Publications by authors named "Maribel González-Acosta"

6Publications

Quality of colonoscopy is associated with adenoma detection and post-colonoscopy colorectal cancer prevention in Lynch syndrome.

Authors:
Ariadna Sánchez Victorine H Roos Matilde Navarro Marta Pineda Berta Caballol Lorena Moreno Sabela Carballal Lorena Rodríguez-Alonso Teresa Ramon Y Cajal Gemma Llort Virginia Piñol Adria Lopez Fernandez Inmaculada Salces Maria Dolores Picó Laura Rivas Luis Bujanda Marta Garzon Angeles Pizarro Eva Martinez de Castro Maria Jesus López-Arias Carmen Poves Catalina Garau Daniel Rodriguez-Alcalde Maite Herraiz Cristina Alvarez-Urrutia Andres Dacal Marta Carrillo-Palau Lucia Cid Marta Ponce Eva Barreiro-Alonso Esteban Saperas Elena Aguirre Cristina Romero Barbara Bastiaansen Maribel Gonzalez-Acosta Blai Morales-Romero Teresa Ocaña Liseth Rivero-Sánchez Gerhard Jung Xavier Bessa Joaquin Cubiella Rodrigo Jover Francisco Rodríguez-Moranta Judith Balmaña Joan Brunet Antoni Castells Evelien Dekker Gabriel Capella Miquel Serra-Burriel Leticia Moreira Maria Pellise Francesc Balaguer

Clin Gastroenterol Hepatol 2020 Nov 3. Epub 2020 Nov 3.

Department of Gastroenterology, Hospital Clínic Barcelona, Centro de Investigación Biomédica en Red en Enfermedades Hepáticas y Digestivas (CIBEREHD), IDIBAPS (Institut d'Investigacions Biomèdiques August Pi i Sunyer), University of Barcelona, Barcelona, Spain. Electronic address:

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November 2020

Comprehensive Constitutional Genetic and Epigenetic Characterization of Lynch-Like Individuals.

Authors:
Estela Dámaso Maribel González-Acosta Gardenia Vargas-Parra Matilde Navarro Judith Balmaña Teresa Ramon Y Cajal Noemí Tuset Bryony A Thompson Fátima Marín Anna Fernández Carolina Gómez Àngela Velasco Ares Solanes Sílvia Iglesias Gisela Urgel Consol López Jesús Del Valle Olga Campos Maria Santacana Xavier Matias-Guiu Conxi Lázaro Laura Valle Joan Brunet Marta Pineda Gabriel Capellá

Cancers (Basel) 2020 Jul 5;12(7). Epub 2020 Jul 5.

Hereditary Cancer Program, Catalan Institute of Oncology, Insititut d'Investigació Biomèdica de Bellvitge (IDIBELL), ONCOBELL Program. Avinguda de la Gran Via de l'Hospitalet 199-203, 08908 L'Hospitalet de Llobregat, Barcelona, Spain.

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July 2020

Validation of an in Vitro Mismatch Repair Assay Used in the Functional Characterization of Mismatch Repair Variants.

Authors:
Maribel González-Acosta Inga Hinrichsen Anna Fernández Conxi Lázaro Marta Pineda Guido Plotz Gabriel Capellá

J Mol Diagn 2020 03 25;22(3):376-385. Epub 2019 Dec 25.

Hereditary Cancer Program, the Catalan Institute of Oncology (ICO), Hereditary Cancer Group, Molecular Mechanisms and Experimental Therapy in Oncology Program, Institut d'Investigació Biomèdica de Bellvitge (IDIBELL), Ciber Oncología (CIBERONC) Instituto Salud Carlos III, L'Hospitalet de Llobregat, Barcelona, Spain. Electronic address:

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March 2020

High-sensitivity microsatellite instability assessment for the detection of mismatch repair defects in normal tissue of biallelic germline mismatch repair mutation carriers.

Authors:
Maribel González-Acosta Fátima Marín Benjamin Puliafito Nuria Bonifaci Anna Fernández Matilde Navarro Hector Salvador Francesc Balaguer Silvia Iglesias Angela Velasco Elia Grau Garces Victor Moreno Luis Ignacio Gonzalez-Granado Pilar Guerra-García Rosa Ayala Benoît Florkin Christian Kratz Tim Ripperger Thorsten Rosenbaum Danuta Januszkiewicz-Lewandowska Amedeo A Azizi Iman Ragab Michaela Nathrath Hans-Jürgen Pander Stephan Lobitz Manon Suerink Karin Dahan Thomas Imschweiler Ugur Demirsoy Joan Brunet Conxi Lázaro Daniel Rueda Katharina Wimmer Gabriel Capellá Marta Pineda

J Med Genet 2020 04 7;57(4):269-273. Epub 2019 Sep 7.

Hereditary Cancer Program, Catalan Institute of Oncology - ICO, Hereditary Cancer Group, Molecular Mechanisms and Experimental Therapy in Oncology Program, Institut d'Investigació Biomèdica de Bellvitge - IDIBELL, Ciber Oncología (CIBERONC) - Instituto de Salud Carlos III, L'Hospitalet de Llobregat, Barcelona, Spain

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April 2020

Elucidating the molecular basis of MSH2-deficient tumors by combined germline and somatic analysis.

Authors:
Gardenia M Vargas-Parra Maribel González-Acosta Bryony A Thompson Carolina Gómez Anna Fernández Estela Dámaso Tirso Pons Monika Morak Jesús Del Valle Silvia Iglesias Àngela Velasco Ares Solanes Xavier Sanjuan Natàlia Padilla Xavier de la Cruz Alfonso Valencia Elke Holinski-Feder Joan Brunet Lídia Feliubadaló Conxi Lázaro Matilde Navarro Marta Pineda Gabriel Capellá

Int J Cancer 2017 10 3;141(7):1365-1380. Epub 2017 Jul 3.

Hereditary Cancer Program, Catalan Institute of Oncology, IDIBELL, CIBERONC, Hospitalet de Llobregat, Spain.

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October 2017

Elucidating the clinical significance of two PMS2 missense variants coexisting in a family fulfilling hereditary cancer criteria.

Authors:
Maribel González-Acosta Jesús Del Valle Matilde Navarro Bryony A Thompson Sílvia Iglesias Xavier Sanjuan María José Paúles Natàlia Padilla Anna Fernández Raquel Cuesta Àlex Teulé Guido Plotz Juan Cadiñanos Xavier de la Cruz Francesc Balaguer Conxi Lázaro Marta Pineda Gabriel Capellá

Fam Cancer 2017 Oct;16(4):501-507

Hereditary Cancer Program, Catalan Institute of Oncology (ICO), IDIBELL and CIBERONC, Av. Gran Via de l'Hospitalet, 199-203, 08908, Hospitalet de Llobregat (Barcelona), Spain.

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October 2017