Philippe Burlet
Impact in
- Genetics top 0.05%
- Neurogenetic and Muscular Disorders Research
- Molecular Biology top 1%
- RNA modifications and cancer
- RNA Research and Splicing
- Muscle Physiology and Disorders
- Cancer-related gene regulation
- Mitochondrial Function and Pathology
Papers in
-
- RNA modifications and cancer 12
- RNA Research and Splicing 8
- Mitochondrial Function and Pathology 5
- Genetics 14
- Neurogenetic and Muscular Disorders Research 14
- Co-authors
- Olivier Clermont (9 shared papers)Judith Melki (7 shared papers)Arnold Münnich (18 shared papers)Lydie Bürglen (4 shared papers)Louis Viollet (4 shared papers)Corinne Cruaud (3 shared papers)Denis Le Paslier (3 shared papers)Bernard Bénichou (2 shared papers)
- Journals
- Genomics (5 papers)Human Molecular Genetics (2 papers)Human Mutation (2 papers)Scientific Reports (1 paper)Nature Genetics (1 paper)
- Partner nations
- FranceUnited StatesPortugal
In The Last Decade
Philippe Burlet
23 papers receiving 4.8k citations
Hit Papers
Peers
Comparison fields: 5 of 81
- Genetics 4.1k
- Molecular Biology 4.1k
- Surgery 1.5k
- Neurology 331
- Clinical Biochemistry 127
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 24 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 | 3069 |
| 2 | Correlation between severity and SMN protein level in spinal muscular atrophy Hit paper breakdown → | 1997 | 876 |
| 3 | 1994 | 265 | |
| 4 | 1996 | 207 | |
| 5 | 2010 | 87 | |
| 6 | 2013 | 64 | |
| 7 | 2004 | 61 | |
| 8 | 1997 | 59 | |
| 9 | 2004 | 39 | |
| 10 | 2002 | 35 | |
| 11 | Use of genetic and physical mapping to locate the spinal muscular atrophy locus between two new highly polymorphic DNA markers. | 1994 | 35 |
| 12 | 2011 | 30 | |
| 13 | 1994 | 28 | |
| 14 | 2004 | 23 | |
| 15 | 2012 | 22 | |
| 16 | 2005 | 15 | |
| 17 | 1993 | 14 | |
| 18 | 2018 | 10 | |
| 19 | 2009 | 5 | |
| 20 | 2021 | 3 |
About Philippe Burlet
Philippe Burlet is a scholar working on Molecular Biology, Genetics, Pediatrics, Perinatology and Child Health, Clinical Biochemistry and Surgery, having authored 24 papers that have together received 5.0k indexed citations. Recurring topics across this work include Neurogenetic and Muscular Disorders Research (14 papers), RNA modifications and cancer (12 papers), RNA Research and Splicing (8 papers), Prenatal Screening and Diagnostics (5 papers), Mitochondrial Function and Pathology (5 papers), Metabolism and Genetic Disorders (4 papers), Congenital Anomalies and Fetal Surgery (3 papers) and Parvovirus B19 Infection Studies (2 papers). The work is most often cited by research in Genetics (4.1k citations), Molecular Biology (4.1k citations), Surgery (1.5k citations), Neurology (331 citations) and Clinical Biochemistry (127 citations). Philippe Burlet has collaborated with scholars based in France, United States and Portugal. Frequent co-authors include Olivier Clermont, Judith Melki, Arnold Münnich, Lydie Bürglen, Louis Viollet, Corinne Cruaud, Denis Le Paslier, Bernard Bénichou, Massimo Zeviani and Philippe Millasseau. Their work appears in journals such as Genomics, Human Molecular Genetics, Human Mutation, Scientific Reports and Nature 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.