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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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M. Muglia
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173
Publications
2,909
Citation Statements Received
3,511
Citation Statements Given
How they've been cited
4,206
131
2,763
15
How they cite others
3,643
237
3,270
4
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
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Cite
Charcot-Marie-Tooth type 4B is caused by mutations in the gene encoding myotubularin-related protein-2
Bolino
1
,
Muglia
2
,
Conforti
3
et al.
2000
Nat Genet
Abstract
Show
470
5
282
0
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Cite
Loss-of-function mutations in the
SIGMAR1
gene cause distal hereditary motor neuropathy by impairing ER-mitochondria tethering and Ca
2+
signalling
Gregianin
1
,
Pallafacchina
2
,
Zanin
3
et al.
2016
Hum. Mol. Genet.
Abstract
Show
102
11
113
1
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Cite
Monoamine Oxidase-A Genetic Variations Influence Brain Activity Associated with Inhibitory Control: New Insight into the Neural Correlates of Impulsivity
Passamonti
1
,
Fera
2
,
Magariello
3
et al.
2006
Biological Psychiatry
157
8
102
0
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Cite
Clinical and genetic studies in hereditary spastic paraplegia with thin corpus callosum
Casali
1
,
Valente
2
,
Bertini
3
et al.
2004
Neurology
Abstract
Show
75
20
68
0
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Cite
The natural history of spinal neurofibromatosis: a critical review of clinical and genetic features
Ruggieri
1
,
Polizzi
2
,
Spalice
3
et al.
2014
Clinical Genetics
Abstract
Show
100
3
80
1
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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
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Cite
A mosaic pattern of INI1/SMARCB1 protein expression distinguishes Schwannomatosis and NF2-associated peripheral schwannomas from solitary peripheral schwannomas and NF2-associated vestibular schwannomas
Caltabiano
1
,
Magro
2
,
Polizzi
3
et al.
2017
Childs Nerv Syst
Abstract
Show
68
2
56
1
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Cite
1
2
3