Davide Mei

7.1k citations
81 papers · 2.4k indexed · h-index 30

Impact in

    • Epilepsy research and treatment
  • Genetics top 1%
    • Genetics and Neurodevelopmental Disorders
    • Genomics and Rare Diseases
    • Genomic variations and chromosomal abnormalities

Papers in

Davide Mei

79 papers receiving 2.4k citations

Peers

Davide Mei
Comparison fields: 5 of 76
  • Psychiatry and Mental health 1.0k
  • Genetics 1.2k
  • Clinical Biochemistry 227
  • Pediatrics, Perinatology and Child Health 577
  • Cellular and Molecular Neuroscience 482
Replace Jun Tohyama with:
Jun Tohyama Japan
Eric Leguern France
László Sztriha United Arab Emirates
Angelika Mühlebner Netherlands
Xinhua Bao China
Agathe Roubertie France
Laura Flores‐Sarnat Canada
Byung Chan Lim South Korea
Francesco Nicita Italy
Mathilde Chipaux France
Davide Mei relative to Jun Tohyama Japan Jun Tohyama's profile →
Citations per field
00.5×1.5×
Jun Tohyama · 1×
Citations per year

Countries citing papers authored by Davide Mei

Since Specialization
Citations

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

Fields of papers citing papers by Davide Mei

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network

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

All Works

20 of 20 papers shown
#Work
1 20251
2 20250
3 20242
4 20241
5 20242
6 202310
7 20232
8 20235
9 20223
10 202126
11 202119
12 202115
13 202125
14 202012
15 202045
16 201717
17 201224
18 200724
19 200435
20
Analisi della variabilita’ genetica della razza Chianina attraverso i dati genealogici e molecolari: Il confronto tra parentele e rassomiglianza genetica
20012

About Davide Mei

Davide Mei is a scholar working on Psychiatry and Mental health, Clinical Biochemistry, Genetics, Cellular and Molecular Neuroscience and Pediatrics, Perinatology and Child Health, having authored 81 papers that have together received 2.4k indexed citations. Recurring topics across this work include Epilepsy research and treatment (29 papers), Genetics and Neurodevelopmental Disorders (28 papers), Genomics and Rare Diseases (25 papers), Metabolism and Genetic Disorders (12 papers), Fetal and Pediatric Neurological Disorders (10 papers), Neuroscience and Neuropharmacology Research (9 papers), Genomic variations and chromosomal abnormalities (9 papers) and Amino Acid Enzymes and Metabolism (4 papers). The work is most often cited by research in Psychiatry and Mental health (1.0k citations), Genetics (1.2k citations), Clinical Biochemistry (227 citations), Pediatrics, Perinatology and Child Health (577 citations) and Cellular and Molecular Neuroscience (482 citations). Davide Mei has collaborated with scholars based in Italy, United States and United Kingdom. Frequent co-authors include Renzo Guerrini, Carla Marini, Elena Parrini, Federico Sicca, Anna Rita Ferrari, Tiziana Pisano, Francesca Moro, Domenica Battaglia, J. Helen Cross and Nicola Specchio. Their work appears in journals such as Epilepsia, Neurology, Epilepsy Research, Cerebral Cortex and Human Molecular Genetics.

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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2026