C. Verlingue
Impact in
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- Cystic Fibrosis Research Advances
- Neonatal Respiratory Health Research
- Tracheal and airway disorders
- Genetics top 5%
- Congenital Ear and Nasal Anomalies
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
Papers in
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- Cystic Fibrosis Research Advances 28
- Neonatal Respiratory Health Research 16
- Tracheal and airway disorders 4
- Genetics 6
- Congenital Ear and Nasal Anomalies 5
- Genomics and Rare Diseases 4
- Genetics and Neurodevelopmental Disorders 2
- Digestive system and related health 1
- Co-authors
- Bernard Mercier (23 shared papers)Claude Férec (24 shared papers)Willy Lissens (2 shared papers)Teresa Casals (1 shared paper)Lluís Bassas (1 shared paper)Marie‐Catherine Romey (1 shared paper)S. Silber (1 shared paper)M. Claustres (1 shared paper)
In The Last Decade
C. Verlingue
30 papers receiving 1.4k citations
C. Verlingue's Hit Papers
Peers
Comparison fields: 5 of 70
- Pulmonary and Respiratory Medicine 1.1k
- Genetics 180
- Reproductive Medicine 129
- Genetics 234
- Pediatrics, Perinatology and Child Health 140
Countries citing papers authored by C. Verlingue
This map shows the geographic impact of C. Verlingue'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 C. Verlingue with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites C. Verlingue more than expected).
Fields of papers citing papers by C. Verlingue
This network shows the impact of papers produced by C. Verlingue. 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 C. Verlingue. The network helps show where C. Verlingue may publish in the future.
Co-authors
The 25 scholars most cited alongside C. Verlingue, 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 31 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 | 751 |
| 2 | 1992 | 146 | |
| 3 | Is congenital bilateral absence of vas deferens a primary form of cystic fibrosis? Analyses of the CFTR gene in 67 patients. | 1995 | 121 |
| 4 | 2000 | 88 | |
| 5 | 1993 | 60 | |
| 6 | 1995 | 34 | |
| 7 | 2001 | 30 | |
| 8 | 1996 | 30 | |
| 9 | 1994 | 30 | |
| 10 | 1993 | 26 | |
| 11 | 1998 | 26 | |
| 12 | 1993 | 26 | |
| 13 | 1994 | 24 | |
| 14 | 1998 | 19 | |
| 15 | 1993 | 16 | |
| 16 | 1988 | 8 | |
| 17 | 1994 | 8 | |
| 18 | Clinical features of cystic fibrosis patients with rare genotypes in Saguenay Lac-Saint-Jean (Quebec, Canada). | 1997 | 8 |
| 19 | 1994 | 7 | |
| 20 | 1995 | 7 |
About C. Verlingue
C. Verlingue is a scholar working on Pulmonary and Respiratory Medicine, Genetics, Genetics, Molecular Biology and Immunology, having authored 31 papers that have together received 1.5k indexed citations. Recurring topics across this work include Cystic Fibrosis Research Advances (28 papers), Neonatal Respiratory Health Research (16 papers), Congenital Ear and Nasal Anomalies (5 papers), Genomics and Rare Diseases (4 papers), Tracheal and airway disorders (4 papers), Genetics and Neurodevelopmental Disorders (2 papers), Advanced biosensing and bioanalysis techniques (2 papers) and Digestive system and related health (1 paper). The work is most often cited by research in Pulmonary and Respiratory Medicine (1.1k citations), Genetics (180 citations), Reproductive Medicine (129 citations), Genetics (234 citations) and Pediatrics, Perinatology and Child Health (140 citations). C. Verlingue has collaborated with scholars based in France, Canada and Italy. Frequent co-authors include Bernard Mercier, Claude Férec, Willy Lissens, Teresa Casals, Lluís Bassas, Marie‐Catherine Romey, S. Silber, M. Claustres, Miguel Chillón and I. Quéré. Their work appears in journals such as Human Genetics, Human Mutation, Clinical Genetics, Human Molecular Genetics 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.