Marco Seri
Impact in
- Hematology top 1%
- Platelet Disorders and Treatments
- Nephrology top 1%
- Renal Diseases and Glomerulopathies
Papers in
-
- RNA regulation and disease 8
- Genetics 65
- Genomic variations and chromosomal abnormalities 12
- Genomics and Rare Diseases 12
- Co-authors
- Isabella Ceccherini (15 shared papers)Renata Bocciardi (7 shared papers)Margherita Lerone (19 shared papers)Virginia Barone (7 shared papers)Yin Luo (3 shared papers)Barbara Pasini (5 shared papers)Giuseppe Martucciello (8 shared papers)Giovanni Romeo (5 shared papers)
- Journals
- European Journal of Human Genetics (12 papers)Human Genetics (8 papers)Human Mutation (8 papers)International Journal of Molecular Medicine (7 papers)Clinical Genetics (5 papers)
- Partner nations
- ItalyUnited StatesUnited Kingdom
In The Last Decade
Marco Seri
188 papers receiving 5.2k citations
Marco Seri's Hit Papers
Peers
Comparison fields: 5 of 121
- Hematology 585
- Nephrology 356
- Genetics 1.2k
- Immunology and Allergy 233
- Gastroenterology 146
Countries citing papers authored by Marco Seri
This map shows the geographic impact of Marco Seri'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 Marco Seri with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Marco Seri more than expected).
Fields of papers citing papers by Marco Seri
This network shows the impact of papers produced by Marco Seri. 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 Marco Seri. The network helps show where Marco Seri may publish in the future.
Co-authors
The 25 scholars most cited alongside Marco Seri, 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 197 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Point mutations affecting the tyrosine kinase domain of the RET proto-oncogene in Hirschsprung's disease Hit paper breakdown → | 1994 | 532 |
| 2 | RET mutations in exons 13 and 14 of FMTC patients. | 1995 | 185 |
| 3 | 2000 | 176 | |
| 4 | 2013 | 159 | |
| 5 | 1995 | 159 | |
| 6 | DNA polymorphisms and conditions for SSCP analysis of the 20 exons of the ret proto-oncogene. | 1994 | 142 |
| 7 | 2001 | 140 | |
| 8 | 2000 | 120 | |
| 9 | 1997 | 104 | |
| 10 | 2004 | 101 | |
| 11 | 2005 | 89 | |
| 12 | 2002 | 74 | |
| 13 | 2014 | 73 | |
| 14 | 2013 | 70 | |
| 15 | 2010 | 68 | |
| 16 | 2013 | 68 | |
| 17 | 1999 | 65 | |
| 18 | 2016 | 63 | |
| 19 | 1999 | 59 | |
| 20 | 1993 | 56 |
About Marco Seri
Marco Seri is a scholar working on Molecular Biology, Genetics, Surgery, Hematology and Cell Biology, having authored 197 papers that have together received 5.3k indexed citations. Recurring topics across this work include Platelet Disorders and Treatments (21 papers), Cell Adhesion Molecules Research (15 papers), Congenital gastrointestinal and neural anomalies (14 papers), Genomic variations and chromosomal abnormalities (12 papers), Genomics and Rare Diseases (12 papers), Hereditary Neurological Disorders (10 papers), RNA regulation and disease (8 papers) and Renal Diseases and Glomerulopathies (8 papers). The work is most often cited by research in Hematology (585 citations), Nephrology (356 citations), Genetics (1.2k citations), Immunology and Allergy (233 citations) and Gastroenterology (146 citations). Marco Seri has collaborated with scholars based in Italy, United States and United Kingdom. Frequent co-authors include Isabella Ceccherini, Renata Bocciardi, Margherita Lerone, Virginia Barone, Yin Luo, Barbara Pasini, Giuseppe Martucciello, Giovanni Romeo, Tommaso Pippucci and Anna Savoia. Their work appears in journals such as European Journal of Human Genetics, Human Genetics, Human Mutation, International Journal of Molecular Medicine and Clinical 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.