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Nicolaas G.J. Jaspers

Observed names: Jaspers NGJ, Jaspers, Nicolaas, Jaspers, Nicolaas G.J., Jaspers, Nicolaas GJ, N.G.J. Jaspers, Nicolaas G J Jaspers, Nicolaas G J Jaspers (16043933), Nicolaas G. J. Jaspers, Nicolaas G. Jaspers, Nicolaas G.J Jaspers, Nicolaas G.J. Jaspers (16043333), Nicolaas G.J. Jaspers
Institution: Erasmus MC
Observed institutions: Centre National de la Recherche Scientifique, University Medical Center Groningen, University of Sussex, University of Groningen, Cancer Research UK, Erasmus MC, Japan Science and Technology Agency, RIKEN, Martini Ziekenhuis, École Supérieure de Biotechnologie de Strasbourg, National Research Council, Medical Research Council, Erasmus University Rotterdam, The University of Osaka
OpenAlex ID: A5113669484
A new progeroid syndrome reveals that genotoxic stress suppresses the somatotroph axis
2006 · Laura J. Niedernhofer, George A. Garinis, et al. · Nature · 668
Xeroderma Pigmentosum Group F Caused by a Defect in a Structure-Specific DNA Repair Endonuclease
1996 · Anneke M Sijbers, Wouter L de Laat, et al. · Cell · 548
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Three DNA Polymerases, Recruited by Different Mechanisms, Carry Out NER Repair Synthesis in Human Cells
2010 · Tomoo Ogi, Siripan Limsirichaikul, et al. · Molecular Cell · 391
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A new, tenth subunit of TFIIH is responsible for the DNA repair syndrome trichothiodystrophy group A
2004 · Giuseppina Giglia-Mari, Frederic Coin, et al. · Nature Genetics · 335
DNA-binding polarity of human replication protein A positions nucleases in nucleotide excision repair
1998 · Wouter L. de Laat, Esther Appeldoorn, et al. · Genes & Development · 333
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Mutations in ERCC4, Encoding the DNA-Repair Endonuclease XPF, Cause Fanconi Anemia
2013 · Massimo Bogliolo, Beatrice Schuster, et al. · The American Journal of Human Genetics · 307
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SLX4, a coordinator of structure-specific endonucleases, is mutated in a new Fanconi anemia subtype
2011 · Chantal Stoepker, Karolina Hain, et al. · Nature Genetics · 299
Incidence of DNA repair deficiency disorders in western Europe: Xeroderma pigmentosum, Cockayne syndrome and trichothiodystrophy
2008 · Wim J. Kleijer, Vincent Laugel, et al. · DNA repair · 278
Xeroderma pigmentosum and trichothiodystrophy are associated with different mutations in the XPD ( ERCC 2) repair/transcription gene
1997 · Elaine M. Taylor, Bernard C. Broughton, et al. · Proceedings of the National Academy of Sciences · 263
Brca2 (XRCC11) Deficiency Results in Radioresistant DNA Synthesis and a Higher Frequency of Spontaneous Deletions
2002 · Maria Kraakman-van der Zwet, Wilhelmina J. I. Overkamp, et al. · Molecular and Cellular Biology · 254
MicroRNA‐mediated gene silencing modulates the UV‐induced DNA‐damage response
2009 · Joris Pothof, Nicole S Verkaik, et al. · The EMBO Journal · 234
DNA Structural Elements Required for ERCC1-XPF Endonuclease Activity
1998 · Wouter L. de Laat, Esther Appeldoorn, et al. · Journal of Biological Chemistry · 231
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First Reported Patient with Human ERCC1 Deficiency Has Cerebro-Oculo-Facio-Skeletal Syndrome with a Mild Defect in Nucleotide Excision Repair and Severe Developmental Failure
2007 · Nicolaas G.J. Jaspers, Anja Raams, et al. · The American Journal of Human Genetics · 214
Deep phenotyping of 89 xeroderma pigmentosum patients reveals unexpected heterogeneity dependent on the precise molecular defect
2016 · Hiva Fassihi, Mieran Sethi, et al. · Proceedings of the National Academy of Sciences · 199
Complete absence of Cockayne syndrome group B gene product gives rise to UV-sensitive syndrome but not Cockayne syndrome
2004 · Katsuyoshi Horibata, Yuka Iwamoto, et al. · Proceedings of the National Academy of Sciences · 180
Molecular analysis of mutations in DNA polymerase η in xeroderma pigmentosum-variant patients
2002 · Bernard C. Broughton, Agnes Cordonnier, et al. · Proceedings of the National Academy of Sciences · 168
Anti-tumour compounds illudin S and Irofulven induce DNA lesions ignored by global repair and exclusively processed by transcription- and replication-coupled repair pathways
2002 · Nicolaas G.J Jaspers, Anja Raams, et al. · DNA repair · 165
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Cerebro-Oculo-Facio-Skeletal Syndrome with a Nucleotide Excision–Repair Defect and a Mutated XPD Gene, with Prenatal Diagnosis in a Triplet Pregnancy
2001 · John M. Graham, Kwame Anyane-Yeboa, et al. · The American Journal of Human Genetics · 135
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The Structure of the Human ERCC1/XPF Interaction Domains Reveals a Complementary Role for the Two Proteins in Nucleotide Excision Repair
2005 · Konstantinos Tripsianes, Gert Folkers, et al. · Structure · 134
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Immortalization and characterization of Nijmegen Breakage Syndrome fibroblasts
1999 · Maria Kraakman-van der Zwet, Wilhelmina J.I Overkamp, et al. · Mutation Research/DNA Repair · 113
A temperature-sensitive disorder in basal transcription and DNA repair in humans
2001 · Wim Vermeulen, Suzanne Rademakers, et al. · Nature Genetics · 105
Identification of C7orf11 (TTDN1) Gene Mutations and Genetic Heterogeneity in Nonphotosensitive Trichothiodystrophy
2005 · Kazuhiko Nakabayashi, Daniela Amann, et al. · The American Journal of Human Genetics · 90
Definition of a Short Region of XPG Necessary for TFIIH Interaction and Stable Recruitment to Sites of UV Damage
2004 · Fabrizio Thorel, Angelos Constantinou, et al. · Molecular and Cellular Biology · 79
Mislocalization of XPF-ERCC1 Nuclease Contributes to Reduced DNA Repair in XP-F Patients
2010 · Anwaar Ahmad, Jacqueline H. Enzlin, et al. · PLoS Genetics · 78
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An Xpd mouse model for the combined xeroderma pigmentosum/Cockayne syndrome exhibiting both cancer predisposition and segmental progeria
2006 · Jaan-Olle Andressoo, James R. Mitchell, et al. · Cancer Cell · 78
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Works count: 84
Citation count: 6,760
H-index: 35
I10-index: 53
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