Alfredo Brusco

12.5k total citations
141 papers, 3.3k citations indexed

About

Alfredo Brusco is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Genetics. According to data from OpenAlex, Alfredo Brusco has authored 141 papers receiving a total of 3.3k indexed citations (citations by other indexed papers that have themselves been cited), including 100 papers in Molecular Biology, 38 papers in Cellular and Molecular Neuroscience and 36 papers in Genetics. Recurrent topics in Alfredo Brusco's work include Genetic Neurodegenerative Diseases (34 papers), Mitochondrial Function and Pathology (33 papers) and DNA Repair Mechanisms (16 papers). Alfredo Brusco is often cited by papers focused on Genetic Neurodegenerative Diseases (34 papers), Mitochondrial Function and Pathology (33 papers) and DNA Repair Mechanisms (16 papers). Alfredo Brusco collaborates with scholars based in Italy, United States and Russia. Alfredo Brusco's co-authors include Nicola Migone, Alessandro Brussino, Claudia Cagnoli, Simona Cavalieri, Eleonora Di Gregorio, Cinzia Gellera, Elisa Giorgio, Caterina Mariotti, Franco Taroni and Cecilia Mancini and has published in prestigious journals such as SHILAP Revista de lepidopterología, The Journal of Immunology and PLoS ONE.

In The Last Decade

Alfredo Brusco

140 papers receiving 3.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Alfredo Brusco Italy 32 2.2k 859 799 355 223 141 3.3k
Dennis Dooijes Netherlands 38 3.2k 1.5× 598 0.7× 619 0.8× 689 1.9× 265 1.2× 110 5.7k
Tayfun Özçelık Türkiye 30 1.5k 0.7× 541 0.6× 859 1.1× 218 0.6× 405 1.8× 59 3.1k
Anthony Antonellis United States 30 2.4k 1.1× 931 1.1× 716 0.9× 179 0.5× 309 1.4× 75 3.8k
H. David Shine United States 30 1.5k 0.7× 1.2k 1.4× 1.0k 1.3× 238 0.7× 213 1.0× 50 3.7k
Dalil Hamroun France 24 2.1k 1.0× 361 0.4× 976 1.2× 201 0.6× 130 0.6× 60 3.5k
Salmo Raskin Brazil 28 1.5k 0.7× 1.1k 1.3× 578 0.7× 670 1.9× 140 0.6× 147 2.8k
Mary G. Sweeney United Kingdom 34 2.8k 1.3× 1.0k 1.2× 290 0.4× 702 2.0× 189 0.8× 71 4.0k
Bernd Wollnik Germany 36 2.8k 1.3× 306 0.4× 1.6k 2.0× 173 0.5× 206 0.9× 138 4.3k
Kunio Kitamura Japan 32 2.1k 0.9× 538 0.6× 556 0.7× 185 0.5× 378 1.7× 92 3.4k
Philippe Horellou France 24 1.3k 0.6× 1.0k 1.2× 697 0.9× 372 1.0× 174 0.8× 52 2.3k

Countries citing papers authored by Alfredo Brusco

Since Specialization
Citations

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

Fields of papers citing papers by Alfredo Brusco

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Alfredo Brusco

This figure shows the co-authorship network connecting the top 25 collaborators of Alfredo Brusco. A scholar is included among the top collaborators of Alfredo Brusco 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 Alfredo Brusco. Alfredo Brusco 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.
Jokela, Manu, Meriel McEntagart, Tessa Homfray, et al.. (2023). The crucial role of titin in fetal development: recurrent miscarriages and bone, heart and muscle anomalies characterise the severe end of titinopathies spectrum. Journal of Medical Genetics. 60(9). 866–873. 8 indexed citations
2.
Priolo, Manuela, Francesca Clementina Radio, Andrea Ciolfi, et al.. (2023). Natural history of MRAS‐related Noonan syndrome: Evidence of mild adult‐onset left ventricular hypertrophy and neuropsychiatric features. American Journal of Medical Genetics Part C Seminars in Medical Genetics. 193(2). 160–166.
3.
Pavinato, Lisa, Alfredo Brusco, Mara Maldotti, et al.. (2022). The Emerging Roles of Long Non-Coding RNAs in Intellectual Disability and Related Neurodevelopmental Disorders. International Journal of Molecular Sciences. 23(11). 6118–6118. 7 indexed citations
4.
Benussi, Alberto, Valentina Cantoni, Marta Manes, et al.. (2021). Motor and cognitive outcomes of cerebello-spinal stimulation in neurodegenerative ataxia. Brain. 144(8). 2310–2321. 46 indexed citations
5.
Pérez, B., Hannah K. Shorrock, Mónica Báñez-Coronel, et al.. (2021). CCG•CGG interruptions in high‐penetrance SCA8 families increase RAN translation and protein toxicity. EMBO Molecular Medicine. 13(11). e14095–e14095. 16 indexed citations
6.
Machol, Keren, Sundeep G. Keswani, Lorraine Potocki, et al.. (2021). Evidence that FGFRL1 contributes to congenital diaphragmatic hernia development in humans. American Journal of Medical Genetics Part A. 185(3). 836–840. 7 indexed citations
7.
Hoxha, Eriola, Roberta Parolisi, Matteo Audano, et al.. (2021). Elovl5 is required for proper action potential conduction along peripheral myelinated fibers. Glia. 69(10). 2419–2428. 9 indexed citations
8.
Magri, Stefania, Lorenzo Nanetti, Cinzia Gellera, et al.. (2021). Digenic inheritance of STUB1 variants and TBP polyglutamine expansions explains the incomplete penetrance of SCA17 and SCA48. Genetics in Medicine. 24(1). 29–40. 32 indexed citations
9.
Avruscio, Giampiero, et al.. (2020). Challenging arterial calcification disease associated with rare NT5E gene mutation. BMJ Case Reports. 13(6). e235365–e235365. 3 indexed citations
10.
Nardello, Rosaria, Giuseppe Donato Mangano, Vincenzo Antona, et al.. (2020). Electroclinical features and outcome of ANKRD11-related KBG syndrome: A novel report and literature review. Seizure. 85. 151–154. 5 indexed citations
11.
Pozzi, Elisa, Elisa Giorgio, Cecilia Mancini, et al.. (2020). In vitro dexamethasone treatment does not induce alternative ATM transcripts in cells from Ataxia–Telangiectasia patients. Scientific Reports. 10(1). 20182–20182. 2 indexed citations
12.
Richter, Uwe, Fumi Suomi, Paula Marttinen, et al.. (2019). Mitochondrial stress response triggered by defects in protein synthesis quality control. Life Science Alliance. 2(1). e201800219–e201800219. 33 indexed citations
13.
Silengo, Margherita, Claudio Defilippi, Elga Fabia Belligni, et al.. (2013). Progressive extreme heterotopic calcification. American Journal of Medical Genetics Part A. 161(7). 1706–1713. 3 indexed citations
14.
Morone, Simona, Nicola Lo Buono, Rossella Parrotta, et al.. (2012). Overexpression of CD157 Contributes to Epithelial Ovarian Cancer Progression by Promoting Mesenchymal Differentiation. PLoS ONE. 7(8). e43649–e43649. 26 indexed citations
15.
Sacco, Tiziana, Enrica Boda, Eriola Hoxha, et al.. (2010). Mouse brain expression patterns of Spg7, Afg3l1, and Afg3l2 transcripts, encoding for the mitochondrial m-AAA protease. BMC Neuroscience. 11(1). 55–55. 22 indexed citations
16.
Brussino, Alessandro, Giovanna Vaula, Cinzia Cagnoli, et al.. (2009). A family with autosomal dominant leukodystrophy linked to 5q23.2–q23.3 without lamin B1 mutations. European Journal of Neurology. 17(4). 541–549. 31 indexed citations
17.
Giordana, Maria Teresa, Marco Piccinini, L. Palmucci, et al.. (2006). Myelin-Associated Glycoprotein is Altered in a Familial Late-Onset Orthochromatic Leukodystrophy. Brain Pathology. 15(2). 116–123. 7 indexed citations
18.
Brusco, Alfredo, Cinzia Gellera, Claudia Cagnoli, et al.. (2004). Molecular Genetics of Hereditary Spinocerebellar Ataxia. Archives of Neurology. 61(5). 727–727. 109 indexed citations
19.
Brusco, Alfredo, et al.. (1995). Molecular characterization of G2m(n+) and G2m(n−) allotypes. Immunogenetics. 42(5). 414–417. 33 indexed citations
20.
Bottaro, Andrea, et al.. (1993). Familial clustering of IGHC deletions and duplications: functional and molecular analysis. Immunogenetics. 37(5). 356–363. 15 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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