Mattia Gentile

4.7k citations
106 papers · 2.3k indexed · h-index 28
Topics
Genomic variations and chromosomal abnormalities (21 papers)Genetic factors in colorectal cancer (17 papers)Congenital heart defects research (17 papers)

In The Last Decade

Mattia Gentile

102 papers receiving 2.2k citations

Peers

Mattia Gentile
Comparison fields: 5 of 123
  • Genetics 659
  • Molecular Biology 642
  • Pulmonary and Respiratory Medicine 477
  • Surgery 436
  • Pediatrics, Perinatology and Child Health 425
Replace William H. Peranteau with:
William H. Peranteau United States
Celia Moss United Kingdom
Kenneth Ward United States
Paolo Bernasconi Italy
Éric Bieth France
Hart Isaacs United States
Corey Raffel United States
J. Briner Switzerland
Debra L. Kearney United States
Tarra L. McDowell United Kingdom
Mattia Gentile relative to William H. Peranteau United States William H. Peranteau's profile →
Citations per field
00.5×1.5×
William H. Peranteau · 1×
Citations per year

Countries citing papers authored by Mattia Gentile

Since Specialization
Citations

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

Fields of papers citing papers by Mattia Gentile

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Mattia Gentile

This figure shows the co-authorship network connecting the top 25 collaborators of Mattia Gentile. A scholar is included among the top collaborators of Mattia Gentile 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 Mattia Gentile. Mattia Gentile 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
#WorkIndexed citations
1 3
2 2
3 0
4 2
5 2
6 24
7 3
8 11
9 11
10 40
11 95
12 92
13 14
14 20
15 14
16 9
17 27
18 11
19 3
20
Exclusion of the APC gene as the cause of a variant form of familial adenomatous polyposis (FAP)
22

About Mattia Gentile

Mattia Gentile is a scholar working on Genetics, Pathology and Forensic Medicine and Pediatrics, Perinatology and Child Health, having authored 106 papers that have together received 2.3k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (21 papers), Genetic factors in colorectal cancer (17 papers) and Congenital heart defects research (17 papers). The work is most often cited by research in Genetics (659 citations), Pediatrics, Perinatology and Child Health (425 citations) and Pathology and Forensic Medicine (318 citations). Mattia Gentile has collaborated with scholars based in Italy, United States and United Kingdom. Frequent co-authors include Paolo Volpe, G Caruso, Ginevra Guanti, Francesco Susca, Andrea Marzullo, Angela Buonadonna, V. De Robertis, Roberto Castellana, Giuseppe Castellana and M. Marasini. Their work appears in journals such as Nature Communications, PEDIATRICS and Biochemical and Biophysical Research Communications.

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

Rankless by CCL
2026