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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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Els Van Hul
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20
Publications
815
Citation Statements Received
458
Citation Statements Given
How they've been cited
1,004
29
776
10
How they cite others
606
21
431
6
Affiliations
University of Antwerp
,
Antwerp University Hospital
Publications
Order By: Most citations
Mutations in the CCN gene family member WISP3 cause progressive pseudorheumatoid dysplasia
Hurvitz
1
,
Suwairi
2
,
Van Hul
3
et al.
1999
Nat Genet
Abstract
Show
271
5
258
1
Get access via publisher
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Cite
Involvement of PLEKHM1 in osteoclastic vesicular transport and osteopetrosis in incisors absent rats and humans
Van Wesenbeeck
1
,
Odgren
2
,
Coxon
3
et al.
2007
J. Clin. Invest.
Abstract
Show
234
13
196
1
Get access via publisher
Add to collection
Cite
Van Buchem Disease (Hyperostosis Corticalis Generalisata) Maps to Chromosome 17q12-q21
Van Hul
1
,
Balemans
2
,
Van Hul
3
et al.
1998
The American Journal of Human Genetics
Abstract
Show
158
1
89
0
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Cite
Mutation Screening of EXT1 and EXT2 by Denaturing High-Performance Liquid Chromatography, Direct Sequencing Analysis, Fluorescence in Situ Hybridization, and a New Multiplex Ligation-Dependent Probe Amplification Probe Set in Patients with Multiple Osteochondromas
Jennes
1
,
Entius
2
,
Van Hul
3
et al.
2008
The Journal of Molecular Diagnostics
Abstract
Show
51
5
60
7
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Cite
Localization of the Gene Causing Autosomal Dominant Osteopetrosis Type I to Chromosome 11q12-13
Van Hul
1
,
Gram
2
,
Bollerslev
3
et al.
2002
Abstract
Show
93
0
57
0
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Cite
Evaluation of the Role of the SQSTM1 Gene in Sporadic Belgian Patients with Paget’s Disease
Beyens
1
,
Van Hul
2
,
Van Driessche
3
et al.
2004
Calcif Tissue Int
Abstract
Show
54
0
47
1
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Cite
Localization of a Gene for Autosomal Dominant Osteopetrosis (Albers-Schönberg Disease) to Chromosome 1p21
Van Hul
1
,
Bollerslev
2
,
Gram
3
et al.
1997
The American Journal of Human Genetics
Abstract
Show
75
1
26
0
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Cite
RNA‐Seq detects a
SAMD12‐EXT1
fusion transcript and leads to the discovery of an
EXT1
deletion in a child with multiple osteochondromas
Oliver
1
,
Blackburn
2
,
Ellingson
3
et al.
2019
Molec Gen & Gen Med
Abstract
Show
16
1
14
0
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Cite
1
2
3