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Jordi Surralles
Jordi Surralles
Director, Genetics Department, Hospital Sant Pau
Verified email at uab.es - Homepage
Title
Cited by
Cited by
Year
Molecular mechanisms of micronucleus, nucleoplasmic bridge and nuclear bud formation in mammalian and human cells
M Fenech, M Kirsch-Volders, AT Natarajan, J Surralles, JW Crott, J Parry, ...
Mutagenesis 26 (1), 125-132, 2011
14832011
Disease-corrected haematopoietic progenitors from Fanconi anaemia induced pluripotent stem cells
Á Raya, I Rodríguez-Pizà, G Guenechea, R Vassena, S Navarro, ...
Nature 460 (7251), 53-59, 2009
9012009
Report from the in vitro micronucleus assay working group
M Kirsch-Volders, T Sofuni, M Aardema, S Albertini, D Eastmond, ...
Mutation Research/Genetic Toxicology and Environmental Mutagenesis 540 (2 …, 2003
7572003
Induction of micronuclei by five pyrethroid insecticides in whole-blood and isolated human lymphocyte cultures
J Surrallés, N Xamena, A Creus, J Catalan, H Norppa, R Marcos
Mutation Research/Genetic Toxicology 341 (3), 169-184, 1995
4831995
Mutations in ERCC4, encoding the DNA-repair endonuclease XPF, cause Fanconi anemia
M Bogliolo, B Schuster, C Stoepker, B Derkunt, Y Su, A Raams, JP Trujillo, ...
The American Journal of Human Genetics 92 (5), 800-806, 2013
3732013
Report from the in vitro micronucleus assay working group
M Kirsch‐Volders, T Sofuni, M Aardema, S Albertini, D Eastmond, ...
Environmental and molecular mutagenesis 35 (3), 167-172, 2000
3422000
Biallelic mutations in the ubiquitin ligase RFWD3 cause Fanconi anemia
K Knies, S Inano, MJ Ramírez, M Ishiai, J Surrallés, M Takata, D Schindler
The Journal of clinical investigation 127 (8), 3013-3027, 2017
2232017
Intra-and inter-laboratory variation in the scoring of micronuclei and nucleoplasmic bridges in binucleated human lymphocytes: Results of an international slide-scoring …
M Fenech, S Bonassi, J Turner, C Lando, M Ceppi, WP Chang, N Holland, ...
Mutation Research/Genetic Toxicology and Environmental Mutagenesis 534 (1-2 …, 2003
2072003
Fanconi anemia: a model disease for studies on human genetics and advanced therapeutics
M Bogliolo, J Surralles
Current opinion in genetics & development 33, 32-40, 2015
2022015
Histone H2AX and Fanconi anemia FANCD2 function in the same pathway to maintain chromosome stability
M Bogliolo, A Lyakhovich, E Callén, M Castellà, E Cappelli, MJ Ramírez, ...
The EMBO journal 26 (5), 1340-1351, 2007
1742007
Hypomorphic mutations in the gene encoding a key Fanconi anemia protein, FANCD2, sustain a significant group of FA-D2 patients with severe phenotype
R Kalb, K Neveling, H Hoehn, H Schneider, Y Linka, SD Batish, C Hunt, ...
The American Journal of Human Genetics 80 (5), 895-910, 2007
1682007
Origin, functional role, and clinical impact of Fanconi anemia FANCA mutations
M Castella, R Pujol, E Callén, JP Trujillo, JA Casado, H Gille, FP Lach, ...
Blood, The Journal of the American Society of Hematology 117 (14), 3759-3769, 2011
1572011
A common founder mutation in FANCA underlies the world's highest prevalence of Fanconi anemia in Gypsy families from Spain
E Callén, JA Casado, MD Tischkowitz, JA Bueren, A Creus, R Marcos, ...
Blood 105 (5), 1946-1949, 2005
1532005
The suitability of the micronucleus assay in human lymphocytes as a new biomarker of excision repair
J Surrallés, N Xamena, A Creus, R Marcos
Mutation Research/Genetic Toxicology 342 (1-2), 43-59, 1995
1531995
Telomere dysfunction in genome instability syndromes
E Callén, J Surrallés
Mutation Research/Reviews in Mutation Research 567 (1), 85-104, 2004
1472004
Molecular cytogenetic analysis of buccal cells and lymphocytes from benzene-exposed workers.
J Surrallés, K Autio, L Nylund, H Järventaus, H Norppa, T Veidebaum, ...
Carcinogenesis 18 (4), 817-823, 1997
1421997
Successful engraftment of gene-corrected hematopoietic stem cells in non-conditioned patients with Fanconi anemia
P Rio, S Navarro, W Wang, R Sanchez-Dominguez, RM Pujol, ...
Nature medicine 25 (9), 1396-1401, 2019
1392019
Modelling Fanconi anemia pathogenesis and therapeutics using integration-free patient-derived iPSCs
GH Liu, K Suzuki, M Li, J Qu, N Montserrat, C Tarantino, Y Gu, F Yi, X Xu, ...
Nature communications 5 (1), 4330, 2014
1332014
Hematopoietic dysfunction in a mouse model for Fanconi anemia group D1
S Navarro, NW Meza, O Quintana-Bustamante, JA Casado, A Jacome, ...
Molecular Therapy 14 (4), 525-535, 2006
1322006
Germline mutations in FAN1 cause hereditary colorectal cancer by impairing DNA repair
N Seguí, LB Mina, C Lázaro, R Sanz-Pamplona, T Pons, M Navarro, ...
Gastroenterology 149 (3), 563-566, 2015
1262015
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