Søgeresultater - Lemire, Mathieu

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  1. 1
    SUP: an extension to SLINK to allow a larger number of marker loci to be simulated in pedigrees conditional on trait values

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

    Udgivet 2006
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  2. 2
    A simple nonparametric multipoint procedure to test for linkage through mothers or fathers as well as imprinting effects in the presence of linkage

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

    Udgivet 2005
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  3. 3
    On the association between rheumatoid arthritis and classical HLA class I and class II alleles predicted from single-nucleotide polymorphism data

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

    Udgivet 2009
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  4. 4
    Successful identification of rare variants using oligogenic segregation analysis as a prioritizing tool for whole-exome sequencing studies

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

    Udgivet 2011
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  5. 5
    In silico pathway analysis and tissue specific cis-eQTL for colorectal cancer GWAS risk variants

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

    Udgivet 2017
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  6. 6
    Using a higher criticism statistic to detect modest effects in a genome-wide study of rheumatoid arthritis

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

    Udgivet 2009
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  7. 7
    Transmission-Ratio Distortion and Allele Sharing in Affected Sib Pairs: A New Linkage Statistic with Reduced Bias, with Application to Chromosome 6q25.3

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

    Udgivet 2004
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  8. 8
    Coordinated Conditional Simulation with SLINK and SUP of Many Markers Linked or Associated to a Trait in Large Pedigrees

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

    Udgivet 2011
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  9. 9
    The dynamic DNA methylation landscape of the mutL homolog 1 shore is altered by MLH1-93G>A polymorphism in normal tissues and colorectal cancer

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

    Udgivet 2017
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  10. 10
    Association between Variants in Atopy-Related Immunologic Candidate Genes and Pancreatic Cancer Risk

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

    Udgivet 2015
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  11. 11
    MLH1 Region Polymorphisms Show a Significant Association with CpG Island Shore Methylation in a Large Cohort of Healthy Individuals

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

    Udgivet 2012
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  12. 12
    Genetic Variants and Susceptibility to Neurological Complications Following West Nile Virus Infection

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

    Udgivet 2011
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  13. 13
    Discovery of cross-reactive probes and polymorphic CpGs in the Illumina Infinium HumanMethylation450 microarray

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

    Udgivet 2013
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  14. 14
    Influence of leukotriene gene polymorphisms on chronic rhinosinusitis

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

    Udgivet 2008
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  15. 15
    Functional normalization of 450k methylation array data improves replication in large cancer studies

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

    Udgivet 2014
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  16. 16
    Genes to Diseases (G2D) Computational Method to Identify Asthma Candidate Genes

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

    Udgivet 2008
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  17. 17
    SBERIA: Set Based gene EnviRonment InterAction test for rare and common variants in complex diseases

    SBERIA: Set Based gene EnviRonment InterAction test for rare and common variants in complex diseases af 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

    Udgivet 2013
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  18. 18
    Blood triglyceride levels are associated with DNA methylation at the serine metabolism gene PHGDH

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

    Udgivet 2017
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  19. 19
    A Common RET Variant Is Associated with Reduced Newborn Kidney Size and Function

    A Common RET Variant Is Associated with Reduced Newborn Kidney Size and Function af 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

    Udgivet 2008
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  20. 20
    Shared genetic etiology between obsessive-compulsive disorder, obsessive-compulsive symptoms in the population, and insulin signaling

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

    Udgivet 2020
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