Roberto Cerone
Impact in
- Clinical Biochemistry top 0.1%
- Metabolism and Genetic Disorders
- Rheumatology top 0.5%
- Folate and B Vitamins Research
Papers in
-
- Metabolism and Genetic Disorders 57
- Rheumatology 16
- Folate and B Vitamins Research 16
- Co-authors
- Harvey L. Levy (2 shared papers)S. Harvey Mudd (2 shared papers)Generoso Andria (3 shared papers)G. H. J. Boers (1 shared paper)Reed Edwin Pyeritz (1 shared paper)Bridget M Wilcken (1 shared paper)Flemming Skovby (1 shared paper)K. D. Pettigrew (1 shared paper)
- Journals
- Journal of Inherited Metabolic Disease (20 papers)Human Genetics (4 papers)Molecular Genetics and Metabolism (4 papers)Acta Paediatrica (3 papers)Clinical Genetics (2 papers)
- Partner nations
- ItalySwitzerlandUnited States
In The Last Decade
Roberto Cerone
77 papers receiving 3.1k citations
Roberto Cerone's Hit Papers
Peers
Comparison fields: 5 of 98
- Clinical Biochemistry 1.4k
- Rheumatology 1.2k
- Biochemistry 107
- Internal Medicine 30
- Hematology 100
Countries citing papers authored by Roberto Cerone
This map shows the geographic impact of Roberto Cerone'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 Roberto Cerone with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Roberto Cerone more than expected).
Fields of papers citing papers by Roberto Cerone
This network shows the impact of papers produced by Roberto Cerone. 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 Roberto Cerone. The network helps show where Roberto Cerone may publish in the future.
Co-authors
The 25 scholars most cited alongside Roberto Cerone, 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 78 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | The natural history of homocystinuria due to cystathionine beta-synthase deficiency. Hit paper breakdown → | 1985 | 1061 |
| 2 | 2016 | 231 | |
| 3 | The natural history of homocystinuria due to cystathionine β-synthase deficiency | 1985 | 147 |
| 4 | 2001 | 132 | |
| 5 | 2014 | 130 | |
| 6 | 2008 | 80 | |
| 7 | 2013 | 67 | |
| 8 | Early-onset combined methylmalonic aciduria and homocystinuria: neuroradiologic findings. | 2001 | 63 |
| 9 | 1990 | 61 | |
| 10 | 2001 | 61 | |
| 11 | 2019 | 58 | |
| 12 | 1990 | 57 | |
| 13 | 1998 | 55 | |
| 14 | 2019 | 55 | |
| 15 | 1991 | 54 | |
| 16 | 2000 | 53 | |
| 17 | 2010 | 53 | |
| 18 | 2001 | 52 | |
| 19 | 2006 | 50 | |
| 20 | 1982 | 48 |
About Roberto Cerone
Roberto Cerone is a scholar working on Clinical Biochemistry, Rheumatology, Nephrology, Biochemistry and Genetics, having authored 78 papers that have together received 3.3k indexed citations. Recurring topics across this work include Metabolism and Genetic Disorders (57 papers), Folate and B Vitamins Research (16 papers), Dialysis and Renal Disease Management (4 papers), Amino Acid Enzymes and Metabolism (2 papers), Mitochondrial Function and Pathology (2 papers), Ethics in Clinical Research (2 papers), Genomics and Rare Diseases (1 paper) and Maternal and Neonatal Healthcare (1 paper). The work is most often cited by research in Clinical Biochemistry (1.4k citations), Rheumatology (1.2k citations), Biochemistry (107 citations), Internal Medicine (30 citations) and Hematology (100 citations). Roberto Cerone has collaborated with scholars based in Italy, Switzerland and United States. Frequent co-authors include Harvey L. Levy, S. Harvey Mudd, Generoso Andria, G. H. J. Boers, Reed Edwin Pyeritz, Bridget M Wilcken, Flemming Skovby, K. D. Pettigrew, Irvin L. Bromberg and Giuseppe Minniti. Their work appears in journals such as Journal of Inherited Metabolic Disease, Human Genetics, Molecular Genetics and Metabolism, Acta Paediatrica 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.