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Features
Assistant
AI grounded in research
Search
Full-text citation search
Collections
Organize and monitor papers
All Features →
Integrations
MCP
Connect AI agents to Scite
API
Programmatic data access
Holdings
Full-text via your library
Zotero Plugin
Citation data in Zotero
Browser Extension
Citation badges anywhere
All Integrations →
Data
Rankings
Pricing
Log In
Start Free Trial
Klaus Rohrschneider
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227
Publications
5,047
Citation Statements Received
1,575
Citation Statements Given
How they've been cited
7,067
236
4,775
36
How they cite others
3,542
78
1,492
5
Affiliations
Heidelberg University
,
Augenklinik Heidelberg
Publications
Order By: Most citations
Mutations in the CEP290 (NPHP6) Gene Are a Frequent Cause of Leber Congenital Amaurosis
den Hollander
1
,
Koenekoop
2
,
Yzer
3
et al.
2006
The American Journal of Human Genetics
Abstract
Show
661
21
559
1
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Cite
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
Maugeri
1
,
van Driel
2
,
van de Pol
3
et al.
1999
The American Journal of Human Genetics
Abstract
Show
238
20
270
3
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Cite
CDH23 Mutation and Phenotype Heterogeneity: A Profile of 107 Diverse Families with Usher Syndrome and Nonsyndromic Deafness
Astuto
1
,
Bork
2
,
Weston
3
et al.
2002
The American Journal of Human Genetics
Abstract
Show
238
19
243
4
Get access via publisher
Add to collection
Cite
Leber Congenital Amaurosis and Retinitis Pigmentosa with Coats-like Exudative Vasculopathy Are Associated with Mutations in the Crumbs Homologue 1 (CRB1) Gene
Hollander
1
,
Heckenlively
2
,
van den Born
3
et al.
2001
The American Journal of Human Genetics
Abstract
Show
346
6
221
0
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Add to collection
Cite
Mutations in the ABCA4 (ABCR) Gene Are the Major Cause of Autosomal Recessive Cone-Rod Dystrophy
Maugeri
1
,
Klevering
2
,
Rohrschneider
3
et al.
2000
The American Journal of Human Genetics
Abstract
Show
349
9
216
0
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Cite
Multilayer amniotic membrane transplantation for reconstruction of deep corneal ulcers
Kruse
1
,
Rohrschneider
2
,
Völcker
3
1999
Ophthalmology
317
10
182
1
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Cite
Use of fundus perimetry (microperimetry) to quantify macular sensitivity
Rohrschneider
1
,
Bültmann
2
,
Springer
3
2008
Progress in Retinal and Eye Research
210
5
174
1
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Mutations in the VMD2 gene are associated with juvenile-onset vitelliform macular dystrophy (Best disease) and adult vitelliform macular dystrophy but not age-related macular degeneration
Krämer
1
,
White
2
,
Pauleikhoff
3
et al.
2000
Eur J Hum Genet
Abstract
Show
204
4
163
0
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Add to collection
Cite
1
2
3
4
5
6