Ceres
Fernández Rozadilla
University of Illinois at Chicago
Chicago, Estados UnidosPublicacións en colaboración con investigadores/as de University of Illinois at Chicago (15)
2017
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Candidate predisposing germline copy number variants in early onset colorectal cancer patients
Clinical and Translational Oncology, Vol. 19, Núm. 5, pp. 625-632
2014
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A genome-wide association study on copy-number variation identifies a 11q11 loss as a candidate susceptibility variant for colorectal cancer
Human Genetics, Vol. 133, Núm. 5, pp. 525-534
2013
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A colorectal cancer genome-wide association study in a Spanish cohort identifies two variants associated with colorectal cancer risk at 1p33 and 8p12
BMC Genomics, Vol. 14, Núm. 1
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BMP2/BMP4 colorectal cancer susceptibility loci in northern and southern european populations
Carcinogenesis, Vol. 34, Núm. 2, pp. 314-318
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BMPR1A mutations in early-onset colorectal cancer with mismatch repair proficiency
Clinical Genetics
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Genetic susceptibility variants associated with colorectal cancer prognosis
Carcinogenesis, Vol. 34, Núm. 10, pp. 2286-2291
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Meta-Analysis of Mismatch Repair Polymorphisms within the Cogent Consortium for Colorectal Cancer Susceptibility
PLoS ONE, Vol. 8, Núm. 9
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Pharmacogenomics in colorectal cancer: A genome-wide association study to predict toxicity after 5-fluorouracil or FOLFOX administration
Pharmacogenomics Journal, Vol. 13, Núm. 3, pp. 209-217
2012
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COGENT (COlorectal cancer GENeTics) revisited
Mutagenesis, Vol. 27, Núm. 2, pp. 143-151
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Seeking genetic susceptibility variants for colorectal cancer: The EPICOLON consortium experience
Mutagenesis, Vol. 27, Núm. 2, pp. 153-159
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Susceptibility genetic variants associated with early-onset colorectal cancer
Carcinogenesis, Vol. 33, Núm. 3, pp. 613-619
2011
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A two-phase case-control study for colorectal cancer genetic susceptibility: Candidate genes from chromosomal regions 9q22 and 3q22
British Journal of Cancer, Vol. 105, Núm. 6, pp. 870-875
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Case-control study for colorectal cancer genetic susceptibility in EPICOLON: Previously identified variants and mucins
BMC Cancer, Vol. 11
2010
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Colorectal cancer susceptibility quantitative trait loci in mice as a novel approach to detect low-penetrance variants in humans: A two-stage case-control study
Cancer Epidemiology Biomarkers and Prevention, Vol. 19, Núm. 2, pp. 619-623
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Single nucleotide polymorphisms in the wnt and bmp pathways and colorectal cancer risk in a spanish cohort
PLoS ONE, Vol. 5, Núm. 9, pp. 1-9