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Germline variation in RASAL2 may predict survival in patients with RAS‐activated colorectal cancer.
- Published in:
- Genes, Chromosomes & Cancer, 2023, v. 62, n. 6, p. 332, doi. 10.1002/gcc.23133
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- Publication type:
- Article
The silent mutational landscape of infant MLL-AF4 pro-B acute lymphoblastic leukemia.
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- Genes, Chromosomes & Cancer, 2013, v. 52, n. 10, p. 954, doi. 10.1002/gcc.22090
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- Publication type:
- Article
Common germline variation at the TERT locus contributes to familial clustering of myeloproliferative neoplasms.
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- American Journal of Hematology, 2014, v. 89, n. 12, p. 1107, doi. 10.1002/ajh.23842
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- Publication type:
- Article
SNPLINK: multipoint linkage analysis of densely distributed SNP data incorporating automated linkage disequilibrium removal.
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- Bioinformatics, 2005, v. 21, n. 13, p. 3060
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- Publication type:
- Article
Inherited variants in MYH are unlikely to contribute to the risk of lung carcinoma.
- Published in:
- Human Genetics, 2004, v. 114, n. 2, p. 207, doi. 10.1007/s00439-003-1033-2
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- Publication type:
- Article
The future of association studies of common cancers.
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- Human Genetics, 2003, v. 112, n. 4, p. 434, doi. 10.1007/s00439-002-0902-4
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- Publication type:
- Article
Quantifying the heritability of glioma using genome-wide complex trait analysis.
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- Scientific Reports, 2015, v. 5, n. 1, p. 17267, doi. 10.1038/srep17267
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- Article
Genome-wide homozygosity signature and risk of Hodgkin lymphoma.
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- Scientific Reports, 2015, p. 14315, doi. 10.1038/srep14315
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- Publication type:
- Article
Quantifying the heritability of testicular germ cell tumour using both population-based and genomic approaches.
- Published in:
- Scientific Reports, 2015, p. 13889, doi. 10.1038/srep13889
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- Publication type:
- Article
Implementation of genome-wide complex trait analysis to quantify the heritability in multiple myeloma.
- Published in:
- Scientific Reports, 2015, p. 12473, doi. 10.1038/srep12473
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- Publication type:
- Article
Targeted Sequencing in Chromosome 17q Linkage Region Identifies Familial Glioma Candidates in the Gliogene Consortium.
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- Scientific Reports, 2015, p. 8278, doi. 10.1038/srep08278
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- Publication type:
- Article
Contribution of cyclin d1 (CCND1) and E-cadherin (CDH1) polymorphisms to familial and sporadic colorectal cancer.
- Published in:
- Oncogene, 2002, v. 21, n. 12, p. 1928, doi. 10.1038/sj.onc.1205245
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- Publication type:
- Article
Polymorphisms in PTGS1, PTGS2 and IL-10 do not influence colorectal adenoma recurrence in the context of a randomized aspirin intervention trial.
- Published in:
- International Journal of Cancer, 2007, v. 121, n. 9, p. 2001, doi. 10.1002/ijc.22942
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- Publication type:
- Article
MTHFR C677T and colorectal cancer risk: A meta-analysis of 25 populations.
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- International Journal of Cancer, 2007, v. 120, n. 5, p. 1027, doi. 10.1002/ijc.22440
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- Publication type:
- Article
Evaluation of xeroderma pigmentosum XPA, XPC, XPD, XPF, XPB, XPG and DDB2 genes in familial early-onset lung cancer predisposition.
- Published in:
- International Journal of Cancer, 2006, v. 119, n. 4, p. 964, doi. 10.1002/ijc.21931
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- Publication type:
- Article
Case-control study of familial lung cancer risks in UK women.
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- International Journal of Cancer, 2005, v. 116, n. 3, p. 445, doi. 10.1002/ijc.21012
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- Publication type:
- Article
Comprehensive analysis of the contribution of germline MYH variation to early-onset colorectal cancer.
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- International Journal of Cancer, 2004, v. 109, n. 4, p. 554
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- Publication type:
- Article
A Novel Gene for Neonatal Diabetes Maps to Chromosome 10p12.1-p13.
- Published in:
- Diabetes, 2003, v. 52, n. 10, p. 2636, doi. 10.2337/diabetes.52.10.2636
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- Publication type:
- Article
Meta-Analysis of Genome-Wide Linkage Studies in Celiac Disease.
- Published in:
- Human Heredity, 2009, v. 68, n. 4, p. 223, doi. 10.1159/000228920
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- Publication type:
- Article
Prediction of Genetic Risks from Segregation Analyses of Morbid Risks.
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- Human Heredity, 1994, v. 44, n. 1, p. 52, doi. 10.1159/000154189
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- Publication type:
- Article
A genome-wide analysis of loss of heterozygosity and chromosomal copy number variation in Proteus syndrome using high-density SNP microarrays.
- Published in:
- Journal of Human Genetics, 2010, v. 55, n. 9, p. 627, doi. 10.1038/jhg.2010.70
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- Publication type:
- Article
MLH1-93G > A is a risk factor for MSI colorectal cancer.
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- Carcinogenesis, 2011, v. 32, n. 8, p. 1157, doi. 10.1093/carcin/bgr089
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- Publication type:
- Article
Association of a novel functional promoter variant (rs2075533 C>T) in the apoptosis gene TNFSF8 with risk of lung cancer—a finding from Texas lung cancer genome-wide association study.
- Published in:
- Carcinogenesis, 2011, v. 32, n. 4, p. 507, doi. 10.1093/carcin/bgr014
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- Publication type:
- Article
Inherited variation in immune genes and pathways and glioblastoma risk.
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- Carcinogenesis, 2010, v. 31, n. 10, p. 1770, doi. 10.1093/carcin/bgq152
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- Publication type:
- Article
Role of 5p15.33 (TERT-CLPTM1L), 6p21.33 and 15q25.1 (CHRNA5-CHRNA3) variation and lung cancer risk in never-smokers.
- Published in:
- Carcinogenesis, 2010, v. 31, n. 2, p. 234, doi. 10.1093/carcin/bgp287
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- Publication type:
- Article
Risk of non-medullary thyroid cancer influenced by polymorphic variation in the thyroglobulin gene.
- Published in:
- Carcinogenesis, 2004, v. 25, n. 3, p. 369
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- Publication type:
- Article
Fine-scale mapping of the 6p25.3 chronic lymphocytic leukaemia susceptibility locus.
- Published in:
- Human Molecular Genetics, 2010, v. 19, n. 9, p. 1840, doi. 10.1093/hmg/ddq044
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- Publication type:
- Article
Genetic variation in the DNA repair genes is predictive of outcome in lung cancer.
- Published in:
- Human Molecular Genetics, 2007, v. 16, n. 19, p. 2333, doi. 10.1093/hmg/ddm190
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- Publication type:
- Article
MTHFR C677T has differential influence on risk of MSI and MSS colorectal cancer.
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- Human Molecular Genetics, 2007, v. 16, n. 9, p. 1072, doi. 10.1093/hmg/ddm055
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- Publication type:
- Article
Evidence for a colorectal cancer susceptibility locus on chromosome 3q21–q24 from a high-density SNP genome-wide linkage scan.
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- Human Molecular Genetics, 2006, v. 15, n. 24, p. 3592, doi. 10.1093/hmg/ddl435
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- Publication type:
- Article
Search for low penetrance alleles for colorectal cancer through a scan of 1467 non-synonymous SNPs in 2575 cases and 2707 controls with validation by kin-cohort analysis of 14 704 first-degree relatives.
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- Human Molecular Genetics, 2006, v. 15, n. 21, p. 3263, doi. 10.1093/hmg/ddl401
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- Publication type:
- Article
Evidence for a colorectal cancer susceptibility locus on chromosome 3q21–q24 from a high-density SNP genome-wide linkage scan.
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- Human Molecular Genetics, 2006, v. 15, n. 19, p. 2903, doi. 10.1093/hmg/ddl231
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- Publication type:
- Article
Genetic and regulatory mechanism of susceptibility to high-hyperdiploid acute lymphoblastic leukaemia at 10p21.2.
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- Nature Communications, 2017, v. 8, n. 3, p. 14616, doi. 10.1038/ncomms14616
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- Publication type:
- Article
The non-coding variant rs1800734 enhances DCLK3 expression through long-range interaction and promotes colorectal cancer progression.
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- Nature Communications, 2017, v. 8, n. 2, p. 14418, doi. 10.1038/ncomms14418
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- Publication type:
- Article
Rare disruptive mutations in ciliary function genes contribute to testicular cancer susceptibility.
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- Nature Communications, 2016, v. 7, n. 12, p. 13840, doi. 10.1038/ncomms13840
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- Publication type:
- Article
Multiple myeloma risk variant at 7p15.3 creates an IRF4-binding site and interferes with CDCA7L expression.
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- Nature Communications, 2016, v. 7, n. 11, p. 13656, doi. 10.1038/ncomms13656
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- Publication type:
- Article
Rare disruptive mutations and their contribution to the heritable risk of colorectal cancer.
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- Nature Communications, 2016, v. 7, n. 6, p. 11883, doi. 10.1038/ncomms11883
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- Article
Identification of four new susceptibility loci for testicular germ cell tumour.
- Published in:
- Nature Communications, 2015, v. 6, n. 10, p. 8690, doi. 10.1038/ncomms9690
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- Publication type:
- Article
Capture Hi-C identifies the chromatin interactome of colorectal cancer risk loci.
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- Nature Communications, 2015, v. 6, n. 2, p. 6178, doi. 10.1038/ncomms7178
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- Publication type:
- Article
Whole-exome sequencing reveals the mutational spectrum of testicular germ cell tumours.
- Published in:
- Nature Communications, 2015, v. 6, n. 1, p. 5973, doi. 10.1038/ncomms6973
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- Publication type:
- Article
DICER1 Mutations in Familial Multinodular Goiter With and Without Ovarian Sertoli-Leydig Cell Tumors.
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- JAMA: Journal of the American Medical Association, 2011, v. 305, n. 1, p. 68, doi. 10.1001/jama.2010.1910
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- Article
Deciphering associations for lung cancer risk through imputation and analysis of 12 316 cases and 16 831 controls.
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- European Journal of Human Genetics, 2015, v. 23, n. 12, p. 1723, doi. 10.1038/ejhg.2015.48
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- Publication type:
- Article
The use of whole genome amplification to study chromosomal changes in prostate cancer: insights into genome-wide signature of preneoplasia associated with cancer progression.
- Published in:
- BMC Genomics, 2006, v. 7, p. 65, doi. 10.1186/1471-2164-7-65
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- Publication type:
- Article
Sequence changes in predicted promoter elements of STK11/LKB1 are unlikely to contribute to Peutz-Jeghers syndrome.
- Published in:
- BMC Genomics, 2005, v. 6, p. 1, doi. 10.1186/1471-2164-6-38
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- Publication type:
- Article
Role of monoamine-oxidase-A-gene variation in the development of glioblastoma in males: a case control study.
- Published in:
- Journal of Neuro-Oncology, 2019, v. 145, n. 2, p. 287, doi. 10.1007/s11060-019-03294-w
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- Publication type:
- Article
Diffuse gliomas classified by 1p/19q co-deletion, <italic>TERT</italic> promoter and IDH mutation status are associated with specific genetic risk loci.
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- Acta Neuropathologica, 2018, v. 135, n. 5, p. 743, doi. 10.1007/s00401-018-1825-z
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- Article
Investigation of the effects of DNA repair gene polymorphisms on the risk of colorectal cancer.
- Published in:
- Mutagenesis, 2012, v. 27, n. 2, p. 219, doi. 10.1093/mutage/ger070
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- Article
COGENT (COlorectal cancer GENeTics) revisited.
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- Mutagenesis, 2012, v. 27, n. 2, p. 143
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- Publication type:
- Article
Genetic landscape of interval and screen detected breast cancer.
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- NPJ Precision Oncology, 2024, v. 8, n. 1, p. 1, doi. 10.1038/s41698-024-00618-6
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- Publication type:
- Article
Re: MLH1 93G>A promoter polymorphism and the risk of microsatellite-unstable colorectal cancer.
- Published in:
- 2007
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- Publication type:
- letter