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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
Virginia P. Johnson
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36
Publications
927
Citation Statements Received
336
Citation Statements Given
How they've been cited
1,629
49
871
7
How they cite others
613
8
328
0
Affiliations
University of South Dakota
,
University of Sioux Falls
Publications
Order By: Most citations
Magnetic Resonance Imaging of Brain Anomalies in Fetal Alcohol Syndrome
Swayze
1
,
Johnson
2
,
Hanson
3
et al.
1997
Abstract
Show
269
8
146
3
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Add to collection
Cite
Correlation of severity and outcome with plasma sterol levels in variants of the Smith-Lemli-Opitz syndrome
Tint
1
,
Salen
2
,
Batta
3
et al.
1995
The Journal of Pediatrics
151
3
84
0
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Cite
Treatment of Smith-Lemli-Opitz syndrome: Results of a multicenter trial
Irons
1
,
Elias
2
,
Abuelo
3
et al.
1997
Am. J. Med. Genet.
Abstract
Show
135
4
61
0
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Cite
Uniparental isodisomy of chromosome 14 in two cases: An abnormal child and a normal adult
Papenhausen
1
,
Mueller
2
,
Johnson
3
et al.
1995
Am. J. Med. Genet.
Abstract
Show
82
4
60
0
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Cite
Fetal alcohol syndrome: Craniofacial and central nervous system manifestations
Johnson
1
,
Swayze
2
,
Satō
3
et al.
1996
Am. J. Med. Genet.
Abstract
Show
132
2
55
1
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Cite
Natural history of mosaic trisomy 14 syndrome
Fujimoto
1
,
Allanson
2
,
Crowe
3
et al.
1992
Am. J. Med. Genet.
Abstract
Show
57
4
46
0
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Cite
Linkage of a human brain malformation, familial holoprosencephaly, to chromosome 7 and evidence for genetic heterogeneity.
Muenke
1
,
Gurrieri
2
,
Bay
3
et al.
1994
Proc. Natl. Acad. Sci. U.S.A.
Abstract
Show
115
0
49
0
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Cite
A newly recognized neuroectodermal syndrome of familial alopecia, anosmia, deafness, and hypogonadism
Johnson
1
,
McMillin
2
,
Aceto
3
et al.
1983
Am. J. Med. Genet.
Abstract
Show
46
7
38
1
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Cite
1
2
3
4
5