Philippe Burlet

6.4k total citations · 2 hit papers
24 papers, 5.0k citations indexed

About

Philippe Burlet is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Philippe Burlet has authored 24 papers receiving a total of 5.0k indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Molecular Biology, 14 papers in Genetics and 5 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Philippe Burlet's work include Neurogenetic and Muscular Disorders Research (14 papers), RNA modifications and cancer (12 papers) and RNA Research and Splicing (8 papers). Philippe Burlet is often cited by papers focused on Neurogenetic and Muscular Disorders Research (14 papers), RNA modifications and cancer (12 papers) and RNA Research and Splicing (8 papers). Philippe Burlet collaborates with scholars based in France, United States and United Kingdom. Philippe Burlet's co-authors include Olivier Clermont, Judith Melki, Arnold Münnich, Lydie Bürglen, Louis Viollet, Corinne Cruaud, Denis Le Paslier, Bernard Bénichou, Philippe Millasseau and Massimo Zeviani and has published in prestigious journals such as Science, Cell and Nature Genetics.

In The Last Decade

Philippe Burlet

23 papers receiving 4.8k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Identification and characterization of a spinal muscular atrophy-determining gene

1995 3.1k citations Lydie Bürglen, Olivier Clermont et al. profile →
Correlation between severity and SMN protein level in spinal muscular atrophy

1997 876 citations Suzie Lefebvre, Philippe Burlet et al. Nature Genetics profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Philippe Burlet France	16	4.1k	4.1k	1.5k	357	331	24	5.0k
Bernard Bénichou France	17	2.8k 0.7×	2.9k 0.7×	1.1k 0.7×	328 0.9×	259 0.8×	29	4.0k
Lydie Bürglen France	25	3.5k 0.9×	4.2k 1.0×	1.4k 0.9×	1.3k 3.7×	303 0.9×	63	5.6k
Louis Viollet France	19	3.3k 0.8×	3.2k 0.8×	1.2k 0.8×	277 0.8×	284 0.9×	32	4.1k
France Leturcq France	35	639 0.2×	3.4k 0.8×	311 0.2×	657 1.8×	82 0.2×	130	4.0k
Enca Martin‐Rendon United Kingdom	27	1.1k 0.3×	1.6k 0.4×	1.3k 0.9×	388 1.1×	70 0.2×	55	3.1k
Richard J.L.F. Lemmers Netherlands	30	895 0.2×	3.5k 0.9×	246 0.2×	526 1.5×	77 0.2×	65	3.9k
Louise R. Rodino‐Klapac United States	38	741 0.2×	3.8k 0.9×	362 0.2×	1.8k 5.1×	105 0.3×	102	4.5k
M. Mayer France	21	333 0.1×	1.0k 0.3×	202 0.1×	152 0.4×	102 0.3×	49	1.5k
Samiah Al-Zaidy United States	15	614 0.2×	1.3k 0.3×	328 0.2×	652 1.8×	53 0.2×	26	1.8k
Sandra Duqué United States	14	693 0.2×	1.0k 0.3×	233 0.2×	573 1.6×	118 0.4×	24	1.5k

Countries citing papers authored by Philippe Burlet

Since Specialization

Citations

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

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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-authorship network of co-authors of Philippe Burlet

This figure shows the co-authorship network connecting the top 25 collaborators of Philippe Burlet. A scholar is included among the top collaborators of Philippe 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 Philippe Burlet. Philippe Burlet is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Santos, Matthieu Dos, Olivier Biondi, Philippe Burlet, et al.. (2018). Small-molecule flunarizine increases SMN protein in nuclear Cajal bodies and motor function in a mouse model of spinal muscular atrophy. Scientific Reports. 8(1). 2075–2075. 10 indexed citations

Monnot, Sophie, David C. Samuels, Laëtitia Hesters, et al.. (2013). Mutation dependance of the mitochondrial DNA copy number in the first stages of human embryogenesis. Human Molecular Genetics. 22(9). 1867–1872. 64 indexed citations

Renvoisé, Benoît, et al.. (2012). A role for protein phosphatase PP1γ in SMN complex formation and subnuclear localization to Cajal bodies. Journal of Cell Science. 125(Pt 12). 2862–74. 22 indexed citations

Frydman, René, Nelly Frydman, Julie Steffann, et al.. (2011). Diagnostic pré-implantatoire : dix ans d’expérience en région parisienne : impasse actuelle et solutions à venir. Bulletin de l Académie Nationale de Médecine. 195(4-5). 1005–1014. 2 indexed citations

Steffann, Julie, Nelly Frydman, Philippe Burlet, et al.. (2011). Le diagnostic pré-implantatoire couplé au typage HLA : l’expérience française. Bulletin de l Académie Nationale de Médecine. 195(4-5). 1015–1022. 1 indexed citations

Gigarel, Nadine, Laëtitia Hesters, David C. Samuels, et al.. (2011). Poor Correlations in the Levels of Pathogenic Mitochondrial DNA Mutations in Polar Bodies versus Oocytes and Blastomeres in Humans. The American Journal of Human Genetics. 88(4). 494–498. 30 indexed citations

Monnot, Sophie, Nadine Gigarel, David C. Samuels, et al.. (2010). Segregation of mtDNA throughout human embryofetal development: m.3243A>G as a model system. Human Mutation. 32(1). 116–125. 87 indexed citations

Burlet, Philippe, Nadine Gigarel, Séverine Drunat, et al.. (2009). Single-sperm analysis for recurrence risk assessment of spinal muscular atrophy. European Journal of Human Genetics. 18(4). 505–508. 5 indexed citations

Burlet, Philippe, Nelly Frydman, Nadine Gigarel, et al.. (2005). Improved single-cell protocol for preimplantation genetic diagnosis of spinal muscular atrophy. Fertility and Sterility. 84(3). 734–739. 15 indexed citations

10.

Clermont, Olivier, Philippe Burlet, Paule Bénit, et al.. (2004). Molecular analysis of SMA patients without homozygous SMN1 deletions using a new strategy for identification of SMN1 subtle mutations. Human Mutation. 24(5). 417–427. 61 indexed citations

11.

Gigarel, Nadine, Nelly Frydman, Pierre F. Ray, et al.. (2004). Single cell co-amplification of polymorphic markers for the indirect preimplantation genetic diagnosis of hemophilia�A, X-linked adrenoleukodystrophy, X-linked hydrocephalus and incontinentia pigmenti loci on Xq28. Human Genetics. 114(3). 298–305. 39 indexed citations

12.

Gigarel, Nadine, Pierre F. Ray, Philippe Burlet, et al.. (2004). Single cell quantification of the 8993T>G NARP mitochondrial DNA mutation by fluorescent PCR. Molecular Genetics and Metabolism. 84(3). 289–292. 23 indexed citations

13.

Viollet, Louis, A Barois, Ziad Rifai, et al.. (2002). Mapping of autosomal recessive chronic distal spinal muscular atrophy to chromosome 11q13. Annals of Neurology. 51(5). 585–592. 35 indexed citations

14.

Lefebvre, Suzie, Philippe Burlet, Qing Liu, et al.. (1997). Correlation between severity and SMN protein level in spinal muscular atrophy. Nature Genetics. 16(3). 265–269. 876 indexed citations breakdown →

15.

Viollet, Louis, Solange Bertrandy, Ana Lúcia Brunialti Godard, et al.. (1997). cDNA Isolation, Expression, and Chromosomal Localization of the Mouse Survival Motor Neuron Gene (Smn). Genomics. 40(1). 185–188. 59 indexed citations

16.

Bürglen, Lydie, Suzie Lefebvre, Olivier Clermont, et al.. (1996). Structure and Organization of the Human Survival Motor Neurone (SMN) Gene. Genomics. 32(3). 479–482. 207 indexed citations

17.

Sequeiros, Jorge, Isabel Silveira, Patrı́cia Maciel, et al.. (1994). Genetic Linkage Studies of Machado-Joseph Disease with Chromosome 14q STRPs in 16 Portuguese-Azorean Kindreds. Genomics. 21(3). 645–648. 28 indexed citations

18.

Burlet, Philippe, et al.. (1993). Trinucleotide repeat polymorphism at the D5S556 locus. Human Molecular Genetics. 2(8). 1328–1328. 1 indexed citations

19.

Silveira, Isabel, Judith Melki, Astrid Lunkes, et al.. (1993). Machado-Joseph Disease Is Genetically Different from Holguin Dominant Ataxia (SCA2). Genomics. 17(3). 556–559. 2 indexed citations

20.

Melki, Judith, Philippe Burlet, Olivier Clermont, et al.. (1993). Refined Linkage Map of Chromosome 5 in the Region of the Spinal Muscular Atrophy Gene. Genomics. 15(3). 521–524. 14 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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