Laprise C - Search Results

1

Mucolipidosis II: a single causal mutation in the N-acetylglucosamine-1-phosphotransferase gene (GNPTAB) in a French Canadian founder population.

Plante M, Claveau S, Lepage P, Lavoie EM, Brunet S, Roquis D, Morin C, Vézina H, Laprise C. Plante M, et al. Among authors: laprise c. Clin Genet. 2008 Mar;73(3):236-44. doi: 10.1111/j.1399-0004.2007.00954.x. Epub 2008 Jan 7. Clin Genet. 2008. PMID: 18190596

2

Genome-wide search for linkage of bipolar affective disorders in a very large pedigree derived from a homogeneous population in quebec points to a locus of major effect on chromosome 12q23-q24.

Morissette J, Villeneuve A, Bordeleau L, Rochette D, Laberge C, Gagné B, Laprise C, Bouchard G, Plante M, Gobeil L, Shink E, Weissenbach J, Barden N. Morissette J, et al. Among authors: laprise c. Am J Med Genet. 1999 Oct 15;88(5):567-87. doi: 10.1002/(sici)1096-8628(19991015)88:5<567::aid-ajmg24>3.0.co;2-8. Am J Med Genet. 1999. PMID: 10490718

3

Association of urokinase-type plasminogen activator with asthma and atopy.

Bégin P, Tremblay K, Daley D, Lemire M, Claveau S, Salesse C, Kacel S, Montpetit A, Becker A, Chan-Yeung M, Kozyrskyj AL, Hudson TJ, Laprise C. Bégin P, et al. Among authors: laprise c. Am J Respir Crit Care Med. 2007 Jun 1;175(11):1109-16. doi: 10.1164/rccm.200607-1012OC. Epub 2007 Mar 15. Am J Respir Crit Care Med. 2007. PMID: 17363771

4

Contribution of hierarchical clustering techniques to the modeling of the geographic distribution of genetic polymorphisms associated with chronic inflammatory diseases in the Québec population.

Madore AM, Houde L, Vézina H, Vohl MC, Pérusse L, Mior N, Connelly PW, Laberge C, Gaudet D, Laprise C. Madore AM, et al. Among authors: laprise c. Community Genet. 2007;10(4):218-26. doi: 10.1159/000106560. Community Genet. 2007. PMID: 17895627

5

Distribution of CFTR mutations in Saguenay- Lac-Saint-Jean: proposal of a panel of mutations for population screening.

Madore AM, Prévost C, Dorfman R, Taylor C, Durie P, Zielenski J, Laprise C. Madore AM, et al. Among authors: laprise c. Genet Med. 2008 Mar;10(3):201-6. doi: 10.1097/GIM.0b013e318164cb1c. Genet Med. 2008. PMID: 18344710 Free article.

6

Origin and spread of a common deletion causing mucolipidosis type II: insights from patterns of haplotypic diversity.

Coutinho MF, Encarnação M, Gomes R, da Silva Santos L, Martins S, Sirois-Gagnon D, Bargal R, Filocamo M, Raas-Rothschild A, Tappino B, Laprise C, Cury GK, Schwartz IV, Artigalás O, Prata MJ, Alves S. Coutinho MF, et al. Among authors: laprise c. Clin Genet. 2011 Sep;80(3):273-80. doi: 10.1111/j.1399-0004.2010.01539.x. Epub 2010 Sep 29. Clin Genet. 2011. PMID: 20880125

7

Genomic and genealogical investigation of the French Canadian founder population structure.

Roy-Gagnon MH, Moreau C, Bherer C, St-Onge P, Sinnett D, Laprise C, Vézina H, Labuda D. Roy-Gagnon MH, et al. Among authors: laprise c. Hum Genet. 2011 May;129(5):521-31. doi: 10.1007/s00439-010-0945-x. Epub 2011 Jan 15. Hum Genet. 2011. PMID: 21234765

8

Expression signature of epidermolysis bullosa simplex.

Bchetnia M, Tremblay ML, Leclerc G, Dupérée A, Powell J, McCuaig C, Morin C, Legendre-Guillemin V, Laprise C. Bchetnia M, et al. Among authors: laprise c. Hum Genet. 2012 Mar;131(3):393-406. doi: 10.1007/s00439-011-1077-7. Epub 2011 Aug 30. Hum Genet. 2012. PMID: 21877134

9

Genome-wide patterns of identity-by-descent sharing in the French Canadian founder population.

Gauvin H, Moreau C, Lefebvre JF, Laprise C, Vézina H, Labuda D, Roy-Gagnon MH. Gauvin H, et al. Among authors: laprise c. Eur J Hum Genet. 2014 Jun;22(6):814-21. doi: 10.1038/ejhg.2013.227. Epub 2013 Oct 16. Eur J Hum Genet. 2014. PMID: 24129432 Free PMC article.

10

Reduction in keratin aggregates in epidermolysis bullosa simplex keratinocytes after pretreatment with trimethylamine N-oxide.

Bchetnia M, Lacroix J, Farez T, Larouche M, Powell J, McCuaig C, Dupéré A, Morin C, Legendre-Guillemin V, Laprise C. Bchetnia M, et al. Among authors: laprise c. Exp Dermatol. 2016 Mar;25(3):229-30. doi: 10.1111/exd.12821. Epub 2015 Sep 15. Exp Dermatol. 2016. PMID: 26264477 No abstract available.

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