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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
Alex V. Levin
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711
Publications
9,168
Citation Statements Received
9,850
Citation Statements Given
How they've been cited
12,072
387
8,714
67
How they cite others
17,593
385
9,388
77
Affiliations
Wills Eye Hospital
,
Thomas Jefferson University
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
Diagnosis and management of Cornelia de Lange syndrome: first international consensus statement
Kline
1
,
Moss
2
,
Selicorni
3
et al.
2018
Nat Rev Genet
Abstract
Show
400
15
649
3
Get access via publisher
Add to collection
Cite
The genomic landscape of balanced cytogenetic abnormalities associated with human congenital anomalies
Redin
1
,
Brand
2
,
Collins
3
et al.
2016
Nat Genet
Abstract
Show
370
16
423
0
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Cite
Cornelia de Lange syndrome: Clinical review, diagnostic and scoring systems, and anticipatory guidance
Kline
1
,
Krantz
2
,
Sommer
3
et al.
2007
American J of Med Genetics Pt A
Abstract
Show
277
12
345
3
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Add to collection
Cite
Digenic Inheritance of Early-Onset Glaucoma: CYP1B1, a Potential Modifier Gene
Vincent
1
,
Billingsley
2
,
Buys
3
et al.
2002
The American Journal of Human Genetics
Abstract
Show
278
8
231
0
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Add to collection
Cite
Prevalence, risk factors, and outcome of uveitis in juvenile idiopathic arthritis: A long‐term followup study
Saurenmann
1
,
Levin
2
,
Feldman
3
et al.
2007
Arthritis & Rheumatism
Abstract
Show
295
20
180
11
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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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Add to collection
Cite
Correlation between retinal abnormalities and intracranial abnormalities in the shaken baby syndrome
Morad
1
,
Kim
2
,
Armstrong
3
et al.
2002
American Journal of Ophthalmology
246
6
175
1
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Add to collection
Cite
1
2
3
4