J.R.M. Cruysberg - Concepedia

Author

J.R.M. Cruysberg

Also Known As

Cruysberg, J. R., J CRUYSBERG, J Cruysberg, J R Cruysberg, J R M Cruysberg, J R M Hans Cruysberg, J. Cruysberg, J. R M Cruysberg, J. R. Cruysberg, J. R. M. Cruysberg

189

Publications

5.7K

Citations

H-Index

100

Concepts

All Affiliations

Radboud University Nijmegen Radboud University Medical Center Heidelberg University

About

J.R.M. Cruysberg is an author at Radboud University Nijmegen specializing in medicine, ophthalmology, and pathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	23	42	2.8K
2	Social Sciences	4	4	787
3	Health Sciences	2	2	295
4	Public Health	2	2	345
5	Arts	1	1	69

J.R.M. Cruysberg

Publications

4.7K

Citations

H-Index

Page 1

	Year	Citations
Visual hallucinations in psychologically normal people: Charles Bonnet's syndrome Robert J. Teunisse, Frans G. Zitman, J.R.M. Cruysberg, The Lancet NeuropsychologyPsychopathologyPsychiatryPsychotic DisorderNeuropsychiatry	1996	433
Leber Congenital Amaurosis and Retinitis Pigmentosa with Coats-like Exudative Vasculopathy Are Associated with Mutations in the Crumbs Homologue 1 (CRB1) Gene Anneke I. den Hollander, John R. Heckenlively, L. Ingeborgh van den Born, The American Journal of Human Genetics Developmental BiologyMendelian DisorderGenetic DisorderRetinitis PigmentosaGenetics	2001	361
Incidence of retinoblastoma in children born after in-vitro fertilisation Annette C. Moll, Saskia M. Imhof, J.R.M. Cruysberg, The Lancet InfertilityFertilityOphthalmologyIn-vitro FertilisationReproductive Health	2003	311
Mobius syndrome redefined H. T. F. M. Verzijl, Bert van der Zwaag, J.R.M. Cruysberg, Neurology	2003	300
A Spatial Hearing Deficit in Early-Blind Humans Marcel P. Zwiers, A. John Van Opstal, J.R.M. Cruysberg Journal of Neuroscience Auditory ProcessingCompensatory PlasticityCognitive ScienceAuditory ModelingHealth Sciences	2001	280
Splicing Mutations of 54-bp Exons in the COL11A1 Gene Cause Marshall Syndrome, but Other Mutations Cause Overlapping Marshall/Stickler Phenotypes Susanna Annunen, Jarmo Körkkö, Malwina Czarny‐Ratajczak, The American Journal of Human Genetics Systems BiologyMendelian DisorderGenetic DisorderGeneticsPathogenesis	1999	258
The Charles Bonnet Syndrome: A Large Prospective Study in the Netherlands Robert J. Teunisse, J.R.M. Cruysberg, André L. M. Verbeek, The British Journal of Psychiatry	1995	190
Genotype–phenotype studies in nail-patella syndrome show that LMX1B mutation location is involved in the risk of developing nephropathy Ernie M.H.F. Bongers, F.T.M. Huysmans, Elena Levtchenko, European Journal of Human Genetics Mendelian DisorderGenetic DisorderGeneticsInherited Metabolic DiseaseGenetic Epidemiology	2005	158
ARSACS in the Dutch population: a frequent cause of early-onset cerebellar ataxia Sascha Vermeer, Rowdy Meijer, Benjamin J. Pijl, Neurogenetics Neurological DisorderGeneticsGenetic EpidemiologyPathologyDisease Gene Identification	2008	147
Neovascular age‐related macular degeneration and its relationship to antioxidant intake E.L.M. Snellen, A.L.M. Verbeek, G.W.P. Van Den Hoogen, Acta Ophthalmologica Scandinavica	2002	139

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