Bernard Mercier
Impact in
- Internal Medicine top 2%
- Venous Thromboembolism Diagnosis and Management
-
- Cystic Fibrosis Research Advances
- Neonatal Respiratory Health Research
- Tracheal and airway disorders
Papers in
-
- Cystic Fibrosis Research Advances 32
- Neonatal Respiratory Health Research 19
- Tracheal and airway disorders 5
- Genetics 21
- Congenital Ear and Nasal Anomalies 7
- Co-authors
- Claude Férec (54 shared papers)C. Verlingue (23 shared papers)Willy Lissens (4 shared papers)Christine Gaucher (6 shared papers)Claudine Mazurier (6 shared papers)I. Quéré (13 shared papers)Miguel Chillón (1 shared paper)M. Claustres (1 shared paper)
- Journals
- Human Mutation (9 papers)Human Genetics (7 papers)Thrombosis Research (6 papers)Nucleic Acids Research (4 papers)Journal of Medical Genetics (4 papers)
- Partner nations
- FranceSwitzerlandUnited States
In The Last Decade
Bernard Mercier
88 papers receiving 2.8k citations
Bernard Mercier's Hit Papers
Peers
Comparison fields: 5 of 122
- Internal Medicine 163
- Pulmonary and Respiratory Medicine 1.2k
- Hematology 382
- Genetics 293
- Genetics 454
Countries citing papers authored by Bernard Mercier
This map shows the geographic impact of Bernard Mercier'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 Bernard Mercier with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Bernard Mercier more than expected).
Fields of papers citing papers by Bernard Mercier
This network shows the impact of papers produced by Bernard Mercier. 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 Bernard Mercier. The network helps show where Bernard Mercier may publish in the future.
Co-authors
The 25 scholars most cited alongside Bernard Mercier, 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 90 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Mutations in the Cystic Fibrosis Gene in Patients with Congenital Absence of the Vas Deferens Hit paper breakdown → | 1995 | 678 |
| 2 | 1990 | 165 | |
| 3 | 1999 | 143 | |
| 4 | 1992 | 139 | |
| 5 | Is congenital bilateral absence of vas deferens a primary form of cystic fibrosis? Analyses of the CFTR gene in 67 patients. | 1995 | 114 |
| 6 | 1998 | 101 | |
| 7 | 2000 | 85 | |
| 8 | 1996 | 68 | |
| 9 | 2001 | 61 | |
| 10 | 1993 | 60 | |
| 11 | 1991 | 56 | |
| 12 | 2008 | 55 | |
| 13 | 2010 | 51 | |
| 14 | TP53 gene mutation profile in esophageal squamous cell carcinomas. | 1993 | 47 |
| 15 | 1997 | 46 | |
| 16 | 1999 | 45 | |
| 17 | 1997 | 44 | |
| 18 | 1996 | 43 | |
| 19 | 1997 | 40 | |
| 20 | 2010 | 36 |
About Bernard Mercier
Bernard Mercier is a scholar working on Pulmonary and Respiratory Medicine, Genetics, Molecular Biology, Hematology and Genetics, having authored 90 papers that have together received 3.0k indexed citations. Recurring topics across this work include Cystic Fibrosis Research Advances (32 papers), Neonatal Respiratory Health Research (19 papers), Blood Coagulation and Thrombosis Mechanisms (9 papers), Congenital Ear and Nasal Anomalies (7 papers), RNA Interference and Gene Delivery (6 papers), Hepatitis C virus research (5 papers), Tracheal and airway disorders (5 papers) and Advanced biosensing and bioanalysis techniques (5 papers). The work is most often cited by research in Internal Medicine (163 citations), Pulmonary and Respiratory Medicine (1.2k citations), Hematology (382 citations), Genetics (293 citations) and Genetics (454 citations). Bernard Mercier has collaborated with scholars based in France, Switzerland and United States. Frequent co-authors include Claude Férec, C. Verlingue, Willy Lissens, Christine Gaucher, Claudine Mazurier, I. Quéré, Miguel Chillón, M. Claustres, Lluís Bassas and Marie‐Catherine Romey. Their work appears in journals such as Human Mutation, Human Genetics, Thrombosis Research, Nucleic Acids Research and Journal of Medical 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.