Ngā hua rapu - Pita, Guillermo

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

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

    I whakaputaina 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 mā 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

    I whakaputaina 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 mā 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

    I whakaputaina 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 mā 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

    I whakaputaina 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 mā 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

    I whakaputaina 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 mā 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

    I whakaputaina 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 mā 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

    I whakaputaina 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 mā 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

    I whakaputaina 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 mā 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

    I whakaputaina 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 mā 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

    I whakaputaina 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 mā 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

    I whakaputaina 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 mā 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

    I whakaputaina 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 mā 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

    I whakaputaina 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 mā 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

    I whakaputaina 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 mā 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

    I whakaputaina 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 mā 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

    I whakaputaina 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 mā 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

    I whakaputaina 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 mā 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

    I whakaputaina 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 mā 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

    I whakaputaina 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 mā 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

    I whakaputaina 2009
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