Simone Gana

990 citations
49 papers · 662 · h-index 11

Impact in

  • Genetics top 10%
    • Genomics and Rare Diseases
    • Genetics and Neurodevelopmental Disorders
    • Genetic and Kidney Cyst Diseases
    • Genomic variations and chromosomal abnormalities

Papers in

    • Genomics and Rare Diseases 13
    • Genetics and Neurodevelopmental Disorders 13
    • Genomic variations and chromosomal abnormalities 5
    • Genetic and Kidney Cyst Diseases 5
    • Fetal and Pediatric Neurological Disorders 4

Simone Gana

43 papers receiving 650 citations

Peers

Simone Gana
Comparison fields: 5 of 51
  • Genetics 322
  • Developmental Biology 14
  • Cellular and Molecular Neuroscience 103
  • Developmental Neuroscience 11
  • Psychiatry and Mental health 50
Replace Joaquim Sá with:
Joaquim Sá Portugal
Alfonso Caro‐Llopis Spain
Erkan Koparir Türkiye
Ruobing Zou Canada
Naseebullah Kakar Pakistan
Anne K. van Riesen Germany
Shenela Lakhani United States
Yunru Shao United States
Marion Gérard France
Vehap Topçu Türkiye
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Citations per field
00.5×2×2.7×
Joaquim Sá · 1×
Citations per year

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-authors

The 25 scholars most cited alongside Simone Gana, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Simone Gana Line = papers co-authored together Simone Gana links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 49 papers — load more, or switch the sort, to bring in the rest.

#Work
1 2012191
2 202181
3 202257
4 201239
5 201528
6 202125
7 202125
8 201323
9 201117
10 201115
11 202012
12 201911
13 201110
14 202010
15 202110
16 20108
17 20198
18 20218
19
Early onset of a nasal perivascular epithelioid cell neoplasm not related to tuberous sclerosis complex.
20127
20 20206

About Simone Gana

Simone Gana is a scholar working on Genetics, Pediatrics, Perinatology and Child Health, Cellular and Molecular Neuroscience, Psychiatry and Mental health and Neurology, having authored 49 papers that have together received 662 indexed citations. Recurring topics across this work include Genomics and Rare Diseases (13 papers), Genetics and Neurodevelopmental Disorders (13 papers), Epilepsy research and treatment (5 papers), Genomic variations and chromosomal abnormalities (5 papers), Genetic and Kidney Cyst Diseases (5 papers), Fetal and Pediatric Neurological Disorders (4 papers), Hereditary Neurological Disorders (3 papers) and Genetic Neurodegenerative Diseases (2 papers). The work is most often cited by research in Genetics (322 citations), Developmental Biology (14 citations), Cellular and Molecular Neuroscience (103 citations), Developmental Neuroscience (11 citations) and Psychiatry and Mental health (50 citations). Simone Gana has collaborated with scholars based in Italy, United States and Switzerland. Frequent co-authors include Enza Maria Valente, Valentina Serpieri, Orsetta Zuffardi, Roberto Ciccone, Pierangelo Veggiotti, Elena Giulia Rossi, Faustina Lalatta, Renzo Guerrini, Anna Bersano and Veronica Bertini. Their work appears in journals such as Journal of Medical Genetics, European Journal of Human Genetics, Movement Disorders, Genes and European Journal of Paediatric Neurology.

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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