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Oncogene|July 16, 2002
SV40 large T-antigen disturbs the formation of nuclear DNA-repair foci containing MRE11Martin Digweed, Ilja Demuth, Susanne Rothe, et al.
Molecular Cytogenetics|July 23, 2025
A homozygous TRIP13 pathogenic variant associated with familiar oocyte arrest and prematurely condensed sperm chromosomesMichal Schweiger, André Reis, Esen Gümüslü, et al.
American Journal of Human Genetics|February 22, 2002
Premature chromosome condensation in humans associated with microcephaly and mental retardation: a novel autosomal recessive conditionHeidemarie Neitzel, Luitgard M Neumann, Detlev Schindler, et al.
Molecular Vision|March 7, 2006
Sutural cataract associated with a mutation in the ferritin light chain gene (FTL) in a family of Indian originVanita Vanita, James Fielding Hejtmancik, Hans Christian Hennies, et al.
Cortex; a Journal Devoted to the Study of the Nervous System and Behavior|August 23, 2007
Hereditary prosopagnosia: the first case seriesMartina Grueter, Thomas Grueter, Vaughan Bell, et al.
Molecular Cytogenetics|March 10, 2010
Two siblings with immunodeficiency, facial abnormalities and chromosomal instability without mutation in DNMT3B gene but liability towards malignancy; a new chromatin disorder delineation?Anna Polityko, Olga Khurs, Natalia Rumyantseva, et al.
Molecular Cytogenetics|February 16, 2018
Evidence for a pre-malignant cell line in a skin biopsy from a patient with Nijmegen breakage syndromeRaneem Habib, Heidemarie Neitzel, Aurelie Ernst, et al.
Plos One|November 16, 2018
Yeast XRS2 and human NBN gene: Experimental evidence for homology using codon optimized cDNAIlja Demuth, Simon K Krebs, Véronique Dutrannoy, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 26, 2005
Nibrin functions in Ig class-switch recombinationSven Kracker, Yvonne Bergmann, Ilja Demuth, et al.
Melanoma Research|May 15, 2007
Molecular genetic analysis of NBS1 in German melanoma patientsPeter Meyer, Henrike Stapelmann, Bernd Frank, et al.
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