Jordi Surrallés - Concepedia

Author

Jordi Surrallés

Also Known As

Antonis C. Antoniou, J Surralles, J Surrallés, J. Surralles, J. Surrallés, J. Surrallés, Jordi Rosell, Jordi Surralles, Jordi Surrallés, Lesley McGuffog

213

Publications

8.8K

Citations

H-Index

141

Concepts

All Affiliations

Universitat Autònoma de Barcelona Centre for Biomedical Network Research on Rare Diseases Hospital de Sant Pau Centro de Investigaciones Energéticas, Medioambientales y Tecnológicas Instituto de Salud Carlos III

About

Jordi Surrallés is an author at Universitat Autònoma de Barcelona specializing in medicine, genetics, and cell biology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	30	54	4.7K
2	Health Sciences	9	9	976
3	Natural Sciences	6	6	198
4	Public Health	4	4	224
5	Engineering	3	3	238

Jordi Surrallés

Publications

6.6K

Citations

H-Index

Page 1

	Year	Citations
Disease-corrected haematopoietic progenitors from Fanconi anaemia induced pluripotent stem cells Ángel Raya, Ignasi Rodríguez-Pizà, Guillermo Güenechea, Nature Fanconi AnaemiaInduced Pluripotent Stem CellDevelopmental BiologyBone Marrow FailureMedicine	2009	691
Report from the in vitro micronucleus assay working group Micheline Kirsch‐Volders, Toshio Sofuni, Marilyn J. Aardema, Mutation Research/Genetic Toxicology and Environmental Mutagenesis MedicineBioanalysisAnalytical ChemistryLaboratory ProtocolPharmacology	2003	623
Induction of micronuclei by five pyrethroid insecticides in whole-blood and isolated human lymphocyte cultures Jordi Surrallés, N. Xamena, A. Creus, Mutation Research/Genetic Toxicology AllergyBiorational PesticideMedicinePesticide ResistanceToxicology	1995	428
Mutations in ERCC4, Encoding the DNA-Repair Endonuclease XPF, Cause Fanconi Anemia Massimo Bogliolo, Beatrice Schuster, Chantal Stoepker, The American Journal of Human Genetics Genome InstabilityGenetic DisorderGeneticsMolecular BiologyDna-repair Endonuclease Xpf	2013	303
Biallelic mutations in the ubiquitin ligase RFWD3 cause Fanconi anemia Kerstin Knies, Shojiro Inano, Masamichi Ishiai, Journal of Clinical Investigation GeneticsGenomic MechanismMolecular BiologyCell DeathMolecular Genetics	2017	212
Successful engraftment of gene-corrected hematopoietic stem cells in non-conditioned patients with Fanconi anemia Susana Navarro, Wei Wang, Rebeca Sánchez‐Domínguez, Nature Medicine Fanconi AnemiaCell TherapyNon-conditioned PatientsDevelopmental BiologyBone Marrow Failure	2019	170
Chromosome fragility in patients with Fanconi anaemia: diagnostic implications and clinical impact M.J. Ramírez, José Antonio Casado, María Talavera, Journal of Medical Genetics	2011	140
Origin, functional role, and clinical impact of Fanconi anemia FANCA mutations María Castellà, Roser Pujol, Elsa Callén, Blood	2011	136
Hypomorphic Mutations in the Gene Encoding a Key Fanconi Anemia Protein, FANCD2, Sustain a Significant Group of FA-D2 Patients with Severe Phenotype Reinhard Kalb, Kornelia Neveling, Holger Hoehn, The American Journal of Human Genetics Fa-d2 PatientsGenetic DisorderGeneticsMolecular BiologyMolecular Genetics	2007	134
Histone H2AX and Fanconi anemia FANCD2 function in the same pathway to maintain chromosome stability Massimo Bogliolo, Alex Lyakhovich, Elsa Callén, The EMBO Journal ChromatinChromosome StabilityChromatin RemodelingEpigenetic ChangeGenetics	2007	131

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