L. Ingeborgh van den Born

Author

Also Known As

B. Jeroen Klevering, Ine Strubbe, L Born, L I van den Born, L Ingeborgh van den Born, L. Born, L. I. van den Born, L. Ingeborgh van den Born, L. Van den Born, L.I. Van den Born

194

Publications

9.7K

Citations

H-Index

Concepts

All Affiliations

Rotterdam Eye Hospital Radboud University Nijmegen Radboud University Medical Center Erasmus MC Radboud Institute for Molecular Life Sciences

About

L. Ingeborgh van den Born is an author at Rotterdam Eye Hospital specializing in medicine, genetics, and molecular genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	33	41	4.6K
2	Social Sciences	4	4	199
3	Natural Sciences	2	2	257
4	Education	1	1	11
5	Engineering	1	1	10

L. Ingeborgh van den Born

105

Publications

8.8K

Citations

H-Index

Page 1

	Year	Citations
Long-Term Effect of Gene Therapy on Leber’s Congenital Amaurosis James Bainbridge, Manjit Mehat, Venki Sundaram, New England Journal of Medicine	2015	713
Mutations in the CEP290 (NPHP6) Gene Are a Frequent Cause of Leber Congenital Amaurosis Anneke I. den Hollander, Robert K. Koenekoop, Suzanne Yzer, The American Journal of Human Genetics Developmental BiologyGenetic DisorderGeneticsFrequent CauseLeber Hereditary Optic Neuropathy	2006	670
Mutations in a human homologue of Drosophila crumbs cause retinitis pigmentosa (RP12) Anneke I. den Hollander, Jacoline B. ten Brink, Yvette J.M. de Kok, Nature Genetics BiologyDevelopmental BiologyGeneticsGenomic MechanismGenetic Mechanism	1999	470
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
Next‐generation genetic testing for retinitis pigmentosa Kornelia Neveling, Rob W.J. Collin, Christian Gilissen, Human Mutation	2012	284
Homozygosity Mapping Reveals PDE6C Mutations in Patients with Early-Onset Cone Photoreceptor Disorders Alberta A. H. J. Thiadens, Anneke I. den Hollander, Susanne Roosing, The American Journal of Human Genetics Photoreceptor CellMolecular NeuroscienceOphthalmologyGenetic DisorderMolecular Biology	2009	213
Deep-intronic ABCA4 variants explain missing heritability in Stargardt disease and allow correction of splice defects by antisense oligonucleotides Riccardo Sangermano, Alejandro Garanto, Mubeen Khan, Genetics in Medicine	2019	192
Progressive Loss of Cones in Achromatopsia: An Imaging Study Using Spectral-Domain Optical Coherence Tomography Alberta A. H. J. Thiadens, Ville Somervuo, L. Ingeborgh van den Born, Investigative Ophthalmology & Visual Science	2010	175
<i>ABCA4</i>midigenes reveal the full splice spectrum of all reported noncanonical splice site variants in Stargardt disease Riccardo Sangermano, Mubeen Khan, Stéphanie S. Cornelis, Genome Research	2017	170
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

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