B. Jeroen Klevering - Concepedia

Author

B. Jeroen Klevering

Also Known As

B J Klevering, B J. Klevering, B JEROEN KLEVERING, B Jeroen Klevering, B Klevering, B. J. Klevering, B. Jeroen Klevering, B. Klevering, B.J. Klevering, B.Jeroen Klevering

150

Publications

7.5K

Citations

H-Index

Concepts

All Affiliations

Radboud University Nijmegen Radboud University Medical Center Rotterdam Eye Hospital Erasmus MC Leiden University Medical Center

About

B. Jeroen Klevering is an author at Radboud University Nijmegen specializing in medicine, ophthalmology, and genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	20	24	2.4K
2	Biology	4	4	216
3	Engineering	3	3	74
4	Public Health	2	2	255
5	Natural Sciences	1	1	12

B. Jeroen Klevering

Publications

5.3K

Citations

H-Index

Page 1

	Year	Citations
Mutations in the ABCA4 (ABCR) Gene Are the Major Cause of Autosomal Recessive Cone-Rod Dystrophy Alessandra Maugeri, B. Jeroen Klevering, Klaus Rohrschneider, The American Journal of Human Genetics Mendelian DisorderGenetic DisorderGeneticsPathologyDegenerative Disease	2000	343
Next‐generation genetic testing for retinitis pigmentosa Kornelia Neveling, Rob W.J. Collin, Christian Gilissen, Human Mutation	2012	284
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
A functional variant in the CFI gene confers a high risk of age-related macular degeneration Johannes P. H. van de Ven, Sara C. Nilsson, Perciliz L. Tan, Nature Genetics Ocular DiseaseOphthalmologyGeneticsAge-related DiseasesCfi Gene Confers	2013	185
Identification of a 2 Mb Human Ortholog of Drosophila eyes shut/spacemaker that Is Mutated in Patients with Retinitis Pigmentosa Rob W.J. Collin, Karin W. Littink, B. Jeroen Klevering, The American Journal of Human Genetics Ocular DiseaseDevelopmental BiologyRetinaOphthalmologyRetinitis Pigmentosa	2008	164
OCT Angiography Compared to Fluorescein and Indocyanine Green Angiography in Chronic Central Serous Chorioretinopathy Michel M. Teussink, Myrte B. Breukink, Mark J. J. P. van Grinsven, Investigative Ophthalmology & Visual Science	2015	155
Early-Onset Stargardt Disease Stanley Lambertus, Ramon A. C. van Huet, Nathalie M. Bax, Ophthalmology Autoimmune DiseaseSurgical PathologyPathogenesisPathologyDegenerative Disease	2014	152
Risk Alleles in CFH and ARMS2 Are Independently Associated with Systemic Complement Activation in Age-related Macular Degeneration Dženita Smailhodzic, Caroline C. W. Klaver, B. Jeroen Klevering, Ophthalmology Complement SystemOcular DiseaseDisease MechanismOphthalmologySystemic Complement Activation	2011	145
Mutations in the peripherin/RDS gene are an important cause of multifocal pattern dystrophy simulating STGD1/fundus flavimaculatus Camiel J.F. Boon, Mary J. van Schooneveld, A. I den Hollander, British Journal of Ophthalmology	2007	130
BBS1 Mutations in a Wide Spectrum of Phenotypes Ranging From Nonsyndromic Retinitis Pigmentosa to Bardet-Biedl Syndrome Alejandro Estrada‐Cuzcano, Robert K. Koenekoop, Audrey Sénéćhal, Archives of Ophthalmology	2012	125

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