Diego Martinelli
Impact in
- Clinical Biochemistry top 0.02%
- Metabolism and Genetic Disorders
- Genetics top 5%
- Neurogenetic and Muscular Disorders Research
- Genomics and Rare Diseases
Papers in
-
- Metabolism and Genetic Disorders 81
- Rheumatology 14
- Glycogen Storage Diseases and Myoclonus 10
- Co-authors
- Carlo Dionisi‐Vici (61 shared papers)Enrico Bertini (23 shared papers)Vicente Rubio (4 shared papers)Johannes Häberle (4 shared papers)Rosalba Carrozzo (17 shared papers)Martina Huemer (4 shared papers)Marjorie Dixon (2 shared papers)Alberto Burlina (2 shared papers)
- Journals
- Journal of Inherited Metabolic Disease (31 papers)Orphanet Journal of Rare Diseases (9 papers)Molecular Genetics and Metabolism (8 papers)The American Journal of Human Genetics (5 papers)Neurology (5 papers)
- Partner nations
- ItalyGermanyUnited Kingdom
In The Last Decade
Diego Martinelli
142 papers receiving 6k citations
Diego Martinelli's Hit Papers
Peers
Comparison fields: 5 of 121
- Clinical Biochemistry 3k
- Genetics 312
- Biochemistry 177
- Molecular Biology 1.8k
- Rheumatology 349
Countries citing papers authored by Diego Martinelli
This map shows the geographic impact of Diego 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 Diego Martinelli with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Diego Martinelli more than expected).
Fields of papers citing papers by Diego Martinelli
This network shows the impact of papers produced by Diego 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 Diego Martinelli. The network helps show where Diego Martinelli may publish in the future.
Co-authors
The 25 scholars most cited alongside Diego 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 148 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Proposed guidelines for the diagnosis and management of methylmalonic and propionic acidemia Hit paper breakdown → | 2014 | 506 |
| 2 | Suggested guidelines for the diagnosis and management of urea cycle disorders Hit paper breakdown → | 2012 | 461 |
| 3 | Suggested guidelines for the diagnosis and management of urea cycle disorders: First revision Hit paper breakdown → | 2019 | 329 |
| 4 | 2015 | 200 | |
| 5 | Guidelines for the diagnosis and management of methylmalonic acidaemia and propionic acidaemia: First revision Hit paper breakdown → | 2021 | 184 |
| 6 | 2015 | 182 | |
| 7 | 2012 | 181 | |
| 8 | 2010 | 177 | |
| 9 | 2012 | 169 | |
| 10 | 2011 | 154 | |
| 11 | 2013 | 144 | |
| 12 | 2014 | 130 | |
| 13 | 2013 | 128 | |
| 14 | 2010 | 119 | |
| 15 | 2015 | 100 | |
| 16 | 2015 | 91 | |
| 17 | 2011 | 83 | |
| 18 | 2019 | 82 | |
| 19 | 2015 | 69 | |
| 20 | 2018 | 67 |
About Diego Martinelli
Diego Martinelli is a scholar working on Clinical Biochemistry, Rheumatology, Molecular Biology, Genetics and Biochemistry, having authored 148 papers that have together received 6.2k indexed citations. Recurring topics across this work include Metabolism and Genetic Disorders (81 papers), Mitochondrial Function and Pathology (25 papers), Glycogen Storage Diseases and Myoclonus (10 papers), Lysosomal Storage Disorders Research (9 papers), Hereditary Neurological Disorders (9 papers), Epilepsy research and treatment (7 papers), Glycosylation and Glycoproteins Research (5 papers) and Genomics and Rare Diseases (5 papers). The work is most often cited by research in Clinical Biochemistry (3k citations), Genetics (312 citations), Biochemistry (177 citations), Molecular Biology (1.8k citations) and Rheumatology (349 citations). Diego Martinelli has collaborated with scholars based in Italy, Germany and United Kingdom. Frequent co-authors include Carlo Dionisi‐Vici, Enrico Bertini, Vicente Rubio, Johannes Häberle, Rosalba Carrozzo, Martina Huemer, Marjorie Dixon, Alberto Burlina, Anupam Chakrapani and René Santer. Their work appears in journals such as Journal of Inherited Metabolic Disease, Orphanet Journal of Rare Diseases, Molecular Genetics and Metabolism, The American Journal of Human Genetics and Neurology.
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.