Montserrat
Andreu García
Publicacions en què col·labora amb Montserrat Andreu García (48)
2020
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Correction to: Efficacy and safety of endoscopic balloon dilation in inflammatory bowel disease: results of the large multicenter study of the ENEIDA registry (Surgical Endoscopy, (2020), 34, 3, (1112-1122), 10.1007/s00464-019-06858-z)
Surgical Endoscopy
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Efficacy and safety of endoscopic balloon dilation in inflammatory bowel disease: results of the large multicenter study of the ENEIDA registry
Surgical Endoscopy, Vol. 34, Núm. 3, pp. 1112-1122
2019
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Clinical Characteristics, Associated Malignancies and Management of Primary Sclerosing Cholangitis in Inflammatory Bowel Disease Patients: A Multicentre Retrospective Cohort Study
Journal of Crohn's & colitis, Vol. 13, Núm. 12, pp. 1492-1500
2018
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Colorectal cancer molecular classification using BRAF, KRAS, microsatellite instability and CIMP status: Prognostic implications and response to chemotherapy
PLoS ONE, Vol. 13, Núm. 9
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Detection of serrated lesions in proximal colon by simulated sigmoidoscopy vs faecal immunochemical testing in a multicentre, pragmatic, randomised controlled trial
United European Gastroenterology Journal, Vol. 6, Núm. 10, pp. 1527-1537
2017
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Correlation between adenoma detection rate in colonoscopy- and fecal immunochemical testing-based colorectal cancer screening programs
United European Gastroenterology Journal, Vol. 5, Núm. 2, pp. 255-260
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
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Genetic variants associated with colorectal adenoma susceptibility
PLoS ONE, Vol. 11, Núm. 4
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Impact of age- and gender-specific cut-off values for the fecal immunochemical test for hemoglobin in colorectal cancer screening
Digestive and Liver Disease, Vol. 48, Núm. 5, pp. 542-551
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Incidence of advanced neoplasia during surveillance in high- and intermediate-risk groups of the European colorectal cancer screening guidelines
Endoscopy, Vol. 48, Núm. 11, pp. 995-1002
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
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Whole-exome sequencing identifies rare pathogenic variants in new predisposition genes for familial colorectal cancer
Genetics in Medicine, Vol. 17, Núm. 2, pp. 131-142
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
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Effect of oral anticoagulants on the outcome of faecal immunochemical test
British Journal of Cancer, Vol. 110, Núm. 5, pp. 1334-1337
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Erratum: Whole-exome sequencing identifies rare pathogenic variants in new predisposition genes for familial colorectal cancer (Genetics in Medicine (2014) DOI: 10.1038/gim.2014.89)
Genetics in Medicine
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New genes emerging for colorectal cancer predisposition
World Journal of Gastroenterology, Vol. 20, Núm. 8, pp. 1961-1971
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Participation and detection rates by age and sex for colonoscopy versus fecal immunochemical testing in colorectal cancer screening
Cancer Causes and Control, Vol. 25, Núm. 8, pp. 985-997
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Rate of Detection of Advanced Neoplasms in Proximal Colon by Simulated Sigmoidoscopy vs Fecal Immunochemical Tests
Clinical Gastroenterology and Hepatology, Vol. 12, Núm. 10, pp. 1708-1716.e4
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The MLH1c.1852-1853delinsGC (p.K618A) variant in colorectal cancer: Genetic association study in 18,723 individuals
PLoS ONE, Vol. 9, Núm. 4