Marta Pineda

ResearcherID ORCID

Publication Activity (10 Years)

Years Active: 2019-2023
Publications (10 Years): 16

Top Topics

Endometrial Cancer

Ulcerative Colitis

Top Venues

Journal of medical genetics

Journal of personalized medicine

International journal of environmental research and public health

This page only lists publications with an associated author ORCID identifier.

Publications

Ana Beatriz Sanchez-Heras, Teresa Ramon Y Cajal, Marta Pineda, Elena Aguirre, Begoña Graña Suarez, Isabel Chirivella, Judith Balmaña, Joan Brunet, null null
SEOM clinical guideline on heritable TP53-related cancer syndrome (2022). Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico (2023)
Núria Dueñas, Hannah Klinkhammer, Nuria Bonifaci, Isabel Spier, Andreas Mayr, Emadeldin Hassanin, Anna Diez-Villanueva, Victor Moreno, Marta Pineda, Carlo Maj, Gabriel Capellà, Stefan Aretz, Joan Brunet
Ability of a polygenic risk score to refine colorectal cancer risk in Lynch syndrome. Journal of medical genetics (2023)
Sara Fernández-Castillejo, Bàrbara Roig, Mireia Melé, Sara Serrano, Mònica Salvat, Montserrat Querol, Joan Brunet, Marta Pineda, Adela Cisneros, David Parada, Joan Badia, Joan Borràs, Marta Rodriguez-Balada, Josep Gumà
Opportunistic genetic screening increases the diagnostic yield and is medically valuable for care of patients and their relatives with hereditary cancer. Journal of medical genetics (2023)
Laura Costas, Irene Onieva, Beatriz Pelegrina, Fátima Marin, Álvaro Carmona, Marta López-Querol, Jon Frias-Gomez, Paula Peremiquel-Trillas, José Manuel Martínez, Eduard Dorca, Joan Brunet, Marta Pineda, Jordi Ponce Sebastià, Xavier M Guiu, Silvia de Sanjosé, Francesc Xavier Bosch, Laia Alemany Vilches, Sonia Paytubi
Evaluation of somatic mutations in urine samples as a non-invasive method for the detection and molecular classification of endometrial cancer. Clinical cancer research : an official journal of the American Association for Cancer Research (2023)
Monika Morak, Marta Pineda, Alexandra Martins, Pascaline Gaildrat, Hélène Tubeuf, Aurélie Drouet, Carolina Gómez, Estela Dámaso, Kerstin Schaefer, Verena Steinke-Lange, Udo Koehler, Andreas Laner, Julie Hauchard, Karine Chauris, Elke Holinski-Feder, Gabriel Capellá Munar
Splicing analyses for variants in MMR genes: best practice recommendations from the European Mismatch Repair Working Group. European journal of human genetics : EJHG 30 (9) (2022)
Paula Peremiquel-Trillas, Sonia Paytubi, Beatriz Pelegrina, Jon Frias-Gomez, Álvaro Carmona, José Manuel Martínez, Javier de Francisco, Yolanda Benavente, Marc Barahona, Ferran Briansó, Júlia Canet-Hermida, Víctor Caño, August Vidal Bel, Alba Zanca, Núria Baixeras, Axel Rodríguez, Sergi Fernandez, Núria Dueñas, Laura Càrdenas, Álvaro Aytes, Ilaria Bianchi, Miquel Àngel Pavón, Jaume Reventós, Gabriel Capellà, David Gómez, Mireia Diaz, Jordi Ponce Sebastià, Joan Brunet, Xavier Matias-Guiu, Francesc Xavier Bosch, Silvia de Sanjosé, Laia Alemany, Marta Pineda, Fátima Marin, Laura Costas
An Integrated Approach for the Early Detection of Endometrial and Ovarian Cancers (Screenwide Study): Rationale, Study Design and Pilot Study. Journal of personalized medicine 12 (7) (2022)
Paula Peremiquel-Trillas, Jon Frias-Gomez, Laia Alemany, Alberto Ameijide, Mireia Vilardell, Rafael Marcos-Gragera, Sonia Paytubi, Jordi Ponce Sebastià, José Manuel Martínez, Marta Pineda, Joan Brunet, Xavier Matías-Guiu, Marià Carulla, Jaume Galceran, Ángel Izquierdo, Josep Maria Borràs, Laura Costas, Ramon Clèries
Predicting Ovarian-Cancer Burden in Catalonia by 2030: An Age-Period-Cohort Modelling. International journal of environmental research and public health 19 (3) (2022)
Chiara M S Herzog, Fátima Marin, Allison Jones, Iona Evans, Daniel Reisel, Elisa Redl, Lena Schreiberhuber, Sonia Paytubi, Beatriz Pelegrina, Álvaro Carmona, Paula Peremiquel-Trillas, Jon Frias-Gomez, Marta Pineda, Joan Brunet, Jordi Ponce Sebastià, Xavier Matias-Guiu, Silvia de Sanjosé, Laia Alemany, Adeola Olaitan, Michael Wong, Davor Jurkovic, Emma J Crosbie, Adam N Rosenthal, Line Bjorge, Michal Zikan, Lukáš Dostálek, David Cibula, Karin Sundström, Joakim Dillner, Laura Costas, Martin Widschwendter
A Simple Cervicovaginal Epigenetic Test for Screening and Rapid Triage of Women With Suspected Endometrial Cancer: Validation in Several Cohort and Case/Control Sets. Journal of clinical oncology : official journal of the American Society of Clinical Oncology 40 (33) (2022)
Mev Dominguez-Valentin, John-Paul Plazzer, Julian R Sampson, Christoph Engel, Stefan Aretz, Mark A Jenkins, Lone Sunde, Inge Bernstein, Gabriel Capellá Munar, Francesc Balaguer, Finlay Macrae, Ingrid M Winship, Huw Thomas, Dafydd Gareth Evans, John Burn, Marc Greenblatt, Wouter H de Vos Tot Nederveen Cappel, Rolf H Sijmons, Maartje Nielsen, Lucio Bertario, Bernardo Bonanni, Maria Grazia Tibiletti, Giulia Martina Cavestro, Annika Lindblom, Adriana Della Valle, Francisco Lopez-Kostner, Karin Alvarez, Nathan Gluck, Lior Katz, Karl Heinimann, Carlos Alberto Vaccaro, Sigve Nakken, Eivind Hovig, Kate Green, Fiona Lalloo, James Hill, Hans F A Vasen, Claudia Perne, Reinhard Büttner, Heike Görgens, Elke Holinski-Feder, Monika Morak, Stefanie Holzapfel, Robert Hueneburg, Magnus von Knebel Doeberitz, Markus Loeffler, Nils Rahner, Jürgen Weitz, Verena Steinke-Lange, Wolff Schmiegel, Deepak Ben Vangala, Emma J Crosbie, Marta Pineda, Matilde Navarro, Joan Brunet, Leticia Moreira, Ariadna Sánchez, Miquel Serra-Burriel, Miriam Mints, Revital Kariv, Guy Rosner, Tamara Alejandra Piñero, Walter Hernán Pavicic, Pablo Kalfayan, Sanne W Ten Broeke, Jukka-Pekka Mecklin, Kirsi Pylvänäinen, Laura Renkonen-Sinisalo, Anna Lepistö, Päivi Peltomäki, John L Hopper, Aung-Ko Win, Daniel D Buchanan, Noralane M Lindor, Steven Gallinger, Loic Le Marchand, Polly A Newcomb, Jane C Figueiredo, Stephen N Thibodeau, Christina Therkildsen, Thomas V O Hansen, Lars Lindberg, Einar Andreas Rødland, Florencia Neffa, Patricia Esperón, Douglas Tjandra, Gabriela Möslein, Toni T Seppälä, Pål Møller
No Difference in Penetrance between Truncating and Missense/Aberrant Splicing Pathogenic Variants in MLH1 and MSH2: A Prospective Lynch Syndrome Database Study. Journal of clinical medicine 10 (13) (2021)
Núria Dueñas, Matilde Navarro, Alex Teule, Ares Solanes, Mònica Salinas, Sílvia Iglesias, Elisabet Munté, Jordi Ponce Sebastià, Jordi Guardiola, Esther Kreisler, Elvira Carballas, Marta Cuadrado, Xavier Matias-Guiu, Napoleón de la Ossa, Joan Lop Gros, Conxi Lázaro, Gabriel Capellá Munar, Marta Pineda, Joan Brunet
Correction: Dueñas et al. Assessing Effectiveness of Colonic and Gynecological Risk Reducing Surgery in Lynch Syndrome Individuals. Cancers 2020, 12, 3419. Cancers 13 (13) (2021)
Jesús Del Valle, Paula Rofes, José Marcos Moreno-Cabrera, Adriana López-Dóriga, Sami Belhadj, Gardenia Vargas-Parra, Àlex Teulé, Raquel Cuesta, Xavier Muñoz, Olga Campos, Mónica Salinas, Rafael de Cid, Joan Brunet, Sara González, Gabriel Capellá Munar, Marta Pineda, Lídia Feliubadaló, Conxi Lázaro
Exploring the Role of Mutations in Fanconi Anemia Genes in Hereditary Cancer Patients. Cancers 12 (4) (2020)
Mariona Terradas, Pilar Mur, Sami Belhadj, Emma Roisin Woodward, George Joseph Burghel, Pau M Muñoz-Torres, Isabel Quintana, Matilde Navarro, Joan Brunet, Conxi Lazaro Garcia, Marta Pineda, Victor Moreno, Gabriel Capellá Munar, Dafydd Gareth Evans, Laura Valle
TP53, a gene for colorectal cancer predisposition in the absence of Li-Fraumeni-associated phenotypes. Gut 70 (6) (2020)
Miriam Cuatrecasas, Iñigo Gorostiaga, Cristina Riera, Esteban Saperas, Gemma Llort, Irmgard Costa, Xavier Matias-Guiu, Cristina Carrato, Matilde Navarro, Marta Pineda, Núria Dueñas, Joan Brunet, Vicente Marco, Isabel Trias, José Ignacio Busteros, Gemma Mateu, Francesc Balaguer, María-Teresa Fernández-Figueras, Manel Esteller, Eva Musulén
Complete Loss of EPCAM Immunoexpression Identifies EPCAM Deletion Carriers in MSH2-Negative Colorectal Neoplasia. Cancers 12 (10) (2020)
Núria Dueñas, Matilde Navarro, Àlex Teulé, Ares Solanes, Mònica Salinas, Sílvia Iglesias, Elisabet Munté, Jordi Ponce Sebastià, Jordi Guardiola, Esther Kreisler, Elvira Carballas, Marta Cuadrado, Xavier Matias-Guiu, Napoleón de la Ossa, Joan Lop Gros, Conxi Lázaro, Gabriel Capellá, Marta Pineda, Joan Brunet
Assessing Effectiveness of Colonic and Gynecological Risk Reducing Surgery in Lynch Syndrome Individuals. Cancers 12 (11) (2020)
Sanne W Ten Broeke, Mar Rodríguez-Girondo, Manon Suerink, Stefan Aretz, Inge Bernstein, Gabriel Capellá Munar, Christoph Engel, Encarna B Gomez-Garcia, Liselot P van Hest, Magnus von Knebel Doeberitz, Kristina Lagerstedt-Robinson, Tom G W Letteboer, Pal Moller, Theo A van Os, Marta Pineda, Nils Rahner, Maran J W Olderode-Berends, Jenny von Salomé, Hans K Schackert, Liesbeth Spruijt, Verena Steinke-Lange, Anja Wagner, Carli M J Tops, Maartje Nielsen
The Apparent Genetic Anticipation in PMS2-Associated Lynch Syndrome Families Is Explained by Birth-cohort Effect. Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 28 (6) (2019)
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 Munar, Marta Pineda
High-sensitivity microsatellite instability assessment for the detection of mismatch repair defects in normal tissue of biallelic germline mismatch repair mutation carriers. Journal of medical genetics 57 (4) (2019)