Antonio Federico

21.1k total citations · 3 hit papers
473 papers, 13.9k citations indexed

About

Antonio Federico is a scholar working on Molecular Biology, Neurology and Rheumatology. According to data from OpenAlex, Antonio Federico has authored 473 papers receiving a total of 13.9k indexed citations (citations by other indexed papers that have themselves been cited), including 204 papers in Molecular Biology, 110 papers in Neurology and 64 papers in Rheumatology. Recurrent topics in Antonio Federico's work include Mitochondrial Function and Pathology (71 papers), Cerebrovascular and genetic disorders (54 papers) and RNA regulation and disease (43 papers). Antonio Federico is often cited by papers focused on Mitochondrial Function and Pathology (71 papers), Cerebrovascular and genetic disorders (54 papers) and RNA regulation and disease (43 papers). Antonio Federico collaborates with scholars based in Italy, United States and United Kingdom. Antonio Federico's co-authors include Nicola De Stefano, Maria Teresa Dotti, Stephen M. Smith, Carla Battisti, Paul M. Matthews, Patrizia Formichi, Elena Radi, Mark Jenkinson, Yongyue Zhang and Jacqueline Chen and has published in prestigious journals such as Journal of Biological Chemistry, Journal of Clinical Investigation and SHILAP Revista de lepidopterología.

In The Last Decade

Antonio Federico

459 papers receiving 13.6k citations

Hit Papers

align trajectories sort by overperformance

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Accurate, Robust, and Automated Longitudinal and Cross-Sectional Brain Change Analysis

2002 1.7k citations Antonio Federico, Nicola De Stefano et al. profile →
Mitochondria, oxidative stress and neurodegeneration

2012 607 citations Antonio Federico, Elena Cardaioli et al. Journal of the Neurological Sciences profile →
Apoptosis and Oxidative Stress in Neurodegenerative Diseases

2014 512 citations Carla Battisti, Antonio Federico et al. profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Antonio Federico Italy	54	4.7k	3.1k	2.8k	1.7k	1.7k	473	13.9k
Norihiro Suzuki Japan	66	4.8k 1.0×	4.6k 1.5×	1.1k 0.4×	988 0.6×	1.7k 1.0×	749	17.7k
Takaaki Kirino Japan	66	5.0k 1.1×	5.5k 1.7×	1.1k 0.4×	748 0.4×	2.9k 1.7×	273	17.0k
David S. Warner United States	85	3.4k 0.7×	4.3k 1.4×	1.6k 0.6×	471 0.3×	1.7k 1.0×	439	22.1k
Frank M. Faraci United States	75	5.1k 1.1×	3.0k 1.0×	915 0.3×	1.2k 0.7×	2.7k 1.6×	307	19.0k
Gary K. Steinberg United States	86	6.3k 1.3×	10.3k 3.3×	1.4k 0.5×	3.2k 1.9×	4.5k 2.7×	521	26.7k
Xunming Ji China	61	4.6k 1.0×	4.0k 1.3×	1.9k 0.7×	502 0.3×	4.4k 2.6×	657	16.8k
Donald D. Heistad United States	85	5.1k 1.1×	4.4k 1.4×	1.2k 0.4×	1.3k 0.7×	2.3k 1.4×	460	25.5k
Gary A. Rosenberg United States	68	5.1k 1.1×	4.2k 1.3×	993 0.4×	460 0.3×	6.8k 4.1×	201	19.5k
Zoltán Ungvári United States	86	7.0k 1.5×	2.4k 0.8×	1.0k 0.4×	706 0.4×	3.9k 2.3×	412	24.6k
Joab Chapman Israel	48	2.3k 0.5×	1.8k 0.6×	745 0.3×	2.0k 1.1×	1.1k 0.7×	288	7.8k

Countries citing papers authored by Antonio Federico

Since Specialization

Citations

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

Fields of papers citing papers by Antonio Federico

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Antonio Federico

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

All Works

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20 of 20 papers shown

Cortese, Rosa, Domenico Plantone, Jian Zhang, et al.. (2024). Hippocampal atrophy and white matter lesions characteristics can predict evolution to dementia in patients with vascular mild cognitive impairment. Journal of the Neurological Sciences. 464. 123163–123163. 3 indexed citations

Morris, Stephen, Julie Vallortigara, Julie Greenfield, et al.. (2023). Impact of specialist ataxia centres on health service resource utilisation and costs across Europe: cross-sectional survey. Orphanet Journal of Rare Diseases. 18(1). 382–382. 4 indexed citations

Verrips, Aad, et al.. (2019). The safety and effectiveness of chenodeoxycholic acid treatment in patients with cerebrotendinous xanthomatosis: two retrospective cohort studies. Neurological Sciences. 41(4). 943–949. 31 indexed citations

Vinciguerra, Claudia, Antonio Giorgio, Ilaria Di Donato, et al.. (2018). Peak width of skeletonized mean diffusivity (PSMD) as marker of widespread white matter tissue damage in multiple sclerosis. Multiple Sclerosis and Related Disorders. 27. 294–297. 18 indexed citations

Taglia, Ilaria, Vincenzo Bonifati, Andrea Mignarri, Maria Teresa Dotti, & Antonio Federico. (2015). Primary familial brain calcification: update on molecular genetics. Neurological Sciences. 36(5). 787–794. 21 indexed citations

Rosini, Francesca, Elena Pretegiani, Andrea Mignarri, et al.. (2015). Afferent and Efferent Visual System Involvement in Cerebrotendinous Xanthomatosis (P5.310). Neurology. 84(14_supplement). 1 indexed citations

Rubegni, Anna, Elena Cardaioli, Paola Da Pozzo, et al.. (2014). A case of 3243A>G mutation in mtDNA presenting as apparently idiopathic hyperCKemia. Journal of the Neurological Sciences. 338(1-2). 232–234. 3 indexed citations

Mignarri, Andrea, Alessandra Tessa, Alessandra Rufa, et al.. (2013). Cerebellum and neuropsychiatric disorders: insights from ARSACS. Neurological Sciences. 35(1). 95–97. 20 indexed citations

Federico, Antonio. (2011). Italian neurology: past, present and future.. PubMed. 26(2). 73–6. 6 indexed citations

10.

Federico, Antonio, Pierlorenzo Pallante, Mimma Bianco, et al.. (2009). Chromobox Protein Homologue 7 Protein, with Decreased Expression in Human Carcinomas, Positively Regulates E-Cadherin Expression by Interacting with the Histone Deacetylase 2 Protein. Cancer Research. 69(17). 7079–7087. 65 indexed citations

11.

Pescini, Francesca, Francesca Cesari, Betti Giusti, et al.. (2009). Bone Marrow-Derived Progenitor Cells in Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts and Leukoencephalopathy. Stroke. 41(2). 218–223. 24 indexed citations

12.

Federico, Antonio, et al.. (2008). A Short Note on the Earth Pressure and Mobilized Angle of Internal Friction in One-Dimensional Compression of Soils. 3(1). 41–46. 22 indexed citations

13.

Bianchi, Silvia, Maria Teresa Dotti, & Antonio Federico. (2005). Physiology and pathology of notch signalling system. Journal of Cellular Physiology. 207(2). 300–308. 53 indexed citations

14.

Caciotti, Anna, Maria Alice Donati, Avihu Boneh, et al.. (2005). Role of ?-galactosidase and elastin binding protein in lysosomal and nonlysosomal complexes of patients with GM1-gangliosidosis. Human Mutation. 25(3). 285–292. 35 indexed citations

15.

Malandrini, Alessandro, et al.. (2004). A syndrome of bilateral hemorrhage of the thalamus and myocarditis with fatal course. Journal of Clinical Forensic Medicine. 11(4). 208–210. 2 indexed citations

16.

Meloni, Ilaria, Pietro Rubegni, G. De Aloe, et al.. (2001). Pseudoxanthoma elasticum: Point mutations in the ABCC6 gene and a large deletion including also ABCC1 and MYH11. Human Mutation. 18(1). 85–85. 37 indexed citations

17.

Battisti, Carla, Georgios Loudianos, Alessandra Rufa, et al.. (1999). Detection of a rare Wilson disease mutation associated with arylsulfatase A pseudodeficiency. American Journal of Medical Genetics. 85(2). 175–178. 2 indexed citations

18.

Orrico, Alfredo, et al.. (1998). Mosaicism for full mutation and normal-sized allele of the FMR1 gene: A new case. American Journal of Medical Genetics. 78(4). 341–344. 29 indexed citations

19.

Federico, Antonio, et al.. (1990). The strategy of investigating autistic syndromes in childhood. 3. 261–270. 4 indexed citations

20.

Federico, Antonio, et al.. (1975). [Refsum's disease: clinical or biological diagnosis? Discussion of 2 clinical cases].. Munich Personal RePEc Archive (Ludwig Maximilian University of Munich). 30(6). 569–75. 1 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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