Silvia Baratta

974 total citations
11 papers, 246 citations indexed

About

Silvia Baratta is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Clinical Biochemistry. According to data from OpenAlex, Silvia Baratta has authored 11 papers receiving a total of 246 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Molecular Biology, 5 papers in Cellular and Molecular Neuroscience and 4 papers in Clinical Biochemistry. Recurrent topics in Silvia Baratta's work include Hereditary Neurological Disorders (5 papers), Neurological diseases and metabolism (4 papers) and Metabolism and Genetic Disorders (4 papers). Silvia Baratta is often cited by papers focused on Hereditary Neurological Disorders (5 papers), Neurological diseases and metabolism (4 papers) and Metabolism and Genetic Disorders (4 papers). Silvia Baratta collaborates with scholars based in Italy, United States and Spain. Silvia Baratta's co-authors include Franco Taroni, Davide Pareyson, Roser Pons, Barbara Garavaglia, Sara Botti, Angelo Sghirlanzoni, Giuseppe Lauria, Michela Morbin, Federica Invernizzi and Patrizia Cavadini and has published in prestigious journals such as Neurology, The American Journal of Human Genetics and Neuroscience Letters.

In The Last Decade

Silvia Baratta

11 papers receiving 240 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Silvia Baratta Italy	7	111	111	76	65	53	11	246
Celeste Panteghini Italy	13	133 1.2×	79 0.7×	65 0.9×	118 1.8×	106 2.0×	25	329
Claire Guissart France	12	174 1.6×	76 0.7×	42 0.6×	65 1.0×	35 0.7×	22	301
Marie‐France Rioux Canada	6	140 1.3×	117 1.1×	37 0.5×	22 0.3×	48 0.9×	8	270
Fabrizia Stregapede Italy	9	83 0.7×	90 0.8×	41 0.5×	43 0.7×	40 0.8×	17	205
Hannah E. Steele United Kingdom	9	180 1.6×	77 0.7×	53 0.7×	29 0.4×	33 0.6×	14	275
Ilaria D’Amato Italy	6	236 2.1×	68 0.6×	88 1.2×	27 0.4×	85 1.6×	8	320
Kaisu Nikali Finland	7	290 2.6×	150 1.4×	122 1.6×	33 0.5×	32 0.6×	10	388
Tim M. Strom Germany	4	173 1.6×	51 0.5×	50 0.7×	65 1.0×	14 0.3×	4	336
Marina Michelson Israel	8	138 1.2×	56 0.5×	45 0.6×	33 0.5×	12 0.2×	19	239
Salah A. Elmalik Saudi Arabia	9	139 1.3×	63 0.6×	35 0.5×	20 0.3×	78 1.5×	12	232

Countries citing papers authored by Silvia Baratta

Since Specialization

Citations

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

Fields of papers citing papers by Silvia Baratta

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Silvia Baratta

This figure shows the co-authorship network connecting the top 25 collaborators of Silvia Baratta. A scholar is included among the top collaborators of Silvia Baratta 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 Silvia Baratta. Silvia Baratta 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:

11 of 11 papers shown

Magri, Stefania, Federica Rachele Danti, Silvia Baratta, et al.. (2020). Expanding the phenotypic spectrum of TRIM2‐associated Charcot‐Marie‐Tooth disease. Journal of the Peripheral Nervous System. 25(4). 429–432. 5 indexed citations

Bella, Daniela Di, Stefania Magri, Laura Farina, et al.. (2020). Hypomyelinating leukodystrophies in adults: Clinical and genetic features. European Journal of Neurology. 28(3). 934–944. 11 indexed citations

D’Arrigo, Stefano, et al.. (2019). A Case of Severe Early-Onset Neuropathy Caused by a Compound Heterozygous Deletion of the PMP22 Gene: Clinical and Neurographic Aspects. Neuropediatrics. 51(3). 173–177. 6 indexed citations

Bersano, Anna, Gloria Bedini, Caterina Mariotti, et al.. (2017). CADASIL: Treatment and Management Options. Current Treatment Options in Neurology. 19(9). 31–31. 18 indexed citations

Nanetti, Lorenzo, Silvia Baratta, Marta Panzeri, et al.. (2012). Novel and recurrent spastin mutations in a large series of SPG4 Italian families. Neuroscience Letters. 528(1). 42–45. 5 indexed citations

Musumeci, Olimpia, M. Aguennouz, Giacomo P. Comi, et al.. (2007). Identification of the infant-type R631C mutation in patients with the benign muscular form of CPT2 deficiency. Neuromuscular Disorders. 17(11-12). 960–963. 8 indexed citations

Iacobazzi, Vito, Federica Invernizzi, Silvia Baratta, et al.. (2004). Molecular and functional analysis ofSLC25A20 mutations causing carnitine-acylcarnitine translocase deficiency. Human Mutation. 24(4). 312–320. 55 indexed citations

Mostacciuolo, Maria Luisa, Valentina Bosello Travain, Luciano Merlini, et al.. (2001). Charcot-Marie-Tooth disease type I and related demyelinating neuropathies: Mutation analysis in a large cohort of Italian families. Human Mutation. 18(1). 32–41. 37 indexed citations

Pons, Roser, Patrizia Cavadini, Silvia Baratta, et al.. (2000). Clinical and molecular heterogeneity in very–long-chain acyl-coenzyme a dehydrogenase deficiency. Pediatric Neurology. 22(2). 98–105. 31 indexed citations

10.

Pareyson, Davide, Franco Taroni, Sara Botti, et al.. (2000). Cranial nerve involvement in CMT disease type 1 due to early growth response 2 gene mutation. Neurology. 54(8). 1696–1698. 65 indexed citations

11.

Gellera, Cinzia, Patrizia Cavadini, & Silvia Baratta. (1994). Fatal mitochondrial encephalopathy caused by fumarase deficiency: A molecular-genetic study. The American Journal of Human Genetics. 55. 5 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