P Burlet
Impact in
- Genetics top 1%
- Neurogenetic and Muscular Disorders Research
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
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- RNA modifications and cancer
- RNA Research and Splicing
- Muscle Physiology and Disorders
Papers in
- Genetics 14
- Neurogenetic and Muscular Disorders Research 13
- Genetic and Kidney Cyst Diseases 2
- Genetics and Neurodevelopmental Disorders 2
- Genomic variations and chromosomal abnormalities 2
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- RNA modifications and cancer 10
- RNA Research and Splicing 6
- Co-authors
- Arnold Münnich (17 shared papers)Judith Melki (9 shared papers)S. Lefebvre (5 shared papers)Olivier Clermont (4 shared papers)Sonia Abdelhak (5 shared papers)J Frézal (5 shared papers)Lydie Bürglen (4 shared papers)Mark G. Lathrop (1 shared paper)
In The Last Decade
P Burlet
19 papers receiving 783 citations
Peers
Comparison fields: 5 of 50
- Genetics 660
- Molecular Biology 654
- Surgery 264
- Genetics 135
- Pediatrics, Perinatology and Child Health 78
Countries citing papers authored by P Burlet
This map shows the geographic impact of P 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 P Burlet with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites P Burlet more than expected).
Fields of papers citing papers by P Burlet
This network shows the impact of papers produced by P 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 P Burlet. The network helps show where P Burlet may publish in the future.
Co-authors
The 25 scholars most cited alongside P 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 21 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1990 | 185 | |
| 2 | 1998 | 122 | |
| 3 | The gene encoding p44, a subunit of the transcription factor TFIIH, is involved in large-scale deletions associated with Werdnig-Hoffmann disease. | 1997 | 91 |
| 4 | 1996 | 79 | |
| 5 | 1999 | 77 | |
| 6 | 1996 | 56 | |
| 7 | 2006 | 53 | |
| 8 | 2008 | 30 | |
| 9 | Linkage analysis in spinal muscular atrophy, by six closely flanking markers on chromosome 5. | 1991 | 30 |
| 10 | 1992 | 26 | |
| 11 | 2009 | 22 | |
| 12 | Proximal spinal muscular atrophy (SMA) types II and III in the same sibship are not caused by different alleles at the SMA locus on 5q. | 1992 | 19 |
| 13 | 1990 | 8 | |
| 14 | 2011 | 4 | |
| 15 | 2006 | 4 | |
| 16 | 1991 | 4 | |
| 17 | 2005 | 3 | |
| 18 | 1995 | 1 | |
| 19 | 2005 | 1 | |
| 20 | 2008 | 1 |
About P Burlet
P Burlet is a scholar working on Genetics, Molecular Biology, Genetics, Surgery and Pediatrics, Perinatology and Child Health, having authored 21 papers that have together received 816 indexed citations. Recurring topics across this work include Neurogenetic and Muscular Disorders Research (13 papers), RNA modifications and cancer (10 papers), RNA Research and Splicing (6 papers), Congenital Anomalies and Fetal Surgery (5 papers), Prenatal Screening and Diagnostics (5 papers), Genetic and Kidney Cyst Diseases (2 papers), Genetics and Neurodevelopmental Disorders (2 papers) and Genomic variations and chromosomal abnormalities (2 papers). The work is most often cited by research in Genetics (660 citations), Molecular Biology (654 citations), Surgery (264 citations), Genetics (135 citations) and Pediatrics, Perinatology and Child Health (78 citations). P Burlet has collaborated with scholars based in France, Belgium and Italy. Frequent co-authors include Arnold Münnich, Judith Melki, S. Lefebvre, Olivier Clermont, Sonia Abdelhak, J Frézal, Lydie Bürglen, Mark G. Lathrop, Céline Huber and Solange Bertrandy. Their work appears in journals such as Reproductive BioMedicine Online, Human Molecular Genetics, Journal of Medical Genetics, Molecular Human Reproduction 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.