Sara Gutiérrez-Enríquez

Scopus Author ID ORCID

Publication Activity (10 Years)

Years Active: 2018-2023
Publications (10 Years): 15

Top Venues

Human mutation

International journal of cancer

NPJ breast cancer

Cancer research

Vall d´Hebron Institut d´Oncologia

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

Affiliation History

Vall d´Hebron Institut d´Oncologia

Spain

Investigador Miguel Servet

Vall d'Hebron Institut de Recerca

Spain

Investigador postdoctoral

Hospital de la Santa Creu i Sant Pau Institut de Recerca

Spain

Investigador Posdoctoral

International Agency for Research on Cancer

France

Investigador Posdoctoral Marie Curie

Universitat Autònoma de Barcelona

Spain

Profesor asociado e investigador

Pontificia Universidad Católica del Ecuador

Ecuador

Profesor asociado e investigador

Publications

Juan C Rosas, Miguel Elías Aguado-Barrera, David Azria, Erik Briers, Rebecca Elliott, Marie-Pierre Farcy-Jacquet, Alexandra Giraldo, Sara Gutiérrez-Enríquez, Tiziana Rancati, Tim Rattay, Victoria Reyes, Barry Rosenstein, Dirk De Ruysscher, Elena Sperk, Hilary Stobart, Christopher Talbot, Ana Vega, Begoña Taboada-Valladares, Liv Veldeman, Tim Ward, Adam Webb, Catharine West, Jenny Chang-Claude, Petra Seibold, null null
(Pre)treatment risk factors for late fatigue and fatigue trajectories following radiotherapy for breast cancer. International journal of cancer (2023)
Juan C Rosas, Miguel Elías Aguado-Barrera, David Azria, Erik Briers, Rebecca Elliott, Marie-Pierre Farcy-Jacquet, Alexandra Giraldo, Sara Gutiérrez-Enríquez, Tiziana Rancati, Tim Rattay, Victoria Reyes, Barry Rosenstein, Dirk De Ruysscher, Elena Sperk, Hilary Stobart, Christopher Talbot, Ana Vega, Begoña Taboada-Valladares, Liv Veldeman, Tim Ward, Adam Webb, Catharine West, Jenny Chang-Claude, Petra Seibold, null null
Reply to: Comments on "(Pre)treatment risk factors for late fatigue and fatigue trajectories following radiotherapy for breast cancer". International journal of cancer (2023)
Benedetta Pellegrino, Andrea Herencia-Ropero, Alba Llop-Guevara, Flaminia Pedretti, Alejandro Moles-Fernández, Cristina Viaplana, Guillermo Villacampa, Marta Guzmán, Olga Rodríguez, Judit Grueso, Jose Jiménez, Enrique J Arenas, Andrea Degasperi, Joao M L Dias, Josep V Forment, Lenka Oplustil O'Connor, Olivier Déas, Stefano Cairo, Yinghui Zhou, Antonino Musolino, Carlos Caldas, Serena Nik-Zainal, Robert B Clarke, Paolo G Nuciforo, Orland Díez, Xavier Serres-Créixams, Vicente Peg, Martín Espinosa-Bravo, Teresa Macarulla, Ana Oaknin, Joaquin Mateo, Joaquín Arribas, Rodrigo Dienstmann, Meritxell Bellet-Ezquerra, Mafalda Oliveira, Cristina Saura, Sara Gutiérrez-Enríquez, Judith Balmaña, Violeta Serra
Preclinical In Vivo Validation of the RAD51 Test for Identification of Homologous Recombination-Deficient Tumors and Patient Stratification. Cancer research 82 (8) (2022)
Laia Castells-Roca, Sara Gutiérrez-Enríquez, Sandra Bonache, Massimo Bogliolo, Estela Carrasco, Miriam Aza-Carmona, Gemma Montalban, Núria Muñoz-Subirana, Roser Pujol, Cristina Cruz, Alba Llop-Guevara, María J Ramírez, Cristina Saura, Adriana Lasa, Violeta Serra, Orland Diez, Judith Balmaña, Jordi Surralles
Clinical consequences of BRCA2 hypomorphism. NPJ breast cancer 7 (1) (2021)
Na Li, Magnus Zethoven, Simone McInerny, Lisa Devereux, Yu-Kuan Huang, Niko Thio, Dane Cheasley, Sara Gutiérrez-Enríquez, Alejandro Moles-Fernández, Orland Diez, Tu Nguyen-Dumont, Melissa C Southey, John L Hopper, Jacques Simard, Martine Dumont, Penny Soucy, Alfons Meindl, Rita Schmutzler, Marjanka K Schmidt, Muriel A Adank, Irene L Andrulis, Eric Hahnen, Christoph Engel, Fabienne Lesueur, Elodie Girard, Susan L Neuhausen, Elad Ziv, Jamie Allen, Douglas F Easton, Rodney J Scott, Kylie L Gorringe, Paul A James, Ian G Campbell
Evaluation of the association of heterozygous germline variants in NTHL1 with breast cancer predisposition: an international multi-center study of 47,180 subjects. NPJ breast cancer 7 (1) (2021)
Alejandro Moles-Fernández, Joanna Domènech-Vivó, Anna Tenés, Judith Balmaña, Orland Diez, Sara Gutiérrez-Enríquez
Role of Splicing Regulatory Elements and In Silico Tools Usage in the Identification of Deep Intronic Splicing Variants in Hereditary Breast/Ovarian Cancer Genes. Cancers 13 (13) (2021)
Michael T Parsons, Emma Tudini, Hongyan Li, Eric Hahnen, Barbara Wappenschmidt, Lidia Feliubadaló, Cora M Aalfs, Simona Agata, Kristiina Aittomäki, Elisa Alducci, María Concepción Alonso-Cerezo, Norbert Arnold, Bernd Auber, Rachel Austin, Jacopo Azzollini, Judith Balmaña, Elena Barbieri, Claus R Bartram, Ana Blanco, Britta Blümcke, Sandra Bonache, Bernardo Bonanni, Åke Borg, Beatrice Bortesi, Joan Brunet, Carla Bruzzone, Karolin Bucksch, Giulia Cagnoli, Trinidad Caldés, Almuth Caliebe, Maria A Caligo, Mariarosaria Calvello, Gabriele L Capone, Sandrine M Caputo, Ileana Carnevali, Estela Carrasco, Virginie Caux-Moncoutier, Pietro Cavalli, Giulia Cini, Edward M Clarke, Paola Concolino, Elisa J Cops, Laura Cortesi, Fergus J Couch, Esther Darder, Miguel de la Hoya, Michael Dean, Irmgard Debatin, Jesús Del Valle, Capucine Delnatte, Nicolas Derive, Orland Diez, Nina Ditsch, Susan M Domchek, Véronique Dutrannoy, Diana M Eccles, Hans Ehrencrona, Ute Enders, D Gareth Evans, Chantal Farra, Ulrike Faust, Ute Felbor, Irene Feroce, Miriam Fine, William D Foulkes, Henrique C R Galvao, Gaetana Gambino, Andrea Gehrig, Francesca Gensini, Anne-Marie Gerdes, Aldo Germani, Jutta Giesecke, Viviana Gismondi, Carolina Gómez, Encarna B Gómez Garcia, Sara González, Elia Grau, Sabine Grill, Eva Gross, Aliana Guerrieri-Gonzaga, Marine Guillaud-Bataille, Sara Gutiérrez-Enríquez, Thomas Haaf, Karl Hackmann, Thomas V O Hansen, Marion Harris, Jan Hauke, Tilman Heinrich, Heide Hellebrand, Karen N Herold, Ellen Honisch, Judit Horvath, Claude Houdayer, Verena Hübbel, Silvia Iglesias, Angel Izquierdo, Paul A James, Linda A M Janssen, Udo Jeschke, Silke Kaulfuß, Katharina Keupp, Marion Kiechle, Alexandra Kölbl, Sophie Krieger, Torben A Kruse, Anders Kvist, Fiona Lalloo, Mirjam Larsen, Vanessa L Lattimore, Charlotte Lautrup, Susanne Ledig, Elena Leinert, Alexandra L Lewis, Joanna Lim, Markus Loeffler, Adrià López-Fernández, Emanuela Lucci-Cordisco, Nicolai Maass, Siranoush Manoukian, Monica Marabelli, Laura Matricardi, Alfons Meindl, Rodrigo D Michelli, Setareh Moghadasi, Alejandro Moles-Fernández, Marco Montagna, Gemma Montalban, Alvaro N Monteiro, Eva Montes, Luigi Mori, Lidia Moserle, Clemens R Müller, Christoph Mundhenke, Nadia Naldi, Katherine L Nathanson, Matilde Navarro, Heli Nevanlinna, Cassandra B Nichols, Dieter Niederacher, Henriette R Nielsen, Kai-Ren Ong, Nicholas Pachter, Edenir I Palmero, Laura Papi, Inge Sokilde Pedersen, Bernard Peissel, Pedro Perez-Segura, Katharina Pfeifer, Marta Pineda, Esther Pohl-Rescigno, Nicola K Poplawski, Berardino Porfirio, Anne S Quante, Juliane Ramser, Rui M Reis, Françoise Revillion, Kerstin Rhiem, Barbara Riboli, Julia Ritter, Daniela Rivera, Paula Rofes, Andreas Rump, Monica Salinas, Ana María Sánchez de Abajo, Gunnar Schmidt, Ulrike Schoenwiese, Jochen Seggewiß, Ares Solanes, Doris Steinemann, Mathias Stiller, Dominique Stoppa-Lyonnet, Kelly J Sullivan, Rachel Susman, Christian Sutter, Sean V Tavtigian, Soo H Teo, Alex Teulé, Mads Thomassen, Maria Grazia Tibiletti, Marc Tischkowitz, Silvia Tognazzo, Amanda Ewart Toland, Eva Tornero, Therese Törngren, Sara Torres-Esquius, Angela Toss, Alison H Trainer, Katherine M Tucker, Christi J van Asperen, Marion T van Mackelenbergh, Liliana Varesco, Gardenia Vargas-Parra, Raymonda Varon, Ana Vega, Ángela Velasco, Anne-Sophie Vesper, Alessandra Viel, Maaike P G Vreeswijk, Sebastian A Wagner, Anke Waha, Logan C Walker, Rhiannon J Walters, Shan Wang-Gohrke, Bernhard H F Weber, Wilko Weichert, Kerstin Wieland, Lisa Wiesmüller, Isabell Witzel, Achim Wöckel, Emma Roisin Woodward, Silke Zachariae, Valentina Zampiga, Christine Zeder-Göß, null null, Conxi Lázaro, Arcangela De Nicolo, Paolo Radice, Christoph Engel, Rita K Schmutzler, David E Goldgar, Amanda B Spurdle
Large scale multifactorial likelihood quantitative analysis of BRCA1 and BRCA2 variants: An ENIGMA resource to support clinical variant classification. Human mutation 40 (9) (2020)
Natália Padilla, Alejandro Moles-Fernández, Casandra Riera, Gemma Montalban, Selen Özkan, Lars Ootes, Sandra Bonache, Orland Diez, Sara Gutiérrez-Enríquez, Xavier de la Cruz
BRCA1- and BRCA2-specific in silico tools for variant interpretation in the CAGI 5 ENIGMA challenge. Human mutation 40 (9) (2019)
Melissa S Cline, Giulia Babbi, Sandra Bonache, Yue Cao, Rita Casadio, Xavier de la Cruz, Orland Díez, Sara Gutiérrez-Enríquez, Panagiostis Katsonis, Carmen Lai, Olivier Lichtarge, Pier Luigi Martelli, Gilad Mishne, Alejandro Moles-Fernández, Gemma Montalban, Sean D Mooney, Robert O'Conner, Lars Ootes, Selen Özkan, Natalia Padilla, Kymberleigh A Pagel, Vikas Pejaver, Predrag Radivojac, Casandra Riera, Castrense Savojardo, Yang Shen, Yuanfei Sun, Scott Topper, Michael T Parsons, Amanda B Spurdle, David E Goldgar, null null
Assessment of blind predictions of the clinical significance of BRCA1 and BRCA2 variants. Human mutation 40 (9) (2019)
Lídia Feliubadaló, Adrià López-Fernández, Marta Pineda, Orland Díez, Jesús Del Valle, Sara Gutiérrez-Enríquez, Alex Teulé, Sara González, Neda Stjepanovic, Mónica Salinas, Gabriel Capellá, Joan Brunet, Conxi Lázaro, Judith Balmaña, null null
Opportunistic testing of BRCA1, BRCA2 and mismatch repair genes improves the yield of phenotype driven hereditary cancer gene panels. International journal of cancer 145 (10) (2019)
Gemma Montalban, Sandra Bonache, Alejandro Moles-Fernández, Neus Gadea, Anna Tenés, Sara Torres-Esquius, Estela Carrasco, Judith Balmaña, Orland Diez, Sara Gutiérrez-Enríquez
Incorporation of semi-quantitative analysis of splicing alterations for the clinical interpretation of variants in BRCA1 and BRCA2 genes. Human mutation 40 (12) (2019)
Rita D Brandão, Klaas Mensaert, Irene López-Perolio, Demis Tserpelis, Markos Xenakis, Vanessa L Lattimore, Logan C Walker, Anders Kvist, Ana Vega, Sara Gutiérrez-Enríquez, Orland Diez, null null, Miguel de la Hoya, Amanda B Spurdle, Tim De Meyer, Marinus J Blok
Targeted RNA-seq successfully identifies normal and pathogenic splicing events in breast/ovarian cancer susceptibility and Lynch syndrome genes. International journal of cancer 145 (2) (2019)
Laura Duran-Lozano, Gemma Montalban, Sandra Bonache, Alejandro Moles-Fernández, Anna Tenés, Marta Castroviejo-Bermejo, Estela Carrasco, Adrià López-Fernández, Sara Torres-Esquius, Neus Gadea, Neda Stjepanovic, Judith Balmaña, Sara Gutiérrez-Enríquez, Orland Diez
Alternative transcript imbalance underlying breast cancer susceptibility in a family carrying PALB2 c.3201+5G>T. Breast cancer research and treatment 174 (2) (2018)
Gemma Montalban, Eugenia Fraile-Bethencourt, Irene López-Perolio, Pedro Pérez-Segura, Mar Infante, Mercedes Durán, María Concepción Alonso-Cerezo, Adrià López-Fernández, Orland Diez, Miguel de la Hoya, Eladio A Velasco, Sara Gutiérrez-Enríquez
Characterization of spliceogenic variants located in regions linked to high levels of alternative splicing: BRCA2 c.7976+5G > T as a case study. Human mutation 39 (9) (2018)
Sandra Bonache, Irene Esteban, Alejandro Moles-Fernández, Anna Tenés, Laura Duran-Lozano, Gemma Montalban, Vanessa Bach, Estela Carrasco, Neus Gadea, Adrià López-Fernández, Sara Torres-Esquius, Francesco Mancuso, Ginevra Caratú, Ana Vivancos, Noemí Tuset, Judith Balmaña, Sara Gutiérrez-Enríquez, Orland Diez
Multigene panel testing beyond BRCA1/2 in breast/ovarian cancer Spanish families and clinical actionability of findings. Journal of cancer research and clinical oncology 144 (12) (2018)

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Publication Activity (10 Years)

Top Topics

Top Venues

Sara Gutiérrez-Enríquez