Benedetta Toschi

728 total citations
28 papers, 309 citations indexed

About

Benedetta Toschi is a scholar working on Genetics, Molecular Biology and Nephrology. According to data from OpenAlex, Benedetta Toschi has authored 28 papers receiving a total of 309 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Genetics, 9 papers in Molecular Biology and 5 papers in Nephrology. Recurrent topics in Benedetta Toschi's work include Genomic variations and chromosomal abnormalities (7 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (5 papers) and Prenatal Screening and Diagnostics (4 papers). Benedetta Toschi is often cited by papers focused on Genomic variations and chromosomal abnormalities (7 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (5 papers) and Prenatal Screening and Diagnostics (4 papers). Benedetta Toschi collaborates with scholars based in Italy, France and United States. Benedetta Toschi's co-authors include Silvano Bertelloni, Giampiero I. Baroncelli, Paolo Simi, Veronica Bertini, Angelo Valetto, Nicolas Forestier, Francesco Massart, Angela Michelucci, Maurizio Genuardi and Fulvia Baldinotti and has published in prestigious journals such as SHILAP Revista de lepidopterología, Cancer Letters and Clinical Biomechanics.

In The Last Decade

Benedetta Toschi

26 papers receiving 273 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Benedetta Toschi Italy 11 145 117 49 46 32 28 309
Rachel M. Sinders United States 6 234 1.6× 171 1.5× 29 0.6× 174 3.8× 27 0.8× 8 383
Udo Schnitzbauer Switzerland 11 138 1.0× 187 1.6× 46 0.9× 185 4.0× 53 1.7× 17 396
Fuping Zhang China 11 89 0.6× 139 1.2× 29 0.6× 28 0.6× 21 0.7× 26 412
Artemis Doulgeraki Greece 12 89 0.6× 145 1.2× 17 0.3× 14 0.3× 70 2.2× 33 358
Judith Saffran United States 8 102 0.7× 94 0.8× 39 0.8× 52 1.1× 55 1.7× 14 350
C. Dony United States 4 88 0.6× 232 2.0× 12 0.2× 10 0.2× 24 0.8× 9 339
Roger Long United States 10 74 0.5× 210 1.8× 9 0.2× 16 0.3× 66 2.1× 14 377
MP Whyte United States 5 105 0.7× 178 1.5× 12 0.2× 39 0.8× 66 2.1× 9 335
Débora Braslavsky Argentina 12 187 1.3× 239 2.0× 22 0.4× 32 0.7× 16 0.5× 25 454
Linda Gibbs France 8 105 0.7× 154 1.3× 21 0.4× 14 0.3× 29 0.9× 12 335

Countries citing papers authored by Benedetta Toschi

Since Specialization
Citations

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

Fields of papers citing papers by Benedetta Toschi

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Benedetta Toschi

This figure shows the co-authorship network connecting the top 25 collaborators of Benedetta Toschi. A scholar is included among the top collaborators of Benedetta Toschi 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 Benedetta Toschi. Benedetta Toschi 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.
Orsini, Alessandro, Andrea Santangelo, Francesco Massart, et al.. (2024). An Ultra-Rare Mixed Phenotype with Combined AP-4 and ERF Mutations: The First Report in a Pediatric Patient and a Literature Review. Genes. 15(4). 436–436.
2.
Baroncelli, Giampiero I., et al.. (2024). Safety and efficacy of burosumab in improving phosphate metabolism, bone health, and quality of life in adolescents with X-linked hypophosphatemic rickets. European Journal of Medical Genetics. 70. 104958–104958. 5 indexed citations
3.
Baroncelli, Giampiero I., Elena Freri, Maria Rita Giuca, et al.. (2023). The diagnosis of hypophosphatasia in children as a multidisciplinary effort: an expert opinion. Journal of Endocrinological Investigation. 47(3). 739–747. 5 indexed citations
4.
Baroncelli, Giampiero I., Caterina Pelosini, Silvano Bertelloni, et al.. (2023). Intact FGF23 concentration in healthy infants, children, and adolescents, and diagnostic usefulness in patients with X-linked hypophosphatemic rickets. Journal of Endocrinological Investigation. 47(4). 873–882. 2 indexed citations
5.
Gana, Simone, Angelo Valetto, Benedetta Toschi, et al.. (2019). Familial Interstitial 6q23.2 Deletion Including Eya4 Associated With Otofaciocervical Syndrome. Frontiers in Genetics. 10. 650–650. 6 indexed citations
6.
Bertini, Veronica, Angelo Valetto, Fulvia Baldinotti, et al.. (2019). Blepharophimosis, Ptosis, Epicanthus Inversus Syndrome: New Report with a 197-kb Deletion Upstream of FOXL2 and Review of the Literature. Molecular Syndromology. 10(3). 147–153. 8 indexed citations
7.
Aretini, Paolo, Chiara Maria Mazzanti, Sara Franceschi, et al.. (2018). Next generation sequencing technologies for a successful diagnosis in a cold case of Leigh syndrome. BMC Neurology. 18(1). 99–99. 13 indexed citations
8.
9.
Valetto, Angelo, Veronica Bertini, Angela Michelucci, et al.. (2016). Short Stature in Isodicentric Y Chromosome and Three Copies of the SHOX Gene: Clinical Report and Review of Literature. Molecular Syndromology. 7(1). 19–25. 8 indexed citations
10.
Bertini, Veronica, Alessia Azzarà, Benedetta Toschi, Simone Gana, & Angelo Valetto. (2016). 3p26.3 terminal deletions: a challenge for prenatal genetic counseling. Prenatal Diagnosis. 37(2). 197–200. 2 indexed citations
11.
Bertini, Veronica, Rossella Bruno, Benedetta Toschi, et al.. (2015). 625 kb microduplication at Xp22.12 including RPS6KA3 in a child with mild intellectual disability. Journal of Human Genetics. 60(12). 777–780. 7 indexed citations
12.
Bertelloni, Silvano, Giampiero I. Baroncelli, Francesco Massart, & Benedetta Toschi. (2015). Growth in Boys with 45,X/46,XY Mosaicism: Effect of Growth Hormone Treatment on Statural Growth. Sexual Development. 9(4). 183–189. 24 indexed citations
13.
Bruno, Rossella, Angelo Valetto, Veronica Bertini, et al.. (2015). A 17q duplication prenatally detected. Taiwanese Journal of Obstetrics and Gynecology. 54(3). 326–329.
14.
Bertelloni, Silvano, Eleonora Dati, Fulvia Baldinotti, et al.. (2014). NR5A1 Gene Mutations: Clinical, Endocrine and Genetic Features in Two Girls with 46,XY Disorder of Sex Development. Hormone Research in Paediatrics. 81(2). 104–108. 13 indexed citations
15.
Bertelloni, Silvano, Giampiero I. Baroncelli, Eleonora Dati, et al.. (2013). IGF-I generation test in prepubertal children with Noonan syndrome due to mutations in the PTPN11 gene. HORMONES. 12(1). 86–92. 20 indexed citations
16.
Toschi, Benedetta, Angelo Valetto, Veronica Bertini, et al.. (2012). Acro‐cardio‐facial syndrome: A microdeletion syndrome?. American Journal of Medical Genetics Part A. 158A(8). 1994–1999. 10 indexed citations
17.
Baroncelli, Giampiero I., Benedetta Toschi, & Silvano Bertelloni. (2012). Hypophosphatemic rickets. Current Opinion in Endocrinology Diabetes and Obesity. 19(6). 460–467. 23 indexed citations
18.
Valetto, Angelo, Alessandro Orsini, Veronica Bertini, et al.. (2012). Molecular cytogenetic characterization of an interstitial deletion of chromosome 21 (21q22.13q22.3) in a patient with dysmorphic features, intellectual disability and severe generalized epilepsy. European Journal of Medical Genetics. 55(5). 362–366. 41 indexed citations
19.
Maffé, Antonella, Benedetta Toschi, Daniela Giachino, et al.. (2010). Constitutional FLCN mutations in patients with suspected Birt-Hogg-Dubé syndrome ascertained for non-cutaneous manifestations. Clinical Genetics. 79(4). 345–354. 34 indexed citations
20.
Tricarico, Rossella, Paola Bet, Benedetta Ciambotti, et al.. (2008). Endometrial cancer and somatic G>T KRAS transversion in patients with constitutional MUTYH biallelic mutations. Cancer Letters. 274(2). 266–270. 16 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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