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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
Tiziano Pramparo
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139
Publications
6,635
Citation Statements Received
6,037
Citation Statements Given
How they've been cited
7,982
365
6,252
18
How they cite others
5,257
405
5,608
24
Affiliations
University of California, San Diego
,
University of Pavia
Publications
Order By: Most citations
Tbx1 haploinsufficiency in the DiGeorge syndrome region causes aortic arch defects in mice
Lindsay
1
,
Vitelli
2
,
Morishima
3
et al.
2001
Nature
Abstract
Show
1,075
22
791
1
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Cite
Altered proliferation and networks in neural cells derived from idiopathic autistic individuals
Marchetto
1
,
Belinson
2
,
Freitas
3
et al.
2016
Mol Psychiatry
Abstract
Show
553
44
539
1
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Add to collection
Cite
Targeted sequencing identifies 91 neurodevelopmental-disorder risk genes with autism and developmental-disability biases
Stessman
1
,
Xiong
2
,
Coe
3
et al.
2017
Nat Genet
Abstract
Show
618
21
530
1
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Cite
Integrating de novo and inherited variants in 42,607 autism cases identifies mutations in new moderate-risk genes
Zhou
1
,
Feliciano
2
,
Shu
3
et al.
2022
Nat Genet
Abstract
Show
531
13
341
0
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Cite
Neuroepithelial Stem Cell Proliferation Requires LIS1 for Precise Spindle Orientation and Symmetric Division
Yingling
1
,
Youn
2
,
Darling
3
et al.
2008
Cell
Abstract
Show
298
28
311
1
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Cite
The ASD Living Biology: from cell proliferation to clinical phenotype
Courchesne
1
,
Pramparo
2
,
Gazestani
3
et al.
2018
Mol Psychiatry
Abstract
Show
357
15
271
0
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Cite
Cryptic deletions are a common finding in “balanced” reciprocal and complex chromosome rearrangements: a study of 59 patients
De Gregori
1
,
Ciccone
2
,
Magini
3
et al.
2007
J Med Genet
Abstract
Show
336
14
219
3
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Cite
Hotspots of missense mutation identify neurodevelopmental disorder genes and functional domains
Geisheker
1
,
Heymann
2
,
Wang
3
et al.
2017
Nat Neurosci
Abstract
Show
196
9
212
0
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Cite
1
2
3
4
5
6