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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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Frank J. Gareis
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20
Publications
99
Citation Statements Received
50
Citation Statements Given
How they've been cited
418
7
91
1
How they cite others
140
8
42
0
Affiliations
University of Washington
,
Regional Medical Center
Publications
Order By: Most citations
Evidence for Partial 21-Hydroxylase Deficiency Among Heterozygote Carriers of Congenital Adrenal Hyperplasia
Lee
1
,
Gareis
2
1975
The Journal of Clinical Endocrinology & Metabolism
Abstract
Show
61
3
22
0
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Cite
An interdisciplinary study of adolescent obesity
Hammar
1
,
Campbell
2
,
Campbell
3
et al.
1972
The Journal of Pediatrics
75
3
15
1
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Cite
X‐linked mental retardation associated with bilateral clasp thumb anomaly
Gareis
1
,
Mason
2
,
Opitz
3
1984
Am. J. Med. Genet.
Abstract
Show
39
0
12
0
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Cite
Gonadotropin and Sex Steroid Response to Luteinizing Hormone-Releasing Hormone in Patients with Premature Adrenarche
Lee
1
,
Gareis
2
1976
The Journal of Clinical Endocrinology & Metabolism
Abstract
Show
22
1
8
0
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Cite
The Russell-Silver syndrome without asymmetry
Gareis
1
,
Smith
2
,
Summitt
3
1971
The Journal of Pediatrics
41
0
9
0
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Cite
Detection of the heterozygous state in siblings of patientswith congenital adrenal hyperplasia due to 21-hydroxylase deficiency
Gutai
1
,
Lee
2
,
Johnsonbaugh
3
et al.
1979
The Journal of Pediatrics
22
0
7
0
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Cite
Recurrent giant cell granuloma occurring in the mandible of a patient on high dose estrogen therapy for the treatment of Sotos' syndrome
Flaggert
1
,
Heldt
2
,
Gareis
3
1987
Journal of Oral and Maxillofacial Surgery
17
0
7
0
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Clinical and molecular findings in two patients with Russell-Silver syndrome and UPD7: Comparison with non-UPD7 cases
Bernard
1
,
Pe�aherrera
2
,
Van Allen
3
et al.
1999
Am. J. Med. Genet.
Abstract
Show
49
0
7
0
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Cite
1
2