Projects per year
Personal profile
Expertise related to UN Sustainable Development Goals
In 2015, UN member states agreed to 17 global Sustainable Development Goals (SDGs) to end poverty, protect the planet and ensure prosperity for all. This person’s work contributes towards the following SDG(s):
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- 1 Similar Profiles
Projects
- 3 Finished
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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.
1/01/16 → 31/12/18
Project: Research Projects and Other Grants
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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., Pujol Calvet, M. R., Ramirez de Haro, M. J. & Estella Aguado, J.
1/01/13 → 30/06/16
Project: Research Projects and Other Grants
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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.
1/01/10 → 31/12/12
Project: Research Projects and Other Grants
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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. 189-194Research output: Contribution to journal › Article › Research
29 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
7 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
17 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. 458-463Research output: Contribution to journal › Article › Research › peer-review
44 Citations (Scopus) -
Decapping protein EDC4 regulates DNA repair and phenocopies BRCA1
Hernández, G., Ramírez, M. J., Minguillón, J., Quiles, P., Ruiz De Garibay, G., Aza-Carmona, M., Bogliolo, M., Pujol, R., Prados-Carvajal, R., Fernández, J., García, N., López, A., Gutiérrez-Enríquez, S., Diez, O., Benítez, J., Salinas, M., Teulé, A., Brunet, J., Radice, P., Peterlongo, P., & 7 others , 1 Dec 2018, In: Nature Communications. 9, 967.Research output: Contribution to journal › Article › Research
28 Citations (Scopus)