Canlyniadau Chwilio - Lemire, Mathieu

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

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

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

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Successful identification of rare variants using oligogenic segregation analysis as a prioritizing tool for whole-exome sequencing studies gan Gagnon, France, Roslin, Nicole M, Lemire, Mathieu

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In silico pathway analysis and tissue specific cis-eQTL for colorectal cancer GWAS risk variants gan Loo, Lenora W. M., Lemire, Mathieu, Le Marchand, Loïc

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Using a higher criticism statistic to detect modest effects in a genome-wide study of rheumatoid arthritis gan Parkhomenko, Elena, Tritchler, David, Lemire, Mathieu, Hu, Pingzhao, Beyene, Joseph

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Transmission-Ratio Distortion and Allele Sharing in Affected Sib Pairs: A New Linkage Statistic with Reduced Bias, with Application to Chromosome 6q25.3 gan Lemire, Mathieu, Roslin, Nicole M., Laprise, Catherine, Hudson, Thomas J., Morgan, Kenneth

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Coordinated Conditional Simulation with SLINK and SUP of Many Markers Linked or Associated to a Trait in Large Pedigrees gan Schäffer, Alejandro A., Lemire, Mathieu, Ott, Jürg, Lathrop, G. Mark, Weeks, Daniel E.

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The dynamic DNA methylation landscape of the mutL homolog 1 shore is altered by MLH1-93G>A polymorphism in normal tissues and colorectal cancer gan Savio, Andrea J., Mrkonjic, Miralem, Lemire, Mathieu, Gallinger, Steven, Knight, Julia A., Bapat, Bharat

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Association between Variants in Atopy-Related Immunologic Candidate Genes and Pancreatic Cancer Risk gan Cotterchio, Michelle, Lowcock, Elizabeth, Bider-Canfield, Zoe, Lemire, Mathieu, Greenwood, Celia, Gallinger, Steven, Hudson, Thomas

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MLH1 Region Polymorphisms Show a Significant Association with CpG Island Shore Methylation in a Large Cohort of Healthy Individuals gan Savio, Andrea J., Lemire, Mathieu, Mrkonjic, Miralem, Gallinger, Steven, Zanke, Brent W., Hudson, Thomas J., Bapat, Bharati

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Genetic Variants and Susceptibility to Neurological Complications Following West Nile Virus Infection gan Loeb, Mark, Eskandarian, Sasha, Rupp, Mark, Fishman, Neil, Gasink, Leanne, Patterson, Jan, Bramson, Jonathan, Hudson, Thomas J, Lemire, Mathieu

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Discovery of cross-reactive probes and polymorphic CpGs in the Illumina Infinium HumanMethylation450 microarray gan Chen, Yi-an, Lemire, Mathieu, Choufani, Sanaa, Butcher, Darci T., Grafodatskaya, Daria, Zanke, Brent W., Gallinger, Steven, Hudson, Thomas J., Weksberg, Rosanna

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Influence of leukotriene gene polymorphisms on chronic rhinosinusitis gan Al-Shemari, Hasan, Bossé, Yohan, Hudson, Thomas J, Cabaluna, Myrna, Duval, Melanie, Lemire, Mathieu, Vallee-Smedja, Sophie, Frenkiel, Saul, Desrosiers, Martin

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Functional normalization of 450k methylation array data improves replication in large cancer studies gan Fortin, Jean-Philippe, Labbe, Aurélie, Lemire, Mathieu, Zanke, Brent W, Hudson, Thomas J, Fertig, Elana J, Greenwood, Celia MT, Hansen, Kasper D

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

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SBERIA: Set Based gene EnviRonment InterAction test for rare and common variants in complex diseases gan Jiao, Shuo, Hsu, Li, Bézieau, Stéphane, Brenner, Hermann, Chan, Andrew T., Chang-Claude, Jenny, Le Marchand, Loic, Lemire, Mathieu, Newcomb, Polly A., Slattery, Martha L., Peters, Ulrike

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

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A Common RET Variant Is Associated with Reduced Newborn Kidney Size and Function gan Zhang, Zhao, Quinlan, Jackie, Hoy, Wendy, Hughson, Michael D., Lemire, Mathieu, Hudson, Thomas, Hueber, Pierre-Alain, Benjamin, Alice, Roy, Anne, Pascuet, Elena, Goodyer, Meigan, Raju, Chandhana, Houghton, Fiona, Bertram, John, Goodyer, Paul

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

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