Alberto Ponzone
Impact in
- Clinical Biochemistry top 0.5%
- Metabolism and Genetic Disorders
- Physiology top 2%
- Lysosomal Storage Disorders Research
Papers in
-
- Metabolism and Genetic Disorders 22
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- Biochemical and Molecular Research 5
- Mitochondrial Function and Pathology 3
- Co-authors
- Marco Spada (21 shared papers)Severo Pagliardini (3 shared papers)Makiko Yasuda (1 shared paper)Robert J. Desnick (1 shared paper)Hitoshi Sakuraba (1 shared paper)Geetha Thiagarajan (1 shared paper)Turgut Tükel (1 shared paper)Irma Dianzani (9 shared papers)
- Journals
- Human Mutation (4 papers)European Journal of Paediatric Neurology (3 papers)Molecular Genetics and Metabolism (2 papers)PEDIATRICS (2 papers)The American Journal of Human Genetics (2 papers)
- Partner nations
- ItalySwitzerlandAustralia
In The Last Decade
Alberto Ponzone
33 papers receiving 1.7k citations
Alberto Ponzone's Hit Papers
Peers
Comparison fields: 5 of 90
- Clinical Biochemistry 631
- Physiology 850
- Rheumatology 455
- Biochemistry 210
- Pediatrics, Perinatology and Child Health 345
Countries citing papers authored by Alberto Ponzone
This map shows the geographic impact of Alberto 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 Alberto Ponzone with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Alberto Ponzone more than expected).
Fields of papers citing papers by Alberto Ponzone
This network shows the impact of papers produced by Alberto 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 Alberto Ponzone. The network helps show where Alberto Ponzone may publish in the future.
Co-authors
The 25 scholars most cited alongside Alberto 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 34 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | High Incidence of Later-Onset Fabry Disease Revealed by Newborn Screening* Hit paper breakdown → | 2006 | 713 |
| 2 | 1998 | 278 | |
| 3 | 2002 | 185 | |
| 4 | 2008 | 81 | |
| 5 | Molecular genetics of cystinuria: identification of four new mutations and seven polymorphisms, and evidence for genetic heterogeneity. | 1995 | 72 |
| 6 | 2003 | 59 | |
| 7 | 2007 | 56 | |
| 8 | 2009 | 36 | |
| 9 | 1998 | 34 | |
| 10 | Tetrahydrobiopterin and inherited hyperphenylalaninemias. | 1996 | 32 |
| 11 | 1997 | 21 | |
| 12 | 1986 | 21 | |
| 13 | 2001 | 20 | |
| 14 | 2015 | 18 | |
| 15 | 2008 | 14 | |
| 16 | 2009 | 12 | |
| 17 | 2010 | 11 | |
| 18 | 2012 | 11 | |
| 19 | 2017 | 11 | |
| 20 | 2016 | 9 |
About Alberto Ponzone
Alberto Ponzone is a scholar working on Clinical Biochemistry, Molecular Biology, Pediatrics, Perinatology and Child Health, Rheumatology and Cell Biology, having authored 34 papers that have together received 1.8k indexed citations. Recurring topics across this work include Metabolism and Genetic Disorders (22 papers), Folate and B Vitamins Research (9 papers), Neonatal Health and Biochemistry (8 papers), Biochemical and Molecular Research (5 papers), Amino Acid Enzymes and Metabolism (4 papers), Muscle metabolism and nutrition (3 papers), Mitochondrial Function and Pathology (3 papers) and Infant Health and Development (2 papers). The work is most often cited by research in Clinical Biochemistry (631 citations), Physiology (850 citations), Rheumatology (455 citations), Biochemistry (210 citations) and Pediatrics, Perinatology and Child Health (345 citations). Alberto Ponzone has collaborated with scholars based in Italy, Switzerland and Australia. Frequent co-authors include Marco Spada, Severo Pagliardini, Makiko Yasuda, Robert J. Desnick, Hitoshi Sakuraba, Geetha Thiagarajan, Turgut Tükel, Irma Dianzani, Francesco Porta and Manuela Ceccarelli. Their work appears in journals such as Human Mutation, European Journal of Paediatric Neurology, Molecular Genetics and Metabolism, PEDIATRICS and The American Journal of Human 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.