Author

Daniela Corongiu

Observed names: Corongiu D, Corongiu Daniela, D. Corongiu

Institutions: Istituto delle Scienze Neurologiche di Bologna, Ospedale Bellaria

Observed institutions: University of Cagliari, Istituto delle Scienze Neurologiche di Bologna, Ospedale Bellaria

OpenAlex ID: A5004520160

Genome-Wide Analyses Identify KIF5A as a Novel ALS Gene

2018 · Aude Nicolas, Kevin P. Kenna, et al. · Neuron · 681

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mtDNA nt13708A Variant Increases the Risk of Multiple Sclerosis

2008 · Xinhua Yu, Dirk Koczan, et al. · PLoS ONE · 73

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Clinical phenotypes and radiological findings in frontotemporal dementia related to TARDBP mutations

2014 · Gianluca Floris, Giuseppe Borghero, et al. · Journal of Neurology · 57

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TBK1 is associated with ALS and ALS-FTD in Sardinian patients

2016 · Giuseppe Borghero, Maura Pugliatti, et al. · Neurobiology of Aging · 50

Bipolar affective disorder preceding frontotemporal dementia in a patient with C9ORF72 mutation: is there a genetic link between these two disorders?

2013 · Gianluca Floris, Giuseppe Borghero, et al. · Journal of Neurology · 41

Vitamin D Responsive Elements within the HLA-DRB1 Promoter Region in Sardinian Multiple Sclerosis Associated Alleles

2012 · Eleonora Cocco, Alessandra Meloni, et al. · PLoS ONE · 41

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Heat shock protein 27 R127W mutation: evidence of a continuum between axonal Charcot-Marie-Tooth and distal hereditary motor neuropathy

2010 · P. Solla, A. Vannelli, et al. · Journal of Neurology Neurosurgery & Psychiatry · 37

The p.A382T TARDBP gene mutation in Sardinian patients affected by Parkinson's disease and other degenerative parkinsonisms

2013 · Antonino Cannas, Giuseppe Borghero, et al. · Neurogenetics · 36

C9ORF72 intermediate repeat expansion in patients affected by atypical parkinsonian syndromes or Parkinson’s disease complicated by psychosis or dementia in a Sardinian population

2015 · Antonino Cannas, Paolo Solla, et al. · Journal of Neurology · 32

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Genetic loci linked to Type 1 Diabetes and Multiple Sclerosis families in Sardinia

2008 · Maristella Pitzalis, Patrizia Zavattari, et al. · BMC Medical Genetics · 28

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A novel Cx32 mutation causes X-linked Charcot-Marie-Tooth disease with brainstem involvement and brain magnetic resonance spectroscopy abnormalities

2006 · M. R. Murru, A. Vannelli, et al. · Neurological Sciences · 27

Genetic analysis for five LRRK2 mutations in a Sardinian parkinsonian population: Importance of G2019S and R1441C mutations in sporadic Parkinson's disease patients

2008 · Gianluca Floris, Antonino Cannas, et al. · Parkinsonism & Related Disorders · 24

Charcot–Marie–Tooth disease: genetic subtypes in the Sardinian population

2017 · Lorena Lorefice, Maria Rita Murru, et al. · Neurological Sciences · 16

Constructional apraxia in frontotemporal dementia associated with the C9orf72 mutation: Broadening the clinical and neuropsychological phenotype

2014 · Gianluca Floris, Giuseppe Borghero, et al. · Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration · 13

Phenotypic variability related to C9orf72 mutation in a large Sardinian kindred

2015 · Gianluca Floris, Giuseppe Borghero, et al. · Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration · 7

A genetic association study of two genes linked to neurodegeneration in a Sardinian multiple sclerosis population: The TARDBP Ala382Thr mutation and C9orf72 expansion

2015 · L. Lorefice, Murru, et al. · Journal of the Neurological Sciences · 6

ParkinExon Rearrangements and Sequence Variants inLRRK2Mutations Carriers: Analysis on a Possible Modifier Effect onLRRK2Penetrance

2010 · Paolo Solla, Antonino Cannas, et al. · Parkinson s Disease · 4

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Progressive apraxia of speech in a patient with a C9orf72 mutation

2016 · Francesca Di Stefano, Monica Melis, et al. · Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration · 3

Erratum to: Charcot−Marie−Tooth disease: genetic subtypes in the Sardinian population

2017 · Lorena Lorefice, Maria Rita Murru, et al. · Neurological Sciences

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Leucine-rich repeat kinase 2 (LRRK2) gene mutations in degenerative parkinsonism

2010 · Paolo Solla, Antonino Cannas, et al. · UNICA IRIS Institutional Research Information System (University of Cagliari)

Axonal Charcot-Marie-Tooth disease, distal hereditary motor neuropathy and spastic paraplegia in a large Sardinian family with Heat Shock Protein RW mutation: an expression of a common spectrum?

2008 · Paolo Solla, Vannelli Alessandro, et al. · UNICA IRIS Institutional Research Information System (University of Cagliari)

Genetic analysis for five LRRK2 mutations in sardinian patients with familial or sporadic Parkinson’s disease

2007 · Paolo Solla, Antonino Cannas, et al. · UNICA IRIS Institutional Research Information System (University of Cagliari)

Parkin sequence variants in Parkinson’s disease patients with LRRK2 mutations

2007 · Paolo Solla, Antonino Cannas, et al. · UNICA IRIS Institutional Research Information System (University of Cagliari)

Analysis of parkin exon rearrangements and sequence variants in LRRK2 mutations carriers

2007 · Paolo Solla, Antonino Cannas, et al. · UNICA IRIS Institutional Research Information System (University of Cagliari)

Analysis of LRRK2 G2019 mutation in a sardinian cohort of PD patients

2006 · Gianluca Floris, Antonino Cannas, et al. · UNICA IRIS Institutional Research Information System (University of Cagliari)

Works count: 30

Citation count: 1,176

H-index: 13

I10-index: 14