Manuela Priolo
Impact in
- Genetics top 5%
- Genomic variations and chromosomal abnormalities
- Genetic Syndromes and Imprinting
- Genomics and Rare Diseases
- Genetics and Neurodevelopmental Disorders
- Developmental Biology top 10%
Papers in
-
- Hedgehog Signaling Pathway Studies 6
- Congenital heart defects research 5
- dental development and anomalies 5
- Protein Tyrosine Phosphatases 4
- Genetics 25
- Genetics and Neurodevelopmental Disorders 6
- Genomic variations and chromosomal abnormalities 5
- Genetic Syndromes and Imprinting 5
- Co-authors
- Margherita Lerone (10 shared papers)Margherita Silengo (7 shared papers)Roberto Ravazzolo (7 shared papers)Carmelo Laganà (6 shared papers)Isabella Ceccherini (4 shared papers)Corrado Mammì (8 shared papers)Marco Seri (9 shared papers)Andrea Riccio (1 shared paper)
- Journals
- European Journal of Medical Genetics (4 papers)Genes (3 papers)Clinical Genetics (2 papers)European Journal of Human Genetics (2 papers)Orphanet Journal of Rare Diseases (2 papers)
- Partner nations
- ItalyFranceUnited States
In The Last Decade
Manuela Priolo
46 papers receiving 835 citations
Peers
Comparison fields: 5 of 59
- Genetics 377
- Developmental Biology 29
- Oral Surgery 83
- Molecular Biology 490
- Pharmacy 23
Countries citing papers authored by Manuela Priolo
This map shows the geographic impact of Manuela Priolo'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 Manuela Priolo with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Manuela Priolo more than expected).
Fields of papers citing papers by Manuela Priolo
This network shows the impact of papers produced by Manuela Priolo. 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 Manuela Priolo. The network helps show where Manuela Priolo may publish in the future.
Co-authors
The 25 scholars most cited alongside Manuela Priolo, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 48 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2001 | 133 | |
| 2 | The physical map of the human RET proto-oncogene. | 1995 | 76 |
| 3 | 2000 | 75 | |
| 4 | 2006 | 61 | |
| 5 | 2008 | 58 | |
| 6 | 1998 | 55 | |
| 7 | 2019 | 33 | |
| 8 | 2015 | 29 | |
| 9 | 1997 | 28 | |
| 10 | 2012 | 25 | |
| 11 | 2013 | 24 | |
| 12 | 2011 | 24 | |
| 13 | 2009 | 23 | |
| 14 | 2000 | 20 | |
| 15 | 1999 | 20 | |
| 16 | 2007 | 19 | |
| 17 | 2012 | 18 | |
| 18 | 2009 | 17 | |
| 19 | 2015 | 16 | |
| 20 | 2022 | 15 |
About Manuela Priolo
Manuela Priolo is a scholar working on Molecular Biology, Genetics, Surgery, Cell Biology and Genetics, having authored 48 papers that have together received 892 indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (6 papers), Hedgehog Signaling Pathway Studies (6 papers), Congenital heart defects research (5 papers), dental development and anomalies (5 papers), Genomic variations and chromosomal abnormalities (5 papers), Genetic Syndromes and Imprinting (5 papers), Protein Tyrosine Phosphatases (4 papers) and Congenital gastrointestinal and neural anomalies (4 papers). The work is most often cited by research in Genetics (377 citations), Developmental Biology (29 citations), Oral Surgery (83 citations), Molecular Biology (490 citations) and Pharmacy (23 citations). Manuela Priolo has collaborated with scholars based in Italy, France and United States. Frequent co-authors include Margherita Lerone, Margherita Silengo, Roberto Ravazzolo, Carmelo Laganà, Isabella Ceccherini, Corrado Mammì, Marco Seri, Andrea Riccio, Angela Sparago and Flavia Cerrato. Their work appears in journals such as European Journal of Medical Genetics, Genes, Clinical Genetics, European Journal of Human Genetics and Orphanet Journal of Rare Diseases.
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.