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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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Eduardo Silva
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98
Publications
2,542
Citation Statements Received
2,496
Citation Statements Given
How they've been cited
3,094
147
2,384
11
How they cite others
3,422
174
2,293
29
Affiliations
University of Coimbra
,
Hospitais da Universidade de Coimbra
Publications
Order By: Most citations
BBS10 encodes a vertebrate-specific chaperonin-like protein and is a major BBS locus
Stoetzel
1
,
Laurier
2
,
Davis
3
et al.
2006
Nat Genet
Abstract
Show
288
11
247
1
1
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Add to collection
Cite
Mainzer-Saldino Syndrome Is a Ciliopathy Caused by IFT140 Mutations
Perrault
1
,
Saunier
2
,
Hanein
3
et al.
2012
The American Journal of Human Genetics
Abstract
Show
238
11
225
2
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Add to collection
Cite
Extreme hyperopia is the result of null mutations in
MFRP
, which encodes a Frizzled-related protein
Sundin
1
,
Leppert
2
,
Silva
3
et al.
2005
Proc. Natl. Acad. Sci. U.S.A.
Abstract
Show
179
6
144
0
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Cite
Genetic basis of total colourblindness among the Pingelapese islanders
Sundin
1
,
Yang
2
,
Li
3
et al.
2000
Nat Genet
Abstract
Show
229
1
134
0
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Cite
ALDH1A3 Mutations Cause Recessive Anophthalmia and Microphthalmia
Fares‐Taie
1
,
Gerber
2
,
Chassaing
3
et al.
2013
The American Journal of Human Genetics
Abstract
Show
106
6
109
1
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Cite
AON-mediated Exon Skipping Restores Ciliation in Fibroblasts Harboring the Common Leber Congenital Amaurosis CEP290 Mutation
Gérard
1
,
Perrault
2
,
Hanein
3
et al.
2012
Molecular Therapy - Nucleic Acids
Abstract
Show
109
1
111
2
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Cite
Mutations in NMNAT1 cause Leber congenital amaurosis with early-onset severe macular and optic atrophy
Perrault
1
,
Hanein
2
,
Zanlonghi
3
et al.
2012
Nat Genet
Abstract
Show
148
3
102
0
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Add to collection
Cite
Redefining papillorenal syndrome: an underdiagnosed cause of ocular and renal morbidity
Parsa
1
,
Silva
2
,
Sundin
3
et al.
2001
Ophthalmology
105
1
83
0
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Add to collection
Cite
1
2
3
4
5
6