A Ponzone
Impact in
- Clinical Biochemistry top 0.5%
- Metabolism and Genetic Disorders
- Biochemistry top 5%
- Amino Acid Enzymes and Metabolism
Papers in
-
- Metabolism and Genetic Disorders 33
-
- Biochemical and Molecular Research 16
- Co-authors
- Richard G.H. Cotton (10 shared papers)Irma Dianzani (16 shared papers)Ornella Guardamagna (14 shared papers)Marco Spada (15 shared papers)A. Niederwieser (4 shared papers)H.‐Ch. Curtius (3 shared papers)Nenad Blau (12 shared papers)Clara Camaschella (7 shared papers)
- Journals
- Journal of Inherited Metabolic Disease (10 papers)Acta Paediatrica (3 papers)Neurology (2 papers)Journal of Medical Genetics (2 papers)Acta Haematologica (2 papers)
- Partner nations
- ItalySwitzerlandAustralia
In The Last Decade
A Ponzone
55 papers receiving 710 citations
Peers
Comparison fields: 5 of 74
- Clinical Biochemistry 468
- Biochemistry 132
- Rheumatology 127
- Pediatrics, Perinatology and Child Health 160
- Molecular Biology 366
Countries citing papers authored by A Ponzone
This map shows the geographic impact of A Ponzone'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 A Ponzone with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites A Ponzone more than expected).
Fields of papers citing papers by A Ponzone
This network shows the impact of papers produced by A Ponzone. 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 A Ponzone. The network helps show where A Ponzone may publish in the future.
Co-authors
The 25 scholars most cited alongside A Ponzone, 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 56 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Localization, by linkage analysis, of the cystinuria type III gene to chromosome 19q13.1. | 1997 | 68 |
| 2 | 2003 | 60 | |
| 3 | 1993 | 55 | |
| 4 | 2010 | 48 | |
| 5 | 1985 | 42 | |
| 6 | 1985 | 38 | |
| 7 | 1993 | 33 | |
| 8 | 1993 | 31 | |
| 9 | Screening for mutations in the phenylalanine hydroxylase gene from Italian patients with phenylketonuria by using the chemical cleavage method: a new splice mutation. | 1991 | 26 |
| 10 | 1993 | 23 | |
| 11 | 1991 | 21 | |
| 12 | 1996 | 21 | |
| 13 | 2009 | 20 | |
| 14 | 1994 | 19 | |
| 15 | 1993 | 19 | |
| 16 | 1986 | 18 | |
| 17 | 2004 | 15 | |
| 18 | 1993 | 12 | |
| 19 | [Neonatal hyperbilirubinemia and response of lymphocytes to phytohemagglutinin]. | 1968 | 12 |
| 20 | 1994 | 11 |
About A Ponzone
A Ponzone is a scholar working on Clinical Biochemistry, Molecular Biology, Genetics, Pediatrics, Perinatology and Child Health and Rheumatology, having authored 56 papers that have together received 729 indexed citations. Recurring topics across this work include Metabolism and Genetic Disorders (33 papers), Biochemical and Molecular Research (16 papers), Neonatal Health and Biochemistry (10 papers), Amino Acid Enzymes and Metabolism (9 papers), Folate and B Vitamins Research (7 papers), Blood disorders and treatments (5 papers), Digestive system and related health (4 papers) and Animal Genetics and Reproduction (3 papers). The work is most often cited by research in Clinical Biochemistry (468 citations), Biochemistry (132 citations), Rheumatology (127 citations), Pediatrics, Perinatology and Child Health (160 citations) and Molecular Biology (366 citations). A Ponzone has collaborated with scholars based in Italy, Switzerland and Australia. Frequent co-authors include Richard G.H. Cotton, Irma Dianzani, Ornella Guardamagna, Marco Spada, A. Niederwieser, H.‐Ch. Curtius, Nenad Blau, Clara Camaschella, Riccardo Ponzone and L. Kierat. Their work appears in journals such as Journal of Inherited Metabolic Disease, Acta Paediatrica, Neurology, Journal of Medical Genetics and Acta Haematologica.
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.