Jordi Surralles Calonge

Department of Genetics and Microbiology

https://orcid.org/0000-0002-4041-7519

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

Research activity per year

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Personal profile

Education/Academic qualification

Ph. D., Universitat Autònoma de Barcelona (UAB)

Award Date: 17 Dec 1994

Postgraduate, Universitat Autònoma de Barcelona (UAB)

Award Date: 1 Jun 1992

Degree, Universitat Autònoma de Barcelona (UAB)

Award Date: 1 Jun 1990

External positions

Cap de unitat i investigador senior

4 Dec 2006 → …

Professor Agregat de Genètica, Universitat Autònoma de Barcelona (UAB)

15 Feb 2005 → …

Investigador "Ramón y Cajal", Universitat Autònoma de Barcelona (UAB)

1 Jan 2002 → 14 Feb 2005

Professor Ajudant Y2, Universitat Autònoma de Barcelona (UAB)

15 Sep 2000 → 31 Dec 2001

Professor Associat A4/6, Universitat Autònoma de Barcelona (UAB)

1 Apr 2000 → 15 Sep 2000

Contracte de reincorporació de Doctors del MEC, Universitat Autònoma de Barcelona (UAB)

1 Sep 1997 → 31 Mar 2000

Contracte de Reincorporació de Doctors del MEC, Universitat Autònoma de Barcelona (UAB)

1 Apr 1997 → 31 Jul 1997

Becario Postdoc.Progr.Ambiente (UE), University of Leiden

1 Jul 1995 → 31 Dec 1996

Investigador Senior

1 Jan 1995 → 30 Jun 1995

Becario FPI (MEC), Universitat Autònoma de Barcelona (UAB)

1 Jan 1991 → 31 Dec 1994

Col·laborador d'investigació del grup de Mutagènesis

1 Sep 1988 → 31 Jul 1990

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12 Similar Profiles

1 Active
26 Finished

CB06/07/0023: Inestabilidad genética y predisposición al cáncer
Surralles Calonge, J., Pujol Calvet, M. R., Ramirez de Haro, M. J., Hernandez Viedma, G., Lopez de Heredia Alonso, M., Miguillón Pedreño, J., Steigerwarld, D. & Umbert Mestres, G.
6/02/09 → 31/12/30
Project
Inhibitors of DNA damage repair for cancer therapy (FANCONINIB)
Surralles Calonge, J.
1/06/19 → 31/01/20
Project
Drug screening and repurposing in Fanconi anemia therapeutics (REPAIR-FANC)
Surralles Calonge, J., Minguillon Pedreño, J. & Montanuy Escribano, H.
1/04/16 → 31/03/18
Project
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
ANEMIA DE FANCONI: INVESTIGACION GENETICA Y APLICACIONES TERAPEUTICAS
Surralles Calonge, J., Mina Ibarra, L. B., Trujillo Quintero, J. P., Bogliolo, M., Pujol Calvet, R., Ramírez De Haro, M. J. & Umbert Maestre, M. G.
1/01/13 → 31/12/15
Project

7601 Citations
43 h-Index
133 Article
7 Review article
5 Chapter

Biallelic germline BRCA1 mutations in a patient with early onset breast cancer, mild Fanconi anemia-like phenotype, and no chromosome fragility
Keupp, K., Hampp, S., Hübbel, A., Maringa, M., Kostezka, S., Rhiem, K., Waha, A., Wappenschmidt, B., Pujol, R., Surrallés, J., Schmutzler, R. K., Wiesmüller, L. & Hahnen, E., 1 Sep 2019, In: Molecular genetics & genomic medicine. 7, e863.
Research output: Contribution to journal › Article › Research
5 Citations (Scopus)
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
11 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

4 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
6 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
29 Citations (Scopus)