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
Manuela Morleo
Sign up to set email alerts
95
Publications
3,953
Citation Statements Received
3,362
Citation Statements Given
How they've been cited
5,000
127
3,816
10
How they cite others
12,350
103
3,254
5
Affiliations
Telethon Institute Of Genetics And Medicine
,
University of Campania "Luigi Vanvitelli"
Publications
Order By: Most citations
Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition)
1
Klionsky
1
,
Abdel‐Aziz
2
,
Abdelfatah
3
et al.
2021
Autophagy
2,921
61
2,105
6
Get access via publisher
Add to collection
Cite
An organelle-specific protein landscape identifies novel diseases and molecular mechanisms
Boldt
1
,
van Reeuwijk
2
,
Lu
3
et al.
2016
Nat Commun
Abstract
Show
274
10
259
0
Get access via publisher
Add to collection
Cite
Mutations of the Mitochondrial Holocytochrome c–Type Synthase in X-Linked Dominant Microphthalmia with Linear Skin Defects Syndrome
Wimplinger
1
,
Morleo
2
,
Rosenberger
3
et al.
2006
The American Journal of Human Genetics
Abstract
Show
143
5
142
0
Get access via publisher
Add to collection
Cite
Ciliopathy proteins regulate paracrine signaling by modulating proteasomal degradation of mediators
Liu
1
,
Tsai
2
,
Morleo
3
et al.
2014
J. Clin. Invest.
Abstract
Show
101
5
118
0
Get access via publisher
Add to collection
Cite
Mutations in COX7B Cause Microphthalmia with Linear Skin Lesions, an Unconventional Mitochondrial Disease
Indrieri
1
,
Tiranti
2
,
Morleo
3
et al.
2012
The American Journal of Human Genetics
Abstract
Show
165
3
118
1
Get access via publisher
Add to collection
Cite
Fifteen years of research on oral–facial–digital syndromes: from 1 to 16 causal genes
Bruel
1
,
Franco
2
,
Duffourd
3
et al.
2017
J Med Genet
Abstract
Show
134
1
112
0
Get access via publisher
Add to collection
Cite
Germline variants in tumor suppressor FBXW7 lead to impaired ubiquitination and a neurodevelopmental syndrome
Stephenson
1
,
Costain
2
,
Blok
3
et al.
2022
The American Journal of Human Genetics
46
1
71
0
Get access via publisher
Add to collection
Cite
Dosage compensation of the mammalian X chromosome influences the phenotypic variability of X-linked dominant male-lethal disorders
Morleo
1
,
Franco
2
2008
J Med Genet
Abstract
Show
88
3
62
0
Get access via publisher
Add to collection
Cite
1
2
3
4