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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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Sten Andréasson
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215
Publications
5,042
Citation Statements Received
4,926
Citation Statements Given
How they've been cited
6,438
211
4,803
28
How they cite others
5,874
355
4,526
45
Affiliations
Lund University
,
Skåne University Hospital
Publications
Order By: Most citations
Identification of the gene responsible for Best macular dystrophy
Petrukhin
1
,
Koisti
2
,
Bakall
3
et al.
1998
Nat Genet
Abstract
Show
659
6
483
3
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Cite
CNGA3 Mutations in Hereditary Cone Photoreceptor Disorders
Wissinger
1
,
Gamer
2
,
Jägle
3
et al.
2001
The American Journal of Human Genetics
Abstract
Show
316
7
286
1
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Cite
CNGB3 mutations account for 50% of all cases with autosomal recessive achromatopsia
Kohl
1
,
Varsányi
2
,
Antunes
3
et al.
2004
Eur J Hum Genet
Abstract
Show
243
4
201
1
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Cite
The complete form of X-linked congenital stationary night blindness is caused by mutations in a gene encoding a leucine-rich repeat protein
Pusch
1
,
Zeitz
2
,
Brandau
3
et al.
2000
Nat Genet
Abstract
Show
255
4
195
0
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Cite
A homologous genetic basis of the murine
cpfl1
mutant and human achromatopsia linked to mutations in the
PDE6C
gene
Chang
1
,
Grau
2
,
Dangel
3
et al.
2009
Proc. Natl. Acad. Sci. U.S.A.
Abstract
Show
192
7
173
0
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Cite
Null RPGRIP1 Alleles in Patients with Leber Congenital Amaurosis
Dryja
1
,
Adams
2
,
Grimsby
3
et al.
2001
The American Journal of Human Genetics
Abstract
Show
272
1
174
1
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Cite
Premature Truncation of a Novel Protein, RD3, Exhibiting Subnuclear Localization Is Associated with Retinal Degeneration
Friedman
1
,
Chang
2
,
Kannabiran
3
et al.
2006
The American Journal of Human Genetics
Abstract
Show
114
7
159
2
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Cite
A new X linked recessive deafness syndrome with blindness, dystonia, fractures, and mental deficiency is linked to Xq22.
Tranebjærg
1
,
Schwartz
2
,
Eriksen
3
et al.
1995
J Med Genet
Abstract
Show
182
0
122
0
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Cite
1
2
3
4
5