Giovanni Neri

3.6k citations
56 papers · 2.2k indexed · 2 hit papers · h-index 23
Topics
Neurogenetic and Muscular Disorders Research (15 papers)Prenatal Screening and Diagnostics (13 papers)RNA modifications and cancer (9 papers)

In The Last Decade

Giovanni Neri

55 papers receiving 2.1k citations

Hit Papers

Molecular alterations of the AKT2 oncogene in ovarian and...199520262005201519952025200400600

Peers

Giovanni Neri
Comparison fields: 5 of 105
  • Molecular Biology 1.4k
  • Genetics 615
  • Pathology and Forensic Medicine 414
  • Genetics 398
  • Oncology 327
Replace Monique Losekoot with:
Monique Losekoot Netherlands
Digamber S. Borgaonkar United States
Mordechai Shohat Israel
Barbara K. Goodman United States
W. Roy Breg United States
Sigrid Swagemakers Netherlands
Bassem A. Bejjani United States
Barbara A. Christy United States
Maja Di Rocco Italy
Seema R. Lalani United States
Giovanni Neri relative to Monique Losekoot Netherlands Monique Losekoot's profile →
Citations per field
00.5×1.5×
Monique Losekoot · 1×
Citations per year

Countries citing papers authored by Giovanni Neri

Since Specialization
Citations

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

Fields of papers citing papers by Giovanni Neri

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Giovanni Neri

This figure shows the co-authorship network connecting the top 25 collaborators of Giovanni Neri. A scholar is included among the top collaborators of Giovanni Neri 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 Giovanni Neri. Giovanni Neri 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
Suicidal risk among adolescent psychiatric inpatients: the role of insomnia, depression, and social-personal factorsbreakdown →
20
2 42
3 39
4 64
5
Upregulation of SMN2 gene expression by 4-phenylbutyrate: relevance for a therapeutic approach to spinal muscular atrophy.
2
6 38
7 49
8 1
9 4
10 65
11
Molecular alterations of the AKT2 oncogene in ovarian and breast carcinomasbreakdown →
691
12 25
13 5
14 22
15 61
16 68
17 22
18 9
19 21
20 70

About Giovanni Neri

Giovanni Neri is a scholar working on Developmental Biology, Genetics and Pediatrics, Perinatology and Child Health, having authored 56 papers that have together received 2.2k indexed citations. Recurring topics across this work include Neurogenetic and Muscular Disorders Research (15 papers), Prenatal Screening and Diagnostics (13 papers) and RNA modifications and cancer (9 papers). The work is most often cited by research in Genetics (398 citations), Pathology and Forensic Medicine (414 citations) and Genetics (615 citations). Giovanni Neri has collaborated with scholars based in Italy, United States and Netherlands. Frequent co-authors include Alfonso Bellacosa, Maurizio Genuardi, Valeria Masciullo, Deborah A. Altomare, Louis Dubeau, Salvatore Mancuso, Minghong Wan, Andrew K. Godwin, Daphne W. Bell and Jin Q. Cheng. Their work appears in journals such as Proceedings of the National Academy of Sciences, The Lancet and International Journal of Molecular Sciences.

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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