Roberta Biancheri

4.8k total citations
100 papers, 2.5k citations indexed

About

Roberta Biancheri is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, Roberta Biancheri has authored 100 papers receiving a total of 2.5k indexed citations (citations by other indexed papers that have themselves been cited), including 51 papers in Molecular Biology, 20 papers in Genetics and 17 papers in Cellular and Molecular Neuroscience. Recurrent topics in Roberta Biancheri's work include RNA regulation and disease (25 papers), Lysosomal Storage Disorders Research (15 papers) and RNA Research and Splicing (13 papers). Roberta Biancheri is often cited by papers focused on RNA regulation and disease (25 papers), Lysosomal Storage Disorders Research (15 papers) and RNA Research and Splicing (13 papers). Roberta Biancheri collaborates with scholars based in Italy, United States and United Kingdom. Roberta Biancheri's co-authors include Andrea Rossi, Paolo Tortori‐Donati, Mirella Filocamo, Carlo Minetti, Federico Zara, Claudio Bruno, Armando Cama, Maja Di Rocco, Edvige Veneselli and Filippo M. Santorelli and has published in prestigious journals such as Nature Genetics, SHILAP Revista de lepidopterología and PLoS ONE.

In The Last Decade

Roberta Biancheri

98 papers receiving 2.4k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Roberta Biancheri Italy 31 1.3k 453 377 350 339 100 2.5k
Jun Tohyama Japan 29 1.2k 0.9× 332 0.7× 992 2.6× 520 1.5× 263 0.8× 108 2.8k
Erik‐Jan Kamsteeg Netherlands 32 2.2k 1.7× 343 0.8× 470 1.2× 704 2.0× 320 0.9× 124 3.2k
Annick Raas‐Rothschild Israel 34 1.7k 1.3× 982 2.2× 898 2.4× 262 0.7× 781 2.3× 108 3.8k
Gaëtan Lesca France 33 1.2k 0.9× 329 0.7× 1.0k 2.8× 610 1.7× 164 0.5× 160 3.4k
Wafaa Eyaid Saudi Arabia 25 1.5k 1.2× 223 0.5× 889 2.4× 146 0.4× 459 1.4× 55 2.4k
Göknur Haliloğlu Türkiye 23 922 0.7× 189 0.4× 259 0.7× 224 0.6× 183 0.5× 116 1.7k
Fernando Kok Brazil 31 2.1k 1.6× 559 1.2× 1.1k 2.8× 544 1.6× 432 1.3× 177 3.9k
Adeline Vanderver United States 33 2.6k 2.0× 318 0.7× 373 1.0× 305 0.9× 320 0.9× 149 3.5k
Charles Marques Lourenço Brazil 23 883 0.7× 667 1.5× 309 0.8× 347 1.0× 247 0.7× 106 1.9k
Cyril Mignot France 26 844 0.7× 520 1.1× 464 1.2× 194 0.6× 321 0.9× 101 2.0k

Countries citing papers authored by Roberta Biancheri

Since Specialization
Citations

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

Fields of papers citing papers by Roberta Biancheri

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Roberta Biancheri

This figure shows the co-authorship network connecting the top 25 collaborators of Roberta Biancheri. A scholar is included among the top collaborators of Roberta Biancheri 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 Roberta Biancheri. Roberta Biancheri 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.
Tarailo‐Graovac, Maja, Graham Sinclair, Sylvia Stöckler‐Ipsiroglu, et al.. (2015). The genotypic and phenotypic spectrum of PIGA deficiency. Orphanet Journal of Rare Diseases. 10(1). 23–23. 58 indexed citations
2.
Feraco, Paola, Marisol Mirabelli-Badenier, Mariasavina Severino, et al.. (2012). The Shrunken, Bright Cerebellum: A Characteristic MRI Finding in Congenital Disorders of Glycosylation Type 1a. American Journal of Neuroradiology. 33(11). 2062–2067. 35 indexed citations
3.
Capra, Valeria, Roberta Biancheri, Andrea Rossi, et al.. (2011). Immunomodulatory therapy in recurrent acute necrotizing encephalopathy ANE1: Is it useful?. Brain and Development. 34(5). 384–391. 27 indexed citations
4.
Grossi, Serena, Stefano Regis, Roberta Biancheri, et al.. (2011). Molecular Genetic Analysis of the PLP1 Gene in 38 Families with PLP1-related disorders: Identification and Functional Characterization of 11 Novel PLP1 Mutations. Orphanet Journal of Rare Diseases. 6(1). 40–40. 32 indexed citations
5.
Battaglia, Francesca, et al.. (2011). Anti-N-Methyl-d-aspartate-receptor encephalitis: Cognitive profile in two children. European Journal of Paediatric Neurology. 16(1). 79–82. 17 indexed citations
6.
Giribaldi, Gaia, Roberta Biancheri, Mariasavina Severino, et al.. (2011). Intermittent‐relapsing pyruvate dehydrogenase complex deficiency: a case with clinical, biochemical, and neuroradiological reversibility. Developmental Medicine & Child Neurology. 54(5). 472–476. 17 indexed citations
7.
Tappino, Barbara, Roberta Biancheri, Matthew Mort, et al.. (2010). Identification and characterization of 15 novel GALC gene mutations causing Krabbe disease. Human Mutation. 31(12). E1894–E1914. 90 indexed citations
8.
Regis, Stefano, Serena Grossi, Fabio Corsolini, Roberta Biancheri, & Mirella Filocamo. (2009). PLP1 gene duplication causes overexpression and alteration of the PLP/DM20 splicing balance in fibroblasts from Pelizaeus–Merzbacher disease patients. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1792(6). 548–554. 23 indexed citations
9.
Morana, Giovanni, Roberta Biancheri, M. DiRocco, et al.. (2009). Enhancing Cranial Nerves and Cauda Equina: An Emerging Magnetic Resonance Imaging Pattern in Metachromatic Leukodystrophy and Krabbe Disease. Neuropediatrics. 40(6). 291–294. 33 indexed citations
10.
Biancheri, Roberta, Andrea Rossi, Alessandra Tessa, et al.. (2009). White matter lesions in spastic paraplegia with mutations in SPG5/CYP7B1. Neuromuscular Disorders. 19(1). 62–65. 34 indexed citations
11.
Regis, Stefano, Roberta Biancheri, Enrico Bertini, et al.. (2008). Genotype–phenotype correlation in five Pelizaeus–Merzbacher disease patients with PLP1 gene duplications. Clinical Genetics. 73(3). 279–287. 18 indexed citations
12.
Rossi, Andrea, Roberta Biancheri, Federico Zara, et al.. (2007). Hypomyelination and Congenital Cataract: Neuroimaging Features of a Novel Inherited White Matter Disorder. American Journal of Neuroradiology. 29(2). 301–305. 23 indexed citations
13.
Biancheri, Roberta, Andrea Rossi, Mirella Filocamo, et al.. (2007). Cerebellar atrophy without cerebellar cortex hyperintensity in infantile neuroaxonal dystrophy (INAD) due to PLA2G6 mutation. European Journal of Paediatric Neurology. 11(3). 175–177. 28 indexed citations
14.
Assereto, Stefania, Silvia Stringara, Federica Sotgia, et al.. (2005). Pharmacological rescue of the dystrophin-glycoprotein complex in Duchenne and Becker skeletal muscle explants by proteasome inhibitor treatment. American Journal of Physiology-Cell Physiology. 290(2). C577–C582. 56 indexed citations
15.
Rossi, Andrea, Armando Cama, Gianluca Piatelli, et al.. (2004). Spinal dysraphism: MR imaging rationale. Journal of Neuroradiology. 31(1). 3–24. 54 indexed citations
16.
Tortori‐Donati, Paolo, Andrea Rossi, Roberta Biancheri, & Armando Cama. (2001). Magnetic Resonance Imaging of Spinal Dysraphism. Topics in Magnetic Resonance Imaging. 12(6). 375–409. 56 indexed citations
17.
Veneselli, Edvige, Roberta Biancheri, Sabrina Buoni, & A. Fois. (2001). Clinical and EEG findings in 18 cases of late infantile neuronal ceroid lipofuscinosis. Brain and Development. 23(5). 306–311. 19 indexed citations
18.
Veneselli, Edvige, et al.. (2000). Neuronal ceroid lipofuscinoses: clinical and EEG findings in a large study of Italian cases. Neurological Sciences. 21(0). S75–S81. 13 indexed citations
19.
Veneselli, E., et al.. (1999). Unusually prolonged survival and childhood-onset epilepsy in a case of alobar holoprosencephaly. Child s Nervous System. 15(5). 274–277. 7 indexed citations
20.
Veneselli, Edvige, et al.. (1998). Neurophysiological findings in a case of carbohydrate-deficient glycoprotein (CDG) syndrome type I with phosphomannomutase deficiency. European Journal of Paediatric Neurology. 2(5). 239–244. 6 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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