Nicolaas G.J. Jaspers

Author

Also Known As

N.G.J. Jaspers, Nicolaas G J Jaspers, Nicolaas G. J. Jaspers, Nicolaas G. Jaspers, Nicolaas G.J Jaspers, Nicolaas G.J. Jaspers, Nicolaas G.J. Jaspers

Publications

6.7K

Citations

H-Index

Concepts

All Affiliations

Erasmus University Rotterdam Erasmus MC University of Sussex Leiden University Medical Center Istituto di Genetica Molecolare

About

Nicolaas G.J. Jaspers is an author at Erasmus University Rotterdam specializing in medicine, genetics, and genome instability.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	27	34	4.9K
2	Cell Biology	15	17	1.9K
3	Natural Sciences	9	9	2K
4	Allergy	1	1	655
5	Endocrinology	1	1	655

Nicolaas G.J. Jaspers

Publications

6.5K

Citations

H-Index

Page 1

	Year	Citations
A new progeroid syndrome reveals that genotoxic stress suppresses the somatotroph axis Laura J. Niedernhofer, George A. Garinis, Anja Raams, Nature InflammationAllergyAutoimmune DiseaseHuman GrowthStress	2006	655
Xeroderma Pigmentosum Group F Caused by a Defect in a Structure-Specific DNA Repair Endonuclease Anneke M. Sijbers, Wouter de Laat, Rafael R. Ariza, Cell ChromatinGenome InstabilityNatural SciencesGeneticsDna Replication	1996	543
Three DNA Polymerases, Recruited by Different Mechanisms, Carry Out NER Repair Synthesis in Human Cells Tomoo Ogi, Siripan Limsirichaikul, René Overmeer, Molecular Cell Polymerase Chain ReactionGenome InstabilityTranscriptional RegulationChromatinDifferent Mechanisms	2010	376
A new, tenth subunit of TFIIH is responsible for the DNA repair syndrome trichothiodystrophy group A Giuseppina Giglia‐Mari, Frédéric Coin, Jeffrey A. Ranish, Nature Genetics Genome InstabilityTenth SubunitGenetic DisorderNatural SciencesGenetics	2004	331
DNA-binding polarity of human replication protein A positions nucleases in nucleotide excision repair Wouter de Laat, Esther Appeldoorn, Kaoru Sugasawa, Genes & Development	1998	329
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
SLX4, a coordinator of structure-specific endonucleases, is mutated in a new Fanconi anemia subtype Chantal Stoepker, Karolina Hain, Beatrice Schuster, Nature Genetics Genetic DisorderNatural SciencesGeneticsProtein GeneticsMolecular Biology	2011	295
Incidence of DNA repair deficiency disorders in western Europe: Xeroderma pigmentosum, Cockayne syndrome and trichothiodystrophy Wim J. Kleijer, Vincent Laugel, Mark Berneburg, DNA repair Genome InstabilityXeroderma PigmentosumMendelian DisorderGenetic DisorderGenetics	2008	271
Xeroderma pigmentosum and trichothiodystrophy are associated with different mutations in the <i>XPD</i> ( <i>ERCC</i> 2) repair/transcription gene Elaine M. Taylor, Bernard C. Broughton, Elena Botta, Proceedings of the National Academy of Sciences GeneticsPathologyMolecular BiologyMolecular GeneticsDisease Gene Identification	1997	259
Brca2 (XRCC11) Deficiency Results in Radioresistant DNA Synthesis and a Higher Frequency of Spontaneous Deletions Maria Kraakman-van der Zwet, Wilhelmina J. I. Overkamp, Rebecca E. E. van Lange, Molecular and Cellular Biology GeneticsMolecular BiologyMurine Brca2 GeneMolecular GeneticsCell Cycle	2002	248

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