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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
Sharola Dharmaraj
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42
Publications
935
Citation Statements Received
660
Citation Statements Given
How they've been cited
1,229
37
894
4
How they cite others
1,499
9
645
6
Affiliations
Johns Hopkins University
,
Johns Hopkins Medicine
Publications
Order By: Most citations
Mutations in LCA5, encoding the ciliary protein lebercilin, cause Leber congenital amaurosis
den Hollander
1
,
Koenekoop
2
,
Mohamed
3
et al.
2007
Nat Genet
Abstract
Show
193
11
150
0
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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
Prevalence of AIPL1 Mutations in Inherited Retinal Degenerative Disease
Sohocki
1
,
Perrault
2
,
Leroy
3
et al.
2000
Molecular Genetics and Metabolism
150
4
131
1
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Add to collection
Cite
Genotyping Microarray (Disease Chip) for Leber Congenital Amaurosis: Detection of Modifier Alleles
Zernant
1
,
Ku ̈lm
2
,
Dharmaraj
3
et al.
2005
Invest. Ophthalmol. Vis. Sci.
Abstract
Show
162
0
115
2
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Add to collection
Cite
Developmental Basis of Nanophthalmos:
MFRP
Is Required for both Prenatal Ocular Growth and Postnatal Emmetropization
Sundin
1
,
Dharmaraj
2
,
Bhutto
3
et al.
2008
Ophthalmic Genetics
Abstract
Show
82
3
108
0
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Cite
The Phenotype of Leber Congenital Amaurosis in Patients With AIPL1 Mutations
Dharmaraj
1
2004
Arch Ophthalmol
Abstract
Show
105
6
71
1
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Cite
Mutational analysis and clinical correlation in Leber congenital amaurosis
Dharmaraj
1
,
Silva
2
,
Piña
3
et al.
2000
Ophthalmic Genetics
Abstract
Show
110
1
53
0
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Cite
A Novel Locus for Leber Congenital Amaurosis Maps to Chromosome 6q
Dharmaraj
1
,
Li
2
,
Robitaille
3
et al.
2000
The American Journal of Human Genetics
80
3
39
0
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Cite
1
2
3