Andelfinger G - Search Results

1

Rare copy number variants contribute to congenital left-sided heart disease.

Hitz MP, Lemieux-Perreault LP, Marshall C, Feroz-Zada Y, Davies R, Yang SW, Lionel AC, D'Amours G, Lemyre E, Cullum R, Bigras JL, Thibeault M, Chetaille P, Montpetit A, Khairy P, Overduin B, Klaassen S, Hoodless P, Awadalla P, Hussin J, Idaghdour Y, Nemer M, Stewart AF, Boerkoel C, Scherer SW, Richter A, Dubé MP, Andelfinger G. Hitz MP, et al. Among authors: andelfinger g. PLoS Genet. 2012 Sep;8(9):e1002903. doi: 10.1371/journal.pgen.1002903. Epub 2012 Sep 6. PLoS Genet. 2012. PMID: 22969434 Free PMC article.

2

The Kruppel-like transcription factor KLF13 is a novel regulator of heart development.

Lavallée G, Andelfinger G, Nadeau M, Lefebvre C, Nemer G, Horb ME, Nemer M. Lavallée G, et al. Among authors: andelfinger g. EMBO J. 2006 Nov 1;25(21):5201-13. doi: 10.1038/sj.emboj.7601379. Epub 2006 Oct 19. EMBO J. 2006. PMID: 17053787 Free PMC article.

3

Catch me if you can: tracking down the genetic origins of congenital heart disease.

Lemyre E, Andelfinger G. Lemyre E, et al. Among authors: andelfinger g. Eur Heart J. 2007 Nov;28(22):2701-2. doi: 10.1093/eurheartj/ehm479. Epub 2007 Oct 25. Eur Heart J. 2007. PMID: 17965008 No abstract available.

4

Genetic factors in congenital heart malformation.

Andelfinger G. Andelfinger G. Clin Genet. 2008 Jun;73(6):516-27. doi: 10.1111/j.1399-0004.2008.01009.x. Epub 2008 May 6. Clin Genet. 2008. PMID: 18462450 Review.

5

The MTHFD1 p.Arg653Gln variant alters enzyme function and increases risk for congenital heart defects.

Christensen KE, Rohlicek CV, Andelfinger GU, Michaud J, Bigras JL, Richter A, Mackenzie RE, Rozen R. Christensen KE, et al. Hum Mutat. 2009 Feb;30(2):212-20. doi: 10.1002/humu.20830. Hum Mutat. 2009. PMID: 18767138

6

Severe left ventricular dysfunction in infants with ventricular preexcitation.

Cadrin-Tourigny J, Fournier A, Andelfinger G, Khairy P. Cadrin-Tourigny J, et al. Among authors: andelfinger g. Heart Rhythm. 2008 Sep;5(9):1320-2. doi: 10.1016/j.hrthm.2008.05.022. Epub 2008 Aug 3. Heart Rhythm. 2008. PMID: 18774110 No abstract available.

7

Partitioning of copy-number genotypes in pedigrees.

Perreault LP, Andelfinger GU, Asselin G, Dubé MP. Perreault LP, et al. Among authors: andelfinger gu. BMC Bioinformatics. 2010 May 3;11:226. doi: 10.1186/1471-2105-11-226. BMC Bioinformatics. 2010. PMID: 20438641 Free PMC article.

8

Ventricular septal defect and restrictive cardiomyopathy in a paediatric TNNI3 mutation carrier.

Yang SW, Hitz MP, Andelfinger G. Yang SW, et al. Among authors: andelfinger g. Cardiol Young. 2010 Oct;20(5):574-6. doi: 10.1017/S1047951110000715. Epub 2010 Jun 23. Cardiol Young. 2010. PMID: 20569525

9

An endocardial pathway involving Tbx5, Gata4, and Nos3 required for atrial septum formation.

Nadeau M, Georges RO, Laforest B, Yamak A, Lefebvre C, Beauregard J, Paradis P, Bruneau BG, Andelfinger G, Nemer M. Nadeau M, et al. Among authors: andelfinger g. Proc Natl Acad Sci U S A. 2010 Nov 9;107(45):19356-61. doi: 10.1073/pnas.0914888107. Epub 2010 Oct 25. Proc Natl Acad Sci U S A. 2010. PMID: 20974940 Free PMC article.

10

Familial ventricular aneurysms and septal defects map to chromosome 10p15.

Tremblay N, Yang SW, Hitz MP, Asselin G, Ginns J, Riopel K, Gendron R, Montpetit A, Duhig E, Dubé MP, Radford D, Andelfinger G. Tremblay N, et al. Among authors: andelfinger g. Eur Heart J. 2011 Mar;32(5):568-73. doi: 10.1093/eurheartj/ehq447. Epub 2010 Dec 18. Eur Heart J. 2011. PMID: 21169613

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