ct. Nat Genet. 1994 Aug;7(4):546-51. doi: 10.1038/ng0894-546. Nat Genet. 1994. PMID: 7951328

2

Familial Hypertrophic cardiomyopathy with Wolff-Parkinson-White syndrome maps to a locus on chromosome 7q3.

MacRae CA, Ghaisas N, Kass S, Donnelly S, Basson CT, Watkins HC, Anan R, Thierfelder LH, McGarry K, Rowland E, et al. MacRae CA, et al. Among authors: basson ct. J Clin Invest. 1995 Sep;96(3):1216-20. doi: 10.1172/JCI118154. J Clin Invest. 1995. PMID: 7657794 Free PMC article.

3

New understandings in the genetics of congenital heart disease.

Benson DW, Basson CT, MacRae CA. Benson DW, et al. Among authors: basson ct. Curr Opin Pediatr. 1996 Oct;8(5):505-11. doi: 10.1097/00008480-199610000-00015. Curr Opin Pediatr. 1996. PMID: 8946132 Review.

4

Genetic heterogeneity of familial atrial myxoma syndromes (Carney complex).

Basson CT, MacRae CA, Korf B, Merliss A. Basson CT, et al. Am J Cardiol. 1997 Apr 1;79(7):994-5. doi: 10.1016/s0002-9149(97)00033-7. Am J Cardiol. 1997. PMID: 9104925

5

Genetic heterogeneity of heart-hand syndromes.

Basson CT, Solomon SD, Weissman B, MacRae CA, Poznanski AK, Prieto F, Ruiz de la Fuente S, Pease WE, Levin SE, Holmes LB, et al. Basson CT, et al. Circulation. 1995 Mar 1;91(5):1326-9. doi: 10.1161/01.cir.91.5.1326. Circulation. 1995. PMID: 7867169

6

Identification, characterization, and chromosomal localization of the human homolog (hES) of ES/130.

Basson CT, MacRae CA, Schoenberg-Fejzo M, Morton CC, Spinner NB, Genin A, Krug E, Seidman JG, Seidman CE. Basson CT, et al. Genomics. 1996 Aug 1;35(3):628-31. doi: 10.1006/geno.1996.0413. Genomics. 1996. PMID: 8812507 Free article.

7

Mutations in the desmosomal protein plakophilin-2 are common in arrhythmogenic right ventricular cardiomyopathy.

Gerull B, Heuser A, Wichter T, Paul M, Basson CT, McDermott DA, Lerman BB, Markowitz SM, Ellinor PT, MacRae CA, Peters S, Grossmann KS, Drenckhahn J, Michely B, Sasse-Klaassen S, Birchmeier W, Dietz R, Breithardt G, Schulze-Bahr E, Thierfelder L. Gerull B, et al. Among authors: basson ct. Nat Genet. 2004 Nov;36(11):1162-4. doi: 10.1038/ng1461. Epub 2004 Oct 17. Nat Genet. 2004. PMID: 15489853

8

Mutant desmocollin-2 causes arrhythmogenic right ventricular cardiomyopathy.

Heuser A, Plovie ER, Ellinor PT, Grossmann KS, Shin JT, Wichter T, Basson CT, Lerman BB, Sasse-Klaassen S, Thierfelder L, MacRae CA, Gerull B. Heuser A, et al. Among authors: basson ct. Am J Hum Genet. 2006 Dec;79(6):1081-8. doi: 10.1086/509044. Epub 2006 Oct 3. Am J Hum Genet. 2006. PMID: 17186466 Free PMC article.

9

Congenital heart disease caused by mutations in the transcription factor NKX2-5.

Schott JJ, Benson DW, Basson CT, Pease W, Silberbach GM, Moak JP, Maron BJ, Seidman CE, Seidman JG. Schott JJ, et al. Among authors: basson ct. Science. 1998 Jul 3;281(5373):108-11. doi: 10.1126/science.281.5373.108. Science. 1998. PMID: 9651244

10

Mutations in human TBX5 [corrected] cause limb and cardiac malformation in Holt-Oram syndrome.

Basson CT, Bachinsky DR, Lin RC, Levi T, Elkins JA, Soults J, Grayzel D, Kroumpouzou E, Traill TA, Leblanc-Straceski J, Renault B, Kucherlapati R, Seidman JG, Seidman CE. Basson CT, et al. Nat Genet. 1997 Jan;15(1):30-5. doi: 10.1038/ng0197-30. Nat Genet. 1997. PMID: 8988165

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