M.‐P. Audrézet
Impact in
-
- Cystic Fibrosis Research Advances
- Neonatal Respiratory Health Research
- Tracheal and airway disorders
- Genetics top 10%
- Congenital Ear and Nasal Anomalies
- Genomics and Rare Diseases
Papers in
-
- Cystic Fibrosis Research Advances 18
- Neonatal Respiratory Health Research 11
- Tracheal and airway disorders 7
- Genetics 6
- Genomics and Rare Diseases 3
- Congenital Ear and Nasal Anomalies 3
- Genetic and Kidney Cyst Diseases 2
- Co-authors
- Claude Férec (18 shared papers)I. Quéré (5 shared papers)Bernard Mercier (8 shared papers)C. Verlingue (6 shared papers)Odile Raguénès (3 shared papers)H. Guillermit (2 shared papers)Cédric Le Maréchal (2 shared papers)D.N. Cooper (1 shared paper)
- Journals
- Journal of Cystic Fibrosis (8 papers)Human Mutation (3 papers)Human Genetics (2 papers)Journal of Medical Genetics (2 papers)Nature Genetics (1 paper)
- Partner nations
- FranceRussiaUnited Kingdom
In The Last Decade
M.‐P. Audrézet
26 papers receiving 679 citations
Peers
Comparison fields: 5 of 64
- Pulmonary and Respiratory Medicine 379
- Genetics 84
- Oncology 167
- Surgery 223
- Genetics 89
Countries citing papers authored by M.‐P. Audrézet
This map shows the geographic impact of M.‐P. Audrézet'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 M.‐P. Audrézet with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites M.‐P. Audrézet more than expected).
Fields of papers citing papers by M.‐P. Audrézet
This network shows the impact of papers produced by M.‐P. Audrézet. 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 M.‐P. Audrézet. The network helps show where M.‐P. Audrézet may publish in the future.
Co-authors
The 25 scholars most cited alongside M.‐P. Audrézet, 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 26 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1999 | 143 | |
| 2 | 1992 | 139 | |
| 3 | 2001 | 106 | |
| 4 | 2013 | 72 | |
| 5 | 1995 | 32 | |
| 6 | 2014 | 31 | |
| 7 | 2001 | 28 | |
| 8 | 1993 | 25 | |
| 9 | 2007 | 25 | |
| 10 | 1993 | 23 | |
| 11 | 2017 | 21 | |
| 12 | 2020 | 11 | |
| 13 | 1995 | 7 | |
| 14 | 2004 | 7 | |
| 15 | 1994 | 7 | |
| 16 | Autosomal dominant polycystic kidney disease in University Clinic of Nephrology and Haemodialysis of Cotonou: clinical and genetical findings. | 2012 | 5 |
| 17 | 2008 | 4 | |
| 18 | 2005 | 3 | |
| 19 | 2017 | 2 | |
| 20 | 2016 | 2 |
About M.‐P. Audrézet
M.‐P. Audrézet is a scholar working on Pulmonary and Respiratory Medicine, Genetics, Surgery, Genetics and Molecular Biology, having authored 26 papers that have together received 700 indexed citations. Recurring topics across this work include Cystic Fibrosis Research Advances (18 papers), Neonatal Respiratory Health Research (11 papers), Tracheal and airway disorders (7 papers), Genomics and Rare Diseases (3 papers), Congenital Ear and Nasal Anomalies (3 papers), Genetic and Kidney Cyst Diseases (2 papers), Pancreatitis Pathology and Treatment (2 papers) and Gastrointestinal disorders and treatments (2 papers). The work is most often cited by research in Pulmonary and Respiratory Medicine (379 citations), Genetics (84 citations), Oncology (167 citations), Surgery (223 citations) and Genetics (89 citations). M.‐P. Audrézet has collaborated with scholars based in France, Russia and United Kingdom. Frequent co-authors include Claude Férec, I. Quéré, Bernard Mercier, C. Verlingue, Odile Raguénès, H. Guillermit, Cédric Le Maréchal, D.N. Cooper, Emmanuelle Masson and Jian‐Min Chen. Their work appears in journals such as Journal of Cystic Fibrosis, Human Mutation, Human Genetics, Journal of Medical Genetics and Nature 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.