Gerull B - Search Results

1

Novel gene locus for autosomal dominant left ventricular noncompaction maps to chromosome 11p15.

Sasse-Klaassen S, Probst S, Gerull B, Oechslin E, Nürnberg P, Heuser A, Jenni R, Hennies HC, Thierfelder L. Sasse-Klaassen S, et al. Among authors: gerull b. Circulation. 2004 Jun 8;109(22):2720-3. doi: 10.1161/01.CIR.0000131865.21260.56. Epub 2004 Jun 1. Circulation. 2004. PMID: 15173023

2

A rapid protocol for cardiac troponin T gene mutation detection in familial hypertrophic cardiomyopathy.

Gerull B, Osterziel KJ, Witt C, Dietz R, Thierfelder L. Gerull B, et al. Hum Mutat. 1998;11(2):179-82. doi: 10.1002/(SICI)1098-1004(1998)11:2<179::AID-HUMU12>3.0.CO;2-W. Hum Mutat. 1998. PMID: 9482583

3

Hypercontractile properties of cardiac muscle fibers in a knock-in mouse model of cardiac myosin-binding protein-C.

Witt CC, Gerull B, Davies MJ, Centner T, Linke WA, Thierfelder L. Witt CC, et al. Among authors: gerull b. J Biol Chem. 2001 Feb 16;276(7):5353-9. doi: 10.1074/jbc.M008691200. Epub 2000 Nov 28. J Biol Chem. 2001. PMID: 11096095 Free article.

4

Mutations of TTN, encoding the giant muscle filament titin, cause familial dilated cardiomyopathy.

Gerull B, Gramlich M, Atherton J, McNabb M, Trombitás K, Sasse-Klaassen S, Seidman JG, Seidman C, Granzier H, Labeit S, Frenneaux M, Thierfelder L. Gerull B, et al. Nat Genet. 2002 Feb;30(2):201-4. doi: 10.1038/ng815. Epub 2002 Jan 14. Nat Genet. 2002. PMID: 11788824

5

Isolated noncompaction of the left ventricular myocardium in the adult is an autosomal dominant disorder in the majority of patients.

Sasse-Klaassen S, Gerull B, Oechslin E, Jenni R, Thierfelder L. Sasse-Klaassen S, et al. Among authors: gerull b. Am J Med Genet A. 2003 Jun 1;119A(2):162-7. doi: 10.1002/ajmg.a.20075. Am J Med Genet A. 2003. PMID: 12749056

6

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. Nat Genet. 2004 Nov;36(11):1162-4. doi: 10.1038/ng1461. Epub 2004 Oct 17. Nat Genet. 2004. PMID: 15489853

7

Identification of a novel frameshift mutation in the giant muscle filament titin in a large Australian family with dilated cardiomyopathy.

Gerull B, Atherton J, Geupel A, Sasse-Klaassen S, Heuser A, Frenneaux M, McNabb M, Granzier H, Labeit S, Thierfelder L. Gerull B, et al. J Mol Med (Berl). 2006 Jun;84(6):478-83. doi: 10.1007/s00109-006-0060-6. Epub 2006 May 6. J Mol Med (Berl). 2006. PMID: 16733766

8

A novel locus for dilated cardiomyopathy, diffuse myocardial fibrosis, and sudden death on chromosome 10q25-26.

Ellinor PT, Sasse-Klaassen S, Probst S, Gerull B, Shin JT, Toeppel A, Heuser A, Michely B, Yoerger DM, Song BS, Pilz B, Krings G, Coplin B, Lange PE, Dec GW, Hennies HC, Thierfelder L, MacRae CA. Ellinor PT, et al. Among authors: gerull b. J Am Coll Cardiol. 2006 Jul 4;48(1):106-11. doi: 10.1016/j.jacc.2006.01.079. Epub 2006 Jun 21. J Am Coll Cardiol. 2006. PMID: 16814656 Free article.

9

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: gerull b. 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.

10

Mutations in sarcomere protein genes in left ventricular noncompaction.

Klaassen S, Probst S, Oechslin E, Gerull B, Krings G, Schuler P, Greutmann M, Hürlimann D, Yegitbasi M, Pons L, Gramlich M, Drenckhahn JD, Heuser A, Berger F, Jenni R, Thierfelder L. Klaassen S, et al. Among authors: gerull b. Circulation. 2008 Jun 3;117(22):2893-901. doi: 10.1161/CIRCULATIONAHA.107.746164. Epub 2008 May 27. Circulation. 2008. PMID: 18506004

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