Simone Gana

976 total citations
34 papers, 255 citations indexed

About

Simone Gana is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Simone Gana has authored 34 papers receiving a total of 255 indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Genetics, 15 papers in Molecular Biology and 7 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Simone Gana's work include Genetics and Neurodevelopmental Disorders (8 papers), Genomic variations and chromosomal abnormalities (5 papers) and Genomics and Rare Diseases (4 papers). Simone Gana is often cited by papers focused on Genetics and Neurodevelopmental Disorders (8 papers), Genomic variations and chromosomal abnormalities (5 papers) and Genomics and Rare Diseases (4 papers). Simone Gana collaborates with scholars based in Italy, United States and United Kingdom. Simone Gana's co-authors include Enza Maria Valente, Orsetta Zuffardi, Roberto Ciccone, Elena Rossi, Pierangelo Veggiotti, Cesare Danesino, Erika Della Mina, Jyotsna Sudi, Faustina Lalatta and Angelo Valetto and has published in prestigious journals such as International Journal of Molecular Sciences, Movement Disorders and Journal of Medical Genetics.

In The Last Decade

Simone Gana

29 papers receiving 251 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Simone Gana Italy 9 151 125 50 25 24 34 255
Liesbeth Backx Belgium 10 196 1.3× 183 1.5× 34 0.7× 22 0.9× 26 1.1× 14 333
Ikumi Hori Japan 11 158 1.0× 157 1.3× 28 0.6× 18 0.7× 14 0.6× 25 258
Chloe Stutterd Australia 9 135 0.9× 109 0.9× 64 1.3× 31 1.2× 30 1.3× 18 283
Carissa Adams United States 2 124 0.8× 171 1.4× 32 0.6× 38 1.5× 29 1.2× 3 275
Erika Della Mina Italy 8 167 1.1× 124 1.0× 24 0.5× 27 1.1× 20 0.8× 16 263
Zhengjun Jia China 9 112 0.7× 106 0.8× 86 1.7× 13 0.5× 29 1.2× 23 262
Filip Roelens Belgium 10 141 0.9× 160 1.3× 46 0.9× 53 2.1× 34 1.4× 17 346
Syed K. Rafi United States 8 137 0.9× 107 0.9× 25 0.5× 12 0.5× 18 0.8× 14 264
Jane Juusola United States 13 192 1.3× 218 1.7× 33 0.7× 11 0.4× 34 1.4× 22 390
Linda Manwaring United States 8 175 1.2× 136 1.1× 31 0.6× 18 0.7× 17 0.7× 15 374

Countries citing papers authored by Simone Gana

Since Specialization
Citations

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

Fields of papers citing papers by Simone Gana

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Simone Gana

This figure shows the co-authorship network connecting the top 25 collaborators of Simone Gana. A scholar is included among the top collaborators of Simone Gana 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 Simone Gana. Simone Gana 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.
Vegezzi, Elisa, Roberta Zangaglia, Ilaria Palmieri, et al.. (2024). Bilateral Dentate Nuclei Hyperintensities and Response to 4-Aminopyridine in a Patient With Childhood-Onset GAA- FGF14 -Related Ataxia. Neurology Genetics. 10(6). e200208–e200208. 2 indexed citations
2.
Mauri, Lucia, Simone Gana, Alessandra Longo, et al.. (2024). Novel molecular, structural and clinical findings in an Italian cohort of congenital cataract. Clinical Genetics. 106(4). 403–412. 2 indexed citations
3.
Pasca, Ludovica, Francesca Ferraro, Simone Gana, et al.. (2024). Cerebellar heterotopia in an 11‐year‐old child with KDM6B‐related neurodevelopmental disorder: A case report and review of the literature. American Journal of Medical Genetics Part A. 194(6). e63555–e63555.
4.
Avenali, Micol, Silvia Cerri, Ilaria Palmieri, et al.. (2024). Functional Study of SNCA p.V15A Variant: Further Linking α‐Synuclein and Glucocerebrosidase. Movement Disorders. 39(6). 1060–1065.
5.
Gana, Simone, G. Catalano, Elisa Rognone, et al.. (2024). Novel HYLS1 variants associated with Joubert syndrome suggest potential genotype-phenotype correlates. Journal of Medical Genetics. 62(1). 3–5. 1 indexed citations
6.
Varesio, Costanza, Elena Freri, Francesca Darra, et al.. (2021). CDKL5 deficiency disorder in males: Five new variants and review of the literature. European Journal of Paediatric Neurology. 33. 9–20. 19 indexed citations
7.
Giorgis, Valentina De, Matteo Paoletti, Costanza Varesio, et al.. (2021). Novel insights into the clinico-radiological spectrum of phenotypes associated to PIGN mutations. European Journal of Paediatric Neurology. 33. 21–28. 1 indexed citations
8.
Palmieri, Ilaria, Marialuisa Valente, Lisa Maria Farina, et al.. (2021). PSEN1 Compound Heterozygous Mutations Associated with Cerebral Amyloid Angiopathy and Cognitive Decline Phenotype. International Journal of Molecular Sciences. 22(8). 3870–3870. 5 indexed citations
9.
Varesio, Costanza, Simone Gana, Elena Ballante, et al.. (2021). Diagnostic Yield and Cost-Effectiveness of “Dynamic” Exome Analysis in Epilepsy with Neurodevelopmental Disorders: A Tertiary-Center Experience in Northern Italy. Diagnostics. 11(6). 948–948. 8 indexed citations
10.
Todisco, Massimiliano, Simone Gana, Giuseppe Cosentino, et al.. (2020). KCTD17-related myoclonus-dystonia syndrome: clinical and electrophysiological findings of a patient with atypical late onset. Parkinsonism & Related Disorders. 78. 129–133. 5 indexed citations
11.
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
12.
13.
Gana, Simone, et al.. (2016). Assessment of Genetic Diversity among Newly Selected Roselle (Hibiscus sabdariffa Linn.) Genotypes in Nigeria Using Rapd-Pcr Molecular Analysis. World Journal of Agricultural Research. 4(3). 64–69. 2 indexed citations
14.
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
15.
Gana, Simone, et al.. (2013). Prenatal phenotype of Nager syndrome and Rodriguez syndrome. Clinical Dysmorphology. 22(4). 135–139. 4 indexed citations
16.
Novara, Francesca, Gloria Bedini, Silvia Esposito, et al.. (2013). MEF2C deletions and mutations versus duplications: A clinical comparison. European Journal of Medical Genetics. 56(5). 260–265. 18 indexed citations
17.
Mari, Francesco, Simone Gana, Francesca Piras, & Renzo Guerrini. (2011). Extremely sustained startle-induced clonus: Non epileptic motor attacks mimicking clonic seizures in children with encephalopathy. Seizure. 21(2). 147–150. 1 indexed citations
18.
Gana, Simone, Laura Sainati, F. Poli, et al.. (2011). Shwachman-Diamond Syndrome and Type 1 Diabetes Mellitus: More Than a Chance Association?. Experimental and Clinical Endocrinology & Diabetes. 119(10). 610–612. 16 indexed citations
19.
Conti, Valerio, Carla Marini, Simone Gana, et al.. (2011). Corpus callosum agenesis, severe mental retardation, epilepsy, and dyskinetic quadriparesis due to a novel mutation in the homeodomain of ARX. American Journal of Medical Genetics Part A. 155(4). 892–897. 13 indexed citations
20.
Gana, Simone, et al.. (2010). Nicolaides–Baraitser syndrome. Clinical Dysmorphology. 20(1). 38–41. 8 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

Breakdown of academic impact, for papers by Liesbeth Backx Breakdown of academic impact, for papers by Ikumi Hori Breakdown of academic impact, for papers by Chloe Stutterd Breakdown of academic impact, for papers by Carissa Adams Breakdown of academic impact, for papers by Erika Della Mina Breakdown of academic impact, for papers by Zhengjun Jia Breakdown of academic impact, for papers by Filip Roelens Breakdown of academic impact, for papers by Syed K. Rafi Breakdown of academic impact, for papers by Jane Juusola Breakdown of academic impact, for papers by Linda Manwaring
Rankless by CCL
2026