Simone Martinelli
Impact in
- Molecular Biology top 2%
- Protein Tyrosine Phosphatases
- Protein Kinase Regulation and GTPase Signaling
- DNA Repair Mechanisms
- Genetics top 5%
- Genomics and Rare Diseases
- Genetics and Neurodevelopmental Disorders
Papers in
-
- Protein Tyrosine Phosphatases 27
- DNA Repair Mechanisms 7
- Genetics 18
- Genomics and Rare Diseases 12
- Genetics and Neurodevelopmental Disorders 8
- Co-authors
- Marco Tartaglia (28 shared papers)Elisabetta Flex (11 shared papers)Gianfranco Bocchinfuso (9 shared papers)Bruce D. Gelb (5 shared papers)Antonio Palleschi (5 shared papers)Mariella Sorcini (4 shared papers)Lorenzo Stella (7 shared papers)Viviana Cordeddu (3 shared papers)
- Journals
- The American Journal of Human Genetics (7 papers)Human Mutation (4 papers)Clinical Genetics (3 papers)Nature Genetics (3 papers)British Journal of Haematology (3 papers)
- Partner nations
- ItalyUnited StatesGermany
In The Last Decade
Simone Martinelli
68 papers receiving 4.5k citations
Simone Martinelli's Hit Papers
Peers
Comparison fields: 5 of 97
- Molecular Biology 2.5k
- Genetics 792
- Hematology 302
- Psychiatry and Mental health 235
- Neurology 179
Countries citing papers authored by Simone Martinelli
This map shows the geographic impact of Simone Martinelli'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 Simone Martinelli with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Simone Martinelli more than expected).
Fields of papers citing papers by Simone Martinelli
This network shows the impact of papers produced by Simone Martinelli. 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 Simone Martinelli. The network helps show where Simone Martinelli may publish in the future.
Co-authors
The 25 scholars most cited alongside Simone Martinelli, 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 72 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2007 | 558 | |
| 2 | 2006 | 474 | |
| 3 | High Rate of Recurrent De Novo Mutations in Developmental and Epileptic Encephalopathies Hit paper breakdown → | 2017 | 364 |
| 4 | 2006 | 339 | |
| 5 | 2009 | 336 | |
| 6 | 2008 | 291 | |
| 7 | 2010 | 201 | |
| 8 | 2019 | 167 | |
| 9 | 2011 | 159 | |
| 10 | 2018 | 155 | |
| 11 | 2014 | 117 | |
| 12 | 2009 | 86 | |
| 13 | 2008 | 77 | |
| 14 | 2020 | 69 | |
| 15 | 2015 | 68 | |
| 16 | 2005 | 67 | |
| 17 | N-(2-chloroethyl)-N'-cyclohexyl-N-nitrosourea sensitivity in mismatch repair-defective human cells. | 1998 | 65 |
| 18 | 2009 | 65 | |
| 19 | 2004 | 57 | |
| 20 | 2018 | 54 |
About Simone Martinelli
Simone Martinelli is a scholar working on Molecular Biology, Genetics, Neurology, Hematology and Clinical Biochemistry, having authored 72 papers that have together received 4.6k indexed citations. Recurring topics across this work include Protein Tyrosine Phosphatases (27 papers), Genomics and Rare Diseases (12 papers), Genetics and Neurodevelopmental Disorders (8 papers), DNA Repair Mechanisms (7 papers), Neurological disorders and treatments (4 papers), Lysosomal Storage Disorders Research (3 papers), Acute Myeloid Leukemia Research (3 papers) and Parkinson's Disease Mechanisms and Treatments (3 papers). The work is most often cited by research in Molecular Biology (2.5k citations), Genetics (792 citations), Hematology (302 citations), Psychiatry and Mental health (235 citations) and Neurology (179 citations). Simone Martinelli has collaborated with scholars based in Italy, United States and Germany. Frequent co-authors include Marco Tartaglia, Elisabetta Flex, Gianfranco Bocchinfuso, Bruce D. Gelb, Antonio Palleschi, Mariella Sorcini, Lorenzo Stella, Viviana Cordeddu, Giuseppe Zampino and Tamara Corinna Petrucci. Their work appears in journals such as The American Journal of Human Genetics, Human Mutation, Clinical Genetics, Nature Genetics and British Journal of Haematology.
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.