Mathieu Lemire

Ontology type: schema:Person     

Person Info





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
  • JSON-LD is the canonical representation for SciGraph data.

    TIP: You can open this SciGraph record using an external JSON-LD service: JSON-LD Playground Google SDTT

        "@context": "", 
        "affiliation": [
            "affiliation": {
              "id": "", 
              "type": "Organization"
            "isCurrent": true, 
            "type": "OrganizationRole"
            "id": "", 
            "type": "Organization"
            "id": "", 
            "type": "Organization"
            "id": "", 
            "type": "Organization"
            "id": "", 
            "type": "Organization"
            "id": "", 
            "type": "Organization"
        "familyName": "Lemire", 
        "givenName": "Mathieu", 
        "id": "sg:person.01125660254.82", 
        "sameAs": [
        "sdDataset": "persons", 
        "sdDatePublished": "2019-03-07T14:58", 
        "sdLicense": "", 
        "sdPublisher": {
          "name": "Springer Nature - SN SciGraph project", 
          "type": "Organization"
        "sdSource": "s3://com-uberresearch-data-dimensions-researchers-20181010/20181011/dim_researchers/base/researchers_673.json", 
        "type": "Person"

    Download the RDF metadata as:  json-ld nt turtle xml License info


    JSON-LD is a popular format for linked data which is fully compatible with JSON.

    curl -H 'Accept: application/ld+json' ''

    N-Triples is a line-based linked data format ideal for batch operations.

    curl -H 'Accept: application/n-triples' ''

    Turtle is a human-readable linked data format.

    curl -H 'Accept: text/turtle' ''

    RDF/XML is a standard XML format for linked data.

    curl -H 'Accept: application/rdf+xml' ''


    This table displays all metadata directly associated to this object as RDF triples.

    26 TRIPLES      10 PREDICATES      16 URIs      7 LITERALS      2 BLANK NODES

    Subject Predicate Object
    1 sg:person.01125660254.82 schema:affiliation N7c72206f69724b128dbaeb5a5bd183bc
    7 schema:familyName Lemire
    8 schema:givenName Mathieu
    9 schema:sameAs
    10 schema:sdDatePublished 2019-03-07T14:58
    11 schema:sdLicense
    12 schema:sdPublisher N861c96006c9f435d99c5847eb5606e21
    13 sgo:license sg:explorer/license/
    14 sgo:sdDataset persons
    15 rdf:type schema:Person
    16 N7c72206f69724b128dbaeb5a5bd183bc schema:affiliation
    17 sgo:isCurrent true
    18 rdf:type schema:OrganizationRole
    19 N861c96006c9f435d99c5847eb5606e21 schema:name Springer Nature - SN SciGraph project
    20 rdf:type schema:Organization
    21 schema:Organization
    22 schema:Organization
    23 schema:Organization
    24 schema:Organization
    25 schema:Organization
    26 schema:Organization

    Preview window. Press ESC to close (or click here)