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Page 1
Mutations in DCC cause congenital mirror movements.
Srour M, Rivière JB, Pham JM, Dubé MP, Girard S, Morin S, Dion PA, Asselin G, Rochefort D, Hince P, Diab S, Sharafaddinzadeh N, Chouinard S, Théoret H, Charron F, Rouleau GA. Srour M, et al. Among authors: asselin g. Science. 2010 Apr 30;328(5978):592. doi: 10.1126/science.1186463. Science. 2010. PMID: 20431009
Partitioning of copy-number genotypes in pedigrees.
Perreault LP, Andelfinger GU, Asselin G, Dubé MP. Perreault LP, et al. Among authors: asselin g. BMC Bioinformatics. 2010 May 3;11:226. doi: 10.1186/1471-2105-11-226. BMC Bioinformatics. 2010. PMID: 20438641 Free PMC article.
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: asselin 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
Mutations in a novel serine protease PRSS56 in families with nanophthalmos.
Orr A, Dubé MP, Zenteno JC, Jiang H, Asselin G, Evans SC, Caqueret A, Lakosha H, Letourneau L, Marcadier J, Matsuoka M, Macgillivray C, Nightingale M, Papillon-Cavanagh S, Perry S, Provost S, Ludman M, Guernsey DL, Samuels ME. Orr A, et al. Among authors: asselin g. Mol Vis. 2011;17:1850-61. Epub 2011 Jul 12. Mol Vis. 2011. PMID: 21850159 Free PMC article.
Identification of the genetic determinants responsible for retinal degeneration in families of Mexican descent.
Villanueva A, Biswas P, Kishaba K, Suk J, Tadimeti K, Raghavendra PB, Nadeau K, Lamontagne B, Busque L, Geoffroy S, Mongrain I, Asselin G, Provost S, Dubé MP, Nudleman E, Ayyagari R. Villanueva A, et al. Among authors: asselin g. Ophthalmic Genet. 2018 Jan-Feb;39(1):73-79. doi: 10.1080/13816810.2017.1373830. Epub 2017 Sep 25. Ophthalmic Genet. 2018. PMID: 28945494 Free PMC article.
CKM and LILRB5 are associated with serum levels of creatine kinase.
Dubé MP, Zetler R, Barhdadi A, Brown AM, Mongrain I, Normand V, Laplante N, Asselin G, Zada YF, Provost S, Bergeron J, Kouz S, Dufour R, Diaz A, de Denus S, Turgeon J, Rhéaume E, Phillips MS, Tardif JC. Dubé MP, et al. Among authors: asselin g. Circ Cardiovasc Genet. 2014 Dec;7(6):880-6. doi: 10.1161/CIRCGENETICS.113.000395. Epub 2014 Sep 11. Circ Cardiovasc Genet. 2014. PMID: 25214527
Pharmacogenomic determinants of the cardiovascular effects of dalcetrapib.
Tardif JC, Rhéaume E, Lemieux Perreault LP, Grégoire JC, Feroz Zada Y, Asselin G, Provost S, Barhdadi A, Rhainds D, L'Allier PL, Ibrahim R, Upmanyu R, Niesor EJ, Benghozi R, Suchankova G, Laghrissi-Thode F, Guertin MC, Olsson AG, Mongrain I, Schwartz GG, Dubé MP. Tardif JC, et al. Among authors: asselin g. Circ Cardiovasc Genet. 2015 Apr;8(2):372-82. doi: 10.1161/CIRCGENETICS.114.000663. Epub 2015 Jan 11. Circ Cardiovasc Genet. 2015. PMID: 25583994 Clinical Trial.
35 results