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Mutation Research|September 3, 2004
Telomere dysfunction in genome instability syndromesElsa Callén, Jordi Surrallés
Nucleic Acids Research|April 29, 2015
Ectopic expression of RNF168 and 53BP1 increases mutagenic but not physiological non-homologous end joiningDali Zong, Elsa Callén, Gianluca Pegoraro, et al.
Mutation Research|July 11, 2002
Relationship between chromosome fragility, aneuploidy and severity of the haematological disease in Fanconi anaemiaElsa Callén, María J Ramírez, Amadeu Creus, et al.
Human Molecular Genetics|February 21, 2002
Breaks at telomeres and TRF2-independent end fusions in Fanconi anemiaElsa Callén, Enrique Samper, María J Ramírez, et al.
The EMBO Journal|February 17, 2007
Histone H2AX and Fanconi anemia FANCD2 function in the same pathway to maintain chromosome stabilityMassimo Bogliolo, Alex Lyakhovich, Elsa Callén, et al.
Molecular Cell|May 20, 2009
Essential role for DNA-PKcs in DNA double-strand break repair and apoptosis in ATM-deficient lymphocytesElsa Callén, Mila Jankovic, Nancy Wong, et al.
Cell Cycle (Georgetown, Tex.)|June 27, 2009
Chimeric IgH-TCRalpha/delta translocations in T lymphocytes mediated by RAGElsa Callén, Sam Bunting, Ching-Yu Huang, et al.
Cell|June 30, 2007
ATM prevents the persistence and propagation of chromosome breaks in lymphocytesElsa Callén, Mila Jankovic, Simone Difilippantonio, et al.
Genes & Development|August 5, 2008
A chromatin-wide transition to H4K20 monomethylation impairs genome integrity and programmed DNA rearrangements in the mouseGunnar Schotta, Roopsha Sengupta, Stefan Kubicek, et al.
Molecular Cell|March 27, 2012
BRCA1 functions independently of homologous recombination in DNA interstrand crosslink repairSamuel F Bunting, Elsa Callén, Marina L Kozak, et al.
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