Fundación Pública Galega de Medicina Xenómica
Centro de investigación
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Academy of Sciences of the Czech Republic
Praga, República ChecaPublicacións en colaboración con investigadores/as de Academy of Sciences of the Czech Republic (14)
2024
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Fine-mapping analysis including over 254,000 East Asian and European descendants identifies 136 putative colorectal cancer susceptibility genes
Nature Communications, Vol. 15, Núm. 1
2023
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Author Correction: Deciphering colorectal cancer genetics through multi-omic analysis of 100,204 cases and 154,587 controls of European and east Asian ancestries (Nature Genetics, (2023), 55, 1, (89-99), 10.1038/s41588-022-01222-9)
Nature Genetics
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Combining Asian and European genome-wide association studies of colorectal cancer improves risk prediction across racial and ethnic populations
Nature Communications, Vol. 14, Núm. 1
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Deciphering colorectal cancer genetics through multi-omic analysis of 100,204 cases and 154,587 controls of European and east Asian ancestries
Nature Genetics, Vol. 55, Núm. 1, pp. 89-99
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ENIGMA CHEK2gether Project: A Comprehensive Study Identifies Functionally Impaired CHEK2 Germline Missense Variants Associated with Increased Breast Cancer Risk
Clinical cancer research : an official journal of the American Association for Cancer Research, Vol. 29, Núm. 16, pp. 3037-3050
2018
2017
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Evidence for genetic association between chromosome 1q loci and predisposition to colorectal neoplasia
British Journal of Cancer, Vol. 117, Núm. 6, pp. 876-884
2014
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Association between CASP8 -652 6N del polymorphism (rs3834129) and colorectal cancer risk: Results from a multi-centric study
PLoS ONE, Vol. 9, Núm. 1
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Correction: Association between CASP8 -652 6N del polymorphism (rs3834129) and colorectal cancer risk: Results from a multi-centric study (PLoS ONE)
PLoS ONE
2013
2012
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Refinement of the associations between risk of colorectal cancer and polymorphisms on chromosomes 1q41 and 12q13.13
Human Molecular Genetics, Vol. 21, Núm. 4, pp. 934-946
2010
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COGENT (COlorectal cancer GENeTics): An international consortium to study the role of polymorphic variation on the risk of colorectal cancer
British Journal of Cancer, Vol. 102, Núm. 2, pp. 447-454
2008
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A genome-wide association study identifies colorectal cancer susceptibility loci on chromosomes 10p14 and 8q23.3
Nature Genetics, Vol. 40, Núm. 5, pp. 623-630
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Refinement of the basis and impact of common 11q23.1 variation to the risk of developing colorectal cancer
Human Molecular Genetics, Vol. 17, Núm. 23, pp. 3720-3727