Massimo Bogliolo

Department of Genetics and Microbiology

EmailMassimo.Bogliolo@uab.cat

Source: Scopus
Calculated based on no. of publications stored in Pure and citations from Scopus

Research output per year

If you made any changes in Pure these will be visible here soon.

Fingerprint

Dive into the research topics where Massimo Bogliolo is active. These topic labels come from the works of this person. Together they form a unique fingerprint.

17 Similar Profiles

3 Finished

Reparación del DNA y anemia de Fanconi: investigación genética y aplicaciones terapéuticas
Surralles Calonge, J., Umbert Maestre, M. G., Bogliolo , M., Castells Roca, L., Pujol Calvet, M. R. & Ramirez De Haro, M. J.
Ministerio de Economia y Competitividad (MINECO)
1/01/16 → 31/12/18
Project
Regenerative medicine for Fanconi anemia: generation of disease-free patient-specific iPS cells, and iPSC-derived hematopoietic progenitors and platelets.
Surralles Calonge, J., Bogliolo , M., Estella Aguado, J., Pujol Calvet, M. R. & Ramirez De Haro, M. J.
Fundació La Marató de TV3
1/01/13 → 30/06/16
Project
Genética Funcional y Biología Molecular del Síndrome de Predisposición al Cáncer Anemia de Fanconi
Surralles Calonge, J., Villa Fontes, J., Bogliolo , M., Cabré Fabré, O., Castella Castella, M., Castillo Bosch, P., Minguillon Pedreño, J., Pujol Calvet, M. R., Ramirez De Haro, M. J. & Umbert Maestre, M. G.
Ministerio de Ciencia e Innovación
1/01/10 → 31/12/12
Project

766 Citations
13 h-Index
18 Article
2 Review article
1 Chapter

From exome analysis in idiopathic azoospermia to the identification of a high-risk subgroup for occult Fanconi anemia
Krausz, C., Riera-Escamilla, A., Chianese, C., Moreno-Mendoza, D., Ars, E., Rajmil, O., Pujol, R., Bogliolo, M., Blanco, I., Rodríguez, I., Badell, I., Ruiz-Castañé, E. & Surrallés, J., 1 Jan 2019, In : Genetics in Medicine. 21, p. 189-194
Research output: Contribution to journal › Article › Research
9 Citations (Scopus)
Functional comparison of XPF missense mutations associated to multiple DNA repair disorders
Marín, M., Ramírez, M. J., Carmona, M. A., Jia, N., Ogi, T., Bogliolo, M. & Surrallés, J., 1 Jan 2019, In : Genes. 10, 60.
Research output: Contribution to journal › Article › Research
3 Citations (Scopus)
Functional comparison of XPF missense mutations associated to multiple DNA repair disorders.
Marín, M., Ramírez, M. J., Carmona, M. A., Jia, N., Ogi, T., Bogliolo, M. & Surrallés, J., 1 Jan 2019, In : Genes. p. -
Research output: Contribution to journal › Article › Research

3 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, Bañez, F., Arrizabalaga, B., López Almaraz, R., Lopez, M., Figuera, Á., Molinés, A., Pérez De Soto, I., Hernando, I., Muñoz, J. A., Del Rosario Marin, M., Balmaña, J., Stjepanovic, N., Carrasco, E., Cuesta, I., Cosuelo, J. M., Regueiro, A., Moraleda Jimenez, J., Galera-Miñarro, A. M., Rosiñol, L., Carrió, A., Beléndez-Bieler, C., Escudero Soto, A., Cela, E., De La Mata, G., Fernández-Delgado, R., Garcia-Pardos, M. C., Sáez-Villaverde, R., Barragaño, M., Portugal, R., Lendinez, F., Hernadez, I., Vagace, J. M., Tapia, M., Nieto, J., Garcia, M., Gonzalez, M., Vicho, C., Galvez, E., Valiente, A., Antelo, M. L., Ancliff, P., Garcia, F., Dopazo, J., Sevilla, J., Paprotka, T., Pérez-Jurado, L. A., Bueren, J. & Surralles, J., 1 Jan 2019, In : Journal of Medical Genetics.
Research output: Contribution to journal › Article › Research
5 Citations (Scopus)
Biallelic truncating FANCM mutations cause early-onset cancer but not Fanconi anemia
Bogliolo, M., Bluteau, D., Lespinasse, J., Pujol, R., Vasquez, N., D'Enghien, C. D., Stoppa-Lyonnet, D., Leblanc, T., Soulier, J. & Surrallés, J., 1 Apr 2018, In : Genetics in Medicine. 20, 4, p. 458-463
Research output: Contribution to journal › Article › Research › peer-review
26 Citations (Scopus)