P Burlet

1.5k total citations
21 papers, 816 citations indexed

About

P Burlet is a scholar working on Genetics, Molecular Biology and Genetics. According to data from OpenAlex, P Burlet has authored 21 papers receiving a total of 816 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Genetics, 12 papers in Molecular Biology and 6 papers in Genetics. Recurrent topics in P Burlet's work include Neurogenetic and Muscular Disorders Research (13 papers), RNA modifications and cancer (10 papers) and RNA Research and Splicing (6 papers). P Burlet is often cited by papers focused on Neurogenetic and Muscular Disorders Research (13 papers), RNA modifications and cancer (10 papers) and RNA Research and Splicing (6 papers). P Burlet collaborates with scholars based in France, Belgium and Italy. P Burlet's co-authors include Arnold Münnich, Judith Melki, S. Lefebvre, Olivier Clermont, Sonia Abdelhak, J Frézal, Lydie Bürglen, Mark G. Lathrop, Solange Bertrandy and Céline Huber and has published in prestigious journals such as The Lancet, Nucleic Acids Research and Journal of Clinical Investigation.

In The Last Decade

P Burlet

19 papers receiving 783 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
P Burlet France 12 660 654 264 135 78 21 816
David Schorling Germany 10 408 0.6× 325 0.5× 241 0.9× 76 0.6× 13 0.2× 18 526
Laura Alías Spain 16 886 1.3× 766 1.2× 495 1.9× 60 0.4× 20 0.3× 28 981
Tamara Dangouloff Belgium 9 399 0.6× 276 0.4× 257 1.0× 50 0.4× 23 0.3× 21 468
Paul Porensky United States 8 505 0.8× 574 0.9× 195 0.7× 196 1.5× 7 0.1× 17 786
Ksenija Gorni Switzerland 13 761 1.2× 500 0.8× 443 1.7× 51 0.4× 11 0.1× 63 833
Agata Robertson United Kingdom 5 521 0.8× 355 0.5× 311 1.2× 36 0.3× 10 0.1× 6 596
Tiziana Vitali Italy 7 407 0.6× 462 0.7× 149 0.6× 81 0.6× 5 0.1× 12 560
Mondher Chouchane France 9 95 0.1× 184 0.3× 74 0.3× 224 1.7× 56 0.7× 14 426
Muna El-Khairi Switzerland 8 469 0.7× 334 0.5× 251 1.0× 36 0.3× 7 0.1× 20 526
Chiara Palka Italy 10 95 0.1× 255 0.4× 48 0.2× 210 1.6× 136 1.7× 34 468

Countries citing papers authored by P Burlet

Since Specialization
Citations

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

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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-authorship network of co-authors of P Burlet

This figure shows the co-authorship network connecting the top 25 collaborators of P Burlet. A scholar is included among the top collaborators of P Burlet based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with P Burlet. P Burlet is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Steffann, Julie, Nelly Frydman, P Burlet, et al.. (2011). Diagnostic préimplantatoire avec typage HLA : naissance du premier enfant du double espoir en France. Journal de gynécologie, obstétrique et biologie de la reproduction. Supplément. 40(7). 682–686. 4 indexed citations
2.
Renvoisé, Benoît, Sabrina Colasse, P Burlet, et al.. (2009). The loss of the snoRNP chaperone Nopp140 from Cajal bodies of patient fibroblasts correlates with the severity of spinal muscular atrophy. Human Molecular Genetics. 18(7). 1181–1189. 22 indexed citations
3.
Gigarel, Nadine, Nelly Frydman, P Burlet, et al.. (2008). Preimplantation genetic diagnosis for autosomal recessive polycystic kidney disease. Reproductive BioMedicine Online. 16(1). 152–158. 30 indexed citations
4.
Gigarel, Nadine, Nelly Frydman, P Burlet, et al.. (2008). Successful preimplantation genetic diagnosis for autosomal recessive polycystic kidney disease by haplotype analysis. Reproductive BioMedicine Online. 16(3). 463–463.
5.
Burlet, P, Nelly Frydman, Nadine Gigarel, et al.. (2006). Multiple displacement amplification improves PGD for fragile X syndrome. Molecular Human Reproduction. 12(10). 647–652. 53 indexed citations
6.
Feyereisen, E., Serge Romana, Violaine Kerbrat, et al.. (2006). Indications et résultats du diagnostic pré-implantatoire (DPI). Journal de gynécologie, obstétrique et biologie de la reproduction. Supplément. 35(4). 356–372. 4 indexed citations
7.
Steffann, Julie, Nelly Frydman, P Burlet, et al.. (2005). Le diagnostic préimplantatoire couplé au typage HLA : l'expérience parisienne. Gynécologie Obstétrique & Fertilité. 33(10). 824–827. 3 indexed citations
8.
Steffann, Julie, Nadine Gigarel, Nelly Frydman, et al.. (2005). O▪26 Preimplantation diagnosis of the NARP mitochondrial DNA mutation. Reproductive BioMedicine Online. 10. 9–9. 1 indexed citations
9.
Bertrandy, Solange, P Burlet, Olivier Clermont, et al.. (1999). The RNA-Binding Properties of SMN: Deletion Analysis of the Zebrafish Orthologue Defines Domains Conserved in Evolution. Human Molecular Genetics. 8(5). 775–782. 77 indexed citations
10.
Burlet, P, Céline Huber, Solange Bertrandy, et al.. (1998). The distribution of SMN protein complex in human fetal tissues and its alteration in spinal muscular atrophy. Human Molecular Genetics. 7(12). 1927–1933. 122 indexed citations
11.
Bürglen, Lydie, Thierry Seroz, Pierre Miniou, et al.. (1997). The gene encoding p44, a subunit of the transcription factor TFIIH, is involved in large-scale deletions associated with Werdnig-Hoffmann disease.. PubMed. 60(1). 72–9. 91 indexed citations
12.
Bürglen, Lydie, Jeanne Amiel, Louis Viollet, et al.. (1996). Survival motor neuron gene deletion in the arthrogryposis multiplex congenita-spinal muscular atrophy association.. Journal of Clinical Investigation. 98(5). 1130–1132. 56 indexed citations
13.
Burlet, P, Lydie Bürglen, Olivier Clermont, et al.. (1996). Large scale deletions of the 5q13 region are specific to Werdnig-Hoffmann disease.. Journal of Medical Genetics. 33(4). 281–283. 79 indexed citations
14.
Bürglen, Lydie, S. Lefébvre, P Burlet, et al.. (1995). Dernière heure : identification et caractérisation d'un gène déterminant dans les amyotrophies spinales. médecine/sciences. 11(1). 149–149. 1 indexed citations
15.
Melki, Judith, Sonia Abdelhak, P Burlet, et al.. (1992). Prenatal prediction of Werdnig-Hoffmann disease using linked polymorphic DNA probes.. Journal of Medical Genetics. 29(3). 171–174. 26 indexed citations
16.
Müller, B., Judith Melki, P Burlet, & Françoise Clerget‐Darpoux. (1992). 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.. PubMed. 50(5). 892–5. 19 indexed citations
17.
Mattéi, Marie‐Geneviève, Judith Melki, Sonia Abdelhak, et al.. (1991). In situ hybridization of two markers closely flanking the spinal muscular atrophy gene to 5q12→q13.3. Cytogenetic and Genome Research. 57(2-3). 112–113. 4 indexed citations
18.
Abdelhak, Sonia, P Burlet, Dominique Hillaire, et al.. (1991). Linkage analysis in spinal muscular atrophy, by six closely flanking markers on chromosome 5.. PubMed. 48(4). 764–8. 30 indexed citations
19.
Abdelhak, Sonia, et al.. (1990). A PstI polymorphism at the D5S39 locus. Nucleic Acids Research. 18(18). 5580–5580. 8 indexed citations
20.
Melki, Judith, Sonia Abdelhak, P Burlet, et al.. (1990). Mapping of acute (type I) spinal muscular atrophy to chromosome 5q12-q14. The Lancet. 336(8710). 271–273. 185 indexed citations

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.

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