Imma Castaldo

1.3k total citations
27 papers, 973 citations indexed

About

Imma Castaldo is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology and Neurology. According to data from OpenAlex, Imma Castaldo has authored 27 papers receiving a total of 973 indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Cellular and Molecular Neuroscience, 20 papers in Molecular Biology and 6 papers in Neurology. Recurrent topics in Imma Castaldo's work include Genetic Neurodegenerative Diseases (22 papers), Mitochondrial Function and Pathology (15 papers) and Neurological diseases and metabolism (3 papers). Imma Castaldo is often cited by papers focused on Genetic Neurodegenerative Diseases (22 papers), Mitochondrial Function and Pathology (15 papers) and Neurological diseases and metabolism (3 papers). Imma Castaldo collaborates with scholars based in Italy, United States and Sweden. Imma Castaldo's co-authors include Alessandro Filla, Antonella Monticelli, Giuseppe De Michele, Sergio Cocozza, Olga Calabrese, Michele Pinelli, Alessandro Filla, Fabio Acquaviva, Enrico V. Avvedimento and G Campanella and has published in prestigious journals such as Neurology, Diabetes Care and Annals of Neurology.

In The Last Decade

Imma Castaldo

27 papers receiving 949 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Imma Castaldo Italy 18 820 723 307 72 70 27 973
Warunee Dansithong United States 19 1.0k 1.2× 732 1.0× 218 0.7× 49 0.7× 82 1.2× 35 1.2k
Katrin S. Lindenberg Germany 14 942 1.1× 817 1.1× 295 1.0× 121 1.7× 34 0.5× 32 1.2k
Sharan Paul United States 19 1.0k 1.2× 688 1.0× 220 0.7× 63 0.9× 81 1.2× 37 1.2k
Christopher A. Ross United States 7 610 0.7× 563 0.8× 265 0.9× 35 0.5× 55 0.8× 7 763
Joline Dalton United States 10 898 1.1× 817 1.1× 290 0.9× 81 1.1× 98 1.4× 18 1.1k
Isabella Palazzolo United States 10 655 0.8× 516 0.7× 218 0.7× 102 1.4× 67 1.0× 11 915
Marcy R. Weatherspoon United States 7 701 0.9× 588 0.8× 157 0.5× 165 2.3× 90 1.3× 8 919
Lisa Bertram Canada 7 572 0.7× 467 0.6× 149 0.5× 79 1.1× 37 0.5× 8 782
Isabel Nascimento-Ferreira Portugal 10 566 0.7× 579 0.8× 217 0.7× 71 1.0× 61 0.9× 10 850
Olivier Didierjean France 10 1.4k 1.7× 1.5k 2.0× 697 2.3× 63 0.9× 80 1.1× 13 1.7k

Countries citing papers authored by Imma Castaldo

Since Specialization
Citations

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

Fields of papers citing papers by Imma Castaldo

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Imma Castaldo

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

All Works

20 of 20 papers shown
1.
Cocozza, Sergio, Giovanni Scala, Gennaro Miele, Imma Castaldo, & Antonella Monticelli. (2013). A distinct group of CpG islands shows differential DNA methylation between replicas of the same cell line in vitro. BMC Genomics. 14(1). 692–692. 5 indexed citations
2.
Rinaldi, Carlo, Elena Salvatore, Ilaria Giordano, et al.. (2012). Predictors of Survival in a Huntington's Disease Population from Southern Italy. Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques. 39(1). 48–51. 26 indexed citations
3.
Ragno, Michele, Luigi Pianese, Michele Pinelli, et al.. (2011). Shorter telomeres in patients with cerebral autosomal dominant arteriopathy and leukoencephalopathy (CADASIL). Neurogenetics. 12(4). 337–343. 8 indexed citations
4.
Castaldo, Imma, Michele Pinelli, Antonella Monticelli, et al.. (2008). DNA methylation in intron 1 of the frataxin gene is related to GAA repeat length and age of onset in Friedreich ataxia patients. Journal of Medical Genetics. 45(12). 808–812. 82 indexed citations
5.
Acquaviva, Fabio, Imma Castaldo, Alessandro Filla, et al.. (2008). Recombinant Human Erythropoietin Increases Frataxin Protein Expression Without Increasing mRNA Expression. The Cerebellum. 7(3). 360–365. 50 indexed citations
6.
Rosa, Anna De, Elena Salvatore, Imma Castaldo, et al.. (2008). Autonomic nervous system abnormalities in spinocerebellar ataxia type 2: A cardiovascular neurophysiologic study. Journal of the Neurological Sciences. 275(1-2). 60–63. 25 indexed citations
7.
Livigni, Alessandra, Antonella Scorziello, Annagrazia Adornetto, et al.. (2005). Mitochondrial AKAP121 Links cAMP and src Signaling to Oxidative Metabolism. Molecular Biology of the Cell. 17(1). 263–271. 131 indexed citations
8.
Titomanlio, Luigi, Alfonso Romano, Melissa Borrelli, et al.. (2005). Cerebellar vermis aplasia: Patient report and exclusion of the candidate genes EN2 and ZIC1. American Journal of Medical Genetics Part A. 136A(2). 198–200. 6 indexed citations
9.
10.
Varrone, Andrea, Elena Salvatore, Giuseppe De Michele, et al.. (2004). Reduced striatal [123I]FP‐CIT binding in SCA2 patients without parkinsonism. Annals of Neurology. 55(3). 426–430. 43 indexed citations
11.
Filla, Alessandro, Giuseppe De Michele, Sergio Cocozza, et al.. (2002). Early onset autosomal dominant dementia with ataxia, extrapyramidal features, and epilepsy. Neurology. 58(6). 922–928. 20 indexed citations
12.
Barbieri, F, Maria Teresa Pellecchia, Emanuela Esposito, et al.. (2001). Adult-onset familial laryngeal abductor paralysis, cerebellar ataxia, and pure motor neuropathy. Neurology. 56(10). 1412–1414. 11 indexed citations
13.
Filla, Alessandro, Caterina Mariotti, Giuseppe Caruso, et al.. (2000). Relative Frequencies of CAG Expansions in Spinocerebellar Ataxia and Dentatorubropallidoluysian Atrophy in 116 Italian Families. European Neurology. 44(1). 31–36. 49 indexed citations
14.
Filla, Alessandro, Giuseppe De Michele, Lucio Santoro, et al.. (1999). Spinocerebellar ataxia type 2 in southern Italy: a clinical and molecular study of 30 families. Journal of Neurology. 246(6). 467–471. 48 indexed citations
15.
Trojano, Luigi, Laura Chiacchio, Dario Grossi, et al.. (1998). Determinants of cognitive disorders in Autosomal Dominant Cerebellar Ataxia type 1. Journal of the Neurological Sciences. 157(2). 162–167. 14 indexed citations
16.
Giovannone, Barbara, G. Sabbadini, Luigi Di Maio, et al.. (1997). Analysis of (CAG)n size heterogeneity in somatic and sperm cell DNA from intermediate and expanded Huntington disease gene carriers. Human Mutation. 10(6). 458–464. 25 indexed citations
17.
Filla, Alessandro, Giuseppe De Michele, G Campanella, et al.. (1996). Autosomal dominant cerebellar ataxia type I. Clinical and molecular study in 36 Italian families including a comparison between SCA1 and SCA2 phenotypes. Journal of the Neurological Sciences. 142(1-2). 140–147. 28 indexed citations
18.
Telenius, H., E. Almqvist, B Kremer, et al.. (1995). Somatic mosaicism in sperm is associated with intergenerational (CAG)n changes in Huntington disease. Human Molecular Genetics. 4(2). 189–195. 67 indexed citations
19.
Filla, Alessandro, Giovanna De Michele, Sandro Banfi, et al.. (1995). Has spinocerebellar ataxia type 2 a distinct phenotype? Genetic and clinical study of an Italian family. Neurology. 45(4). 793–796. 38 indexed citations
20.
Pianese, Luigi, Sergio Cocozza, G Campanella, et al.. (1994). Linkage disequilibrium between FD1-D9S202 haplotypes and the Friedreich's ataxia locus in a central-southern Italian population.. Journal of Medical Genetics. 31(2). 133–135. 4 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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