eQTL colocalization analysis highlights novel susceptibility genes in Autism Spectrum Disorders (ASD)

por Dominguez-Alonso, S., Carracedo, A., Rodriguez-Fontenla, C.
Publicado 2023

ZBTB7 HapMap in a worldwide population study

por Salas, A, Vega, A, Phillips, C, Torres, M, Quintela, I, Carracedo, A
Publicado 2005

Medical genomics: The intricate path from genetic variant identification to clinical interpretation

por Quintáns, B., Ordóñez-Ugalde, A., Cacheiro, P., Carracedo, A., Sobrido, M.J.
Publicado 2014

Neurofibromatosis without Neurofibromas: Confirmation of a Genotype-Phenotype Correlation and Implications for Genetic Testing

por Quintáns, B., Pardo, J., Campos, B., Barros, F., Volpini, V., Carracedo, Á., Sobrido, M.J.
Publicado 2011

High-density screening of the Zbtb7 gene in breast cancer patients

por Salas, A, Vega, A, Torres, M, Quintela, I, Phillips, C, Rodríguez-López, R, Rivas, G, Benítez, J, Carracedo, A
Publicado 2005

Psychiatric polygenic risk as a predictor of COVID-19 risk and severity: insight into the genetic overlap between schizophrenia and COVID-19

por Alemany-Navarro, M., Diz-de Almeida, S., Cruz, R., Riancho, J. A., Rojas-Martínez, A., Lapunzina, P., Flores, C., Carracedo, A.
Publicado 2023

How is COVID-19 affecting patients with obsessive–compulsive disorder? A longitudinal study on the initial phase of the pandemic in a Spanish cohort

por Alonso, P., Bertolín, S., Segalàs, J., Tubío-Fungueiriño, M., Real, E., Mar-Barrutia, L., Fernández-Prieto, M., Carvalho, S., Carracedo, A., Menchón, JM.
Publicado 2021

Large-scale single nucleotide polymorphism analysis of candidates for low-penetrance breast cancer genes

por Vega, A, Salas, A, Phillips, C, Sobrino, B, Carracedo, B, Ruíz-Ponte, C, Rodríguez-López, R, Rivas, G, Benítez, J, Carracedo, A
Publicado 2005

FAS system deregulation in T-cell lymphoblastic lymphoma

por Villa-Morales, M, Cobos, M A, González-Gugel, E, Álvarez-Iglesias, V, Martínez, B, Piris, M A, Carracedo, A, Benítez, J, Fernández-Piqueras, J
Publicado 2014

Mutational analysis of BRCA1 and BRCA2 genes in Spanish women with early-onset breast cancer

por Martínez-Ferrandis, JI, Vega, A, Marín-Garcia, P, Barros, F, Chaves, FJ, Carracedo, A, Armengod, ME, Chirivella, I, Lluch, A, García-Conde, J, Cervantes, A
Publicado 2000

Exploring the biological role of postzygotic and germinal de novo mutations in ASD

por Alonso-Gonzalez, A., Calaza, M., Amigo, J., González-Peñas, J., Martínez-Regueiro, R., Fernández-Prieto, M., Parellada, M., Arango, C., Rodriguez-Fontenla, Cristina, Carracedo, A.
Publicado 2021

HRAS1 minisatellite alleles and breast cancer in Spanish women under age forty years

por Vega, A, Martínez, JI, Barros, F, Marín-García, P, Chavez, FJ, Ruiz-Ponte, C, Chirivella, I, Lluch, A, Cervantes, A, García-Conde, I, Armengod, ME, Carracedo, A
Publicado 2000

Gravedad de COVID-19 atribuible a obesidad según IMC y CUN-BAE

por Fernández Crespo, S., Pérez-Matute, P., Íñiguez Martínez, M., Fernández-Villa, T., Domínguez-Garrido, E., Oteo, J.A., Marcos-Delgado, A., Flores, C., Riancho, J.A., Rojas-Martínez, A., Lapunzina, P., Carracedo, Á.
Publicado 2022

Exon-focused genome-wide association study of obsessive-compulsive disorder and shared polygenic risk with schizophrenia

por Costas, J, Carrera, N, Alonso, P, Gurriarán, X, Segalàs, C, Real, E, López-Solà, C, Mas, S, Gassó, P, Domènech, L, Morell, M, Quintela, I, Lázaro, L, Menchón, J M, Estivill, X, Carracedo, Á
Publicado 2016

Exome sequencing of early-onset patients supports genetic heterogeneity in colorectal cancer

por Fernández-Rozadilla, C., Álvarez-Barona, M., Quintana, I., López-Novo, A., Amigo, J., Cameselle-Teijeiro, J. M., Roman, E., Gonzalez, D., Llor, X., Bujanda, L., Bessa, X., Jover, R., Balaguer, F., Castells, A., Castellví-Bel, S., Capellá, G., Carracedo, A., Valle, L., Ruiz-Ponte, Clara
Publicado 2021

A two-phase case–control study for colorectal cancer genetic susceptibility: candidate genes from chromosomal regions 9q22 and 3q22

por Abulí, A, Fernández-Rozadilla, C, Giráldez, M D, Muñoz, J, Gonzalo, V, Bessa, X, Bujanda, L, Reñé, J M, Lanas, A, García, A M, Saló, J, Argüello, L, Vilella, À, Carreño, R, Jover, R, Xicola, R M, Llor, X, Carvajal-Carmona, L, Tomlinson, I P M, Kerr, D J, Houlston, R S, Piqué, J M, Carracedo, A, Castells, A, Andreu, M, Ruiz-Ponte, C, Castellví-Bel, S
Publicado 2011

COGENT (COlorectal cancer GENeTics): an international consortium to study the role of polymorphic variation on the risk of colorectal cancer

por Tomlinson, I P M, Dunlop, M, Campbell, H, Zanke, B, Gallinger, S, Hudson, T, Koessler, T, Pharoah, P D, Niittymäkix, I, Tuupanenx, S, Aaltonen, L A, Hemminki, K, Lindblom, A, Försti, A, Sieber, O, Lipton, L, van Wezel, T, Morreau, H, Wijnen, J T, Devilee, P, Matsuda, K, Nakamura, Y, Castellví-Bel, S, Ruiz-Ponte, C, Castells, A, Carracedo, A, Ho, J W C, Sham, P, Hofstra, R M W, Vodicka, P, Brenner, H, Hampe, J, Schafmayer, C, Tepel, J, Schreiber, S, Völzke, H, Lerch, M M, Schmidt, C A, Buch, S, Moreno, V, Villanueva, C M, Peterlongo, P, Radice, P, Echeverry, M M, Velez, A, Carvajal-Carmona, L, Scott, R, Penegar, S, Broderick, P, Tenesa, A, Houlston, R S
Publicado 2010

COGENT (COlorectal cancer GENeTics): an international consortium to study the role of polymorphic variation on the risk of colorectal cancer

por Tomlinson, I P M, Dunlop, M, Campbell, H, Zanke, B, Gallinger, S, Hudson, T, Koessler, T, Pharoah, P D, Niittymäki, I, Tuupanen, S, Aaltonen, L A, Hemminki, K, Lindblom, A, Försti, A, Sieber, O, Lipton, L, van Wezel, T, Morreau, H, Wijnen, J T, Devilee, P, Matsuda, K, Nakamura, Y, Castellví-Bel, S, Ruiz-Ponte, C, Castells, A, Carracedo, A, Ho, J W C, Sham, P, Hofstra, R M W, Vodicka, P, Brenner, H, Hampe, J, Schafmayer, C, Tepel, J, Schreiber, S, Völzke, H, Lerch, M M, Schmidt, C A, Buch, S, Moreno, V, Villanueva, C M, Peterlongo, P, Radice, P, Echeverry, M M, Velez, A, Carvajal-Carmona, L, Scott, R, Penegar, S, Broderick, P, Tenesa, A, Houlston, R S
Publicado 2010

Examining the independent and joint effects of genomic and exposomic liabilities for schizophrenia across the psychosis spectrum

por Pries, L.-K., Dal Ferro, G. A., van Os, J., Delespaul, P., Kenis, G., Lin, B. D., Luykx, J. J., Richards, A. L., Akdede, B., Binbay, T., Altınyazar, V., Yalınçetin, B., Gümüş-Akay, G., Cihan, B., Soygür, H., Ulaş, H., Şahin Cankurtaran, E., Ulusoy Kaymak, S., Mihaljevic, M. M., Andric Petrovic, S., Mirjanic, T., Bernardo, M., Mezquida, G., Amoretti, S., Bobes, J., Saiz, P. A., García-Portilla, M. Paz, Sanjuan, J., Aguilar, E. J., Santos, J. L., Jiménez-López, E., Arrojo, M., Carracedo, A., López, G., González-Peñas, J., Parellada, M., Maric, N. P., Atbaşoğlu, C., Ucok, A., Alptekin, K., Can Saka, M., Arango, C., O'Donovan, M., Tosato, S., Rutten, B. P. F., Guloksuz, S.
Publicado 2020

Stem cell-like transcriptional reprogramming mediates metastatic resistance to mTOR inhibition

por Mateo, F, Arenas, E J, Aguilar, H, Serra-Musach, J, de Garibay, G Ruiz, Boni, J, Maicas, M, Du, S, Iorio, F, Herranz-Ors, C, Islam, A, Prado, X, Llorente, A, Petit, A, Vidal, A, Català, I, Soler, T, Venturas, G, Rojo-Sebastian, A, Serra, H, Cuadras, D, Blanco, I, Lozano, J, Canals, F, Sieuwerts, A M, de Weerd, V, Look, M P, Puertas, S, García, N, Perkins, A S, Bonifaci, N, Skowron, M, Gómez-Baldó, L, Hernández, V, Martínez-Aranda, A, Martínez-Iniesta, M, Serrat, X, Cerón, J, Brunet, J, Barretina, M P, Gil, M, Falo, C, Fernández, A, Morilla, I, Pernas, S, Plà, M J, Andreu, X, Seguí, M A, Ballester, R, Castellà, E, Nellist, M, Morales, S, Valls, J, Velasco, A, Matias-Guiu, X, Figueras, A, Sánchez-Mut, J V, Sánchez-Céspedes, M, Cordero, A, Gómez-Miragaya, J, Palomero, L, Gómez, A, Gajewski, T F, Cohen, E E W, Jesiotr, M, Bodnar, L, Quintela-Fandino, M, López-Bigas, N, Valdés-Mas, R, Puente, X S, Viñals, F, Casanovas, O, Graupera, M, Hernández-Losa, J, Ramón y Cajal, S, García-Alonso, L, Saez-Rodriguez, J, Esteller, M, Sierra, A, Martín-Martín, N, Matheu, A, Carracedo, A, González-Suárez, E, Nanjundan, M, Cortés, J, Lázaro, C, Odero, M D, Martens, J W M, Moreno-Bueno, G, Barcellos-Hoff, M H, Villanueva, A, Gomis, R R, Pujana, M A
Publicado 2017