Wim J. Kleijer - Concepedia

Author

Wim J. Kleijer

Also Known As

W J Kleijer, W KLEIJER, W. J. KLEIJER, W. J. Kleijer, W. JONGMANS M. VUILLAUME W. J. KLEIJER, W. Kleijer, W.J Kleijer, W.J. Kleijer, Wim J Kleijer, Wim J. Kleijer

161

Publications

10.3K

Citations

H-Index

131

Concepts

All Affiliations

Erasmus University Rotterdam Erasmus MC Leiden University University of Amsterdam Erasmus MC - Sophia Children’s Hospital

About

Wim J. Kleijer is an author at Erasmus University Rotterdam specializing in medicine, pathology, and genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	35	66	5.6K
2	Natural Sciences	7	7	299
3	Public Health	6	6	1.7K
4	Health Sciences	2	2	61
5	Engineering	1	1	56

Wim J. Kleijer

114

Publications

9.2K

Citations

H-Index

Page 1

	Year	Citations
Senescence‐associated β‐galactosidase is lysosomal β‐galactosidase Bo Yun Lee, Jung A Han, Jun Sub Im, Aging Cell	2006	1.4K
Heterozygosity for Homocystinuria in Premature Peripheral and Cerebral Occlusive Arterial Disease Godfried H.J. Boers, Antony G.H. Smals, Frans J.M. Trijbels, New England Journal of Medicine Vascular DiseaseGeneticsGenetic EpidemiologyPathologyHyperlipidemia	1985	740
The frequency of lysosomal storage diseases in The Netherlands Ben J. H. M. Poorthuis, Ron A. Wevers, Wim J. Kleijer, Human Genetics Lysosomal Storage DiseasesMendelian DisorderGenetic DisorderPathogenesisGenetic Epidemiology	1999	724
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
Loss of ZMPSTE24 (FACE-1) causes autosomal recessive restrictive dermopathy and accumulation of Lamin A precursors Claire Navarro, Juan Cadiñanos, Annachiara De Sandre‐Giovannoli, Human Molecular Genetics	2005	290
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
Mutations in the Gene Encoding Capillary Morphogenesis Protein 2 Cause Juvenile Hyaline Fibromatosis and Infantile Systemic Hyalinosis Sandra Hanks, Sarah Adams, Jenny Douglas, The American Journal of Human Genetics FibrosisDevelopmental BiologyInfantile Systemic HyalinosisPathologyCraniofacial Development	2003	240
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 Silengo, The American Journal of Human Genetics Developmental AnomalySevere Developmental FailureGenetic DisorderGeneticsPathology	2007	210
Inversion of the IDS gene resulting from recombination with IDS-related sequences in a common cause of the Hunter syndrome Maire-Louise Bondeson, Niklas Dahl, Helena Malmgren, Human Molecular Genetics Mendelian DisorderGenetic DisorderGeneticsEvolutionary BiologyPathogenesis	1995	176
Presence of ATM protein and residual kinase activity correlates with the phenotype in ataxia-telangiectasia: A genotype-phenotype study Mijke M.M. Verhagen, James I. Last, Frans B.L. Hogervorst, Human Mutation	2011	166

Page 1