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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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A. Patitucci
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122
Publications
1,689
Citation Statements Received
1,210
Citation Statements Given
How they've been cited
2,506
59
1,620
10
How they cite others
2,013
76
1,134
0
Affiliations
Institute of Neurological Sciences
,
National Research Council
Publications
Order By: Most citations
Mutations in the mitochondrial GTPase mitofusin 2 cause Charcot-Marie-Tooth neuropathy type 2A
Zuchner
1
,
Mersiyanova
2
,
Muglia
3
et al.
2004
Nat Genet
Abstract
Show
1,585
31
1,091
2
1
Get access via publisher
Add to collection
Cite
Ataxin-1 and ataxin-2 intermediate-length PolyQ expansions in amyotrophic lateral sclerosis
Conforti
1
,
Spataro
2
,
Sproviero
3
et al.
2012
Neurology
Abstract
Show
86
3
55
1
Get access via publisher
Add to collection
Cite
A novel Angiogenin gene mutation in a sporadic patient with amyotrophic lateral sclerosis from southern Italy
Conforti
1
,
Sprovieri
2
,
Mazzei
3
et al.
2008
Neuromuscular Disorders
55
1
38
0
Get access via publisher
Add to collection
Cite
Further evidence that
SPG3A
gene mutations cause autosomal dominant hereditary spastic paraplegia
Muglia
1
,
Magariello
2
,
Nicoletti
3
et al.
2002
Annals of Neurology
50
4
33
1
Get access via publisher
Add to collection
Cite
A longitudinal observation of Brain-Derived Neurotrophic Factor mRNA levels in patients with Relapsing–Remitting Multiple Sclerosis
Liguori
1
,
Fera
2
,
Patitucci
3
et al.
2009
Brain Research
34
4
32
1
Get access via publisher
Add to collection
Cite
Juvenile Huntington’s disease presenting as progressive myoclonic epilepsy
Gambardella
1
,
Muglia
2
,
Labate
3
et al.
2001
Neurology
Abstract
Show
67
1
31
0
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Add to collection
Cite
TARDBP gene mutations in south Italian patients with amyotrophic lateral sclerosis
Conforti
1
,
Sproviero
2
,
Simone
3
et al.
2010
Journal of Neurology, Neurosurgery & Psychiatry
35
1
25
0
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Add to collection
Cite
CADASIL: Extended polymorphisms and mutational analysis of the NOTCH3 gene
Ungaro
1
,
Mazzei
2
,
Conforti
3
et al.
2008
J of Neuroscience Research
Abstract
Show
29
1
20
2
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Add to collection
Cite
1
2
3