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Molecular Biology

D-Index
53
Citations
11487
World Ranking
2384
National Ranking
35

Overview

Jordi Surrallés is affiliated with the Autonomous University of Barcelona in Spain. Their research primarily falls within the broad field of Biochemistry, Genetics and Molecular Biology, with a particular focus on Molecular Biology, Genetics, Oncology, Cancer Research, and Plant Science.

Their work concentrates on several main topics, including:

  • DNA Repair Mechanisms
  • CRISPR and Genetic Engineering
  • Cancer-related Molecular Pathways
  • Genomics and Rare Diseases
  • Genetic factors in colorectal cancer
  • Cancer Genomics and Diagnostics
  • BRCA gene mutations in cancer

Jordi Surrallés has contributed to multiple peer-reviewed publications. Noteworthy recent papers include:

  • Genomic signature of Fanconi anaemia DNA repair pathway deficiency in cancer (2022), published in Nature
  • CSVS, a crowdsourcing database of the Spanish population genetic variability (2020), published in Nucleic Acids Research
  • Mosaicism in Fanconi anemia: concise review and evaluation of published cases with focus on clinical course of blood count normalization (2020), published in Annals of Hematology
  • Gefitinib and Afatinib Show Potential Efficacy for Fanconi Anemia-Related Head and Neck Cancer (2020), published in Clinical Cancer Research
  • CRISPR Screens in Synthetic Lethality and Combinatorial Therapies for Cancer (2021), published in Cancers

The scientist has published extensively in venues such as bioRxiv (Cold Spring Harbor Laboratory), Cancers, American Journal of Hematology, Frontiers in Genetics, and Orphanet Journal of Rare Diseases.

Jordi Surrallés frequently collaborates with several co-authors including Roser Pujol, Paula Río, Juan A. Bueren, Jordi Minguillón, and Massimo Bogliolo, with collaborative works numbering in the double digits for many of these colleagues.

Best Publications

  • Molecular mechanisms of micronucleus, nucleoplasmic bridge and nuclear bud formation in mammalian and human cells

    M. Fenech;M. Kirsch-Volders;A. T. Natarajan;J. Surralles

  • Disease-corrected haematopoietic progenitors from Fanconi anaemia induced pluripotent stem cells

    Ángel Raya;Ignasi Rodríguez-Pizà;Guillermo Guenechea;Rita Vassena

  • Report from the in vitro micronucleus assay working group

    Micheline Kirsch-Volders;Toshio Sofuni;Marilyn Aardema;Silvio Albertini

  • Induction of micronuclei by five pyrethroid insecticides in whole-blood and isolated human lymphocyte cultures.

    J. Surrallés;N. Xamena;A. Creus;J. Catalán

  • Mutations in ERCC4, encoding the DNA-repair endonuclease XPF, cause Fanconi anemia.

    Massimo Bogliolo;Beatrice Schuster;Chantal Stoepker;Burak Derkunt

  • Report from the in vitro micronucleus assay working group

    M. Kirsch-Volders;T. Sofuni;M. Aardema;S. Albertini

  • Intra- and inter-laboratory variation in the scoring of micronuclei and nucleoplasmic bridges in binucleated human lymphocytes. Results of an international slide-scoring exercise by the HUMN project

    Michael Fenech;Stefano Bonassi;Julie Turner;Cecilia Lando

  • Biallelic mutations in the ubiquitin ligase RFWD3 cause Fanconi anemia

    Kerstin Knies;Shojiro Inano;María J. Ramírez;Masamichi Ishiai

  • Fanconi anemia: a model disease for studies on human genetics and advanced therapeutics

    Massimo Bogliolo;Jordi Surrallés

  • Histone H2AX and Fanconi anemia FANCD2 function in the same pathway to maintain chromosome stability

    Massimo Bogliolo;Alex Lyakhovich;Elsa Callén;Maria Castellà

  • 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;Hildegard Schneider

  • A common founder mutation in FANCA underlies the world's highest prevalence of Fanconi anemia in Gypsy families from Spain

    Elsa Callén;José A. Casado;Marc D. Tischkowitz;Juan A. Bueren

  • Origin, functional role, and clinical impact of Fanconi anemia FANCA mutations

    Maria Castella;Maria Castella;Roser Pujol;Roser Pujol;Elsa Callén;Elsa Callén;Juan P. Trujillo

  • Telomere dysfunction in genome instability syndromes

    Elsa Callén;Jordi Surrallés

  • Successful engraftment of gene-corrected hematopoietic stem cells in non-conditioned patients with Fanconi anemia.

    Paula Río;Susana Navarro;Wei Wang;Rebeca Sánchez-Domínguez

  • The suitability of the micronucleus assay in human lymphocytes as a new biomarker of excision repair.

    Jordi Surrallés;Noel Xamena;Amadeu Creus;Ricard Marcos

  • Hematopoietic dysfunction in a mouse model for Fanconi anemia group D1.

    Susana Navarro;Nestor W. Meza;Oscar Quintana-Bustamante;José A. Casado

  • Molecular cytogenetic analysis of buccal cells and lymphocytes from benzene-exposed workers.

    J Surrallés;K Autio;L Nylund;H Järventaus

  • Modelling Fanconi anemia pathogenesis and therapeutics using integration-free patient-derived iPSCs

    Guang Hui Liu;Guang Hui Liu;Keiichiro Suzuki;Mo Li;Jing Qu

  • Accelerated Telomere Shortening in the Human Inactive X Chromosome

    Jordi Surrallés;M. Prakash Hande;Ricard Marcos;Peter M. Lansdorp

Frequent Co-Authors

Ricard Marcos
Ricard Marcos Autonomous University of Barcelona
Amadeu Creus
Amadeu Creus Autonomous University of Barcelona
Elsa Callen
Elsa Callen National Institutes of Health
Helmut Hanenberg
Helmut Hanenberg University of Duisburg-Essen
Detlev Schindler
Detlev Schindler University of Würzburg
Hannu Norppa
Hannu Norppa Finnish Institute of Occupational Health
Adayapalam T. Natarajan
Adayapalam T. Natarajan Leiden University
Javier Benitez
Javier Benitez Instituto de Salud Carlos III
Conxi Lázaro
Conxi Lázaro Institut d'Investigació Biomédica de Bellvitge

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