Simone Pizzi

2.0k citations
31 papers · 313 · h-index 11

Impact in

    • Genomics and Rare Diseases
    • Genetics and Neurodevelopmental Disorders
    • Neurogenetic and Muscular Disorders Research
    • Neurological diseases and metabolism

Papers in

    • RNA modifications and cancer 4
    • Mitochondrial Function and Pathology 3
    • Epigenetics and DNA Methylation 3
    • Genetics and Neurodevelopmental Disorders 5
    • Genomic variations and chromosomal abnormalities 4
    • Genomics and Rare Diseases 4

Simone Pizzi

31 papers receiving 305 citations

Peers

Simone Pizzi
Comparison fields: 5 of 56
  • Genetics 123
  • Genetics 45
  • Neurology 28
  • Cellular and Molecular Neuroscience 53
  • Molecular Biology 185
Replace Tahir Naeem Khan with:
Tahir Naeem Khan Pakistan
Kristin McDonald Gibson United States
Aziza Sbiti Morocco
Rachel Gillespie United Kingdom
Cristina Villanueva‐Mendoza Mexico
Robea Ballo South Africa
Christin Collins United States
Magdalena Badura‐Stronka Poland
Florence Renaldo France
Sharan Goobie Canada
Simone Pizzi relative to Tahir Naeem Khan Pakistan Tahir Naeem Khan's profile →
Citations per field
00.5×3.6×
Tahir Naeem Khan · 1×
Citations per year

Countries citing papers authored by Simone Pizzi

Since Specialization
Citations

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

Fields of papers citing papers by Simone Pizzi

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Simone Pizzi, 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 Pizzi Line = papers co-authored together Simone Pizzi links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 31 papers — load more, or switch the sort, to bring in the rest.

#Work
1 201843
2 202028
3 201623
4 201920
5 201719
6 201718
7 201816
8 201915
9 201814
10 201611
11 201910
12 201810
13 201710
14 20229
15 20188
16 20217
17 20206
18 20176
19 20226
20 20105

About Simone Pizzi

Simone Pizzi is a scholar working on Molecular Biology, Genetics, Pathology and Forensic Medicine, Cellular and Molecular Neuroscience and Cell Biology, having authored 31 papers that have together received 313 indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (5 papers), RNA modifications and cancer (4 papers), Genomic variations and chromosomal abnormalities (4 papers), Genomics and Rare Diseases (4 papers), Genetic factors in colorectal cancer (3 papers), Mitochondrial Function and Pathology (3 papers), Epigenetics and DNA Methylation (3 papers) and Genetic Neurodegenerative Diseases (3 papers). The work is most often cited by research in Genetics (123 citations), Genetics (45 citations), Neurology (28 citations), Cellular and Molecular Neuroscience (53 citations) and Molecular Biology (185 citations). Simone Pizzi has collaborated with scholars based in Italy, Canada and Netherlands. Frequent co-authors include Marco Tartaglia, Sabina Barresi, Andrea Ciolfi, Alessandro Bruselles, Bruno Dallapiccola, Maria Lisa Dentici, Marcello Niceta, M. Cristina Digilio, Emilia Stellacci and Adele D’Amico. Their work appears in journals such as Genes, Clinical Genetics, Frontiers in Neurology, Frontiers in Genetics and Clinical Epigenetics.

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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