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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
Grazia Nardella
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42
Publications
305
Citation Statements Received
1,063
Citation Statements Given
How they've been cited
382
18
285
2
How they cite others
1,293
37
1,014
12
Affiliations
Casa Sollievo della Sofferenza
,
Sapienza University of Rome
Publications
Order By: Most citations
Inter-observer variability in the delineation of pharyngo-laryngeal tumor, parotid glands and cervical spinal cord: Comparison between CT-scan and MRI
Geets
1
,
Daisne
2
,
Arcangeli
3
et al.
2005
Radiotherapy and Oncology
190
8
141
1
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Cite
A single-center study on 140 patients with cerebral cavernous malformations: 28 new pathogenic variants and functional characterization of a
PDCD10
large deletion
Nardella
1
,
Visci
2
,
Guarnieri
3
et al.
2018
Human Mutation
Abstract
Show
18
0
25
0
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Cite
Mutational spectrum and clinical signatures in 114 families with hereditary multiple osteochondromas: insights into molecular properties of selected exostosin variants
Fusco
1
,
Nardella
2
,
Fischetto
3
et al.
2019
19
3
17
0
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Cite
Insights into the molecular pathogenesis of cardiospondylocarpofacial syndrome: MAP3K7 c.737-7A > G variant alters the TGFβ-mediated α-SMA cytoskeleton assembly and autophagy
Micale
1
,
Morlino
2
,
Biagini
3
et al.
2020
Biochimica et Biophysica Acta (BBA) - Molecular Basis of Diseas
14
1
14
0
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Cite
Pro-Fibrotic Phenotype in a Patient with Segmental Stiff Skin Syndrome via TGF-β Signaling Overactivation
Fusco
1
,
Nardella
2
,
Augello
3
et al.
2020
IJMS
Abstract
Show
18
0
12
0
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Cite
A novel dominant-negative FGFR1 variant causes Hartsfield syndrome by deregulating RAS/ERK1/2 pathway
Palumbo
1
,
Petracca
2
,
Maggi
3
et al.
2019
Eur J Hum Genet
Abstract
Show
21
1
10
0
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Review of clinical and molecular variability in autosomal recessive cutis laxa
2A
Morlino
1
,
Nardella
2
,
Castellana
3
et al.
2020
American J of Med Genetics Pt A
Abstract
Show
8
3
7
0
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Cite
Exon-Trapping Assay Improves Clinical Interpretation of COL11A1 and COL11A2 Intronic Variants in Stickler Syndrome Type 2 and Otospondylomegaepiphyseal Dysplasia
Micale
1
,
Morlino
2
,
Schirizzi
3
et al.
2020
Genes
Abstract
Show
19
1
8
0
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Cite
1
2
3
4