Philippe Burlet
Impact in
- Genetics top 0.1%
- Neurogenetic and Muscular Disorders Research
- Genomics and Rare Diseases
-
- Prenatal Screening and Diagnostics
Papers in
- Genetics 24
- Neurogenetic and Muscular Disorders Research 24
- Genomics and Rare Diseases 4
-
- Prenatal Screening and Diagnostics 17
- Co-authors
- Arnold Münnich (41 shared papers)Suzie Lefebvre (17 shared papers)Judith Melki (19 shared papers)Olivier Clermont (15 shared papers)Lydie Bürglen (9 shared papers)Louis Viollet (8 shared papers)Corinne Cruaud (4 shared papers)Jean Frézal (6 shared papers)
- Journals
- Human Molecular Genetics (5 papers)Genomics (5 papers)Reproductive BioMedicine Online (4 papers)Journal of Medical Genetics (3 papers)The Lancet (2 papers)
- Partner nations
- FranceUnited StatesUnited Kingdom
In The Last Decade
Philippe Burlet
44 papers receiving 6.2k citations
Philippe Burlet's Hit Papers
Peers
Comparison fields: 5 of 88
- Genetics 4.5k
- Pediatrics, Perinatology and Child Health 365
- Neurology 334
- Molecular Biology 1.2k
- Cellular and Molecular Neuroscience 252
Countries citing papers authored by Philippe Burlet
This map shows the geographic impact of Philippe Burlet'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 Burlet with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Philippe Burlet more than expected).
Fields of papers citing papers by Philippe Burlet
This network shows the impact of papers produced by Philippe Burlet. 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 Burlet. The network helps show where Philippe Burlet may publish in the future.
Co-authors
The 25 scholars most cited alongside Philippe Burlet, 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 49 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Identification and characterization of a spinal muscular atrophy-determining gene Hit paper breakdown → | 1995 | 3338 |
| 2 | Correlation between severity and SMN protein level in spinal muscular atrophy Hit paper breakdown → | 1997 | 934 |
| 3 | 1994 | 281 | |
| 4 | 1996 | 222 | |
| 5 | 1990 | 200 | |
| 6 | 1998 | 132 | |
| 7 | 2005 | 114 | |
| 8 | 2010 | 97 | |
| 9 | The gene encoding p44, a subunit of the transcription factor TFIIH, is involved in large-scale deletions associated with Werdnig-Hoffmann disease. | 1997 | 89 |
| 10 | 1996 | 78 | |
| 11 | 1999 | 75 | |
| 12 | 1996 | 71 | |
| 13 | 2013 | 70 | |
| 14 | 1995 | 67 | |
| 15 | 2004 | 67 | |
| 16 | 1997 | 58 | |
| 17 | 2006 | 55 | |
| 18 | 2008 | 44 | |
| 19 | 2004 | 42 | |
| 20 | 2002 | 41 |
About Philippe Burlet
Philippe Burlet is a scholar working on Genetics, Pediatrics, Perinatology and Child Health, Cellular and Molecular Neuroscience, Genetics and Public Health, Environmental and Occupational Health, having authored 49 papers that have together received 6.4k indexed citations. Recurring topics across this work include Neurogenetic and Muscular Disorders Research (24 papers), Prenatal Screening and Diagnostics (17 papers), Mitochondrial Function and Pathology (7 papers), Genomics and Rare Diseases (4 papers), Reproductive Biology and Fertility (3 papers), Genetic Neurodegenerative Diseases (3 papers), Hereditary Neurological Disorders (2 papers) and Medical and Health Sciences Research (2 papers). The work is most often cited by research in Genetics (4.5k citations), Pediatrics, Perinatology and Child Health (365 citations), Neurology (334 citations), Molecular Biology (1.2k citations) and Cellular and Molecular Neuroscience (252 citations). Philippe Burlet has collaborated with scholars based in France, United States and United Kingdom. Frequent co-authors include Arnold Münnich, Suzie Lefebvre, Judith Melki, Olivier Clermont, Lydie Bürglen, Louis Viollet, Corinne Cruaud, Jean Frézal, Jean Weissenbach and Daniel Cohen. Their work appears in journals such as Human Molecular Genetics, Genomics, Reproductive BioMedicine Online, Journal of Medical Genetics and The Lancet.
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.