SUP: an extension to SLINK to allow a larger number of marker loci to be simulated in pedigrees conditional on trait values

por Lemire, Mathieu
Publicado 2006

A simple nonparametric multipoint procedure to test for linkage through mothers or fathers as well as imprinting effects in the presence of linkage

por Lemire, Mathieu
Publicado 2005

On the association between rheumatoid arthritis and classical HLA class I and class II alleles predicted from single-nucleotide polymorphism data

por Lemire, Mathieu
Publicado 2009

Successful identification of rare variants using oligogenic segregation analysis as a prioritizing tool for whole-exome sequencing studies

por Gagnon, France, Roslin, Nicole M, Lemire, Mathieu
Publicado 2011

In silico pathway analysis and tissue specific cis-eQTL for colorectal cancer GWAS risk variants

por Loo, Lenora W. M., Lemire, Mathieu, Le Marchand, Loïc
Publicado 2017

Using a higher criticism statistic to detect modest effects in a genome-wide study of rheumatoid arthritis

por Parkhomenko, Elena, Tritchler, David, Lemire, Mathieu, Hu, Pingzhao, Beyene, Joseph
Publicado 2009

The dynamic DNA methylation landscape of the mutL homolog 1 shore is altered by MLH1-93G>A polymorphism in normal tissues and colorectal cancer

por Savio, Andrea J., Mrkonjic, Miralem, Lemire, Mathieu, Gallinger, Steven, Knight, Julia A., Bapat, Bharat
Publicado 2017

Association between Variants in Atopy-Related Immunologic Candidate Genes and Pancreatic Cancer Risk

por Cotterchio, Michelle, Lowcock, Elizabeth, Bider-Canfield, Zoe, Lemire, Mathieu, Greenwood, Celia, Gallinger, Steven, Hudson, Thomas
Publicado 2015

MLH1 Region Polymorphisms Show a Significant Association with CpG Island Shore Methylation in a Large Cohort of Healthy Individuals

por Savio, Andrea J., Lemire, Mathieu, Mrkonjic, Miralem, Gallinger, Steven, Zanke, Brent W., Hudson, Thomas J., Bapat, Bharati
Publicado 2012

Genetic Variants and Susceptibility to Neurological Complications Following West Nile Virus Infection

por Loeb, Mark, Eskandarian, Sasha, Rupp, Mark, Fishman, Neil, Gasink, Leanne, Patterson, Jan, Bramson, Jonathan, Hudson, Thomas J, Lemire, Mathieu
Publicado 2011

Discovery of cross-reactive probes and polymorphic CpGs in the Illumina Infinium HumanMethylation450 microarray

por Chen, Yi-an, Lemire, Mathieu, Choufani, Sanaa, Butcher, Darci T., Grafodatskaya, Daria, Zanke, Brent W., Gallinger, Steven, Hudson, Thomas J., Weksberg, Rosanna
Publicado 2013

Influence of leukotriene gene polymorphisms on chronic rhinosinusitis

por Al-Shemari, Hasan, Bossé, Yohan, Hudson, Thomas J, Cabaluna, Myrna, Duval, Melanie, Lemire, Mathieu, Vallee-Smedja, Sophie, Frenkiel, Saul, Desrosiers, Martin
Publicado 2008

Functional normalization of 450k methylation array data improves replication in large cancer studies

por Fortin, Jean-Philippe, Labbe, Aurélie, Lemire, Mathieu, Zanke, Brent W, Hudson, Thomas J, Fertig, Elana J, Greenwood, Celia MT, Hansen, Kasper D
Publicado 2014

Genes to Diseases (G2D) Computational Method to Identify Asthma Candidate Genes

por Tremblay, Karine, Lemire, Mathieu, Potvin, Camille, Tremblay, Alexandre, Hunninghake, Gary M., Raby, Benjamin A., Hudson, Thomas J., Perez-Iratxeta, Carolina, Andrade-Navarro, Miguel A., Laprise, Catherine
Publicado 2008

Blood triglyceride levels are associated with DNA methylation at the serine metabolism gene PHGDH

por Truong, Vinh, Huang, Siying, Dennis, Jessica, Lemire, Mathieu, Zwingerman, Nora, Aïssi, Dylan, Kassam, Irfahan, Perret, Claire, Wells, Philip, Morange, Pierre-Emmanuel, Wilson, Michael, Trégouët, David-Alexandre, Gagnon, France
Publicado 2017

Shared genetic etiology between obsessive-compulsive disorder, obsessive-compulsive symptoms in the population, and insulin signaling

por Bralten, Janita, Widomska, Joanna, Witte, Ward De, Yu, Dongmei, Mathews, Carol A., Scharf, Jeremiah M., Buitelaar, Jan, Crosbie, Jennifer, Schachar, Russell, Arnold, Paul, Lemire, Mathieu, Burton, Christie L., Franke, Barbara, Poelmans, Geert
Publicado 2020

Asthma and genes encoding components of the vitamin D pathway

por Bossé, Yohan, Lemire, Mathieu, Poon, Audrey H, Daley, Denise, He, Jian-Qing, Sandford, Andrew, White, John H, James, Alan L, Musk, Arthur William, Palmer, Lyle J, Raby, Benjamin A, Weiss, Scott T, Kozyrskyj, Anita L, Becker, Allan, Hudson, Thomas J, Laprise, Catherine
Publicado 2009

Long-range epigenetic regulation is conferred by genetic variation located at thousands of independent loci

por Lemire, Mathieu, Zaidi, Syed H.E., Ban, Maria, Ge, Bing, Aïssi, Dylan, Germain, Marine, Kassam, Irfahan, Wang, Mike, Zanke, Brent W., Gagnon, France, Morange, Pierre-Emmanuel, Trégouët, David-Alexandre, Wells, Philip S., Sawcer, Stephen, Gallinger, Steven, Pastinen, Tomi, Hudson, Thomas J.
Publicado 2015

Obsessive-compulsive disorder and attention-deficit/hyperactivity disorder: distinct associations with DNA methylation and genetic variation

por Goodman, Sarah J., Burton, Christie L., Butcher, Darci T., Siu, Michelle T., Lemire, Mathieu, Chater-Diehl, Eric, Turinsky, Andrei L., Brudno, Michael, Soreni, Noam, Rosenberg, David, Fitzgerald, Kate D., Hanna, Gregory L., Anagnostou, Evdokia, Arnold, Paul D., Crosbie, Jennifer, Schachar, Russell, Weksberg, Rosanna
Publicado 2020

Whole genomes define concordance of matched primary, xenograft, and organoid models of pancreas cancer

por Gendoo, Deena M. A., Denroche, Robert E., Zhang, Amy, Radulovich, Nikolina, Jang, Gun Ho, Lemire, Mathieu, Fischer, Sandra, Chadwick, Dianne, Lungu, Ilinca M., Ibrahimov, Emin, Cao, Ping-Jiang, Stein, Lincoln D., Wilson, Julie M., Bartlett, John M. S., Tsao, Ming-Sound, Dhani, Neesha, Hedley, David, Gallinger, Steven, Haibe-Kains, Benjamin
Publicado 2019