Skip to main content
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
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
Lucia Perone
Sign up to set email alerts
51
Publications
389
Citation Statements Received
1,198
Citation Statements Given
How they've been cited
507
11
376
2
How they cite others
920
62
1,133
3
Affiliations
Telethon Institute Of Genetics And Medicine
,
University of Naples Federico II
Publications
Order By: Most citations
The KCNQ1OT1 imprinting control region and non-coding RNA: new properties derived from the study of Beckwith–Wiedemann syndrome and Silver–Russell syndrome cases
Chiesa
1
,
De Crescenzo
2
,
Mishra
3
et al.
2011
Abstract
Show
125
3
106
0
Get access via publisher
Add to collection
Cite
Characterization of the most frequent ATP7B mutation causing Wilson disease in hepatocytes from patient induced pluripotent stem cells
Parisi
1
,
Polishchuk
2
,
Allocca
3
et al.
2018
Sci Rep
Abstract
Show
51
3
61
0
2
Get access via publisher
Add to collection
Cite
Microphthalmia with linear skin defects (MLS) syndrome: Clinical, cytogenetic, and molecular characterization of 11 cases
Morleo
1
,
Pramparo
2
,
Perone
3
et al.
2005
American J of Med Genetics Pt A
Abstract
Show
44
2
48
0
Get access via publisher
Add to collection
Cite
MePR: A Novel Human Mesenchymal Progenitor Model with Characteristics of Pluripotency
Miceli
1
,
Franci
2
,
Dell’Aversana
3
et al.
2013
Stem Cells and Development
Abstract
Show
20
1
34
0
Get access via publisher
Add to collection
Cite
Contiguous gene syndrome due to an interstitial deletion in Xp22.3 in a boy with ichthyosis, chondrodysplasia punctata, mental retardation and ADHD
Lonardo
1
,
Parenti
2
,
Luquetti
3
et al.
2007
European Journal of Medical Genetics
41
1
23
0
Get access via publisher
Add to collection
Cite
Clinical, cytogenetic and molecular-cytogenetic characterization of a patient with a de novo tandem proximal-intermediate duplication of 16q and review of the literature
Lonardo
1
,
Perone
2
,
Maioli
3
et al.
2011
Am. J. Med. Genet.
Abstract
Show
40
1
22
0
Get access via publisher
Add to collection
Cite
Relaxation of Insulin-like Growth Factor 2 Imprinting and Discordant Methylation at KvDMR1 in Two First Cousins Affected by Beckwith-Wiedemann and Klippel-Trenaunay-Weber Syndromes
Sperandeo
1
,
Ungaro
2
,
Vernucci
3
et al.
2000
The American Journal of Human Genetics
Abstract
Show
30
0
15
0
Get access via publisher
Add to collection
Cite
Mild phenotype associated with an interstitial deletion of the long arm of chromosome 1.
Melis
1
,
Perone
2
,
Sperandeo
3
et al.
1998
J Med Genet
Abstract
Show
11
0
13
2
Get access via publisher
Add to collection
Cite
1
2
3
4
5