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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
Jenneke van den Ende
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104
Publications
3,355
Citation Statements Received
2,265
Citation Statements Given
How they've been cited
3,980
147
3,191
17
How they cite others
2,516
137
2,104
24
Affiliations
Antwerp University Hospital
,
University of Antwerp
Publications
Order By: Most citations
A SWI/SNF-related autism syndrome caused by de novo mutations in ADNP
Helsmoortel
1
,
Vulto‐van Silfhout
2
,
Coe
3
et al.
2014
Nat Genet
Abstract
Show
396
19
379
2
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Cite
Clinical Presentation of a Complex Neurodevelopmental Disorder Caused by Mutations in ADNP
Van Dijck
1
,
Vulto‐van Silfhout
2
,
Cappuyns
3
et al.
2019
Biological Psychiatry
Abstract
Show
195
9
242
2
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Cite
Stickler syndrome caused by COL2A1 mutations: genotype–phenotype correlation in a series of 100 patients
Hoornaert
1
,
Vereecke
2
,
Dewinter
3
et al.
2010
Eur J Hum Genet
Abstract
Show
154
5
165
0
1
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Cite
Fourteen new cases contribute to the characterization of the 7q11.23 microduplication syndrome
Van der Aa
1
,
Rooms
2
,
Vandeweyer
3
et al.
2009
European Journal of Medical Genetics
193
10
151
1
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Cite
The genetic basis of DOORS syndrome: an exome-sequencing study
Campeau
1
,
Kasperavičiūtė
2
,
Lu
3
et al.
2014
The Lancet Neurology
Abstract
Show
244
2
160
0
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Cite
Phenotype and genotype in 103 patients with tricho-rhino-phalangeal syndrome
Maas
1
,
Shaw
2
,
Bikker
3
et al.
2015
European Journal of Medical Genetics
Abstract
Show
115
9
138
0
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Cite
Clinical spectrum of individuals with pathogenic
N
F1
missense variants affecting p.Met1149, p.Arg1276, and p.Lys1423: genotype–phenotype study in neurofibromatosis type 1
Koczkowska
1
,
Callens
2
,
Chen
3
et al.
2019
Human Mutation
Abstract
Show
142
5
120
1
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Cite
Myhre and LAPS syndromes: clinical and molecular review of 32 patients
Michot
1
,
Le Goff
2
,
Mahaut
3
et al.
2014
Eur J Hum Genet
Abstract
Show
57
1
122
1
1
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Cite
1
2
3
4
5