N.G.J. Jaspers - Concepedia

Author

N.G.J. Jaspers

Erasmus University Rotterdam

Also Known As

C M McConville, N G Jaspers, N. G. J. Jaspers, N.G. Jaspers, N.G.J. Jaspers, NGJ Jaspers, Nova Jaspers

Publications

Citations

H-Index

Concepts

All Affiliations

Erasmus University Rotterdam Leiden University Erasmus MC University of Sussex Tel Aviv University

About

N.G.J. Jaspers is an author at Erasmus University Rotterdam specializing in medicine, pathology, and genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	13	14	1K
2	Cell Biology	7	7	348
3	Natural Sciences	3	3	286
4	Health Sciences	2	2	82
5	Biochemistry	1	1	183

N.G.J. Jaspers

Publications

1.9K

Citations

H-Index

Page 1

	Year	Citations
The Structure-Specific Endonuclease Ercc1-Xpf Is Required To Resolve DNA Interstrand Cross-Link-Induced Double-Strand Breaks Laura J. Niedernhofer, Hanny Odijk, Magda Budzowska, Molecular and Cellular Biology	2004	484
Evidence for a repair enzyme complex involving ERCC1 and complementing activities of ERCC4, ERCC11 and xeroderma pigmentosum group F. Anneke J. van Vuuren, Esther Appeldoorn, Hanny Odijk, The EMBO Journal Protein FunctionBiochemistryNatural SciencesBiochemical GeneticsMolecular Biology	1993	183
A seventh complementation group in excision-deficient xeroderma pigmentosum W. Keijzer, N.G.J. Jaspers, P. J. Abrahams, Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis Surgical PathologyHistopathologyPathologyMolecular GeneticsDermatology	1979	164
Three Unusual Repair Deficiencies Associated with Transcription Factor BTF2(TFIIH): Evidence for the Existence of a Transcription Syndrome Wim Vermeulen, Anneke J. van Vuuren, M. Chipoulet, Cold Spring Harbor Symposia on Quantitative Biology Dna DamageGeneticsPathologyMolecular GeneticsDisease Gene Identification	1994	143
Neurological symptoms and natural course of xeroderma pigmentosum Anu Anttinen, Leena Koulu, Eeva Nikoskelainen, Brain Ocular DiseaseComplementation AnalysisNeurological DisorderBrain LesionDermatology	2008	130
Phenotypic heterogeneity in the XPB DNA helicase gene (<i>ERCC3</i>): xeroderma pigmentosum without and with Cockayne syndrome Kyu‐Seon Oh, Sikandar G. Khan, N.G.J. Jaspers, Human Mutation	2006	117
Correction of xeroderma pigmentosum repair defect by basal transcription factor BTF2 (TFIIH). Anneke J. van Vuuren, Wim Vermeulen, Lanping Ma, The EMBO Journal GeneticsPathologyMolecular GeneticsGene ExpressionMedicine	1994	113
The rate of DNA synthesis in normal human and ataxia telangiectasia cells after exposure to X-irradiation J. de Witt, N.G.J. Jaspers, D. Bootsma Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis ChromatinGenome InstabilityRadiation MedicineDna DamageGenetics	1981	107
Abnormal regulation of DNA replication and increased lethality in ataxia telangiectasia cells exposed to carcinogenic agents. N.G.J. Jaspers, Jan de Wit, Michael Regulski, PubMed Dna DamagePathologyCell DeathMolecular BiologyAbnormal Regulation	1982	78
AT‐related disorder R.‐D. Wegner, Marc J. Metzger, F. Hanefeld, Clinical Genetics	1988	70

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