Isabel Badell Serra

Department of Paediatrics, Obstetrics and Gynaecology and Preventive Medicine and Public Health

Source: Scopus
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Personal profile

Education/Academic qualification

Degree, Universitat de Barcelona

Award Date: 1 Jan 1976

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1 Finished

Anemia de Fanconi: cap a un nou diagnòstic citogenètic molecular i relació entre longitud telomèrica, fragilitat cromosòmica i pancitopenia progressiva.
Creus Capdevila, A., Blasco Marhuenda, M. A., Ortega Aramburu, J. J., Puerto Navarro, S., Badell Serra, I., Suarez Figueras, S. & Surralles Calonge, J.
2/03/99 → 31/12/00
Project

799 Citations
15 h-Index
54 Article
3 Chapter
1 Review article

Long-term outcome after allogeneic hematopoietic stem cell transplantation for Shwachman–Diamond syndrome: a retrospective analysis and a review of the literature by the Severe Aplastic Anemia Working Party of the European Society for Blood and Marrow Transplantation (SAAWP-EBMT)
Cesaro, S., Pillon, M., Sauer, M., Smiers, F., Faraci, M., de Heredia, C. D., Wynn, R., Greil, J., Locatelli, F., Veys, P., Uyttebroeck, A., Ljungman, P., Chevalier, P., Ansari, M., Badell, I., Güngör, T., Salim, R., Tischer, J., Tecchio, C., Russell, N. & 13 others, Chybicka, A., Styczynski, J., Krivan, G., Smith, O., Stein, J., Afanasyev, B., Pochon, C., Menconi, M. C., Bosman, P., Mauro, M., Tridello, G., de Latour, R. P. & Dufour, C., 1 Sep 2020, In: Bone Marrow Transplantation. 55, 9, p. 1796-1809 14 p.
Research output: Contribution to journal › Article › Research › peer-review
3 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)
Genetic analyses of aplastic anemia and idiopathic pulmonary fibrosis patients with short telomeres, possible implication of DNA-repair genes
Arias-Salgado, E. G., Galvez, E., Planas-Cerezales, L., Pintado-Berninches, L., Vallespin, E., Martinez, P., Carrillo, J., Iarriccio, L., Ruiz-Llobet, A., Catalá, A., Badell-Serra, I., Gonzalez-Granado, L. I., Martín-Nalda, A., Martínez-Gallo, M., Galera-Miñarro, A., Rodríguez-Vigil, C., Bastos-Oreiro, M., Perez De Nanclares, G., Leiro-Fernández, V., Uria, M. L. & 8 others, Diaz-Heredia, C., Valenzuela, C., López-Muñiz, B., Lapunzina, P., Sevilla, J., Molina-Molina, M., Perona, R. & Sastre, L., 17 Apr 2019, In: Orphanet Journal of Rare Diseases. 14, 1, p. 82 12 p., 82.
Research output: Contribution to journal › Article › Research
8 Citations (Scopus)
Hematopoietic stem cell transplantation in pediatric patients with thalassemia and sickle cell disease: An experience of the Spanish Working Group for Bone Marrow Transplantation in Children (GETMON)
Alonso, L., González-Vicent, M., Belendez, C., Badell, I., Sastre, A., Rodríguez-Villa, A., Bermúdez-Cortés, M., Hladun, R. & Díaz de Heredia, C., 15 Feb 2019, In: Medicina Clinica. 152, p. 135-140
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
6 Citations (Scopus)

Education/Academic qualification

Anemia de Fanconi: cap a un nou diagnòstic citogenètic molecular i relació entre longitud telomèrica, fragilitat cromosòmica i pancitopenia progressiva.

Long-term outcome after allogeneic hematopoietic stem cell transplantation for Shwachman–Diamond syndrome: a retrospective analysis and a review of the literature by the Severe Aplastic Anemia Working Party of the European Society for Blood and Marrow Transplantation (SAAWP-EBMT)

From exome analysis in idiopathic azoospermia to the identification of a high-risk subgroup for occult Fanconi anemia

Genetic analyses of aplastic anemia and idiopathic pulmonary fibrosis patients with short telomeres, possible implication of DNA-repair genes

Hematopoietic stem cell transplantation in pediatric patients with thalassemia and sickle cell disease: An experience of the Spanish Working Group for Bone Marrow Transplantation in Children (GETMON)

Optimised molecular genetic diagnostics of Fanconi anaemia by whole exome sequencing and functional studies