Nel Tijmes - Concepedia

Author

Nel Tijmes

Combined Ophthalmic Research Rotterdam

Also Known As

N Tijmes, N. T TIJMES, N. Tijmes, N.T. Tijmes, Nel T. Tijmes, Nel Tijmes

Publications

886

Citations

H-Index

Concepts

All Affiliations

Combined Ophthalmic Research Rotterdam Radboud University Nijmegen Amsterdam UMC Location University of Amsterdam

About

Nel Tijmes is an author at Combined Ophthalmic Research Rotterdam specializing in genetics, medicine, and ophthalmology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	5	5	359
2	Molecular Genetics	4	4	347
3	Neurology	2	2	23
4	Pathology	1	1	259
5	Clinical Genetics	1	1	259

Nel Tijmes

Publications

779

Citations

H-Index

Page 1

	Year	Citations
The 2588G→C Mutation in the ABCR Gene Is a Mild Frequent Founder Mutation in the Western European Population and Allows the Classification of ABCR Mutations in Patients with Stargardt Disease Alessandra Maugeri, Marc A. van Driel, Dorien J.R. van de Pol, The American Journal of Human Genetics Mendelian DisorderGenetic DisorderAbcr GeneGeneticsMedicine	1999	259
Retinal arterial changes correlate with cerebral small-vessel disease Vincent I.H. Kwa, J.J. van der Sande, J. Stam, Neurology	2002	221
Prevalence of Symptomatic Intracranial Aneurysm and Ischaemic Stroke in Pseudoxanthoma Elasticum JanS.P. vandenBerg, Raoul C. M. Hennekam, J.R.M. Cruysberg, Cerebrovascular Diseases	2000	112
Changes in causes of low vision between 1988 and 2009 in a Dutch population of children Nienke Boonstra, Hans Limburg, Nel Tijmes, Acta Ophthalmologica	2011	87
A Gene for X-Linked Optic Atrophy Is Closely Linked to the Xp11.4-Xp11.2 Region of the X Chromosome Jacqueline J.M. Assink, Nel Tijmes, Jacoline B. ten Brink, The American Journal of Human Genetics OphthalmologyCytogeneticsX ChromosomeGeneticsGenetic Disorder	1997	67
On the many faces of Leber hereditary optic neuropathy Roelof‐Jan Oostra, Nel Tijmes, Jan-Maarten Cobben, Clinical Genetics Mendelian DisorderOphthalmologyMtdna AnalysisNeuroanatomyGenetics	1997	12
Conclusive evidence for a distinct congenital stationary night blindness locus in Xp21.1. Arthur A. Bergen, Jacoline B. ten Brink, Frans C. C. Riemslag, Journal of Medical Genetics Decreased Visual AcuityOcular DiseaseNon-progressive Retinal DisorderGeneticsGenetic Epidemiology	1996	11
Localization of a novel X-linked congenital stationary night blindness locus: close linkage to the RP3 type retinitis pigmentosa gene region Arthur A. Bergen, Jacoline B. ten Brink, Frans C. C. Riemslag, Human Molecular Genetics Close LinkageOcular DiseaseDevelopmental BiologyPhotoreceptor CellOphthalmology	1995	10

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