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M. Nardella · SciRah

Researcher profile · Semantic Scholar

M. Nardella

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M. Nardella — researcher profile on SciRah

h-index: 12
Works: 23
Citations: 420

Most-cited papers

Missense mutations of CACNA1A are a frequent cause of autosomal dominant nonprogressive congenital ataxia.
L. Travaglini, M. Nardella, E. Bellacchio, A. D'Amico +13 more
2017European journal of paediatric neurology49 citations
Semantic Scholar
LMNA Knock-Down Affects Differentiation and Progression of Human Neuroblastoma Cells
G. Maresca, Manuela Natoli, M. Nardella, I. Arisi +11 more
2012PLoS ONE48 citations Open access
Semantic Scholar
MYCN gene expression is required for the onset of the differentiation programme in neuroblastoma cells
L. Guglielmi, C. Cinnella, M. Nardella, G. Maresca +4 more
2014Cell Death and Disease45 citations Open access
Semantic Scholar
Conditioned medium of primary lung cancer cells induces EMT in A549 lung cancer cell line by TGF-ß1 and miRNA21 cooperation
R. Camerlingo, Roberta Miceli, L. Marra, Giuseppina Rea +7 more
2019PLoS ONE38 citations Open access
Semantic Scholar
Age and sex prevalence estimate of Joubert syndrome in Italy
S. Nuovo, I. Bacigalupo, M. Ginevrino, R. Battini +10 more
2020Neurology37 citations Open access
Semantic Scholar
Heterozygous missense variants of SPTBN2 are a frequent cause of congenital cerebellar ataxia
F. Nicita, M. Nardella, E. Bellacchio, P. Alfieri +7 more
2019Clinical Genetics31 citations
Semantic Scholar
Identification of novel and hotspot mutations in the channel domain of ITPR1 in two patients with Gillespie syndrome
M. Dentici, S. Barresi, M. Nardella, E. Bellacchio +9 more
2017Gene30 citations Open access
Semantic Scholar
Down-regulation of the Lamin A/C in neuroblastoma triggers the expansion of tumor initiating cells
M. Nardella, L. Guglielmi, Carla Musa, Ilaria Iannetti +17 more
2015OncoTarget25 citations Open access
Semantic Scholar
De novo p.T362R mutation in MORC2 causes early onset cerebellar ataxia, axonal polyneuropathy and nocturnal hypoventilation.
G. Zanni, M. Nardella, S. Barresi, E. Bellacchio +6 more
2017Brain : a journal of neurology20 citations
Semantic Scholar
Novel Homozygous KCNJ10 Mutation in a Patient with Non-syndromic Early-Onset Cerebellar Ataxia
F. Nicita, G. Tasca, M. Nardella, E. Bellacchio +5 more
2018Cerebellum16 citations Open access
Semantic Scholar
A novel PMCA3 mutation in an ataxic patient with hypomorphic phosphomannomutase 2 (PMM2) heterozygote mutations: Biochemical characterization of the pump defect.
Mattia Vicario, Tito Calì, Domenico Cieri, F. Vallese +12 more
2017Biochimica et Biophysica Acta - Molecular Basis of Disease16 citations Open access
Semantic Scholar
Defining the clinical-genetic and neuroradiological features in SPG54: description of eight additional cases and nine novel DDHD2 variants
F. Nicita, Fabrizia Stregapede, A. Tessa, M. Bassi +16 more
2019Journal of Neurology14 citations
Semantic Scholar
Circulating miRNAs in Small Extracellular Vesicles Secreted by a Human Melanoma Xenograft in Mouse Brains
L. Guglielmi, M. Nardella, Carla Musa, I. Cifola +16 more
2020Cancers11 citations Open access
Semantic Scholar
Biallelic Variants in the Nuclear Pore Complex Protein NUP93 Are Associated with Non-progressive Congenital Ataxia
G. Zanni, P. De Magistris, M. Nardella, E. Bellacchio +9 more
2019Cerebellum10 citations
Semantic Scholar
Differentiation of Caco-2 cells requires both transcriptional and post-translational down-regulation of Myc.
B. D. Leoni, Manuela Natoli, M. Nardella, B. Bucci +3 more
2012Differentiation; research in biological diversity10 citations
Semantic Scholar
Human placenta-derived neurospheres are susceptible to transformation after extensive in vitro expansion
D. Amendola, M. Nardella, L. Guglielmi, L. Cerquetti +10 more
2014Stem cell research & therapeutics7 citations Open access
Semantic Scholar
Lamin A/C Is Required for ChAT-Dependent Neuroblastoma Differentiation
L. Guglielmi, M. Nardella, Carla Musa, Ilaria Iannetti +9 more
2016Molecular Neurobiology6 citations
Semantic Scholar
Teaching Video NeuroImages: Palatal tremor associated with SPG7 variants
G. Primiano, G. Zanni, M. Nardella, S. Servidei
2020Neurology2 citations Open access
Semantic Scholar
Novel Homozygous KCNJ10 Mutation in a Patient with Non-syndromic Early-Onset Cerebellar Ataxia
F. Nicita, G. Tasca, M. Nardella, E. Bellacchio +5 more
2018Cerebellum2 citations Open access
Semantic Scholar
De novo T362R mutation in MORC2 causes early onset cerebellar ataxia, axonal polyneuropathy and nocturnal hypoventilation
G. Zanni, M. Nardella, M. Niceta, E. Bellacchio +5 more
20172 citations
Semantic Scholar
Lamin A/C regulates cerebellar granule cell maturation
Laura Vilardo, I. Cifola, M. Nardella, Paride Pelucchi +12 more
2025Cell Biology and Toxicology0 citations Open access
Semantic Scholar
Correction to: Biallelic Variants in the Nuclear Pore Complex Protein NUP93 Are Associated with Non-progressive Congenital Ataxia
G. Zanni, P. De Magistris, M. Nardella, E. Bellacchio +9 more
2019Cerebellum0 citations Open access
Semantic Scholar
Author response for "Heterozygous missense variants of SPTBN2 are a frequent cause of congenital cerebellar ataxia"
F. Nicita, M. Nardella, E. Bellacchio, P. Alfieri +7 more
20190 citations
Semantic Scholar

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