Gabriel Capellá Munar (Gabriel Capellá, Gabriel Capella)

ResearcherID ORCID

Publication Activity (10 Years)

Years Active: 2015-2024
Publications (10 Years): 23

Top Venues

European journal of human genetics : EJHG

Human mutation

Journal of clinical medicine

Cancers

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

Publications

Mariona Terradas, Stephanie A Schubert, Julen Viana-Errasti, Dina Ruano, Gemma Aiza, Maartje Nielsen, Paula Marciel, Carli M Tops, Genís Parra, Hans Morreau, David Torrents, Monique E van Leerdam, Gabriel Capellá Munar, Noel F C C de Miranda, Laura Valle, J Tom van Wezel
Germline NPAT inactivating variants as cause of hereditary colorectal cancer. European journal of human genetics : EJHG 32 (7) (2024)
Mariona Terradas, Stephanie A Schubert, Julen Viana-Errasti, Dina Ruano, Gemma Aiza, Maartje Nielsen, Paula Marciel, Carli M Tops, Genís Parra, Hans Morreau, David Torrents, Monique E van Leerdam, Gabriel Capellá Munar, Noel F C C de Miranda, Laura Valle, J Tom van Wezel
Germline NPAT inactivating variants as cause of hereditary colorectal cancer. European journal of human genetics : EJHG 32 (7) (2024)
Mariona Terradas, Stephanie A Schubert, Julen Viana-Errasti, Dina Ruano, Gemma Aiza, Maartje Nielsen, Paula Marciel, Carli M Tops, Genís Parra, Hans Morreau, David Torrents, Monique E van Leerdam, Gabriel Capellá Munar, Noel F C C de Miranda, Laura Valle, J Tom van Wezel
Germline NPAT inactivating variants as cause of hereditary colorectal cancer. European journal of human genetics : EJHG (2024)
Mariona Terradas, Stephanie A Schubert, Julen Viana-Errasti, Dina Ruano, Gemma Aiza, Maartje Nielsen, Paula Marciel, Carli M Tops, Genís Parra, Hans Morreau, David Torrents, Monique E van Leerdam, Gabriel Capellá Munar, Noel F C C de Miranda, Laura Valle, J Tom van Wezel
Germline NPAT inactivating variants as cause of hereditary colorectal cancer. European journal of human genetics : EJHG 32 (7) (2024)
Mariona Terradas, Stephanie A Schubert, Julen Viana-Errasti, Dina Ruano, Gemma Aiza, Maartje Nielsen, Paula Marciel, Carli M Tops, Genís Parra, Hans Morreau, David Torrents, Monique E van Leerdam, Gabriel Capellá Munar, Noel F C C de Miranda, Laura Valle, J Tom van Wezel
Germline NPAT inactivating variants as cause of hereditary colorectal cancer. European journal of human genetics : EJHG 32 (7) (2024)
Laura Valle, Lior H Katz, Andrew Latchford, Pilar Mur, Victor Moreno, Ian M Frayling, Brandie H Leach, Gabriel Capellá Munar, null null
Position statement of the International Society for Gastrointestinal Hereditary Tumours (InSiGHT) on APC I1307K and cancer risk. Journal of medical genetics (2023)
Mariona Terradas, Noemi Gonzalez-Abuin, Sandra García-Mulero, Julen Viana-Errasti, Gemma Aiza, Josep M Piulats, Joan Brunet, Gabriel Capellá Munar, Laura Valle
MBD4-associated neoplasia syndrome: screening of cases with suggestive phenotypes. European journal of human genetics : EJHG (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)
Pilar Mur, Lorena Magraner-Pardo, Sandra García-Mulero, Anna Díez-Villanueva, Jesús Del Valle, Elsa Ezquerro, Conxi Lazaro Garcia, Gabriel Capellá Munar, Victor Moreno, Rebeca Sanz-Pamplona, Tirso Pons, Laura Valle
Solving the enigma of POLD1 p.V295M as a potential cause of increased cancer risk. European journal of human genetics : EJHG (2021)
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)
Paula Rofes, Jesús Del Valle, Sara Torres-Esquius, Lidia Feliubadaló, Agostina Stradella, José Marcos Moreno-Cabrera, Adriana López-Doriga, Elisabet Munté, Rafael De Cid, Olga Campos, Raquel Cuesta, Álex Teulé, Èlia Grau, Judit Sanz, Gabriel Capellá Munar, Orland Díez, Joan Brunet, Judith Balmaña, Conxi Lázaro
BARD1 Pathogenic Variants are Associated with Triple-Negative Breast Cancer in a Spanish Hereditary Breast and Ovarian Cancer Cohort. Genes 12 (2) (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)
Sami Belhadj, Mariona Terradas, Pau M Muñoz-Torres, Gemma Aiza, Matilde Navarro, Gabriel Capellá Munar, Laura Valle
Candidate genes for hereditary colorectal cancer: Mutational screening and systematic review. Human mutation 41 (9) (2020)
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)
Mev Dominguez-Valentin, Toni T Seppälä, Christoph Engel, Stefan Aretz, Finlay Macrae, Ingrid Winship, Gabriel Capellá Munar, Huw Thomas, Eivind Hovig, Maartje Nielsen, Rolf H Sijmons, Lucio Bertario, Bernardo Bonanni, Maria Grazia Tibiletti, Giulia Martina Cavestro, Miriam Mints, Nathan Gluck, Lior Katz, Karl Heinimann, Carlos Alberto Vaccaro, Kate Green, Fiona Lalloo, James Hill, Wolff Schmiegel, Deepak Ben Vangala, Claudia Perne, Hans-Georg Strauß, Johanna Tecklenburg, Elke Holinski-Feder, Verena Steinke-Lange, Jukka-Pekka Mecklin, John-Paul Plazzer, Marta Pineda, Matilde Navarro, Joan Brunet Vidal, Revital Kariv, Guy Rosner, Tamara Alejandra Piñero, María Laura Gonzalez, Pablo Kalfayan, Julian R Sampson, Neil A J Ryan, D Gareth Evans, Pål Møller, Emma J Crosbie
Risk-Reducing Gynecological Surgery in Lynch Syndrome: Results of an International Survey from the Prospective Lynch Syndrome Database. Journal of clinical medicine 9 (7) (2020)
Natalia Guillén Díaz-Maroto, Rebeca Sanz-Pamplona, Mireia Berdiel-Acer, Francisco J Cimas, Elena García, Samuel Gonçalves-Ribeiro, Nerea Albert, Gemma Garcia-Vicién, Gabriel Capellá Munar, Victor Moreno, Ramon Salazar, Alberto Villanueva, David G Molleví
Noncanonical TGFβ Pathway Relieves the Blockade of IL1β/TGFβ-Mediated Crosstalk between Tumor and Stroma: TGFBR1 and TAK1 Inhibition in Colorectal Cancer. Clinical cancer research : an official journal of the American Association for Cancer Research 25 (14) (2019)
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)
Manon Suerink, Mar Rodríguez-Girondo, Heleen M van der Klift, Chrystelle Colas, Laurence Brugieres, Noémie Lavoine, Marjolijn Jongmans, Gabriel Capellá Munar, D Gareth Evans, Michael P Farrell, Maurizio Genuardi, Yael Goldberg, Encarna Gomez-Garcia, Karl Heinimann, Jessica I Hoell, Stefan Aretz, Kory W Jasperson, Inbal Kedar, Mitul B Modi, Sergey Nikolaev, Theo A M van Os, Tim Ripperger, Daniel Rueda, Leigha Senter, Wenche Sjursen, Lone Sunde, Christina Therkildsen, Maria G Tibiletti, Alison H Trainer, Yvonne J Vos, Anja Wagner, Ingrid M Winship, Katharina Wimmer, Stefanie Y Zimmermann, Hans F Vasen, Christi J van Asperen, Jeanine J Houwing-Duistermaat, Sanne W Ten Broeke, Maartje Nielsen
An alternative approach to establishing unbiased colorectal cancer risk estimation in Lynch syndrome. Genetics in medicine : official journal of the American College of Medical Genetics 21 (12) (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)
Mariona Terradas, Pau M Muñoz-Torres, Sami Belhadj, Gemma Aiza, Matilde Navarro, Joan Brunet, Gabriel Capellá Munar, Laura Valle
Contribution to colonic polyposis of recently proposed predisposing genes and assessment of the prevalence of NTHL1- and MSH3-associated polyposes. Human mutation 40 (11) (2019)
Estela Dámaso, Júlia Canet-Hermida, Gardenia Vargas-Parra, Àngela Velasco, Fátima Marín, Esther Darder, Jesús Del Valle, Anna Fernández, Àngel Izquierdo, Gemma Mateu, Glòria Oliveras, Carmen Escribano, Virgínia Piñol, Hugo-Ikuo Uchima, José Luis Soto, Megan Hitchins, Ramon Farrés, Conxi Lázaro, Bernat Queralt, Joan Brunet, Gabriel Capellá Munar, Marta Pineda
Highly sensitive MLH1 methylation analysis in blood identifies a cancer patient with low-level mosaic MLH1 epimutation. Clinical epigenetics 11 (1) (2019)
Pilar Mur, Ann-Sofie Jemth, Luka Bevc, Nuno Amaral, Matilde Navarro, Rafael Valdés-Mas, Tirso Pons, Gemma Aiza, Miguel Urioste, Alfonso Valencia, Conxi Lazaro Garcia, Victor Moreno, Xose S Puente, Pål Stenmark, Ulrika Warpman-Berglund, Gabriel Capellá Munar, Thomas Helleday, Laura Valle
Germline variation in the oxidative DNA repair genes NUDT1 and OGG1 is not associated with hereditary colorectal cancer or polyposis. Human mutation 39 (9) (2018)
Manon Suerink, Heleen M van der Klift, Sanne W Ten Broeke, Olaf M Dekkers, Inge Bernstein, Gabriel Capellá Munar, Encarna Gomez Garcia, Nicoline Hoogerbrugge, Tom G W Letteboer, Fred H Menko, Annika Lindblom, Arjen Mensenkamp, Pal Moller, Theo A van Os, Nils Rahner, Bert J W Redeker, M J W Olderode-Berends, Maran Olderode, Liesbeth Spruijt, Yvonne J Vos, Anja Wagner, Hans Morreau, Frederik J Hes, Hans F A Vasen, Carli M Tops, Juul T Wijnen, Maartje Nielsen
The effect of genotypes and parent of origin on cancer risk and age of cancer development in PMS2 mutation carriers. Genetics in medicine : official journal of the American College of Medical Genetics 18 (4) (2015)

Gabriel Capellá Munar.css-eqlu8i{font-size:small;padding-left:4px;} (Gabriel Capellá, Gabriel Capella)

Publication Activity (10 Years)

Top Topics

Top Venues

Gabriel Capellá Munar (Gabriel Capellá, Gabriel Capella)