about
COL11A1 in FAP polyps and in sporadic colorectal tumorsA widely expressed transcription factor with multiple DNA sequence specificity, CTCF, is localized at chromosome segment 16q22.1 within one of the smallest regions of overlap for common deletions in breast and prostate cancersNew common variants affecting susceptibility to basal cell carcinomaRevised Bethesda Guidelines for hereditary nonpolyposis colorectal cancer (Lynch syndrome) and microsatellite instabilityGenome-wide association studies identify four ER negative-specific breast cancer risk lociDifferential expression of aquaporin 8 in human colonic epithelial cells and colorectal tumorsThe clinical phenotype of Lynch syndrome due to germ-line PMS2 mutationsA screen for germline mutations in the gene encoding CCCTC-binding factor (CTCF) in familial non-BRCA1/BRCA2 breast cancerLow frequency of E-cadherin alterations in familial breast cancerNo mutations in the BACH1 gene in BRCA1 and BRCA2 negative breast-cancer families linked to 17q22Tumor-associated zinc finger mutations in the CTCF transcription factor selectively alter tts DNA-binding specificityMutation analysis of the DBC2 gene in sporadic and familial breast cancerCandidate locus analysis of the TERT-CLPTM1L cancer risk region on chromosome 5p15 identifies multiple independent variants associated with endometrial cancer riskGenome-Wide Meta-Analyses of Breast, Ovarian, and Prostate Cancer Association Studies Identify Multiple New Susceptibility Loci Shared by at Least Two Cancer TypesPALB2, CHEK2 and ATM rare variants and cancer risk: data from COGSLarge-scale genotyping identifies 41 new loci associated with breast cancer risk.Common variation near CDKN1A, POLD3 and SHROOM2 influences colorectal cancer risk.Genetically Predicted Body Mass Index and Breast Cancer Risk: Mendelian Randomization Analyses of Data from 145,000 Women of European DescentNo clinical utility of KRAS variant rs61764370 for ovarian or breast cancer.Comparison of 6q25 breast cancer hits from Asian and European Genome Wide Association Studies in the Breast Cancer Association Consortium (BCAC)Mutation analyses of KRAS exon 1 comparing three different techniques: temporal temperature gradient electrophoresis, constant denaturant capillary electrophoresis and allele specific polymerase chain reaction.CHEK2 1100delC is prevalent in Swedish early onset familial breast cancer.Genome-wide linkage scan for colorectal cancer susceptibility genes supports linkage to chromosome 3q.ASIP and TYR pigmentation variants associate with cutaneous melanoma and basal cell carcinoma.TP53-based interaction analysis identifies cis-eQTL variants for TP53BP2, FBXO28, and FAM53A that associate with survival and treatment outcome in breast cancerMixed lineage kinase 3 gene mutations in mismatch repair deficient gastrointestinal tumours.Ancestry-shift refinement mapping of the C6orf97-ESR1 breast cancer susceptibility locus.Familial cancer among consecutive uterine cancer patients in Sweden.2q36.3 is associated with prognosis for oestrogen receptor-negative breast cancer patients treated with chemotherapy.Fine scale mapping of the breast cancer 16q12 locus.Frameshift-mutation-derived peptides as tumor-specific antigens in inherited and spontaneous colorectal cancerThe biology of inherited cancer.Hereditary breast cancer: a review.Identification of susceptibility loci for colorectal cancer in a genome-wide meta-analysisA sequence variant at 4p16.3 confers susceptibility to urinary bladder cancer.Missense variants in ATM in 26,101 breast cancer cases and 29,842 controls.Association studies on 11 published colorectal cancer risk loci.Lack of HIN-1 methylation in BRCA1-linked and "BRCA1-like" breast tumors.Parent-of-origin-specific allelic associations among 106 genomic loci for age at menarcheBreast cancer risk and 6q22.33: combined results from Breast Cancer Association Consortium and Consortium of Investigators on Modifiers of BRCA1/2
P50
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P50
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Annika Lindblom
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Annika Lindblom
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Annika Lindblom
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Annika Lindblom
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Annika Lindblom
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Annika Lindblom
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Annika Lindblom
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Annika Lindblom
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