Research output per year
Research output per year
Fingerprint
Dive into the research topics where Lídia Gonzalez Quereda is active. These topic labels come from the works of this person. Together they form a unique fingerprint.
- 1 Similar Profiles
Network
Recent external collaboration on country/territory level. Dive into details by clicking on the dots or
Research output
- 108 Citations
- 5 h-Index
- 6 Article
-
Novel Somatic Genetic Variants as Predictors of Resistance to EGFR-Targeted Therapies in Metastatic Colorectal Cancer Patients
Riera, P., Rodríguez-Santiago, B., Lasa, A., Gonzalez-Quereda, L., Martín, B., Salazar, J., Sebio, A., Virgili, A. C., Minguillón, J., Camps, C., Surrallés, J. & Páez, D., 11 Aug 2020, In: Cancers. 12, 8Research output: Contribution to journal › Article › Research › peer-review
1 Citation (Scopus) -
Muscle MRI in a large cohort of patients with oculopharyngeal muscular dystrophy
Alonso-Jimenez, A., Kroon, R. H. M. J. M., Alejaldre-Monforte, A., Nuñez-Peralta, C., Horlings, C. G. C., Van Engelen, B. G. M., Olive, M., González, L., Verges-Gil, E., Paradas, C., Márquez, C., Garibaldi, M., Gallano, P., Rodriguez, M. J., Gonzalez-Quereda, L., Dominguez Gonzalez, C., Vissing, J., Fornander, F., Eisum, A. S. V., García-Sobrino, T. & 30 others, , 1 May 2019, In: Journal of Neurology, Neurosurgery and Psychiatry. 90, 5, p. 576-585 10 p.Research output: Contribution to journal › Article › Research
22 Citations (Scopus) -
Optimised molecular genetic diagnostics of Fanconi anaemia by whole exome sequencing and functional studies
Bogliolo, M., Pujol, R., Aza-Carmona, M., Muñoz-Subirana, N., Rodriguez-Santiago, B., Casado, J. A., Rio, P., Bauser, C., Reina-Castillón, J., Lopez-Sanchez, M., Gonzalez-Quereda, L., Gallano, P., Catalá, A., Ruiz-Llobet, A., Badell, I., Diaz-Heredia, C., Hladun, R., Senent, L., Argiles, B., Bergua Burgues, J. M. & 48 others, , 1 Jan 2019, In: Journal of Medical Genetics.Research output: Contribution to journal › Article › Research
15 Citations (Scopus) -
A new mutation of the SCGA gene is the cause of a late onset mild phenotype limb girdle muscular dystrophy type 2D with axial involvement
Gonzalez-Quereda, L., Gallardo, E., Töpf, A., Alonso-Jimenez, A., Straub, V., Rodriguez, M. J., Lleixa, C., Illa, I., Gallano, P. & Diaz-Manera, J., 1 Aug 2018, In: Neuromuscular Disorders. 28, 8, p. 633-638Research output: Contribution to journal › Article › Research › peer-review
11 Citations (Scopus) -
Muscle imaging in muscle dystrophies produced by mutations in the EMD and LMNA genes
Díaz-Manera, J., Alejaldre, A., González, L., Olivé, M., Gómez-Andrés, D., Muelas, N., Vílchez, J. J., Llauger, J., Carbonell, P., Márquez-Infante, C., Fernández-Torrón, R., Poza, J. J., López de Munáin, A., González-Quereda, L., Mirabet, S., Clarimon, J., Gallano, P., Rojas-García, R., Gallardo, E. & Illa, I., 1 Jan 2016, In: Neuromuscular Disorders. 26, 1, p. 33-40Research output: Contribution to journal › Article › Research › peer-review
27 Citations (Scopus)