Pages that link to "Q53226230"
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The following pages link to Colon Cancer Family Registry: an international resource for studies of the genetic epidemiology of colon cancer. (Q53226230):
Displaying 50 items.
- Multiple common susceptibility variants near BMP pathway loci GREM1, BMP4, and BMP2 explain part of the missing heritability of colorectal cancer (Q21144952) (← links)
- Molecular pathological epidemiology of colorectal neoplasia: an emerging transdisciplinary and interdisciplinary field (Q24620628) (← links)
- Two-phase and family-based designs for next-generation sequencing studies (Q26828744) (← links)
- Collaborative cancer epidemiology in the 21st century: the model of cancer consortia (Q27022338) (← links)
- Prediagnostic Physical Activity and Colorectal Cancer Survival: Overall and Stratified by Tumor Characteristics. (Q27347219) (← links)
- Colorectal carcinomas with KRAS mutation are associated with distinctive morphological and molecular features (Q28284149) (← links)
- Genome-wide diet-gene interaction analyses for risk of colorectal cancer (Q29417001) (← links)
- A genome-wide association study of early-onset breast cancer identifies PFKM as a novel breast cancer gene and supports a common genetic spectrum for breast cancer at any age. (Q29417036) (← links)
- Proceedings of the third international molecular pathological epidemiology (MPE) meeting (Q30238962) (← links)
- Prevalence and Penetrance of Major Genes and Polygenes for Colorectal Cancer (Q30275554) (← links)
- Cancer risks for monoallelic MUTYH mutation carriers with a family history of colorectal cancer (Q30461804) (← links)
- Risks of Lynch syndrome cancers for MSH6 mutation carriers (Q30492977) (← links)
- The PREMM(1,2,6) model predicts risk of MLH1, MSH2, and MSH6 germline mutations based on cancer history (Q30501708) (← links)
- Body mass index in early adulthood and colorectal cancer risk for carriers and non-carriers of germline mutations in DNA mismatch repair genes (Q30502502) (← links)
- The TERT variant rs2736100 is associated with colorectal cancer risk (Q30525527) (← links)
- Metachronous colorectal cancer risk for mismatch repair gene mutation carriers: the advantage of more extensive colon surgery (Q30558412) (← links)
- Cancer risks for MLH1 and MSH2 mutation carriers (Q30563768) (← links)
- Red meat and poultry intake, polymorphisms in the nucleotide excision repair and mismatch repair pathways and colorectal cancer risk (Q33386678) (← links)
- On combining triads and unrelated subjects data in candidate gene studies: an application to data on testicular cancer (Q33392516) (← links)
- On combining family-based and population-based case-control data in association studies (Q33531899) (← links)
- Communication of genetic test results to family and health-care providers following disclosure of research results (Q33563539) (← links)
- Genetic variability in the MTHFR gene and colorectal cancer risk using the colorectal cancer family registry (Q33586578) (← links)
- Does risk of endometrial cancer for women without a germline mutation in a DNA mismatch repair gene depend on family history of endometrial cancer or colorectal cancer? (Q33593851) (← links)
- Integrated analysis of genome-wide copy number alterations and gene expression in microsatellite stable, CpG island methylator phenotype-negative colon cancer (Q33604452) (← links)
- Family history of colorectal cancer in BRAF p.V600E-mutated colorectal cancer cases (Q33625221) (← links)
- Risk factors for colorectal cancer in patients with multiple serrated polyps: a cross-sectional case series from genetics clinics (Q33641289) (← links)
- Genetic variation in the vitamin D receptor (VDR) and the vitamin D-binding protein (GC) and risk for colorectal cancer: results from the Colon Cancer Family Registry (Q33643330) (← links)
- Smoking and colorectal cancer in Lynch syndrome: results from the Colon Cancer Family Registry and the University of Texas M.D. Anderson Cancer Center (Q33658220) (← links)
- Risk of metachronous colon cancer following surgery for rectal cancer in mismatch repair gene mutation carriers (Q33699887) (← links)
- Specific variants in the MLH1 gene region may drive DNA methylation, loss of protein expression, and MSI-H colorectal cancer (Q33725467) (← links)
- Case-control study of overweight, obesity, and colorectal cancer risk, overall and by tumor microsatellite instability status (Q33736763) (← links)
- Lynch syndrome-associated breast cancers: clinicopathologic characteristics of a case series from the colon cancer family registry (Q33767027) (← links)
- Estimating the heritability of colorectal cancer (Q33784483) (← links)
- Convergence of genes and cellular pathways dysregulated in autism spectrum disorders (Q33794546) (← links)
- Parent of origin effects on age at colorectal cancer diagnosis (Q33879359) (← links)
- Role of inflammation and inflammatory mediators in colorectal cancer (Q33957824) (← links)
- Confirmation of linkage to and localization of familial colon cancer risk haplotype on chromosome 9q22. (Q33959070) (← links)
- Family history of colorectal cancer is not associated with colorectal cancer survival regardless of microsatellite instability status (Q33992074) (← links)
- Characterisation of familial colorectal cancer Type X, Lynch syndrome, and non-familial colorectal cancer (Q33994353) (← links)
- Genes involved with folate uptake and distribution and their association with colorectal cancer risk (Q33994469) (← links)
- Bayesian mixture models for the incorporation of prior knowledge to inform genetic association studies (Q34022116) (← links)
- Genetic variation in the retinoid X receptor and calcium-sensing receptor and risk of colorectal cancer in the Colon Cancer Family Registry. (Q34042369) (← links)
- Meat intake, cooking methods, dietary carcinogens, and colorectal cancer risk: findings from the Colorectal Cancer Family Registry (Q34043663) (← links)
- Identification of susceptibility loci for colorectal cancer in a genome-wide meta-analysis (Q34048230) (← links)
- The Family Health Promotion Project (FHPP): design and baseline data from a randomized trial to increase colonoscopy screening in high risk families (Q34078901) (← links)
- Meta-analysis of 8q24 for seven cancers reveals a locus between NOV and ENPP2 associated with cancer development (Q34091855) (← links)
- Cancer risks for the relatives of colorectal cancer cases with a methylated MLH1 promoter region: data from the Colorectal Cancer Family Registry (Q34092337) (← links)
- Genetic variation in prostaglandin synthesis and related pathways, NSAID use and colorectal cancer risk in the Colon Cancer Family Registry (Q34096843) (← links)
- Informatics and data quality at collaborative multicenter Breast and Colon Cancer Family Registries (Q34155880) (← links)
- Risk of endometrial cancer for women diagnosed with HNPCC-related colorectal carcinoma (Q34163849) (← links)