M.‐P. Audrézet
Impact in
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- Cystic Fibrosis Research Advances
- Neonatal Respiratory Health Research
- Tracheal and airway disorders
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- Congenital Ear and Nasal Anomalies
- Genomics and Rare Diseases
Papers in
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- Cystic Fibrosis Research Advances 18
- Neonatal Respiratory Health Research 10
- Tracheal and airway disorders 5
- Genetics 5
- Congenital Ear and Nasal Anomalies 3
- Genomics and Rare Diseases 2
- 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)Emmanuelle Masson (1 shared paper)
- Journals
- Journal of Cystic Fibrosis (8 papers)Human Mutation (3 papers)Human Genetics (2 papers)Journal of Medical Genetics (2 papers)Journal of Neurology (1 paper)
- Partner nations
- FranceRussiaSwitzerland
In The Last Decade
M.‐P. Audrézet
26 papers receiving 701 citations
Peers
Comparison fields: 5 of 58
- Pulmonary and Respiratory Medicine 380
- Genetics 71
- Surgery 211
- Oncology 116
- Clinical Biochemistry 18
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 | 147 | |
| 2 | 1992 | 146 | |
| 3 | 2001 | 110 | |
| 4 | 2013 | 72 | |
| 5 | 2014 | 36 | |
| 6 | 1995 | 34 | |
| 7 | 2001 | 30 | |
| 8 | 1993 | 26 | |
| 9 | 1993 | 26 | |
| 10 | 2007 | 25 | |
| 11 | 2017 | 21 | |
| 12 | 2020 | 11 | |
| 13 | 1994 | 7 | |
| 14 | 1995 | 7 | |
| 15 | 2004 | 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 | 2015 | 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 728 indexed citations. Recurring topics across this work include Cystic Fibrosis Research Advances (18 papers), Neonatal Respiratory Health Research (10 papers), Tracheal and airway disorders (5 papers), Congenital Ear and Nasal Anomalies (3 papers), Genomics and Rare Diseases (2 papers), Pancreatic and Hepatic Oncology Research (2 papers), Genetic and Kidney Cyst Diseases (2 papers) and Gastrointestinal disorders and treatments (2 papers). The work is most often cited by research in Pulmonary and Respiratory Medicine (380 citations), Genetics (71 citations), Surgery (211 citations), Oncology (116 citations) and Clinical Biochemistry (18 citations). M.‐P. Audrézet has collaborated with scholars based in France, Russia and Switzerland. Frequent co-authors include Claude Férec, I. Quéré, Bernard Mercier, C. Verlingue, Odile Raguénès, H. Guillermit, Cédric Le Maréchal, Emmanuelle Masson, D.N. Cooper and Claude Férec. Their work appears in journals such as Journal of Cystic Fibrosis, Human Mutation, Human Genetics, Journal of Medical Genetics and Journal of Neurology.
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.