Mathieu Lemire


Ontology type: schema:Person     


Person Info

NAME

Mathieu

SURNAME

Lemire

Publications in SciGraph latest 50 shown

  • 2019-01 Discovery of common and rare genetic risk variants for colorectal cancer in NATURE GENETICS
  • 2018-06 Mendelian randomisation study of age at menarche and age at menopause and the risk of colorectal cancer in BRITISH JOURNAL OF CANCER
  • 2017-12 Blood triglyceride levels are associated with DNA methylation at the serine metabolism gene PHGDH in SCIENTIFIC REPORTS
  • 2017-12 In silico pathway analysis and tissue specific cis-eQTL for colorectal cancer GWAS risk variants in BMC GENOMICS
  • 2017-12 The dynamic DNA methylation landscape of the mutL homolog 1 shore is altered by MLH1-93G>A polymorphism in normal tissues and colorectal cancer in CLINICAL EPIGENETICS
  • 2017-01 Disease variants alter transcription factor levels and methylation of their binding sites in NATURE GENETICS
  • 2016-10 A renewed model of pancreatic cancer evolution based on genomic rearrangement patterns in NATURE
  • 2016-05 Analysis of 589,306 genomes identifies individuals resilient to severe Mendelian childhood diseases in NATURE BIOTECHNOLOGY
  • 2016-01 CYP24A1 variant modifies the association between use of oestrogen plus progestogen therapy and colorectal cancer risk in BRITISH JOURNAL OF CANCER
  • 2015-12 Genome-wide association study of colorectal cancer identifies six new susceptibility loci in NATURE COMMUNICATIONS
  • 2015-12 Long-range epigenetic regulation is conferred by genetic variation located at thousands of independent loci in NATURE COMMUNICATIONS
  • 2015-11 A genome-wide association study for colorectal cancer identifies a risk locus in 14q23.1 in HUMAN GENETICS
  • 2014-12 Trans-ethnic genome-wide association study of colorectal cancer identifies a new susceptibility locus in VTI1A in NATURE COMMUNICATIONS
  • 2014-11 Functional normalization of 450k methylation array data improves replication in large cancer studies in GENOME BIOLOGY
  • 2012-02 Meta-analysis of new genome-wide association studies of colorectal cancer risk in HUMAN GENETICS
  • 2011-12 Successful identification of rare variants using oligogenic segregation analysis as a prioritizing tool for whole-exome sequencing studies in BMC PROCEEDINGS
  • 2011-05 Defining rare variants by their frequencies in controls may increase type I error in NATURE GENETICS
  • 2010-03 Fine mapping and association studies of a high-density lipoprotein cholesterol linkage region on chromosome 16 in French-Canadian subjects in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2009-12 On the association between rheumatoid arthritis and classical HLA class I and class II alleles predicted from single-nucleotide polymorphism data in BMC PROCEEDINGS
  • 2009-12 Using a higher criticism statistic to detect modest effects in a genome-wide study of rheumatoid arthritis in BMC PROCEEDINGS
  • 2009-12 Asthma and genes encoding components of the vitamin D pathway in RESPIRATORY RESEARCH
  • 2009-06 Common variants of the glial cell-derived neurotrophic factor gene do not influence kidney size of the healthy newborn in PEDIATRIC NEPHROLOGY
  • 2009-05 Analyses of associations with asthma in four asthma population samples from Canada and Australia in HUMAN GENETICS
  • 2009-01 Common variants in the NLRP3 region contribute to Crohn's disease susceptibility in NATURE GENETICS
  • 2008-12 Influence of leukotriene gene polymorphisms on chronic rhinosinusitis in BMC MEDICAL GENETICS
  • 2008-01 Identification of a chromosome 8p locus for early-onset coronary heart disease in a French Canadian population in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2006-12 SUP: an extension to SLINK to allow a larger number of marker loci to be simulated in pedigrees conditional on trait values in BMC GENETICS
  • 2006-12 Association study between the CX3CR1 gene and asthma in GENES & IMMUNITY
  • 2005-12 A simple nonparametric multipoint procedure to test for linkage through mothers or fathers as well as imprinting effects in the presence of linkage in BMC GENETICS
  • 2005-09 NRAMP1 is not associated with asthma, atopy, and serum immunoglobulin E levels in the French Canadian population in GENES & IMMUNITY
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