Fundación Pública Galega de Medicina Xenómica
Centro de investigación
![Foto de Cristina](/img/nophoto.png)
Cristina
Alenda González
Publicacións nas que colabora con Cristina Alenda González (10)
2021
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XDEEP-MSI: Explainable bias-rejecting microsatellite instability deep learning system in colorectal cancer
Biomolecules, Vol. 11, Núm. 12
2016
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Association of a let-7 miRNA binding region of TGFBR1 with hereditary mismatch repair proficient colorectal cancer (MSS HNPCC)
Carcinogenesis, Vol. 37, Núm. 8, pp. 751-758
2015
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Prevalence of MLH1 constitutional epimutations as a cause of Lynch syndrome in unselected versus selected consecutive series of patients with colorectal cancer
Journal of Medical Genetics, Vol. 52, Núm. 7, pp. 498-502
2014
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High incidence of large deletions in the PMS2 gene in Spanish Lynch syndrome families
Clinical Genetics, Vol. 85, Núm. 6, pp. 583-588
2013
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Risk of cancer in cases of suspected lynch syndrome without germline mutation
Gastroenterology, Vol. 144, Núm. 5
2012
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COGENT (COlorectal cancer GENeTics) revisited
Mutagenesis, Vol. 27, Núm. 2, pp. 143-151
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Comparison between universal molecular screening for Lynch syndrome and revised Bethesda guidelines in a large population-based cohort of patients with colorectal cancer
Gut, Vol. 61, Núm. 6, pp. 865-872
2011
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Evidence for classification of c.1852_1853AA>GC in MLH1 as a neutral variant for Lynch syndrome
BMC Medical Genetics, Vol. 12
2010
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Susceptibility genetic variants associated with colorectal cancer risk correlate with cancer phenotype
Gastroenterology, Vol. 139, Núm. 3
2007
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Association of the ARLTS1 Cys148Arg variant with sporadic and familial colorectal cancer
Carcinogenesis, Vol. 28, Núm. 8, pp. 1687-1691