Genotyping Platform

Serre D, Hudson TJ. Resources for Genetic Variation Studies.Annu Rev Genomics Hum Genet. 2006 Jun 7.

Saarela J, Kallio SP, Chen D, Montpetit A, Jokiaho A, Choi E, Asselta R, Bronnikov D, Lincoln MR, Sadovnick AD, Tienari PJ, Koivisto K, Palotie A, Ebers GC, Hudson TJ, Peltonen L. PRKCA and multiple sclerosis: association in two independent populations. PLoS Genet. 2006 Mar;2(3):e42.

Montpetit A, Nelis M, Laflamme P, Magi R, Ke X, Remm M, Cardon L, Hudson TJ, Metspalu A. An evaluation of the performance of tag SNPs derived from HapMap in a Caucasian population. PLoS Genet. 2006 Mar;2(3):e27.

Tessier MC, Qu HQ, Frechette R, Bacot F, Grabs R, Taback SP, Lawson ML, Kirsch SE, Hudson TJ, Polychronakos C. Type 1 diabetes and the OAS gene cluster: association with splicing polymorphism or haplotype? J Med Genet. 2006 Feb;43(2):129-32.

Serre D, Nadon R, Hudson TJ. Large-scale recombination rate patterns are conserved among human populations. Genome Res. 2005 Nov;15(11):1547-52.

International HapMap Consortium (A. Montpetit, T. J. Hudson, F. Chagnon, V. Ferretti, M. Leboeuf, M. S. Phillips and A. Verner as co-authors and members of the Canadian group). A haplotype map of the human genome. Nature. 2005 Oct 27;437(7063):1299-320.

Lincoln MR, Montpetit A, Cader MZ, Saarela J, Dyment DA, Tiislar M, Ferretti V, Tienari PJ, Sadovnick AD, Peltonen L, Ebers GC, Hudson TJ. A predominant role for the HLA class II region in the association of the MHC region with multiple sclerosis. Nat Genet. 2005 Oct;37(10):1108-12.

Poon AH, Laprise C, Lemire M, Hudson TJ, Schurr E. NRAMP1 is not associated with asthma, atopy, and serum immunoglobulin E levels in the French Canadian population. Genes Immun. 2005 Sep;6(6):519-27.

Qu H, Tessier MC, Hudson TJ, Polychronakos C. Confirmation of the association of the R620W polymorphism in the protein tyrosine phosphatase PTPN22 with type 1 diabetes in a family based study. J Med Genet. 2005 Mar;42(3):266-70.

Saba TG, Montpetit A, Verner A, Rioux P, Hudson TJ, Drouin R, Drouin CA. An atypical form of erythrokeratodermia variabilis maps to chromosome 7q22. Hum Genet. 2005 Feb;116(3):167-71.

Lemire M, Roslin NM, Laprise C, Hudson TJ, Morgan K. Transmission-ratio distortion and allele sharing in affected sib pairs: a new linkage statistic with reduced bias, with application to chromosome 6q25.3. Am J Hum Genet. 2004 Oct;75(4):571-86.

Poon AH, Laprise C, Lemire M, Montpetit A, Sinnett D, Schurr E, Hudson TJ. Association of vitamin D receptor genetic variants with susceptibility to asthma and atopy. Am J Respir Crit Care Med. 2004 Nov 1;170(9):967-73.

Laitinen T, Polvi A, Rydman P, Vendelin J, Pulkkinen V, Salmikangas P, Makela S, Rehn M, Pirskanen A, Rautanen A, Zucchelli M, Gullsten H, Leino M, Alenius H, Petays T, Haahtela T, Laitinen A, Laprise C, Hudson TJ, Laitinen LA, Kere J. Characterization of a common susceptibility locus for asthma-related traits. Science. 2004 Apr 9;304(5668):300-4.

M. T. Mira, A. Alcaïs, N. V. Thuc, M. O. Moraes, C. Di Flumeri, V. H. Thai, M. C. Phuong, N. T. Huong, N. Ngoc Ba, E.N. Sarno, A. Alter, A. Montpetit, M. E. Moraes, J. R. Moraes, C. Doré, C. J. Gallant, P. Lepage, A. Verner, E. Van de Vosse, T. J. Hudson, L. Abel, E. Schurr (2004) The 5-prime regulatory region shared by the PARK2 and PACRG genes is associated with susceptibility to leprosy. Nature 2004 427(6975): 636-640

M.-T. Berthier, P. Couture, A. Houde, A.-M. Paradis, A. Sammak, A. Verner, J.-P. Deprés, C. Gagné, D. Gaudet, and M.-C. Vohl. The c. 419-420insA in the MTP gene is associated with abetalipoproteinemia among French-Canadians. Molecular Genetics and Metabolism 2004 81(2): 140-143.

C. N. Pato, M. T. Pato, A. Kirby, T. L. Petryshen , H. Medeiros, C. Carvalho, A. Madeco, A. Dourado, I. Coelho, J. Valente, M. J. Soares, C. P. Ferreira, M. Lei, A. Verner, T. J. Hudson, C. P. Morley, J. L. Kennedy, M. H. Azevedo, M. J. Daly, P. Sklar. Genome-wide scan in Portuguese Island families implicates multiple loci in bipolar disorder: fine mapping adds support on chromosomes 6 and 11. American Journal of Medical Genetics 2004 May 15, 127B(1):30-34.

P. Sklar, M.T. Pato, A. Kirby, T.L. Petryshen, H. Medeiros, C. Carvalho, A. Macedo, A. Dourado, I. CoelhoI, J. Valente, M.J. Soares, C.P. Ferreira, M. Lei, A. Verner, T.J. Hudson, C.P. Morley, J.L. Kennedy, M.H. Azevedo, E. Lander, M.J. Daly, C.N. Pato. Genome-Wide Scan in Portuguese Island Families Identifies 5q31-5q35 as a Susceptibility Locus for Schizophrenia and Psychosis. Molecular Psychiatry 2004 9(2): 213-218.

The International HapMap Consortium (A. Montpetit, T. J. Hudson, F. Chagnon, V. Ferretti, M. Leboeuf, M. S. Phillips and A. Verner as co-authors and members of the Canadian group.) The International HapMap Project. Nature 2003 426(6998): 789-79.

M.T. Mira, A, Alcais, N,Van Thuc, V.H, Thai, N.T, Huong, N.N, Ba A. Verner, T.J. Hudson, L. Abel, E. Schurr. Chromosome 6q25 is linked to susceptibility to leprosy in a Vietnamese population. Nature Genetics 2003 33(3): 412-415.