Philippe Parent
Impact in
- Genetics top 10%
- Genomic variations and chromosomal abnormalities
- Genetic and Kidney Cyst Diseases
- Genomics and Rare Diseases
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- Cystic Fibrosis Research Advances
- Neonatal Respiratory Health Research
- Tracheal and airway disorders
Papers in
- Genetics 15
- Genomic variations and chromosomal abnormalities 9
- Congenital Ear and Nasal Anomalies 2
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- Cystic Fibrosis Research Advances 9
- Neonatal Respiratory Health Research 3
- Co-authors
- Marc De Braekeleer (11 shared papers)Claude Férec (12 shared papers)Nathalie Douet‐Guilbert (6 shared papers)Fréderic Morel (7 shared papers)I. Duguépéroux (8 shared papers)Virginie Scotet (8 shared papers)Marie‐Pierre Audrézet (8 shared papers)Bernard Mercier (4 shared papers)
- Journals
- Journal of Cystic Fibrosis (3 papers)Human Genetics (2 papers)Pediatric Surgery International (2 papers)Andrologia (1 paper)Human Molecular Genetics (1 paper)
- Partner nations
- FranceUnited KingdomItaly
In The Last Decade
Philippe Parent
29 papers receiving 486 citations
Peers
Comparison fields: 5 of 50
- Genetics 195
- Pulmonary and Respiratory Medicine 203
- Pediatrics, Perinatology and Child Health 87
- Genetics 41
- Neurology 23
Countries citing papers authored by Philippe Parent
This map shows the geographic impact of Philippe Parent'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 Parent with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Philippe Parent more than expected).
Fields of papers citing papers by Philippe Parent
This network shows the impact of papers produced by Philippe Parent. 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 Parent. The network helps show where Philippe Parent may publish in the future.
Co-authors
The 25 scholars most cited alongside Philippe Parent, 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 30 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2000 | 88 | |
| 2 | 2007 | 54 | |
| 3 | 2005 | 46 | |
| 4 | 2008 | 41 | |
| 5 | 1995 | 34 | |
| 6 | 1997 | 33 | |
| 7 | 2001 | 30 | |
| 8 | 2014 | 29 | |
| 9 | 2002 | 24 | |
| 10 | 2013 | 20 | |
| 11 | 2008 | 19 | |
| 12 | 1995 | 18 | |
| 13 | 2004 | 15 | |
| 14 | 2016 | 14 | |
| 15 | 2014 | 12 | |
| 16 | 2016 | 10 | |
| 17 | 2011 | 8 | |
| 18 | 2010 | 8 | |
| 19 | 1988 | 8 | |
| 20 | 1996 | 7 |
About Philippe Parent
Philippe Parent is a scholar working on Genetics, Pulmonary and Respiratory Medicine, Molecular Biology, Surgery and Plant Science, having authored 30 papers that have together received 546 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (9 papers), Cystic Fibrosis Research Advances (9 papers), Chromosomal and Genetic Variations (4 papers), Genomics and Chromatin Dynamics (3 papers), Prenatal Screening and Diagnostics (3 papers), Neonatal Respiratory Health Research (3 papers), Congenital heart defects research (2 papers) and Congenital Ear and Nasal Anomalies (2 papers). The work is most often cited by research in Genetics (195 citations), Pulmonary and Respiratory Medicine (203 citations), Pediatrics, Perinatology and Child Health (87 citations), Genetics (41 citations) and Neurology (23 citations). Philippe Parent has collaborated with scholars based in France, United Kingdom and Italy. Frequent co-authors include Marc De Braekeleer, Claude Férec, Nathalie Douet‐Guilbert, Fréderic Morel, I. Duguépéroux, Virginie Scotet, Marie‐Pierre Audrézet, Bernard Mercier, G. Rault and C. Verlingue. Their work appears in journals such as Journal of Cystic Fibrosis, Human Genetics, Pediatric Surgery International, Andrologia and Human Molecular 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.