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Chimeric EWSR1-FLI1 regulates the Ewing sarcoma susceptibility gene EGR2 via a GGAA microsatelliteAnalysis of heritability and shared heritability based on genome-wide association studies for thirteen cancer typesCloning of the SCA7 gene reveals a highly unstable CAG repeat expansionCloning of the gene for spinocerebellar ataxia 2 reveals a locus with high sensitivity to expanded CAG/glutamine repeatsClose associations between prevalences of dominantly inherited spinocerebellar ataxias with CAG-repeat expansions and frequencies of large normal CAG alleles in Japanese and Caucasian populationsA candidate gene approach within the susceptibility region PCaP on 1q42.2-43 excludes deleterious mutations of the PCTA-1 gene to be responsible for hereditary prostate cancerGenome-wide association study identifies multiple loci associated with bladder cancer riskGenome-wide interaction study of smoking and bladder cancer riskA multi-stage genome-wide association study of bladder cancer identifies multiple susceptibility lociMultiple loci identified in a genome-wide association study of prostate cancer[CCAFU french national guidelines 2016-2018 on prostate cancer].Characterisation of the unstable expanded CAG repeat in the MJD1 gene in four Brazilian families of Portuguese descent with Machado-Joseph diseaseGenome-wide association study identifies multiple risk loci for renal cell carcinoma.Refining the prostate cancer genetic association within the JAZF1 gene on chromosome 7p15.2.Analysis of Xq27-28 linkage in the international consortium for prostate cancer genetics (ICPCG) families.Olfactory detection of prostate cancer by dogs sniffing urine: a step forward in early diagnosis.Large-scale exploration of gene-gene interactions in prostate cancer using a multistage genome-wide association study.Region 2 of 8q24 is associated with the risk of aggressive prostate cancer in Caribbean men of African descent from Guadeloupe (French West Indies)Fine mapping the KLK3 locus on chromosome 19q13.33 associated with prostate cancer susceptibility and PSA levels.Impact of genotyping on outcome of prostatic biopsies: a multicenter prospective study.Fine mapping of a region of chromosome 11q13 reveals multiple independent loci associated with risk of prostate cancer.Large-scale fine mapping of the HNF1B locus and prostate cancer riskTwo susceptibility loci identified for prostate cancer aggressiveness.Application of a novel score test for genetic association incorporating gene-gene interaction suggests functionality for prostate cancer susceptibility regions.A genome-wide association study identifies a novel susceptibility locus for renal cell carcinoma on 12p11.23Y chromosome haplogroups and prostate cancer in populations of European and Ashkenazi Jewish ancestryAssociations of prostate cancer risk variants with disease aggressiveness: results of the NCI-SPORE Genetics Working Group analysis of 18,343 cases.Identification of a new prostate cancer susceptibility locus on chromosome 8q24.Prostate cancer genetics.Genetic susceptibility to prostate cancer.HOXB13 is a susceptibility gene for prostate cancer: results from the International Consortium for Prostate Cancer Genetics (ICPCG).Validation of prostate cancer risk-related loci identified from genome-wide association studies using family-based association analysis: evidence from the International Consortium for Prostate Cancer Genetics (ICPCG)Low penetrance genetic susceptibility to kidney cancer.Chromosomes 4 and 8 implicated in a genome wide SNP linkage scan of 762 prostate cancer families collected by the ICPCGIdentification of a novel susceptibility locus at 13q34 and refinement of the 20p12.2 region as a multi-signal locus associated with bladder cancer risk in individuals of European ancestry.Fine mapping and functional analysis of a common variant in MSMB on chromosome 10q11.2 associated with prostate cancer susceptibility.REVEL: An Ensemble Method for Predicting the Pathogenicity of Rare Missense Variants.Association analysis of 9,560 prostate cancer cases from the International Consortium of Prostate Cancer Genetics confirms the role of reported prostate cancer associated SNPs for familial disease.Detection of specific chromosomal aberrations in urine using BCA-1 (oligo-CGH-array) enhances diagnostic sensitivity and predicts the aggressiveness of non-muscle-invasive bladder transitional cell carcinoma.Genetic pathways involved in carcinogenesis of clear cell renal cell carcinoma: genomics towards personalized medicine.
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P50
description
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onderzoeker
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հետազոտող
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Geraldine Cancel-Tassin
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Geraldine Cancel-Tassin
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Geraldine Cancel-Tassin
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Geraldine Cancel-Tassin
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Geraldine Cancel-Tassin
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Geraldine Cancel-Tassin
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Geraldine Cancel-Tassin
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Geraldine Cancel-Tassin
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Geraldine Cancel-Tassin
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Geraldine Cancel-Tassin
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Cancel-Tassin G
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Geraldine Cancel
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Géraldine Cancel-Tassin
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Geraldine Cancel-Tassin
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Geraldine Cancel-Tassin
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Geraldine Cancel-Tassin
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Geraldine Cancel-Tassin
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Geraldine Cancel-Tassin
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P106
P21
P31
P496
0000-0002-9583-6382