Chiara Reale

713 total citations
19 papers, 320 citations indexed

About

Chiara Reale is a scholar working on Neurology, Molecular Biology and Neurology. According to data from OpenAlex, Chiara Reale has authored 19 papers receiving a total of 320 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Neurology, 5 papers in Molecular Biology and 5 papers in Neurology. Recurrent topics in Chiara Reale's work include Neurological disorders and treatments (6 papers), Parkinson's Disease Mechanisms and Treatments (6 papers) and Neurological diseases and metabolism (5 papers). Chiara Reale is often cited by papers focused on Neurological disorders and treatments (6 papers), Parkinson's Disease Mechanisms and Treatments (6 papers) and Neurological diseases and metabolism (5 papers). Chiara Reale collaborates with scholars based in Italy, United Kingdom and Germany. Chiara Reale's co-authors include Barbara Garavaglia, Celeste Panteghini, Nardo Nardocci, Chiara Barzaghi, Miryam Carecchio, Maria Regoni, Jenny Sassone, Maria Teresa Pellecchia, Luisa Chiapparini and Enza Maria Valente and has published in prestigious journals such as Neurology, Journal of Neuroscience Research and European Journal of Neurology.

In The Last Decade

Chiara Reale

18 papers receiving 316 citations

Peers

Chiara Reale
Comparison fields: 5 of 65
  • Neurology 157
  • Molecular Biology 121
  • Cellular and Molecular Neuroscience 113
  • Neurology 87
  • Clinical Biochemistry 41
Janel O. Johnson United States
Gia Tuong Tran Norway
Milena Janković Serbia
Elena Sánchez-Ferrero Spain
Ilhem Turki Tunisia
Viorica Chelban United Kingdom
Chiara Barzaghi Italy
Edoardo Monfrini Italy
Mika H. Martikainen Finland
Gamze Güven Türkiye
Janel O. Johnson United States View profile →
Citations per field, relative to Chiara Reale
Chiara Reale · 1×
Citations per year, relative to Chiara Reale
Chiara Reale · 1×

Countries citing papers authored by Chiara Reale

Since Specialization
Citations

This map shows the geographic impact of Chiara Reale'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 Chiara Reale with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Chiara Reale more than expected).

Fields of papers citing papers by Chiara Reale

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Chiara Reale. 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 Chiara Reale. The network helps show where Chiara Reale may publish in the future.

Co-authorship network of co-authors of Chiara Reale

This figure shows the co-authorship network connecting the top 25 collaborators of Chiara Reale. A scholar is included among the top collaborators of Chiara Reale 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 Chiara Reale. Chiara Reale is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

19 of 19 papers shown
# Title Journal Authors Indexed citations
1 Could we Safely Perform Liver Ablation Without Deep Sedation or General Anesthesia? Preliminary Experience on Erector Spinae Plane Block (Espb) in the Management of Intra- and Post-Procedural Pain for Liver Microwave Ablation (with video) CardioVascular and Interventional Radiology Pierleone Lucatelli, Fabrizio Basilico et al. 0
2 CLN6‐related continuum phenotype caused by aberrant splicing Epilepsia Open Federica Invernizzi, Barbara Castellotti et al. 1
3 Two Cases of TMEM151A‐Associated Paroxysmal Dyskinesia in a Single‐Center Series of PRRT2‐Negative Patients Movement Disorders Clinical Practice Federica Invernizzi, Federica Rachele Danti et al. 2
4 Sex distribution and classification of GBA1 variants in an Italian cohort of Parkinson's disease patients analyzed over the last seventeen years Parkinsonism & Related Disorders Celeste Panteghini, Chiara Reale et al. 3
5 DNAJB2‐related Charcot‐Marie‐Tooth disease type 2: Pathomechanism insights and phenotypic spectrum widening European Journal of Neurology Paola Saveri, Stefania Magri et al. 11
6 Novel deep intronic mutation in PLA2G6 causing early-onset Parkinson’s disease with brain iron accumulation through pseudo-exon activation Neurogenetics Celeste Panteghini, Chiara Reale et al. 4
7 Genetics, sex, and gender Journal of Neuroscience Research Chiara Reale, Federica Invernizzi et al. 17
8 The Role of VPS35 in the Pathobiology of Parkinson’s Disease Cellular and Molecular Neurobiology Jenny Sassone, Chiara Reale et al. 46
9 Idiopathic brain calcification in a patient with hereditary hemochromatosis BMC Neurology Francesco Cavallieri, Elisa Menozzi et al. 2
10 Pallidal Deep Brain Stimulation in DYT6 Dystonia: Clinical Outcome and Predictive Factors for Motor Improvement Journal of Clinical Medicine Miryam Carecchio, Laura Cif et al. 24
11 Encephalopathies with intracranial calcification in children: clinical and genetic characterization Orphanet Journal of Rare Diseases Davide Tonduti, Celeste Panteghini et al. 14
12 The relevance of gene panels in movement disorders diagnosis: A lab perspective European Journal of Paediatric Neurology Chiara Reale, Celeste Panteghini et al. 18
13 DYT2 screening in early-onset isolated dystonia European Journal of Paediatric Neurology Miryam Carecchio, Chiara Reale et al. 9
14 Novel GNAL mutation with intra-familial clinical heterogeneity: Expanding the phenotype Parkinsonism & Related Disorders Miryam Carecchio, Celeste Panteghini et al. 28
15 Mitochondrial dysfunction in Parkinson disease: evidence in mutant PARK2 fibroblasts Frontiers in Genetics Chiara Barzaghi, Chiara Reale et al. 57
16 Novel DYT11 gene mutation in patients without dopaminergic deficit (SWEDD) screened for dystonia Neurology Roberto Cilia, Chiara Reale et al. 15
17 Expanding the clinical phenotype of DYT5 mutations: Is multiple system atrophy a possible one? Neurology Roberto Ceravolo, Valentina Nicoletti et al. 8
18 C19orf12 and FA2H Mutations Are Rare in Italian Patients With Neurodegeneration With Brain Iron Accumulation Seminars in Pediatric Neurology Celeste Panteghini, Giovanna Zorzi et al. 31
19 The “Eye-of-the-Tiger” Sign may be Absent in the Early Stages of Classic Pantothenate Kinase Associated Neurodegeneration Neuropediatrics Luisa Chiapparini, M. Savoiardo et al. 30

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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