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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
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August F. Deutman
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170
Publications
3,304
Citation Statements Received
1,336
Citation Statements Given
How they've been cited
7,058
128
3,159
17
How they cite others
2,356
56
1,272
8
Affiliations
Radboud University Nijmegen
,
Radboud University Medical Center
Publications
Order By: Most citations
Mutations in a human homologue of Drosophila crumbs cause retinitis pigmentosa (RP12)
den Hollander
1
,
ten Brink
2
,
de Kok
3
et al.
1999
Nat Genet
Abstract
Show
456
9
314
0
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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
239
20
270
3
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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
347
6
222
0
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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
350
9
216
0
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Cite
Acute Macular Neuroretinopathy
Bos
1
,
Deutman
2
1975
American Journal of Ophthalmology
282
0
185
2
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Cite
Arteriovenous Communications of the Retina
Archer
1
,
Deutman
2
,
Ernest
3
et al.
1973
American Journal of Ophthalmology
218
4
128
0
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Cite
Disruption of the 11-
cis
-Retinol Dehydrogenase Gene Leads to Accumulation of
cis
-Retinols and
cis
-Retinyl Esters
Driessen
1
,
Winkens
2
,
Hoffmann
3
et al.
2000
Mol Cell Biol
Abstract
Show
125
9
97
0
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Cite
The spectrum of retinal phenotypes caused by mutations in the ABCA4 gene
Klevering
1
,
Deutman
2
,
Maugeri
3
et al.
2004
Graefe's Arch Clin Exp Ophthalmol
Abstract
Show
121
1
83
0
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Cite
1
2
3
4
5
6