Philippe Vago
- Sensory Systems top 2%
- Hearing, Cochlea, Tinnitus, Genetics 15
- Genetics top 10%
- Genomic variations and chromosomal abnormalities 24
- Neurology top 10%
- Otorhinolaryngology top 10%
- Genetics top 10%
- Genomic variations and chromosomal abnormalities 24
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- Prenatal Screening and Diagnostics 15
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- Chromosomal and Genetic Variations 10
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- Telomeres, Telomerase, and Senescence 6
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- Congenital heart defects research 5
- Genomics and Chromatin Dynamics 5
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- Hearing Loss and Rehabilitation 5
- Co-authors
- Andréï TchirkovMarc LenoirLauren VéronèseCarole GoumyLaëtitia GouasRémy PujolPierre VerrelleB. Irthum
- Cited by
- Sensory SystemsGeneticsNeurology
- Journals
- European Journal of Medical Genetics (4 papers)Prenatal Diagnosis (3 papers)Birth Defects Research Part A Clinical and Molecular Teratology (3 papers)
- Partner nations
- FranceHungaryUnited States
In The Last Decade
Philippe Vago
84 papers receiving 1.1k citations
Peers
Comparison fields: 5 of 103
- Sensory Systems 262
- Genetics 297
- Neurology 81
- Otorhinolaryngology 42
- Genetics 101
Countries citing papers authored by Philippe Vago
This map shows the geographic impact of Philippe Vago'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 Philippe Vago with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Philippe Vago more than expected).
Fields of papers citing papers by Philippe Vago
This network shows the impact of papers produced by Philippe Vago. 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 Philippe Vago. The network helps show where Philippe Vago may publish in the future.
Co-authorship network
The 25 scholars most cited alongside Philippe Vago, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 2022 | 5 | |
| 2 | 2014 | 19 | |
| 3 | 2014 | 2 | |
| 4 | 2013 | 31 | |
| 5 | 2013 | 0 | |
| 6 | 2010 | 6 | |
| 7 | 2010 | 0 | |
| 8 | 2010 | 2 | |
| 9 | 2010 | 38 | |
| 10 | 2009 | 17 | |
| 11 | 2008 | 10 | |
| 12 | 2004 | 8 | |
| 13 | 2003 | 31 | |
| 14 | Du caryotype « monocouleur » au caryotype « multicouleur » : applications de la M-Fish en hématologie et en oncologie | 2002 | 1 |
| 15 | 2002 | 67 | |
| 16 | [Regional epidemiologic examination of dental health status]. | 2000 | 1 |
| 17 | 1998 | 8 | |
| 18 | Distribution of actin and tubulin in outer hair cells isolated from developing rat cochlea: a quantitative study. | 1996 | 7 |
| 19 | 1993 | 8 | |
| 20 | Chronobiologie de l'inflammation. | 1987 | 5 |
About Philippe Vago
Philippe Vago is a scholar working on Sensory Systems, Periodontics, Genetics, Genetics and Pediatrics, Perinatology and Child Health, having authored 89 papers that have together received 1.2k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (24 papers), Hearing, Cochlea, Tinnitus, Genetics (15 papers), Prenatal Screening and Diagnostics (15 papers), Chromosomal and Genetic Variations (10 papers), Telomeres, Telomerase, and Senescence (6 papers), Congenital heart defects research (5 papers), Genomics and Chromatin Dynamics (5 papers) and Hearing Loss and Rehabilitation (5 papers). The work is most often cited by research in Sensory Systems (262 citations), Genetics (297 citations), Neurology (81 citations), Otorhinolaryngology (42 citations) and Genetics (101 citations). Philippe Vago has collaborated with scholars based in France, Hungary and United States. Frequent co-authors include Andréï Tchirkov, Marc Lenoir, Lauren Véronèse, Carole Goumy, Laëtitia Gouas, Rémy Pujol, Pierre Verrelle, B. Irthum, Christine Francannet and T. Khalil. Their work appears in journals such as European Journal of Medical Genetics, Prenatal Diagnosis, Birth Defects Research Part A Clinical and Molecular Teratology, Human Reproduction and Oncotarget.
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.