Posch MG - Search Results

1

Mutations in GATA4, NKX2.5, CRELD1, and BMP4 are infrequently found in patients with congenital cardiac septal defects.

Posch MG, Perrot A, Schmitt K, Mittelhaus S, Esenwein EM, Stiller B, Geier C, Dietz R, Gessner R, Ozcelik C, Berger F. Posch MG, et al. Am J Med Genet A. 2008 Jan 15;146A(2):251-3. doi: 10.1002/ajmg.a.32042. Am J Med Genet A. 2008. PMID: 18076106 No abstract available.

2

A gain-of-function TBX20 mutation causes congenital atrial septal defects, patent foramen ovale and cardiac valve defects.

Posch MG, Gramlich M, Sunde M, Schmitt KR, Lee SH, Richter S, Kersten A, Perrot A, Panek AN, Al Khatib IH, Nemer G, Mégarbané A, Dietz R, Stiller B, Berger F, Harvey RP, Ozcelik C. Posch MG, et al. J Med Genet. 2010 Apr;47(4):230-5. doi: 10.1136/jmg.2009.069997. Epub 2009 Sep 16. J Med Genet. 2010. PMID: 19762328 Free PMC article.

3

Molecular genetics of congenital atrial septal defects.

Posch MG, Perrot A, Berger F, Ozcelik C. Posch MG, et al. Clin Res Cardiol. 2010 Mar;99(3):137-47. doi: 10.1007/s00392-009-0095-0. Epub 2009 Dec 11. Clin Res Cardiol. 2010. PMID: 20012542 Free PMC article. Review.

4

Mutations in the cardiac transcription factor GATA4 in patients with lone atrial fibrillation.

Posch MG, Boldt LH, Polotzki M, Richter S, Rolf S, Perrot A, Dietz R, Ozcelik C, Haverkamp W. Posch MG, et al. Eur J Med Genet. 2010 Jul-Aug;53(4):201-3. doi: 10.1016/j.ejmg.2010.03.008. Epub 2010 Apr 2. Eur J Med Genet. 2010. PMID: 20363377

5

We need a detailed phenome in the phenomenon of genetics and congenital heart disease.

Posch MG, Berger F, Perrot A, Ozcelik C. Posch MG, et al. J Med Genet. 2008 May;45(5):320. doi: 10.1136/jmg.2007.057117. J Med Genet. 2008. PMID: 18443152 No abstract available.

6

Mutational analysis of the PITX2 and NKX2-5 genes in patients with idiopathic atrial fibrillation.

Boldt LH, Posch MG, Perrot A, Polotzki M, Rolf S, Parwani AS, Huemer M, Wutzler A, Özcelik C, Haverkamp W. Boldt LH, et al. Among authors: posch mg. Int J Cardiol. 2010 Nov 19;145(2):316-317. doi: 10.1016/j.ijcard.2009.11.023. Int J Cardiol. 2010. PMID: 20022124

7

CCN1 mutation is associated with atrial septal defect.

Perrot A, Schmitt KR, Roth EM, Stiller B, Posch MG, Browne EN, Timmann C, Horstmann RD, Berger F, Özcelik C. Perrot A, et al. Among authors: posch mg. Pediatr Cardiol. 2015 Feb;36(2):295-9. doi: 10.1007/s00246-014-1001-8. Epub 2014 Aug 19. Pediatr Cardiol. 2015. PMID: 25135600

8

Mutations in the EGF-CFC gene cryptic are an infrequent cause of congenital heart disease.

Ozcelik C, Bit-Avragim N, Panek A, Gaio U, Geier C, Lange PE, Dietz R, Posch MG, Perrot A, Stiller B. Ozcelik C, et al. Among authors: posch mg. Pediatr Cardiol. 2006 Nov-Dec;27(6):695-8. doi: 10.1007/s00246-006-1082-0. Epub 2006 Oct 27. Pediatr Cardiol. 2006. PMID: 17072672

9

Beyond the sarcomere: CSRP3 mutations cause hypertrophic cardiomyopathy.

Geier C, Gehmlich K, Ehler E, Hassfeld S, Perrot A, Hayess K, Cardim N, Wenzel K, Erdmann B, Krackhardt F, Posch MG, Osterziel KJ, Bublak A, Nägele H, Scheffold T, Dietz R, Chien KR, Spuler S, Fürst DO, Nürnberg P, Ozcelik C. Geier C, et al. Among authors: posch mg. Hum Mol Genet. 2008 Sep 15;17(18):2753-65. doi: 10.1093/hmg/ddn160. Epub 2008 May 27. Hum Mol Genet. 2008. PMID: 18505755

10

Sequence analysis of myozenin 2 in 438 European patients with familial hypertrophic cardiomyopathy.

Posch MG, Thiemann L, Tomasov P, Veselka J, Cardim N, Garcia-Castro M, Coto E, Perrot A, Geier C, Dietz R, Haverkamp W, Ozcelik C. Posch MG, et al. Med Sci Monit. 2008 Jul;14(7):CR372-4. Med Sci Monit. 2008. PMID: 18591919

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

48 results

Search Page

Filters