World's Best Scientists 2026 revealed!

D-Index & Metrics

Genetics

D-Index
56
Citations
11469
World Ranking
3505
National Ranking
124

Overview

Wim J. Kleijer is affiliated with Erasmus University Rotterdam in the Netherlands. The scholar's research profile shows a connection to this institution, which is known for its work in social sciences, economics, and medical research among other fields.

Although specific publications, co-authors, and detailed research topics related to Wim J. Kleijer are not publicly listed, the affiliation with Erasmus University Rotterdam suggests potential involvement in research areas commonly explored at this institution. Erasmus University has a strong focus on interdisciplinary studies spanning health sciences, economics, business, and social sciences.

No recent papers or defined areas of study are available to further detail the main fields or subfields of study for Wim J. Kleijer. Similarly, there is no publicly available data on frequent publication venues or awards associated with this researcher.

The absence of detailed information on book publications or citation metrics may indicate either early career stage or a specific research focus with limited indexing in the commonly surveyed databases.

Given this context, the profile remains focused on the identified affiliation, allowing for the possibility that Wim J. Kleijer's work contributes to the broader academic environment of Erasmus University Rotterdam, which encompasses a variety of scholarly disciplines and collaborative research initiatives.

Best Publications

  • Senescence‐associated β‐galactosidase is lysosomal β‐galactosidase

    Bo Yun Lee;Jung A. Han;Jun Sub Im;Amelia Morrone

  • A new progeroid syndrome reveals that genotoxic stress suppresses the somatotroph axis

    Laura J. Niedernhofer;George A. Garinis;Anja Raams;Astrid S. Lalai

  • Loss of ZMPSTE24 (FACE-1) causes autosomal recessive restrictive dermopathy and accumulation of Lamin A precursors

    Claire L. Navarro;Juan Cadiñanos;Annachiara De Sandre-Giovannoli;Rafaëlle Bernard

  • Genotype and phenotype in patients with dihydropyrimidine dehydrogenase deficiency.

    A. B. van Kuilenburg;P. Vreken;N. G. Abeling;H. D. Bakker

  • Incidence of DNA repair deficiency disorders in western Europe: Xeroderma pigmentosum, Cockayne syndrome and trichothiodystrophy.

    Wim J. Kleijer;Vincent Laugel;Mark Berneburg;Tiziana Nardo

  • Genotype versus phenotype in families with androgen insensitivity syndrome.

    Annemie L. M. Boehmer;Annemie L. M. Boehmer;Hennie Brüggenwirth;Cissy van Assendelft;Barto J. Otten

  • 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

    Nicolaas G.J. Jaspers;Anja Raams;Margherita Cirillo Silengo;Nils Wijgers

  • Mutations in the gene encoding capillary morphogenesis protein 2 cause juvenile hyaline fibromatosis and infantile systemic hyalinosis.

    Sandra Hanks;Sarah Adams;Jenny Douglas;Laura Arbour

  • Molecular analysis of mutations in DNA polymerase η in xeroderma pigmentosum-variant patients

    Bernard C. Broughton;Agnes Cordonnier;Wim J. Kleijer;Nicolaas G. J. Jaspers

  • Inversion of the IDS gene resulting from recombination with IDS-related sequences is a common cause of the Hunter syndrome.

    Maire-Louise Bondeson;Niklas Dahl;Helena Malmgren;Wim J. Kleijer

  • Twenty-two novel mutations in the lysosomal alpha-glucosidase gene (GAA) underscore the genotype-phenotype correlation in glycogen storage disease type II.

    Monique M.P. Hermans;Dik van Leenen;Marian A. Kroos;Clare E. Beesley

  • Presence of ATM protein and residual kinase activity correlates with the phenotype in ataxia-telangiectasia: a genotype-phenotype study.

    Mijke M. M. Verhagen;Frans B. L. Hogervorst;Dominique F. C. M. Smeets

  • Clinical heterogeneity within xeroderma pigmentosum associated with mutations in the DNA repair and transcription gene ERCC3

    W. Vermeulen;R. J. Scott;S. Rodgers;H. J. Müller

  • Cerebro-oculo-facio-skeletal syndrome with a nucleotide excision-repair defect and a mutated XPD gene, with prenatal diagnosis in a triplet pregnancy.

    John M. Graham;Kwame Anyane-Yeboa;Anja Raams;Esther Appeldoorn

  • Mucopolysaccharidosis type I: identification of 8 novel mutations and determination of the frequency of the two common α-L-iduronidase mutations (W402X and Q70X) among European patients

    Bunge S;Kleijer Wj;Steglich C;Beck M

  • A temperature-sensitive disorder in basal transcription and DNA repair in humans

    Wim Vermeulen;Suzanne Rademakers;Nicolaas G.J. Jaspers;Esther Appeldoorn

  • Genetic heterogeneity of the excision repair defect associated with trichothiodystrophy.

    Miria Stefanini;Paola Lagomarsini;Silvia Giliani;Tiziana Nardo

  • Different Removal of Ultraviolet Photoproducts in Genetically Related Xeroderma Pigmentosum and Trichothiodystrophy Diseases

    Eric Eveno;François Bourre;Xavier Quilliet;Odile Chevallier-Lagente

  • Genotype-phenotype correlations in mucopolysaccharidosis type I using enzyme kinetics, immunoquantification and in vitro turnover studies.

    Susanna Bunge;Peter R. Clements;Sharon Byers;Wim J. Kleijer

  • Molecular basis of androgen insensitivity.

    H.T. Brüggenwirth;A.L.M. Boehmer;M.C.T. Verleun-Mooijman;T. Hoogenboezem

Frequent Co-Authors

Nicolaas G. J. Jaspers
Nicolaas G. J. Jaspers Erasmus University Rotterdam
Ronald J.A. Wanders
Ronald J.A. Wanders University of Amsterdam
Arnold J. J. Reuser
Arnold J. J. Reuser Erasmus University Rotterdam
Dirk Bootsma
Dirk Bootsma Erasmus University Rotterdam
John J. Hopwood
John J. Hopwood University of Adelaide
Jan H.J. Hoeijmakers
Jan H.J. Hoeijmakers Erasmus University Rotterdam
Ulf Pettersson
Ulf Pettersson Uppsala University
Alain Sarasin
Alain Sarasin Institut Gustave Roussy
Wim Vermeulen
Wim Vermeulen Erasmus University Rotterdam
Alan R. Lehmann
Alan R. Lehmann University of Sussex

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Best Scientists Citing Wim J. Kleijer