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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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Charles J. Wolock
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51
Publications
1,011
Citation Statements Received
1,722
Citation Statements Given
How they've been cited
1,261
53
956
2
How they cite others
1,507
80
1,636
6
Affiliations
University of Pennsylvania
,
Columbia University
Publications
Order By: Most citations
Statistical analysis of iron geochemical data suggests limited late Proterozoic oxygenation
Sperling
1
,
Wolock
2
,
Morgan
3
et al.
2015
Nature
Abstract
Show
647
35
418
1
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Add to collection
Cite
Whole‐exome sequencing in 20,197 persons for rare variants in Alzheimer's disease
Raghavan
1
,
Brickman
2
,
Andrews
3
et al.
2018
Ann Clin Transl Neurol
Abstract
Show
173
7
120
0
2
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Add to collection
Cite
Convergence between the microcosms of Southeast Asian and North American pitcher plants
Bittleston
1
,
Wolock
2
,
Yahya
3
et al.
2018
Abstract
Show
61
6
93
1
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Add to collection
Cite
Serine biosynthesis defect due to haploinsufficiency of PHGDH causes retinal disease
Eade
1
,
Gantner
2
,
Hostyk
3
et al.
2021
Nat Metab
Abstract
Show
71
4
85
0
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Cite
Exome-Based Rare-Variant Analyses in CKD
Cameron‐Christie
1
,
Wolock
2
,
Groopman
3
et al.
2019
JASN
Abstract
Show
60
0
59
0
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Cite
Improved Pathogenic Variant Localization via a Hierarchical Model of Sub-regional Intolerance
Hayeck
1
,
Stong
2
,
Wolock
3
et al.
2019
The American Journal of Human Genetics
Abstract
Show
43
0
44
0
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Cite
A new approach for rare variation collapsing on functional protein domains implicates specific genic regions in ALS
Gelfman
1
,
Dugger
2
,
Moreno
3
et al.
2019
Genome Res.
Abstract
Show
35
0
37
0
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Cite
A case–control collapsing analysis identifies retinal dystrophy genes associated with ophthalmic disease in patients with no pathogenic ABCA4 variants
Wolock
1
,
Stong
2
,
Jian
3
et al.
2019
Genetics in Medicine
Abstract
Show
32
0
35
0
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Cite
1
2
3
4
5
6