Manuela Priolo
Impact in
- Developmental Biology top 10%
- Genetics top 5%
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
- Genetic Syndromes and Imprinting
- Genetics and Neurodevelopmental Disorders
Papers in
-
- Congenital heart defects research 7
- Hedgehog Signaling Pathway Studies 6
- dental development and anomalies 5
- Genetics 26
- Genetic Syndromes and Imprinting 6
- Genetics and Neurodevelopmental Disorders 6
- Genomics and Rare Diseases 6
- Genomic variations and chromosomal abnormalities 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)Flavia Cerrato (1 shared paper)
- Journals
- European Journal of Medical Genetics (4 papers)Genes (3 papers)Orphanet Journal of Rare Diseases (2 papers)European Journal of Human Genetics (2 papers)American Journal of Medical Genetics Part C Seminars in Medical Genetics (2 papers)
- Partner nations
- ItalyFranceUnited States
In The Last Decade
Manuela Priolo
46 papers receiving 826 citations
Peers
Comparison fields: 5 of 62
- Developmental Biology 32
- Genetics 404
- Oral Surgery 90
- Molecular Biology 542
- Pharmacy 25
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 | 57 | |
| 6 | 1998 | 55 | |
| 7 | 2019 | 32 | |
| 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 | 2008 | 15 | |
| 20 | 2015 | 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 882 indexed citations. Recurring topics across this work include Congenital heart defects research (7 papers), Genetic Syndromes and Imprinting (6 papers), Hedgehog Signaling Pathway Studies (6 papers), Genetics and Neurodevelopmental Disorders (6 papers), Genomics and Rare Diseases (6 papers), Genomic variations and chromosomal abnormalities (5 papers), dental development and anomalies (5 papers) and Congenital gastrointestinal and neural anomalies (4 papers). The work is most often cited by research in Developmental Biology (32 citations), Genetics (404 citations), Oral Surgery (90 citations), Molecular Biology (542 citations) and Pharmacy (25 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, Flavia Cerrato, Andrea Riccio and Angela Sparago. Their work appears in journals such as European Journal of Medical Genetics, Genes, Orphanet Journal of Rare Diseases, European Journal of Human Genetics and American Journal of Medical Genetics Part C Seminars in 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.