Generoso Andria
Impact in
- Clinical Biochemistry top 0.1%
- Metabolism and Genetic Disorders
- Rheumatology top 0.2%
- Folate and B Vitamins Research
- Glycogen Storage Diseases and Myoclonus
Papers in
-
- Metabolism and Genetic Disorders 44
- Rheumatology 77
- Folate and B Vitamins Research 36
- Glycogen Storage Diseases and Myoclonus 32
- Co-authors
- Giancarlo ParentiAndrea BallabioGianfranco SebastioMaria Pia SperandeoR. CeroneS. Harvey MuddReed E. PyeritzFlemming Skovby
- Journals
- Journal of Inherited Metabolic Disease (14 papers)Clinical Genetics (8 papers)Journal of Medical Genetics (7 papers)European Journal of Pediatrics (7 papers)The American Journal of Human Genetics (6 papers)
- Partner nations
- ItalyUnited StatesUnited Kingdom
In The Last Decade
Generoso Andria
212 papers receiving 8.2k citations
Hit Papers
Peers
Comparison fields: 5 of 128
- Clinical Biochemistry 1.3k
- Rheumatology 2.6k
- Biochemistry 999
- Physiology 2.3k
- Genetics 1.7k
Countries citing papers authored by Generoso Andria
This map shows the geographic impact of Generoso Andria'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 Generoso Andria with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Generoso Andria more than expected).
Fields of papers citing papers by Generoso Andria
This network shows the impact of papers produced by Generoso Andria. 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 Generoso Andria. The network helps show where Generoso Andria may publish in the future.
Co-authors
The 25 scholars most cited alongside Generoso Andria, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 2020 | 5 | |
| 2 | 2018 | 4 | |
| 3 | 2017 | 5 | |
| 4 | 2014 | 5 | |
| 5 | 2012 | 4 | |
| 6 | 2011 | 30 | |
| 7 | 2011 | 75 | |
| 8 | 2006 | 103 | |
| 9 | 2004 | 31 | |
| 10 | [Anderson-Fabry's disease: diagnostic problems, therapeutic relevance, and clinical experience in the treatment of the disease with enzyme replacement therapy in nephropathic patients]. | 2003 | 3 |
| 11 | 2002 | 13 | |
| 12 | 2002 | 17 | |
| 13 | 2001 | 108 | |
| 14 | 1998 | 42 | |
| 15 | Low circulating vitamin B12, B6 and folate leading to marked hyperhomocysteinemia - associations with premature cerebral and peripheral vascular disease | 1998 | 1 |
| 16 | 1995 | 233 | |
| 17 | 1990 | 40 | |
| 18 | 1988 | 5 | |
| 19 | 1987 | 115 | |
| 20 | Dégénérescence maculaire juvénile chez une famille atteinte de cystinurie. | 1980 | 1 |
About Generoso Andria
Generoso Andria is a scholar working on Clinical Biochemistry, Rheumatology, Biochemistry, Physiology and Genetics, having authored 215 papers that have together received 8.5k indexed citations. Recurring topics across this work include Lysosomal Storage Disorders Research (45 papers), Metabolism and Genetic Disorders (44 papers), Folate and B Vitamins Research (36 papers), Glycogen Storage Diseases and Myoclonus (32 papers), Amino Acid Enzymes and Metabolism (26 papers), Carbohydrate Chemistry and Synthesis (17 papers), Genetics and Neurodevelopmental Disorders (13 papers) and Genomic variations and chromosomal abnormalities (13 papers). The work is most often cited by research in Clinical Biochemistry (1.3k citations), Rheumatology (2.6k citations), Biochemistry (999 citations), Physiology (2.3k citations) and Genetics (1.7k citations). Generoso Andria has collaborated with scholars based in Italy, United States and United Kingdom. Frequent co-authors include Giancarlo Parenti, Andrea Ballabio, Gianfranco Sebastio, Maria Pia Sperandeo, R. Cerone, S. Harvey Mudd, Reed E. Pyeritz, Flemming Skovby, Irvin L. Bromberg and Bridget Wilcken. Their work appears in journals such as Journal of Inherited Metabolic Disease, Clinical Genetics, Journal of Medical Genetics, European Journal of 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.