Amedeo Bianchi

2.2k total citations
32 papers, 507 citations indexed

About

Amedeo Bianchi is a scholar working on Genetics, Psychiatry and Mental health and Molecular Biology. According to data from OpenAlex, Amedeo Bianchi has authored 32 papers receiving a total of 507 indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Genetics, 17 papers in Psychiatry and Mental health and 10 papers in Molecular Biology. Recurrent topics in Amedeo Bianchi's work include Epilepsy research and treatment (17 papers), Genetics and Neurodevelopmental Disorders (15 papers) and Neuroscience and Neuropharmacology Research (6 papers). Amedeo Bianchi is often cited by papers focused on Epilepsy research and treatment (17 papers), Genetics and Neurodevelopmental Disorders (15 papers) and Neuroscience and Neuropharmacology Research (6 papers). Amedeo Bianchi collaborates with scholars based in Italy, Germany and Austria. Amedeo Bianchi's co-authors include Federico Zara, Giuseppe Gobbi, Diéter Janz, Stefano Viaggi, Elena Di Gennaro, Pasquale Striano, Antonio Gambardella, Thomas Hildmann, Francesca Madia and Roberto Michelucci and has published in prestigious journals such as Neurology, Annals of Neurology and Epilepsia.

In The Last Decade

Amedeo Bianchi

32 papers receiving 495 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Amedeo Bianchi Italy 15 289 230 168 167 103 32 507
Manyee Gee United States 6 178 0.6× 151 0.7× 104 0.6× 111 0.7× 56 0.5× 9 341
Gregorio Pineda Spain 5 252 0.9× 156 0.7× 131 0.8× 118 0.7× 97 0.9× 6 408
Lia Santulli Italy 11 138 0.5× 138 0.6× 93 0.6× 77 0.5× 73 0.7× 14 347
Hideyuki Ohtani Japan 8 240 0.8× 111 0.5× 135 0.8× 140 0.8× 108 1.0× 17 375
C Dravet Italy 14 588 2.0× 173 0.8× 220 1.3× 125 0.7× 366 3.6× 31 761
Tojo Nakayama Japan 12 164 0.6× 165 0.7× 134 0.8× 240 1.4× 57 0.6× 29 472
Jan‐Peter Ernst Germany 5 463 1.6× 65 0.3× 237 1.4× 134 0.8× 271 2.6× 6 555
Goryu Fukuma Japan 13 751 2.6× 367 1.6× 545 3.2× 677 4.1× 155 1.5× 15 1.1k
Jason Coryell United States 10 247 0.9× 89 0.4× 139 0.8× 172 1.0× 160 1.6× 13 532
Tine Van Dyck Belgium 6 332 1.1× 156 0.7× 179 1.1× 188 1.1× 61 0.6× 6 472

Countries citing papers authored by Amedeo Bianchi

Since Specialization
Citations

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

Fields of papers citing papers by Amedeo Bianchi

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Amedeo Bianchi

This figure shows the co-authorship network connecting the top 25 collaborators of Amedeo Bianchi. A scholar is included among the top collaborators of Amedeo Bianchi 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 Amedeo Bianchi. Amedeo Bianchi 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.
Licchetta, Laura, Tommaso Pippucci, Sara Baldassari, et al.. (2019). Sleep-related hypermotor epilepsy (SHE): Contribution of known genes in 103 patients. Seizure. 74. 60–64. 30 indexed citations
2.
Pozzo, Paola Da, Elena Cardaioli, Anna Rubegni, et al.. (2017). Novel POLG mutations and variable clinical phenotypes in 13 Italian patients. Neurological Sciences. 38(4). 563–570. 16 indexed citations
3.
Canafoglia, Laura, Edoardo Ferlazzo, Roberto Michelucci, et al.. (2017). Variable course of Unverricht-Lundborg disease. Neurology. 89(16). 1691–1697. 15 indexed citations
4.
Capovilla, Giuseppe, Francesca Beccaria, Amedeo Bianchi, et al.. (2010). Ictal EEG patterns in epilepsy with centro-temporal spikes. Brain and Development. 33(4). 301–309. 7 indexed citations
5.
Zara, Federico & Amedeo Bianchi. (2009). The impact of genetics on the classification of epilepsy syndromes. Epilepsia. 50(s5). 11–14. 9 indexed citations
6.
Baykan, Betül, Francesca Madia, Nerses Bebek, et al.. (2004). Autosomal Recessive Idiopathic Epilepsy in an Inbred Family from Turkey: Identification of a Putative Locus on Chromosome 9q32‐33. Epilepsia. 45(5). 479–487. 9 indexed citations
7.
Bianchi, Amedeo, et al.. (2003). Family study of epilepsy in first degree relatives: data from the Italian Episcreen Study. Seizure. 12(4). 203–210. 27 indexed citations
8.
Nabbout, Rima, Elena Di Gennaro, Nadia Bahi‐Buisson, et al.. (2003). Absence of mutations in major GEFS+ genes in myoclonic astatic epilepsy. Epilepsy Research. 56(2-3). 127–133. 24 indexed citations
9.
Gennaro, Elena Di, Pierangelo Veggiotti, Francesca Madia, et al.. (2003). Familial severe myoclonic epilepsy of infancy: truncation of Na v 1.1 and genetic heterogeneity. Epileptic Disorders. 5(1). 21–25. 29 indexed citations
10.
Windemuth, Christine, Herbert Schulz, Kathrin Saar, et al.. (2002). No evidence for a susceptibility locus for idiopathic generalized epilepsy on chromosome 5 in families with typical absence seizures. Epilepsy Research. 51(1-2). 23–29. 5 indexed citations
11.
Gennaro, Elena Di, Michela Malacarne, Ilaria Carbone, et al.. (1999). No Evidence of a Major Locus for Benign Familial Infantile Convulsions on Chromosome 19q12‐q13.1. Epilepsia. 40(12). 1799–1803. 16 indexed citations
12.
Sander, T., Christian Peters, Diéter Janz, et al.. (1998). The gene encoding the α1A-voltage-dependent calcium channel (CACN1A4) is not a candidate for causing common subtypes of idiopathic generalized epilepsy. Epilepsy Research. 29(2). 115–122. 16 indexed citations
13.
Sander, Thomas, Thomas Hildmann, Diéter Janz, et al.. (1996). Exclusion of linkage between idiopathic generalized epilepsies and the GABAA receptor α1 and γ2 subunit gene cluster on chromosome 5. Epilepsy Research. 23(3). 235–244. 9 indexed citations
14.
Sander, Thomas, Thomas Hildmann, Thomas F. Wienker, et al.. (1996). Common subtypes of idiopathic generalized epilepsies: Lack of linkage to D20S19 close to candidate loci (EBN1, EEGV1) on chromosome 20. American Journal of Medical Genetics. 67(1). 31–39. 7 indexed citations
15.
Sander, T., Thomas Hildmann, Diéter Janz, et al.. (1995). The phenotypic spectrum related to the human epilepsy susceptibility gene “EJM1”. Annals of Neurology. 38(2). 210–217. 34 indexed citations
16.
Sander, T., Diéter Janz, Christian Ramel, et al.. (1995). Refinement of map position of the human GluR6 kainate receptor gene (GRIK2) and lack of association and linkage with idiopathic generalized epilepsies. Neurology. 45(9). 1713–1720. 17 indexed citations
17.
Bianchi, Amedeo, P. Zolo, R. Canger, et al.. (1994). Allopurinol as Add‐on Therapy in Refractory Epilepsy: A Double‐Blind Placebo‐Controlled Randomized Study Italy, on his retirement.. Epilepsia. 35(1). 107–112. 35 indexed citations
18.
Zaccara, Gaetano, Andrea Messori, Giovanni Muscas, et al.. (1989). Predictive performance of pharmacokinetic methods for phenytoin dosing: a multi-center evaluation in 282 patients with epilepsy. Epilepsy Research. 3(3). 253–261. 9 indexed citations
19.
Bianchi, Amedeo, et al.. (1970). Behaviour and linkage relationship of gametophyte factors in chromosome 9 of maize.. 22. 2 indexed citations
20.
Bianchi, Amedeo, et al.. (1967). Linkage relationship betweenGa-factors and genetic markers of maize chromosome 9. Der Züchter. 37(7-8). 359–364. 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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