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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
Elias I. Traboulsi
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740
Publications
10,687
Citation Statements Received
7,370
Citation Statements Given
How they've been cited
14,846
446
10,169
72
How they cite others
22,753
305
7,008
57
Affiliations
Cleveland Clinic
,
Cleveland Eye Clinic
Publications
Order By: Most citations
Human TUBB3 Mutations Perturb Microtubule Dynamics, Kinesin Interactions, and Axon Guidance
Tischfield
1
,
Baris
2
,
Wu
3
et al.
2010
Cell
Abstract
Show
623
39
680
1
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Add to collection
Cite
Mutations in a Human
ROBO
Gene Disrupt Hindbrain Axon Pathway Crossing and Morphogenesis
Jen
1
,
Chan
2
,
Bosley
3
et al.
2004
Science
Abstract
Show
395
11
336
1
Get access via publisher
Add to collection
Cite
Bietti Crystalline Corneoretinal Dystrophy Is Caused by Mutations in the Novel Gene CYP4V2
Li
1
,
Jiao
2
,
Munier
3
et al.
2004
The American Journal of Human Genetics
Abstract
Show
287
11
306
2
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Add to collection
Cite
Identifying photoreceptors in blind eyes caused by
RPE65
mutations: Prerequisite for human gene therapy success
Jacobson
1
,
Alemán
2
,
Cideciyan
3
et al.
2005
Proc. Natl. Acad. Sci. U.S.A.
Abstract
Show
279
8
297
1
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Add to collection
Cite
Aberrant accumulation of EFEMP1 underlies drusen formation in Malattia Leventinese and age-related macular degeneration
Marmorstein
1
,
Munier
2
,
Arsenijévic
3
et al.
2002
Proc. Natl. Acad. Sci. U.S.A.
Abstract
Show
248
17
222
3
Get access via publisher
Add to collection
Cite
The Natural History of the Progression of Atrophy Secondary to Stargardt Disease (ProgStar) Studies
Strauß
1
,
Ho
2
,
Muñoz
3
et al.
2016
Ophthalmology
171
3
231
0
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Add to collection
Cite
Heterozygous mutations of the kinesin KIF21A in congenital fibrosis of the extraocular muscles type 1 (CFEOM1)
Yamada
1
,
Andrews
2
,
Chan
3
et al.
2003
Nat Genet
Abstract
Show
268
4
213
0
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Cite
GPR179 Is Required for Depolarizing Bipolar Cell Function and Is Mutated in Autosomal-Recessive Complete Congenital Stationary Night Blindness
Peachey
1
,
Ray
2
,
Florijn
3
et al.
2012
The American Journal of Human Genetics
Abstract
Show
166
16
193
0
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Cite
1
2
3
4
5