Search Results - Pita, Guillermo

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  1. 1
    Human Genomic Diversity Where the Mediterranean Joins the Atlantic

    Human Genomic Diversity Where the Mediterranean Joins the Atlantic by Hernández, Candela L, Pita, Guillermo, Cavadas, Bruno, López, Saioa, Sánchez-Martínez, Luis J, Dugoujon, Jean-Michel, Novelletto, Andrea, Cuesta, Pedro, Pereira, Luisa, Calderón, Rosario

    Published 2020
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  2. 2
    Effect of ABCB1 and ABCC3 Polymorphisms on Osteosarcoma Survival after Chemotherapy: A Pharmacogenetic Study

    Effect of ABCB1 and ABCC3 Polymorphisms on Osteosarcoma Survival after Chemotherapy: A Pharmacogenetic Study by Caronia, Daniela, Patiño-Garcia, Ana, Peréz-Martínez, Antonio, Pita, Guillermo, Moreno, Leticia Tais, Zalacain-Díez, Marta, Molina, Blanca, Colmenero, Isabel, Sierrasesúmaga, Luis, Benítez, Javier, Gonzalez-Neira, Anna

    Published 2011
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  3. 3
    Identification of genetic variants associated with capecitabine-induced hand-foot syndrome through integration of patient and cell-line genomic analyses

    Identification of genetic variants associated with capecitabine-induced hand-foot syndrome through integration of patient and cell-line genomic analyses by Wheeler, Heather E., Gonzalez-Neira, Anna, Pita, Guillermo, de la Torre- Montero, Julio-Cesar, Alonso, Rosario, Lopez-Fernandez, Luis A., Alba, Emilio, Martín, Miguel, Dolan, M. Eileen

    Published 2014
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  4. 4
    Deep Sequencing of Target Linkage Assay-Identified Regions in Familial Breast Cancer: Methods, Analysis Pipeline and Troubleshooting

    Deep Sequencing of Target Linkage Assay-Identified Regions in Familial Breast Cancer: Methods, Analysis Pipeline and Troubleshooting by Rosa-Rosa, Juan Manuel, Gracia-Aznárez, Francisco Javier, Hodges, Emily, Pita, Guillermo, Rooks, Michelle, Xuan, Zhenyu, Bhattacharjee, Arindam, Brizuela, Leonardo, Silva, José M., Hannon, Gregory J., Benitez, Javier

    Published 2010
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  5. 5
    Exome sequencing of three cases of familial exceptional longevity

    Exome sequencing of three cases of familial exceptional longevity by Cash, Timothy P, Pita, Guillermo, Domínguez, Orlando, Alonso, Maria R, Moreno, Leticia T, Borrás, Consuelo, Rodríguez-Mañas, Leocadio, Santiago, Catalina, Garatachea, Nuria, Lucia, Alejandro, Avellana, Juan A, Viña, Jose, González-Neira, Anna, Serrano, Manuel

    Published 2014
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  6. 6
    Genomewide high-density SNP linkage analysis of non-BRCA1/2 breast cancer families identifies various candidate regions and has greater power than microsatellite studies

    Genomewide high-density SNP linkage analysis of non-BRCA1/2 breast cancer families identifies various candidate regions and has greater power than microsatellite studies by Gonzalez-Neira, Anna, Rosa-Rosa, Juan Manuel, Osorio, Ana, Gonzalez, Emilio, Southey, Melissa, Sinilnikova, Olga, Lynch, Henry, Oldenburg, Rogier A, van Asperen, Christi J, Hoogerbrugge, Nicoline, Pita, Guillermo, Devilee, Peter, Goldgar, David, Benitez, Javier

    Published 2007
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  7. 7
    Genetic analysis of the vitamin D receptor gene in two epithelial cancers: melanoma and breast cancer case-control studies

    Genetic analysis of the vitamin D receptor gene in two epithelial cancers: melanoma and breast cancer case-control studies by Barroso, Eva, Fernandez, Lara P, Milne, Roger L, Pita, Guillermo, Sendagorta, Elena, Floristan, Uxua, Feito, Marta, Aviles, Jose A, Martin-Gonzalez, Manuel, Arias, Jose I, Zamora, Pilar, Blanco, Monserrat, Lazaro, Pablo, Benitez, Javier, Ribas, Gloria

    Published 2008
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  8. 8
    Genome-wide Linkage Scan Reveals Three Putative Breast-Cancer-Susceptibility Loci

    Genome-wide Linkage Scan Reveals Three Putative Breast-Cancer-Susceptibility Loci by Rosa-Rosa, Juan Manuel, Pita, Guillermo, Urioste, Miguel, Llort, Gemma, Brunet, Joan, Lázaro, Conxi, Blanco, Ignacio, Ramón y Cajal, Teresa, Díez, Orland, de la Hoya, Miguel, Caldés, Trinidad, Tejada, Maria-Isabel, González-Neira, Anna, Benítez, Javier

    Published 2009
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  9. 9
    Assessment of Copy Number Variation Using the Illumina Infinium 1M SNP-Array: A Comparison of Methodological Approaches in the Spanish Bladder Cancer/EPICURO Study

    Assessment of Copy Number Variation Using the Illumina Infinium 1M SNP-Array: A Comparison of Methodological Approaches in the Spanish Bladder Cancer/EPICURO Study by Marenne, Gaëlle, Rodríguez-Santiago, Benjamín, Closas, Montserrat García, Pérez-Jurado, Luis, Rothman, Nathaniel, Rico, Daniel, Pita, Guillermo, Pisano, David G., Kogevinas, Manolis, Silverman, Debra T., Valencia, Alfonso, Real, Francisco X., Chanock, Stephen J., Génin, Emmanuelle, Malats, Núria

    Published 2011
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  10. 10
    POLRMT as a Novel Susceptibility Gene for Cardiotoxicity in Epirubicin Treatment of Breast Cancer Patients

    POLRMT as a Novel Susceptibility Gene for Cardiotoxicity in Epirubicin Treatment of Breast Cancer Patients by Velasco-Ruiz, Alejandro, Nuñez-Torres, Rocio, Pita, Guillermo, Wildiers, Hans, Lambrechts, Diether, Hatse, Sigrid, Delombaerde, Danielle, Van Brussel, Thomas, Alonso, M. Rosario, Alvarez, Nuria, Herraez, Belen, Vulsteke, Christof, Zamora, Pilar, Lopez-Fernandez, Teresa, Gonzalez-Neira, Anna

    Published 2021
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  11. 11
    Association Between ABCB1 Genetic Variants and Persistent Chemotherapy-Induced Alopecia in Women With Breast Cancer

    Association Between ABCB1 Genetic Variants and Persistent Chemotherapy-Induced Alopecia in Women With Breast Cancer by Núñez-Torres, Rocío, Martín, Miguel, García-Sáenz, Jose Ángel, Rodrigo-Faus, María, del Monte-Millán, María, Tejera-Pérez, Hugo, Pita, Guillermo, de la Torre-Montero, Julio C., Pinilla, Karen, Herraez, Belén, Peiró-Chova, Lorena, Bermejo, Begoña, Lluch, Anna, González-Neira, Anna

    Published 2020
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  12. 12
    A candidate gene study of capecitabine-related toxicity in colorectal cancer identifies new toxicity variants at DPYD and a putative role for ENOSF1 rather than TYMS

    A candidate gene study of capecitabine-related toxicity in colorectal cancer identifies new toxicity variants at DPYD and a putative role for ENOSF1 rather than TYMS by Rosmarin, Dan, Palles, Claire, Pagnamenta, Alistair, Kaur, Kulvinder, Pita, Guillermo, Martin, Miguel, Domingo, Enric, Jones, Angela, Howarth, Kimberley, Freeman-Mills, Luke, Johnstone, Elaine, Wang, Haitao, Love, Sharon, Scudder, Claire, Julier, Patrick, Fernández-Rozadilla, Ceres, Ruiz-Ponte, Clara, Carracedo, Angel, Castellvi-Bel, Sergi, Castells, Antoni, Gonzalez-Neira, Anna, Taylor, Jenny, Kerr, Rachel, Kerr, David, Tomlinson, Ian

    Published 2015
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  13. 13
    Standard Versus Continuous Administration of Capecitabine in Metastatic Breast Cancer (GEICAM/2009-05): A Randomized, Noninferiority Phase II Trial With a Pharmacogenetic Analysis

    Standard Versus Continuous Administration of Capecitabine in Metastatic Breast Cancer (GEICAM/2009-05): A Randomized, Noninferiority Phase II Trial With a Pharmacogenetic Analysis by Martín, Miguel, Martínez, Noelia, Ramos, Manuel, Calvo, Lourdes, Lluch, Ana, Zamora, Pilar, Muñoz, Montserrat, Carrasco, Eva, Caballero, Rosalía, García-Sáenz, José Ángel, Guerra, Eva, Caronia, Daniela, Casado, Antonio, Ruíz-Borrego, Manuel, Hernando, Blanca, Chacón, José Ignacio, De la Torre-Montero, Julio César, Jimeno, María Ángeles, Heras, Lucía, Alonso, Rosario, De la Haba, Juan, Pita, Guillermo, Constenla, Manuel, González-Neira, Anna

    Published 2015
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  14. 14
    A POGLUT1 mutation causes a muscular dystrophy with reduced Notch signaling and satellite cell loss

    A POGLUT1 mutation causes a muscular dystrophy with reduced Notch signaling and satellite cell loss by Servián‐Morilla, Emilia, Takeuchi, Hideyuki, Lee, Tom V, Clarimon, Jordi, Mavillard, Fabiola, Area‐Gómez, Estela, Rivas, Eloy, Nieto‐González, Jose L, Rivero, Maria C, Cabrera‐Serrano, Macarena, Gómez‐Sánchez, Leonardo, Martínez‐López, Jose A, Estrada, Beatriz, Márquez, Celedonio, Morgado, Yolanda, Suárez‐Calvet, Xavier, Pita, Guillermo, Bigot, Anne, Gallardo, Eduard, Fernández‐Chacón, Rafael, Hirano, Michio, Haltiwanger, Robert S, Jafar‐Nejad, Hamed, Paradas, Carmen

    Published 2016
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  15. 15
    Whole exome sequencing characterization of individuals presenting extreme phenotypes of high and low risk of developing tobacco-induced lung adenocarcinoma

    Whole exome sequencing characterization of individuals presenting extreme phenotypes of high and low risk of developing tobacco-induced lung adenocarcinoma by Patiño-García, Ana, Guruceaga, Elizabeth, Segura, Victor, Sánchez Bayona, Rodrigo, Andueza, Maria Pilar, Tamayo Uria, Ibon, Serrano, Guillermo, Fusco, Juan Pablo, Pajares, María José, Gurpide, Alfonso, Ocón, Marimar, Sanmamed, Miguel F., Rodriguez Ruiz, Maria, Melero, Ignacio, Lozano, Maria Dolores, de Andrea, Carlos, Pita, Guillermo, Gonzalez-Neira, Anna, Gonzalez, Alvaro, Zulueta, Javier J., Montuenga, Luis M., Pio, Ruben, Perez-Gracia, Jose Luis

    Published 2021
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  16. 16
    Recurrent Germline DLST Mutations in Individuals with Multiple Pheochromocytomas and Paragangliomas

    Recurrent Germline DLST Mutations in Individuals with Multiple Pheochromocytomas and Paragangliomas by Remacha, Laura, Pirman, David, Mahoney, Christopher E., Coloma, Javier, Calsina, Bruna, Currás-Freixes, Maria, Letón, Rocío, Torres-Pérez, Rafael, Richter, Susan, Pita, Guillermo, Herráez, Belén, Cianchetta, Giovanni, Honrado, Emiliano, Maestre, Lorena, Urioste, Miguel, Aller, Javier, García-Uriarte, Óscar, Gálvez, María Ángeles, Luque, Raúl M., Lahera, Marcos, Moreno-Rengel, Cristina, Eisenhofer, Graeme, Montero-Conde, Cristina, Rodríguez-Antona, Cristina, Llorca, Óscar, Smolen, Gromoslaw A., Robledo, Mercedes, Cascón, Alberto

    Published 2019
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  17. 17
    Recurrent Germline DLST Mutations in Individuals with Multiple Pheochromocytomas and Paragangliomas

    Recurrent Germline DLST Mutations in Individuals with Multiple Pheochromocytomas and Paragangliomas by Remacha, Laura, Pirman, David, Mahoney, Christopher E., Coloma, Javier, Calsina, Bruna, Currás-Freixes, Maria, Letón, Rocío, Torres-Pérez, Rafael, Richter, Susan, Pita, Guillermo, Herráez, Belén, Cianchetta, Giovanni, Honrado, Emiliano, Maestre, Lorena, Urioste, Miguel, Aller, Javier, García-Uriarte, Óscar, Gálvez, María Ángeles, Luque, Raúl M., Lahera, Marcos, Moreno-Rengel, Cristina, Eisenhofer, Graeme, Montero-Conde, Cristina, Rodríguez-Antona, Cristina, Llorca, Óscar, Smolen, Gromoslaw A., Robledo, Mercedes, Cascón, Alberto

    Published 2019
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  18. 18
    Whole Exome Sequencing Suggests Much of Non-BRCA1/BRCA2 Familial Breast Cancer Is Due to Moderate and Low Penetrance Susceptibility Alleles

    Whole Exome Sequencing Suggests Much of Non-BRCA1/BRCA2 Familial Breast Cancer Is Due to Moderate and Low Penetrance Susceptibility Alleles by Gracia-Aznarez, Francisco Javier, Fernandez, Victoria, Pita, Guillermo, Peterlongo, Paolo, Dominguez, Orlando, de la Hoya, Miguel, Duran, Mercedes, Osorio, Ana, Moreno, Leticia, Gonzalez-Neira, Anna, Rosa-Rosa, Juan Manuel, Sinilnikova, Olga, Mazoyer, Sylvie, Hopper, John, Lazaro, Conchi, Southey, Melissa, Odefrey, Fabrice, Manoukian, Siranoush, Catucci, Irene, Caldes, Trinidad, Lynch, Henry T., Hilbers, Florentine S. M., van Asperen, Christi J., Vasen, Hans F. A., Goldgar, David, Radice, Paolo, Devilee, Peter, Benitez, Javier

    Published 2013
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  19. 19
    Genomic characterization of individuals presenting extreme phenotypes of high and low risk to develop tobacco‐induced lung cancer

    Genomic characterization of individuals presenting extreme phenotypes of high and low risk to develop tobacco‐induced lung cancer by Fusco, Juan Pablo, Pita, Guillermo, Pajares, María José, Andueza, Maria Pilar, Patiño‐García, Ana, de‐Torres, Juan P., Gurpide, Alfonso, Zulueta, Javier, Alonso, Rosario, Alvarez, Nuria, Pio, Ruben, Melero, Ignacio, Sanmamed, Miguel F., Rodriguez Ruiz, Maria, Gil‐Bazo, Ignacio, Lopez‐Picazo, Jose María, Casanova, Ciro, Baz Davila, Rebeca, Agudo, Antonio, Lozano, Maria Dolores, Gonzalez, Alvaro, Sala, Nuria, Ardanaz, Eva, Benitez, Javier, Montuenga, Luis, Gonzalez‐Neira, Anna, Perez‐Gracia, Jose Luis

    Published 2018
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  20. 20
    The Variant rs1867277 in FOXE1 Gene Confers Thyroid Cancer Susceptibility through the Recruitment of USF1/USF2 Transcription Factors

    The Variant rs1867277 in FOXE1 Gene Confers Thyroid Cancer Susceptibility through the Recruitment of USF1/USF2 Transcription Factors by Landa, Iñigo, Ruiz-Llorente, Sergio, Montero-Conde, Cristina, Inglada-Pérez, Lucía, Schiavi, Francesca, Leskelä, Susanna, Pita, Guillermo, Milne, Roger, Maravall, Javier, Ramos, Ignacio, Andía, Víctor, Rodríguez-Poyo, Paloma, Jara-Albarrán, Antonino, Meoro, Amparo, del Peso, Cristina, Arribas, Luis, Iglesias, Pedro, Caballero, Javier, Serrano, Joaquín, Picó, Antonio, Pomares, Francisco, Giménez, Gabriel, López-Mondéjar, Pedro, Castello, Roberto, Merante-Boschin, Isabella, Pelizzo, Maria-Rosa, Mauricio, Didac, Opocher, Giuseppe, Rodríguez-Antona, Cristina, González-Neira, Anna, Matías-Guiu, Xavier, Santisteban, Pilar, Robledo, Mercedes

    Published 2009
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