Giovanni Neri
Impact in
- Genetics top 0.1%
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Genetic Syndromes and Imprinting
- Developmental Biology top 1%
Papers in
- Genetics 194
- Genetics and Neurodevelopmental Disorders 91
- Genomic variations and chromosomal abnormalities 79
- Genetic Syndromes and Imprinting 26
- Co-authors
- Pietro ChiurazziMarcella ZollinoFiorella GurrieriElisabetta TabolacciJohn M. OpitzMaria Grazia PomponiClaudia BagniCharles E. Schwartz
- Journals
- European Journal of Human Genetics (20 papers)American Journal of Medical Genetics (89 papers)Human Genetics (8 papers)American Journal of Medical Genetics Part C Seminars in Medical Genetics (7 papers)Journal of Medical Genetics (5 papers)
- Partner nations
- ItalyUnited StatesGermany
In The Last Decade
Giovanni Neri
296 papers receiving 9.0k citations
Hit Papers
Peers
Comparison fields: 5 of 161
- Genetics 5.5k
- Developmental Biology 257
- Molecular Biology 5.7k
- Genetics 719
- Cognitive Neuroscience 1.2k
Countries citing papers authored by Giovanni Neri
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
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-authors
The 25 scholars most cited alongside Giovanni Neri, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 2025 | 1 | |
| 2 | 2024 | 2 | |
| 3 | 2024 | 0 | |
| 4 | 2022 | 2 | |
| 5 | 2022 | 4 | |
| 6 | 2021 | 26 | |
| 7 | 2020 | 3 | |
| 8 | 2012 | 14 | |
| 9 | 2006 | 3 | |
| 10 | 2004 | 94 | |
| 11 | P63 mutations in the EEC, Hay-Wells, ADULT syndromes and in split hand/foot malformation reveals a genotype-phenotype correlation. | 2000 | 6 |
| 12 | 1999 | 167 | |
| 13 | 1996 | 2 | |
| 14 | Mutations in GPC3, a glypican gene, cause the Simpson-Golabi-Behmel overgrowth syndrome Hit paper breakdown → | 1996 | 593 |
| 15 | 1996 | 46 | |
| 16 | X-linked mental retardation 3 : proceedings of the Third International Workshop on Fragile X and X-linked Mental Retardation held in Troina, Italy, September 13-16, 1987 | 1988 | 1 |
| 17 | 1988 | 4 | |
| 18 | 1982 | 1 | |
| 19 | 1979 | 8 | |
| 20 | Viral expression, oncogenicity, and antigenicity of a mouse salivary gland tumor and two cell lines derived from it. | 1975 | 3 |
About Giovanni Neri
Giovanni Neri is a scholar working on Developmental Biology, Genetics, Molecular Biology, Cognitive Neuroscience and Genetics, having authored 302 papers that have together received 9.4k indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (91 papers), Genomic variations and chromosomal abnormalities (79 papers), Autism Spectrum Disorder Research (35 papers), RNA modifications and cancer (30 papers), Epigenetics and DNA Methylation (28 papers), Prenatal Screening and Diagnostics (27 papers), Congenital heart defects research (26 papers) and Genetic Syndromes and Imprinting (26 papers). The work is most often cited by research in Genetics (5.5k citations), Developmental Biology (257 citations), Molecular Biology (5.7k citations), Genetics (719 citations) and Cognitive Neuroscience (1.2k citations). Giovanni Neri has collaborated with scholars based in Italy, United States and Germany. Frequent co-authors include Pietro Chiurazzi, Marcella Zollino, Fiorella Gurrieri, Elisabetta Tabolacci, John M. Opitz, Maria Grazia Pomponi, Claudia Bagni, Charles E. Schwartz, Maurizio Genuardi and Roberta Pietrobono. Their work appears in journals such as European Journal of Human Genetics, American Journal of Medical Genetics, Human Genetics, American Journal of Medical Genetics Part C Seminars in Medical Genetics and Journal of Medical 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.