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Recurrent Coding Sequence Variation Explains Only A Small Fraction of the Genetic Architecture of Colorectal Cancer.
- Published in:
- Scientific Reports, 2015, p. 16286, doi. 10.1038/srep16286
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- Article
Erratum: A new GWAS and meta-analysis with 1000Genomes imputation identifies novel risk variants for colorectal cancer.
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- Scientific Reports, 2015, p. 12372, doi. 10.1038/srep12372
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- Article
A new GWAS and meta-analysis with 1000Genomes imputation identifies novel risk variants for colorectal cancer.
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- Scientific Reports, 2015, p. 10442, doi. 10.1038/srep10442
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- Article
Identification of susceptibility loci for colorectal cancer in a genome-wide meta-analysis.
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- Human Molecular Genetics, 2014, v. 23, n. 17, p. 4729
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- Article
Evidence for a colorectal cancer susceptibility locus on chromosome 3q21–q24 from a high-density SNP genome-wide linkage scan.
- Published in:
- Human Molecular Genetics, 2006, v. 15, n. 24, p. 3592, doi. 10.1093/hmg/ddl435
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- 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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- Article
Common colorectal cancer risk alleles contribute to the multiple colorectal adenoma phenotype, but do not influence colonic polyposis in FAP.
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- European Journal of Human Genetics, 2015, v. 23, n. 2, p. 260, doi. 10.1038/ejhg.2014.74
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- Article
Deciphering the genetics of hereditary non-syndromic colorectal cancer.
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- European Journal of Human Genetics, 2008, v. 16, n. 12, p. 1477, doi. 10.1038/ejhg.2008.129
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- Article
Germline mutations affecting the proofreading domains of POLE and POLD1 predispose to colorectal adenomas and carcinomas.
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- Nature Genetics, 2013, v. 45, n. 6, p. 713, doi. 10.1038/ng0613-713b
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- Article
Germline mutations affecting the proofreading domains of POLE and POLD1 predispose to colorectal adenomas and carcinomas.
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- Nature Genetics, 2013, v. 45, n. 2, p. 136, doi. 10.1038/ng.2503
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- Article
Common variation near CDKN1A, POLD3 and SHROOM2 influences colorectal cancer risk.
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- Nature Genetics, 2012, v. 44, n. 7, p. 770, doi. 10.1038/ng.2293
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- Article
Meta-analysis of genome-wide association data identifies four new susceptibility loci for colorectal cancer.
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- Nature Genetics, 2008, v. 40, n. 12, p. 1426, doi. 10.1038/ng.262
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- Article
Common genetic variants at the CRAC1 (HMPS) locus on chromosome 15q13.3 influence colorectal cancer risk.
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- Nature Genetics, 2008, v. 40, n. 1, p. 26, doi. 10.1038/ng.2007.41
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- Article
A genome-wide association scan of tag SNPs identifies a susceptibility variant for colorectal cancer at 8q24.21.
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- Nature Genetics, 2007, v. 39, n. 8, p. 984, doi. 10.1038/ng2085
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- Article
Multiple Common Susceptibility Variants near BMP Pathway Loci GREM1, BMP4, and BMP2 Explain Part of the Missing Heritability of Colorectal Cancer.
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- PLoS Genetics, 2011, v. 7, n. 6, p. 1, doi. 10.1371/journal.pgen.1002105
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- Article
Liquid-Immersion Reprocessing Effects on Filtration Efficiency of 'Single-Use' Commercial Medical Face Masks.
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- Annals of Work Exposures & Health, 2022, v. 66, n. 2, p. 246, doi. 10.1093/annweh/wxab079
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- Article
Germline mutations in FH predispose to dominantly inherited uterine fibroids, skin leiomyomata and papillary renal cell cancer.
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- Nature Genetics, 2002, v. 30, n. 4, p. 406
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- Article
Adult Leydig Cell Tumors of the Testis Caused by Germline Fumarate Hydratase Mutations.
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- Journal of Clinical Endocrinology & Metabolism, 2006, v. 91, n. 8, p. 3071, doi. 10.1210/jc.2006-0183
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- Article
Erratum to: The TGFBR1*6A/9A polymorphism is not associated with differential risk of breast cancer.
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- 2012
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- Correction notice
The TGFBR1*6A/9A polymorphism is not associated with differential risk of breast cancer.
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- Breast Cancer Research & Treatment, 2010, v. 119, n. 2, p. 437, doi. 10.1007/s10549-009-0395-0
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- Article
Low penetrance breast cancer predisposition SNPs are site specific.
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- Breast Cancer Research & Treatment, 2009, v. 117, n. 1, p. 151, doi. 10.1007/s10549-008-0235-7
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- Article
Germline APC variants in patients with multiple colorectal adenomas, with evidence for the particular importance of E1317Q.
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- Human Molecular Genetics, 2000, v. 9, n. 15, p. 2215, doi. 10.1093/oxfordjournals.hmg.a018912
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- Article