Fabienne Lesueur


Ontology type: schema:Person     


Person Info

NAME

Fabienne

SURNAME

Lesueur

Publications in SciGraph latest 50 shown

  • 2018-12 Morphology and genomic hallmarks of breast tumours developed by ATM deleterious variant carriers in BREAST CANCER RESEARCH
  • 2017-12 Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer in NATURE GENETICS
  • 2017-12 Investigation of DNA repair-related SNPs underlying susceptibility to papillary thyroid carcinoma reveals MGMT as a novel candidate gene in Belarusian children exposed to radiation in BMC CANCER
  • 2017-05-02 Functional characterization of a multi-cancer risk locus on chr5p15.33 reveals regulation of TERT by ZNF148 in NATURE COMMUNICATIONS
  • 2017-05 Identification of 12 new susceptibility loci for different histotypes of epithelial ovarian cancer in NATURE GENETICS
  • 2017-01 Association of breast cancer risk in BRCA1 and BRCA2 mutation carriers with genetic variants showing differential allelic expression: identification of a modifier of breast cancer risk at locus 11q22.3 in BREAST CANCER RESEARCH AND TREATMENT
  • 2016-12 GENESIS: a French national resource to study the missing heritability of breast cancer in BMC CANCER
  • 2016-12 Identification of independent association signals and putative functional variants for breast cancer risk through fine-scale mapping of the 12p11 locus in BREAST CANCER RESEARCH
  • 2016-09-07 Functional mechanisms underlying pleiotropic risk alleles at the 19p13.1 breast–ovarian cancer susceptibility locus in NATURE COMMUNICATIONS
  • 2016-03 Corrigendum: A SUMOylation-defective MITF germline mutation predisposes to melanoma and renal carcinoma in NATURE
  • 2015-12 Common variants at the 9q22.33, 14q13.3 and ATM loci, and risk of differentiated thyroid cancer in the Cuban population in BMC GENETICS
  • 2015-06 Breast Cancer Risk Gene Discovery: Opportunities and Challenges in CURRENT GENETIC MEDICINE REPORTS
  • 2014-06 Rare key functional domain missense substitutions in MRE11A, RAD50, and NBNcontribute to breast cancer susceptibility: results from a Breast Cancer Family Registry case-control mutation-screening study in BREAST CANCER RESEARCH
  • 2013-06 COMPLEXO: identifying the missing heritability of breast cancer via next generation collaboration in BREAST CANCER RESEARCH
  • 2013-03 Polymorphisms in regulators of xenobiotic transport and metabolism genes PXR and CAR do not affect multiple myeloma risk: a case–control study in the context of the IMMEnSE consortium in JOURNAL OF HUMAN GENETICS
  • 2012-12 Identification of new breast cancer predisposition genes via whole exome sequencing in HEREDITARY CANCER IN CLINICAL PRACTICE
  • 2011-12 Detecting differential allelic expression using high-resolution melting curve analysis: application to the breast cancer susceptibility gene CHEK2 in BMC MEDICAL GENOMICS
  • 2011-10-19 A SUMOylation-defective MITF germline mutation predisposes to melanoma and renal carcinoma in NATURE
  • 2011-02 Rare, evolutionarily unlikely missense substitutions in CHEK2contribute to breast cancer susceptibility: results from a breast cancer family registry case-control mutation-screening study in BREAST CANCER RESEARCH
  • 2009-12 Determining the effectiveness of High Resolution Melting analysis for SNP genotyping and mutation scanning at the TP53 locus in BMC GENETICS
  • 2009-12 Protective effect of copy number polymorphism of glutathione S-transferase T1 gene on melanoma risk in presence of CDKN2A mutations, MC1R variants and host-related phenotypes in FAMILIAL CANCER
  • 2009-11 An Association Study of 22 Candidate Genes in Psoriasis Families Reveals Shared Genetic Factors with Other Autoimmune and Skin Disorders in JOURNAL OF INVESTIGATIVE DERMATOLOGY
  • 2008-07 The contribution of large genomic deletions at the CDKN2A locus to the burden of familial melanoma in BRITISH JOURNAL OF CANCER
  • 2008-06 Effects of common germline genetic variation in cell cycle control genes on breast cancer survival: results from a population-based cohort in BREAST CANCER RESEARCH
  • 2007-06 Confirmation of Psoriasis Susceptibility Loci on Chromosome 6p21 and 20p13 in French Families in JOURNAL OF INVESTIGATIVE DERMATOLOGY
  • 2007-04 Novel Mutations in ALOX12B in Patients with Autosomal Recessive Congenital Ichthyosis and Evidence for Genetic Heterogeneity on Chromosome 17p13 in JOURNAL OF INVESTIGATIVE DERMATOLOGY
  • 2006-12 HapMap-based study of the 17q21 ERBB2 amplicon in susceptibility to breast cancer in BRITISH JOURNAL OF CANCER
  • 2006-06 Single-nucleotide polymorphisms in the RB1 gene and association with breast cancer in the British population in BRITISH JOURNAL OF CANCER
  • 2005-12 Common variation in EMSYand risk of breast and ovarian cancer: a case-control study using HapMap tagging SNPs in BMC CANCER
  • 2005-10 Sipa1 is a candidate for underlying the metastasis efficiency modifier locus Mtes1 in NATURE GENETICS
  • 2005-06 The search for low-penetrance breast cancer genes in BREAST CANCER RESEARCH
  • 2005-04 Common ERBB2 polymorphisms and risk of breast cancer in a white British population: a case–control study in BREAST CANCER RESEARCH
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