Browsing by Author Blanco Guillermo, Ignacio

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Issue DateTitleAuthor(s)
17-Apr-2013Functional and Structural Analysis of C-Terminal BRCA1 Missense VariantsQuiles Vidal, Francisco de Asís; Fernández-Rodríguez, Juana; Mosca, Roberto; Feliubadaló i Elorza, Maria Lídia; Tornero, Eva; Brunet, Joan; Blanco Guillermo, Ignacio; Capellá, G. (Gabriel); Pujana Genestar, M. Ángel; Aloy, Patrick, 1972-; Monteiro, Alvaro N.; Lázaro García, Conxi
20-Oct-2009Gene expression profiling integrated into network modelling reveals heterogeneity in the mechanisms of BRCA1 tumorigenesisFernández-Ramires, Ricardo; Sole, Xavi; De Cecco, Loris; Llort Pursals, Gemma; Cazorla, Alicia; Bonifaci Cano, Núria; Garcia, Maria Jose; Caldés, Trinidad; Blanco Guillermo, Ignacio; Gariboldi, Manuela; Pierotti, Marco Alessandro; Pujana Genestar, M. Ángel; Benitez, Javier; Osorio, Ana
27-Mar-2013Genome-wide association study in BRCA1 mutation carriers identifies novel loci associated with breast and ovarian cancer riskCouch, Fergus J.; Wang, Xianshu; McGuffog, Lesley; Lee, Andrew; Olswold, Curtis; Kuchenbaecker, Karoline B.; Soucy, Penny; Fredericksen, Zachary; Barrowdale, Daniel; Dennis, Joe; Gaudet, Mia M.; Dicks, Ed; Kosel, Matthew; Healey, Sue; Sinilnikova, Olga M.; Bacot, François; Vincent, Daniel; Hogervorst, Frans B. L.; Peock, Susan; Stoppa-Lyonnet, Dominique; Jakubowska, Anna; Radice, Paolo; Schmutzler, Rita Katharina; Domchek, Susan M.; Piedmonte, Marion; Singer, Christian F.; Friedman, Eitan; Thomassen, Mads; Hansen, Thomas V. O.; Neuhausen, Susan L.; Szabo, Csilla I.; Blanco Guillermo, Ignacio; Greene, Mark H.; Karlan, Beth Y.; Garber, Judy; Phelan, Catherine M.; Weitzel, Jeffrey N.; Montagna, Marco; Olah, Edith
1-Dec-2017Geographical distribution of COPD prevalence in Europe, estimated by an inverse distance weighting interpolation techniqueBlanco Guillermo, Ignacio; Diego, Isidro; Bueno, Patricia; Fernández, Eloy; Casas-Maldonado, Francisco; Esquinas López, Cristina; Soriano, Joan B.; Miravitlles Fernández, Marc
2008Guidelines for the clinical management of familial adenomatous polyposis (FAP)Vasen, Hans; Möslein, Gabriela; Alonso, A.; Aretz, S.; Bernstein, Inge; Bertario, Lucio; Blanco Guillermo, Ignacio; Bülow, S.; Burn, John; Capellá, G. (Gabriel); Colas, Chrystelle; Engel, Christoph; Frayling, Ian M.; Friedl, W.; Hes, F. J.; Hodgson, Shirley; Järvinen, Heikki; Mecklin, Jukka-Pekka; Møller, Pål; Myrhoi, T.; Nagengast, F. M.; Parc, Yann; Phillips, R.; Clark, Susan K.; Ponz de Leon, Maurizio; Renkonen-Sinisalo, Laura; Sampson, J. R.; Stormorken, A.; Tejpar, Sabine; Thomas, H. J. W.; Wijnen, Juul
20-May-2011Haplotype structure in Ashkenazi Jewish BRCA1 and BRCA2 mutation carriersLázaro García, Conxi; Blanco Guillermo, Ignacio
27-Mar-2013Identification of a BRCA2-Specific modifier locus at 6p24 related to breast cancer riskGaudet, Mia M.; Kuchenbaecker, Karoline B.; Vijai, Joseph; Klein, Robert J.; Kirchhoff, Tomas; McGuffog, Lesley; Barrowdale, Daniel; Dunning, Alison M.; Lee, Andrew; Dennis, Joe; Healey, Sue; Dicks, Ed; Soucy, Penny; Sinilnikova, Olga M.; Pankratz, Vernon S.; Wang, Xianshu; Eldridge, Ronald C.; Tessier, Daniel C.; Vincent, Daniel; Bacot, François; Hogervorst, Frans B. L.; Peock, Susan; Stoppa-Lyonnet, Dominique; Peterlongo, Paolo; Schmutzler, Rita Katharina; Nathanson, Katherine L.; Piedmonte, Marion; Singer, Christian F.; Thomassen, Mads; Hansen, Thomas V. O.; Neuhausen, Susan L.; Blanco Guillermo, Ignacio; Lázaro García, Conxi
Feb-2015Identification of six new susceptibility loci for invasive epithelial ovarian cancerKuchenbaecker, Karoline B.; Ramus, Susan J.; Tyrer, Jonathan P.; Lee, Andrew; Shen, Howard C.; Beesley, Jonathan; Lawrenson, Kate; McGuffog, Lesley; Healey, Sue; Lee, Janet M.; Spindler, Tassja J.; Lin, Yvonne G.; Pejovic, Tanja; Bean, Yukie; Li, Qiyuan; Coetzee, Simon; Hazelett, Dennis; Miron, Alexander; Southey, Melissa C.; Terry, Mary Beth; Goldgar, David E.; Buys, Saundra S.; Janavicius, Ramunas; Dorfling, Cecilia M.; van Rensburg, Elizabeth J.; Neuhausen, Susan L.; Ding, Yuan Chun; Hansen, Thomas V. O.; Jønson, Lars; Gerdes, Anne Marie; Ejlertsen, Bent; Barrowdale, Daniel; Dennis, Joe; Benitez, Javier; Osorio, Ana; Garcia, Maria Jose; Komenaka, Ian; Blanco Guillermo, Ignacio; Lázaro García, Conxi; Pujana Genestar, M. Ángel
Sep-2017Incidence of and survival after subsequent cancers in carriers of pathogenic MMR variants with previous cancer: a report from the prospective Lynch syndrome databaseMøller, Pål; Seppälä, Toni T.; Bernstein, Inge; Holinski Feder, Elke; Sala, Paulo; Evans, D. Gareth; Lindblom, Annika; Macrae, Finlay; Blanco Guillermo, Ignacio; Sijmons, Rolf H.; Jeffries, Jacqueline; Vasen, Hans; Burn, John; Nakken, Sigve; Hovig, Eivind; Rødland, Einar Andreas; Tharmaratnam, Kukatharmini; de Vos Tot Nederveen Cappel, Wouter H.; Hill, James; Wijnen, Juul T.; Jenkins, Mark A.; Green, Kate; Lalloo, Fiona; Sunde, Lone; Mints, Miriam; Bertario, Lucio; Pineda Riu, Marta; Navarro García, Matilde; Morak, Monika; Renkonen Sinisalo, Laura; Frayling, Ian M.; Plazzer, John Paul; Pylvanainen, Kirsi; Genuardi, Maurizio; Mecklin, Jukka-Pekka; Möslein, Gabriela; Sampson, Julian R.; Capellá, G. (Gabriel); Mallorca Group
2011Interplay between BRCA1 and RHAMM Regulates Epithelial Apicobasal Polarization and May Influence Risk of Breast Cancer.Maxwell, Christopher A.; Gomez-Baldó, Laia; Bonifaci Cano, Núria; Guinó, Elisabet; Català, Isabel; Petit, Anna; Aguilar, Helena; Villanueva Garatachea, Alberto; Aytés Meneses, Álvaro; Serra-Musach, Jordi; Aiza, Gemma; Brunet, Joan; Castellsagué, Joan; Martrat Sànchez, Griselda; Urruticoechea Ribate, Ander; Blanco Guillermo, Ignacio; Lázaro García, Conxi; Capellá, G. (Gabriel); Genestar, Miquel Àngel; Moreno Aguado, Víctor
18-Jan-2000Intron splice acceptor site polymorphism in the hMSH2 gene in sporadic and familial colorectal cancerPalicio, M.; Blanco Guillermo, Ignacio; Tórtola, S.; González, I.; Marcuello, Eugenio; Brunet, Joan; Gonzalez Aguilera, Juan Jose; Peinado Morales, Miguel Á. (Miguel Ángel); Capellá, G. (Gabriel); Lluis, Fèlix
28-Feb-2019Lack of association between screening interval and cancer stage in Lynch syndrome may be accounted for by over-diagnosis; a prospective Lynch syndrome database reportSeppälä, Toni T.; Ahadova, Aysel; Dominguez Valentin, Mev; Macrae, Finlay; Evans, D. Gareth; Therkildsen, Christina; Sampson, Julian R.; Scott, RodneyJ.; Burn, John; Moslein, Gabriela; Bernstein, Inge; Holinski-Feder, Elke; Pylvanainen, Kirsi; Renkonen Sinisalo; Lepisto, Anna; Lautrup, Charlotte K.; Lindblom, Annika; Plazzer, John Paul; Winship, Ingrid; Tjandra, Douglas; Katz, Lior; Aretz, Stefan; Hüneburg, Robert; Holzapfel, Stefanie; Heinimann, Karl; Della Valle, Adriana; Neffa, Florencia; Gluck, Nathan; De Vos Tot Nederveen Cappel, Wouter H. WH.; Vasen, Hans; Morak, Monika; Steinke-Lange, Verena; Engel, Christoph; Rahner, Nils; Schmiegel, Wolff; Vangala, Deepak; Thomas, Huw; Green, Kate; Lalloo, Fiona; Crosbie, Emma J.; Hill, James; Capellá, G. (Gabriel); Pineda Riu, Marta; Navarro, Matilde; Blanco Guillermo, Ignacio; ten Broeke, Sanne W.; Nielsen, Maartje; Ljungmann, Ken; Nakken, Sigve; Lindor, Noralane; Frayling, Ian M.; Hovig, Eivind; Sunde, Lone; Kloor, Matthias; Mecklin, Jukka-Pekka; Kalager, Mette; Møller, Pål
1-Jul-2014Little evidence for association between the TGFBR1*6A variant and colorectal cancer: a family-based association study on non-syndromic family members from Australia and Spain.Ross, Jason P.; Lockett, Linda J.; Tabor, Bruce; Saunders, Ian W.; Young, Graeme P.; Macrae, Finlay; Blanco Guillermo, Ignacio; Capellá, G. (Gabriel); Brown, Glenn S; Lockett, Trevor J.; Hannan, Garry N.
3-Feb-2014Longer telomeres are associated with cancer risk in MMR-proficient hereditary non-polyposis colorectal cancerSeguí Gracia, Nuria; Guinó, Elisabet; Pineda Riu, Marta; Navarro, Matilde; Bellido Molías, Fernando; Lázaro García, Conxi; Blanco Guillermo, Ignacio; Moreno Aguado, Víctor; Capellá, G. (Gabriel); Valle Velasco, Laura
25-Jan-2012MLH1 promoter hypermethylation in the analytical algorithm of Lynch syndrome: a cost-effectiveness studyGausachs Romero, Mireia; Mur, Pilar; Corral, Julieta; Pineda Riu, Marta; González, Sara; Benito-Aracil, Llúcia; Menéndez Vilà, Mireia; Espinàs Piñol, Josep Alfons; Brunet, Joan; Iniesta, María Dolores; Gruber, Stephen B.; Lázaro García, Conxi; Blanco Guillermo, Ignacio; Capellá, G. (Gabriel)
1-Feb-2022Modeling iPSC-derived human neurofibroma-like tumors in mice uncovers the heterogeneity of Schwann cells within plexiform neurofibromasMazuelas, Helena; Magallón Lorenz, Míriam; Fernández Rodríguez, Juana; Uriarte Arrazola, Itziar; Richaud Patin, Yvonne; Terribas, Ernest; Villanueva Garatachea, Alberto; Castellanos, Elisabeth; Blanco Guillermo, Ignacio; Raya Chamorro, Ángel; Chojnacki, Jakub; Heyn, Holger; Romagosa Pérez-Portabella, Cleofé; Lázaro, Conxi; Gel, Bernat; Carrió, Meritxell; Serra Arenas, Eduard
27-Mar-2013Multiple independent variants at the TERT locus are associated with telomere length and risks of breast and ovarian cancerBlanco Guillermo, Ignacio; Australian Cancer Study; Australian Ovarian Cancer Study Group; GENICA (Gene Environment Interaction and Breast Cancer); SWE-BRCA Group; HEBON Investigators; EMBRACE Collaborators; GEMO Study Collaborators
Feb-2020Mutational spectrum by phenotype: panel-based NGS testing of patients with clinical suspition of RASopathy and children with multiple café-au-lait maculesCastellanos, Elisabeth; Rosas, Inma; Negro, Alex; Gel Moreno, Bernat; Alibés, Andreu; Baena, Neus; Pineda Marfà, Mercè; Pi, Graciela; Pintos, Guillem; Salvador, Hector; Lázaro García, Conxi; Blanco Guillermo, Ignacio; Vilageliu i Arqués, Lluïsa; Brems, Hilde; Grinberg Vaisman, Daniel Raúl; Legius, Eric; Serra Arenas, Eduard
1-Jun-2012Neurofibromatosis tipo 2: La historia de LidiaSolanes, Ares; Lázaro García, Conxi; Castellanos, Elisabeth; Serra Arenas, Eduard; Blanco Guillermo, Ignacio
17-Jan-2012Ovarian cancer susceptibility alleles and risk of ovarian cancer in BRCA1 and BRCA2 mutation carriersLázaro García, Conxi; Blanco Guillermo, Ignacio; Tornero, Eva; Navarro, Matilde; CIMBA Consortium