Luisa Bonafé
Impact in
- Clinical Biochemistry top 0.5%
- Metabolism and Genetic Disorders
- Genetics top 1%
- Connective tissue disorders research
- Neurogenetic and Muscular Disorders Research
Papers in
-
- Mitochondrial Function and Pathology 13
- RNA modifications and cancer 7
- Biochemical and Molecular Research 6
- Genetics 43
- Connective tissue disorders research 36
- Co-authors
- Andrea Superti‐Furga (44 shared papers)Nenad Blau (9 shared papers)Beat Thöny (6 shared papers)Sheila Unger (26 shared papers)Diana Ballhausen (17 shared papers)Belinda Campos‐Xavier (20 shared papers)Andreas Zankl (10 shared papers)Ravi Savarirayan (5 shared papers)
- Journals
- Molecular Genetics and Metabolism (6 papers)Journal of Inherited Metabolic Disease (5 papers)The American Journal of Human Genetics (5 papers)European Journal of Pediatrics (4 papers)Clinical Genetics (4 papers)
- Partner nations
- SwitzerlandGermanyUnited States
In The Last Decade
Luisa Bonafé
96 papers receiving 3.6k citations
Luisa Bonafé's Hit Papers
Peers
Comparison fields: 5 of 118
- Clinical Biochemistry 683
- Genetics 1.3k
- Rheumatology 437
- Molecular Biology 1.6k
- Cell Biology 351
Countries citing papers authored by Luisa Bonafé
This map shows the geographic impact of Luisa Bonafé'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 Luisa Bonafé with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Luisa Bonafé more than expected).
Fields of papers citing papers by Luisa Bonafé
This network shows the impact of papers produced by Luisa Bonafé. 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 Luisa Bonafé. The network helps show where Luisa Bonafé may publish in the future.
Co-authors
The 25 scholars most cited alongside Luisa Bonafé, 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 98 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Nosology and classification of genetic skeletal disorders: 2015 revision Hit paper breakdown → | 2015 | 372 |
| 2 | 2001 | 159 | |
| 3 | 2004 | 132 | |
| 4 | 2010 | 132 | |
| 5 | 2001 | 132 | |
| 6 | 2003 | 125 | |
| 7 | 2010 | 106 | |
| 8 | 1998 | 93 | |
| 9 | 2009 | 85 | |
| 10 | 2003 | 85 | |
| 11 | 2011 | 81 | |
| 12 | 2001 | 80 | |
| 13 | 2001 | 72 | |
| 14 | 2000 | 68 | |
| 15 | 2011 | 67 | |
| 16 | 2002 | 61 | |
| 17 | 2015 | 61 | |
| 18 | 2008 | 60 | |
| 19 | 2015 | 55 | |
| 20 | 2005 | 55 |
About Luisa Bonafé
Luisa Bonafé is a scholar working on Molecular Biology, Genetics, Clinical Biochemistry, Rheumatology and Cancer Research, having authored 98 papers that have together received 3.6k indexed citations. Recurring topics across this work include Connective tissue disorders research (36 papers), Metabolism and Genetic Disorders (21 papers), Mitochondrial Function and Pathology (13 papers), RNA modifications and cancer (7 papers), Bone and Dental Protein Studies (6 papers), Biochemical and Molecular Research (6 papers), Protease and Inhibitor Mechanisms (6 papers) and Neonatal Health and Biochemistry (5 papers). The work is most often cited by research in Clinical Biochemistry (683 citations), Genetics (1.3k citations), Rheumatology (437 citations), Molecular Biology (1.6k citations) and Cell Biology (351 citations). Luisa Bonafé has collaborated with scholars based in Switzerland, Germany and United States. Frequent co-authors include Andrea Superti‐Furga, Nenad Blau, Beat Thöny, Sheila Unger, Diana Ballhausen, Belinda Campos‐Xavier, Andreas Zankl, Ravi Savarirayan, Gen Nishimura and Jürgen W. Spranger. Their work appears in journals such as Molecular Genetics and Metabolism, Journal of Inherited Metabolic Disease, The American Journal of Human Genetics, European Journal of Pediatrics 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.