G. Sabbadini

605 total citations
9 papers, 417 citations indexed

About

G. Sabbadini is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology and Neurology. According to data from OpenAlex, G. Sabbadini has authored 9 papers receiving a total of 417 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Cellular and Molecular Neuroscience, 6 papers in Molecular Biology and 5 papers in Neurology. Recurrent topics in G. Sabbadini's work include Genetic Neurodegenerative Diseases (7 papers), Neurological disorders and treatments (4 papers) and Mitochondrial Function and Pathology (4 papers). G. Sabbadini is often cited by papers focused on Genetic Neurodegenerative Diseases (7 papers), Neurological disorders and treatments (4 papers) and Mitochondrial Function and Pathology (4 papers). G. Sabbadini collaborates with scholars based in Italy, United States and Netherlands. G. Sabbadini's co-authors include Marina Frontali, L. Calandriello, Ada Francia, Elide Mantuano, Carla Jodice, Liana Veneziano, Flavia Trettel, M. Spadaro, Francesco Pierelli and Fabrizio Salvi and has published in prestigious journals such as Brain, Human Molecular Genetics and Gene.

In The Last Decade

G. Sabbadini

9 papers receiving 401 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
G. Sabbadini Italy	8	317	315	202	44	43	9	417
L. Calandriello Italy	6	204 0.6×	215 0.7×	147 0.7×	52 1.2×	36 0.8×	9	325
Neven Maksemous Australia	12	89 0.3×	121 0.4×	81 0.4×	50 1.1×	124 2.9×	28	362
Elena D. Markova Russia	14	318 1.0×	320 1.0×	258 1.3×	29 0.7×	9 0.2×	28	560
Chiara Reale Italy	11	113 0.4×	121 0.4×	157 0.8×	87 2.0×	10 0.2×	19	320
Yacen Hu China	11	116 0.4×	118 0.4×	192 1.0×	61 1.4×	9 0.2×	20	317
R. Liane Ramirez United States	8	259 0.8×	247 0.8×	116 0.6×	23 0.5×	14 0.3×	11	366
R.A. Ophoff Netherlands	6	268 0.8×	319 1.0×	111 0.5×	46 1.0×	118 2.7×	6	449
Lumine Matsumoto Japan	5	130 0.4×	206 0.7×	152 0.8×	50 1.1×	10 0.2×	6	373
T. Nishio Japan	8	255 0.8×	173 0.5×	130 0.6×	33 0.8×	10 0.2×	13	325
Gail Eglon United Kingdom	8	190 0.6×	172 0.5×	72 0.4×	82 1.9×	9 0.2×	10	302

Countries citing papers authored by G. Sabbadini

Since Specialization

Citations

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

Fields of papers citing papers by G. Sabbadini

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of G. Sabbadini

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

All Works

Sort: Min cites: Since: Top N: Style:

9 of 9 papers shown

Sabbadini, G., et al.. (2005). Clark???Baraitser syndrome: report of a new case and review of the literature. Clinical Dysmorphology. 14(3). 133–135. 5 indexed citations

Squitieri, Ferdinando, G. Sabbadini, Paola Mandich, et al.. (2000). Family and molecular data for a fine analysis of age at onset in Huntington disease. American Journal of Medical Genetics. 95(4). 366–373. 39 indexed citations

Trettel, Flavia, Elide Mantuano, Valentina Calabresi, et al.. (2000). A fine physical map of the CACNA1A gene region on 19p13.1–p13.2 chromosome. Gene. 241(1). 45–50. 14 indexed citations

Mandich, Paola, Gioia Jacopini, Emilio Di Maria, et al.. (1998). Predictive testing for Huntington’s disease: ten years’ experience in two Italian centres. The Italian Journal of Neurological Sciences. 19(2). 68–74. 20 indexed citations

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

Jodice, Carla, Elide Mantuano, Liana Veneziano, et al.. (1997). Episodic Ataxia Type 2 (EA2) and Spinocerebellar Ataxia Type 6 (SCA6) Due to CAG Repeat Expansion in the CACNA1A Gene on Chromosome 19p. Human Molecular Genetics. 6(11). 1973–1978. 215 indexed citations

Frontali, Marina, G. Sabbadini, Andrea Novelletto, et al.. (1996). Genetic fitness in Huntington's Disease and Spinocerebellar Ataxia 1: a population genetics model for CAG repeat expansions. Annals of Human Genetics. 60(5). 423–435. 17 indexed citations

Sabbadini, G., Ada Francia, L. Calandriello, et al.. (1995). Cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy (CADASIL). Brain. 118(1). 207–215. 49 indexed citations

Novelletto, Andrea, Francesca Persichetti, G. Sabbadini, et al.. (1994). Polymorphism analysis of the huntingtin gene in Italian families affected with Huntington disease. Human Molecular Genetics. 3(7). 1129–1132. 33 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.

Explore authors with similar magnitude of impact