Patrick Edery
Impact in
- Genetics top 0.5%
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
- Molecular Biology top 2%
- Congenital heart defects research
- RNA modifications and cancer
Papers in
- Genetics 109
- Genomic variations and chromosomal abnormalities 56
- Genetics and Neurodevelopmental Disorders 42
- Genomics and Rare Diseases 26
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- Congenital heart defects research 17
- RNA modifications and cancer 15
- Co-authors
- Arnold Münnich (18 shared papers)Stanislas Lyonnet (20 shared papers)Anna Pelet (14 shared papers)Damien Sanlaville (45 shared papers)Audrey Labalme (37 shared papers)Lois M. Mulligan (5 shared papers)Claire Nihoul‐Feketé (7 shared papers)Jeanne Amiel (6 shared papers)
- Journals
- European Journal of Medical Genetics (17 papers)European Journal of Human Genetics (14 papers)Journal of Medical Genetics (13 papers)Clinical Genetics (11 papers)Genetics in Medicine (8 papers)
- Partner nations
- FranceUnited StatesUnited Kingdom
In The Last Decade
Patrick Edery
184 papers receiving 7.9k citations
Patrick Edery's Hit Papers
Peers
Comparison fields: 5 of 136
- Genetics 3.4k
- Molecular Biology 3.9k
- Developmental Neuroscience 186
- Sensory Systems 206
- Surgery 1.6k
Countries citing papers authored by Patrick Edery
This map shows the geographic impact of Patrick Edery'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 Patrick Edery with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Patrick Edery more than expected).
Fields of papers citing papers by Patrick Edery
This network shows the impact of papers produced by Patrick Edery. 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 Patrick Edery. The network helps show where Patrick Edery may publish in the future.
Co-authors
The 25 scholars most cited alongside Patrick Edery, 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 195 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Mutations of the RET proto-oncogene in Hirschsprung's disease Hit paper breakdown → | 1994 | 645 |
| 2 | Meta-analysis of SHANK Mutations in Autism Spectrum Disorders: A Gradient of Severity in Cognitive Impairments Hit paper breakdown → | 2014 | 488 |
| 3 | 1996 | 373 | |
| 4 | 2000 | 314 | |
| 5 | 1995 | 280 | |
| 6 | 2013 | 264 | |
| 7 | 2002 | 254 | |
| 8 | 2014 | 221 | |
| 9 | 2000 | 197 | |
| 10 | 1995 | 190 | |
| 11 | 2009 | 187 | |
| 12 | 2011 | 181 | |
| 13 | 2018 | 161 | |
| 14 | 2012 | 150 | |
| 15 | 2015 | 117 | |
| 16 | 2009 | 109 | |
| 17 | 2011 | 103 | |
| 18 | 2013 | 102 | |
| 19 | 2008 | 98 | |
| 20 | 2017 | 93 |
About Patrick Edery
Patrick Edery is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Surgery and Genetics, having authored 195 papers that have together received 8.4k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (56 papers), Genetics and Neurodevelopmental Disorders (42 papers), Genomics and Rare Diseases (26 papers), Congenital gastrointestinal and neural anomalies (21 papers), Congenital heart defects research (17 papers), RNA modifications and cancer (15 papers), Prenatal Screening and Diagnostics (12 papers) and Chromosomal and Genetic Variations (10 papers). The work is most often cited by research in Genetics (3.4k citations), Molecular Biology (3.9k citations), Developmental Neuroscience (186 citations), Sensory Systems (206 citations) and Surgery (1.6k citations). Patrick Edery has collaborated with scholars based in France, United States and United Kingdom. Frequent co-authors include Arnold Münnich, Stanislas Lyonnet, Anna Pelet, Damien Sanlaville, Audrey Labalme, Lois M. Mulligan, Claire Nihoul‐Feketé, Jeanne Amiel, Tania Attié‐Bitach and Charis Eng. Their work appears in journals such as European Journal of Medical Genetics, European Journal of Human Genetics, Journal of Medical Genetics, Clinical Genetics and Genetics in Medicine.
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.