Daniela Corongiu

1.2k total citations
12 papers, 239 citations indexed

About

Daniela Corongiu is a scholar working on Neurology, Pathology and Forensic Medicine and Cellular and Molecular Neuroscience. According to data from OpenAlex, Daniela Corongiu has authored 12 papers receiving a total of 239 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Neurology, 3 papers in Pathology and Forensic Medicine and 3 papers in Cellular and Molecular Neuroscience. Recurrent topics in Daniela Corongiu's work include Amyotrophic Lateral Sclerosis Research (5 papers), Parkinson's Disease Mechanisms and Treatments (4 papers) and Hereditary Neurological Disorders (3 papers). Daniela Corongiu is often cited by papers focused on Amyotrophic Lateral Sclerosis Research (5 papers), Parkinson's Disease Mechanisms and Treatments (4 papers) and Hereditary Neurological Disorders (3 papers). Daniela Corongiu collaborates with scholars based in Italy, Germany and Finland. Daniela Corongiu's co-authors include Maria Giovanna Marrosu, Stefania Tranquilli, Maria Rita Murru, Stefania Cuccu, Antonino Cannas, Gianluca Floris, Francesco Marrosu, Paolo Solla, Maria Valeria Cherchi and Gianna Costa and has published in prestigious journals such as PLoS ONE, Journal of Neurology Neurosurgery & Psychiatry and Journal of the Neurological Sciences.

In The Last Decade

Daniela Corongiu

11 papers receiving 236 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Daniela Corongiu Italy	8	113	96	61	55	47	12	239
Kimiko Inoue Japan	9	150 1.3×	110 1.1×	49 0.8×	16 0.3×	40 0.9×	22	309
Jinzhi Zhang China	5	146 1.3×	146 1.5×	70 1.1×	16 0.3×	73 1.6×	5	373
Kelby M. Killoy United States	9	136 1.2×	123 1.3×	47 0.8×	11 0.2×	70 1.5×	10	335
M Milani Italy	12	109 1.0×	108 1.1×	236 3.9×	11 0.2×	107 2.3×	18	380
Giorgia Puorro Italy	10	130 1.2×	238 2.5×	196 3.2×	18 0.3×	19 0.4×	14	354
Constanze Depp Germany	7	59 0.5×	111 1.2×	67 1.1×	10 0.2×	117 2.5×	13	295
Xianghua He China	9	136 1.2×	64 0.7×	55 0.9×	6 0.1×	44 0.9×	21	229
Víctor Caraballo-Miralles Spain	8	122 1.1×	179 1.9×	62 1.0×	25 0.5×	58 1.2×	8	340
Antoine Duquette Canada	9	95 0.8×	251 2.6×	214 3.5×	11 0.2×	79 1.7×	21	394
B Dobosz Poland	7	92 0.8×	82 0.9×	30 0.5×	109 2.0×	65 1.4×	9	328

Countries citing papers authored by Daniela Corongiu

Since Specialization

Citations

This map shows the geographic impact of Daniela Corongiu's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Daniela Corongiu with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Daniela Corongiu more than expected).

Fields of papers citing papers by Daniela Corongiu

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Daniela Corongiu. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Daniela Corongiu. The network helps show where Daniela Corongiu may publish in the future.

Co-authorship network of co-authors of Daniela Corongiu

This figure shows the co-authorship network connecting the top 25 collaborators of Daniela Corongiu. A scholar is included among the top collaborators of Daniela Corongiu based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Daniela Corongiu. Daniela Corongiu is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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12 of 12 papers shown

Lorefice, Lorena, Maria Rita Murru, Giancarlo Coghe, et al.. (2017). Charcot–Marie–Tooth disease: genetic subtypes in the Sardinian population. Neurological Sciences. 38(6). 1019–1025. 9 indexed citations

Stefano, Francesca Di, Antonino Cannas, Giuseppe Borghero, et al.. (2016). Progressive apraxia of speech in a patient with a C9orf72 mutation. Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration. 17(7-8). 608–609.

Lorefice, Lorena, Giuseppe Fenu, Daniela Corongiu, et al.. (2015). A genetic association study of two genes linked to neurodegeneration in a Sardinian multiple sclerosis population: The TARDBP Ala382Thr mutation and C9orf72 expansion. Journal of the Neurological Sciences. 357(1-2). 229–234. 4 indexed citations

Floris, Gianluca, Giuseppe Borghero, Francesca Di Stefano, et al.. (2015). Phenotypic variability related to C9orf72 mutation in a large Sardinian kindred. Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration. 17(3-4). 245–248. 5 indexed citations

Floris, Gianluca, Giuseppe Borghero, Antonino Cannas, et al.. (2014). Constructional apraxia in frontotemporal dementia associated with the C9orf72 mutation: Broadening the clinical and neuropsychological phenotype. Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration. 16(1-2). 8–15. 10 indexed citations

Floris, Gianluca, Giuseppe Borghero, Antonino Cannas, et al.. (2014). Clinical phenotypes and radiological findings in frontotemporal dementia related to TARDBP mutations. Journal of Neurology. 262(2). 375–384. 45 indexed citations

Cocco, Eleonora, Alessandra Meloni, Maria Rita Murru, et al.. (2012). Vitamin D Responsive Elements within the HLA-DRB1 Promoter Region in Sardinian Multiple Sclerosis Associated Alleles. PLoS ONE. 7(7). e41678–e41678. 29 indexed citations

Solla, Paolo, Alessandra Bolino, Maria Giovanna Marrosu, et al.. (2010). Heat shock protein 27 R127W mutation: evidence of a continuum between axonal Charcot-Marie-Tooth and distal hereditary motor neuropathy. Journal of Neurology Neurosurgery & Psychiatry. 81(9). 958–962. 30 indexed citations

Solla, Paolo, Antonino Cannas, Gianluca Floris, et al.. (2010). ParkinExon Rearrangements and Sequence Variants inLRRK2Mutations Carriers: Analysis on a Possible Modifier Effect onLRRK2Penetrance. Parkinson s Disease. 2010. 1–5. 4 indexed citations

10.

Yu, Xinhua, Dirk Koczan, Anna-Maija Sulonen, et al.. (2008). mtDNA nt13708A Variant Increases the Risk of Multiple Sclerosis. PLoS ONE. 3(2). e1530–e1530. 63 indexed citations

11.

Floris, Gianluca, Antonino Cannas, Paolo Solla, et al.. (2008). Genetic analysis for five LRRK2 mutations in a Sardinian parkinsonian population: Importance of G2019S and R1441C mutations in sporadic Parkinson's disease patients. Parkinsonism & Related Disorders. 15(4). 277–280. 23 indexed citations

12.

Murru, Maria Rita, Maria Giovanna Marrosu, Eleonora Cocco, et al.. (2006). A novel Cx32 mutation causes X-linked Charcot-Marie-Tooth disease with brainstem involvement and brain magnetic resonance spectroscopy abnormalities. Neurological Sciences. 27(1). 18–23. 17 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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