P Maroteaux is a scholar working on Genetics, Rheumatology and Molecular Biology.
According to data from OpenAlex, P Maroteaux has authored 294 papers receiving a total of 5.8k indexed citations (citations by other indexed papers that have themselves been cited), including 146 papers in Genetics, 77 papers in Rheumatology and 73 papers in Molecular Biology. Recurrent topics in P Maroteaux's work include Connective tissue disorders research (105 papers), Bone health and treatments (50 papers) and Dermatological and Skeletal Disorders (34 papers). P Maroteaux is often cited by papers focused on Connective tissue disorders research (105 papers), Bone health and treatments (50 papers) and Dermatological and Skeletal Disorders (34 papers). P Maroteaux collaborates with scholars based in France, Germany and United States. P Maroteaux's co-authors include Jacky Bonaventure, V. Stănescu, Laurence Legeai‐Mallet, Arnold Münnich, R Stănescu, Jürgen W. Spranger, Maurice Lamy, Francis Rousseau, Anna Pelet and Jean‐Michel Rozet and has published in prestigious journals such as Nature, Cell and The Lancet.
In The Last Decade
P Maroteaux
283 papers
receiving
5.4k citations
Hit Papers
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.
Mutations in the gene encoding fibroblast growth factor receptor-3 in achondroplasia
1994689 citationsJacky Bonaventure, P Maroteaux et al.profile →
Peers — A (Enhanced Table)
Peers by citation overlap · career bar shows stage (early→late)
cites ·
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This map shows the geographic impact of P Maroteaux'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 Maroteaux with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites P Maroteaux more than expected).
This network shows the impact of papers produced by P Maroteaux. 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 Maroteaux. The network helps show where P Maroteaux may publish in the future.
Co-authorship network of co-authors of P Maroteaux
This figure shows the co-authorship network connecting the top 25 collaborators of P Maroteaux.
A scholar is included among the top collaborators of P Maroteaux 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 Maroteaux. P Maroteaux 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.
Maroteaux, P. (2008). Du danger d’être petit: Une taille inférieure à la moyenne devient-elle pathologique dans notre société ?. Archives de Pédiatrie. 15(9). 1381–1382.1 indexed citations
Rousseau, F., Jacky Bonaventure, M Le Merrer, P Maroteaux, & Arnold Munnich. (1996). [Mutations of FGFR3 gene cause 3 types of nanisms with variably severity: achondroplasia, thanatophoric nanism and hypochondroplasia].. PubMed. 57(3). 153–153.5 indexed citations
7.
Maroteaux, P, et al.. (1996). L'odontochondrodysplasie. Archives de Pédiatrie. 3(6). 549–554.8 indexed citations
Verloès, Alain, et al.. (1994). Osteocraniostenosis.. Journal of Medical Genetics. 31(10). 772–778.20 indexed citations
11.
Merrer, M. Le, et al.. (1991). [Autosomal recessive metaphyseal chondrodysplasia and Hirschsprung's disease].. PubMed. 38(1). 27–30.9 indexed citations
12.
Verloès, Alain, Martine Le Merrer, J. P. Farriaux, & P Maroteaux. (1991). Metaphyseal acroscyphodysplasia. Clinical Genetics. 39(5). 362–369.10 indexed citations
Poisson, D.M., et al.. (1983). Maladie des synostoses multiples. Etude de la variation des symptômes dans une même famille.. 40(1).1 indexed citations
16.
Dhermy, P, et al.. (1980). Manifestations oculaires d'une forme particulière de mucolipidose: la néphrosialidose.. Journal Français d Ophtalmologie. 3(4).1 indexed citations
17.
Maroteaux, P, et al.. (1978). [Mucolipidosis type I. Sialidosis due to alpha-2-6-neuraminidase deficiency with neurological symptoms].. Munich Personal RePEc Archive (Ludwig Maximilian University of Munich). 35(3). 280–91.2 indexed citations
18.
Peyron, J, R Stănescu, V. Stănescu, & P Maroteaux. (1978). [Particular electrophoretic distribution of proteoglycans in the zones of regeneration of the arthrotic cartilage and study of their collagen].. Munich Personal RePEc Archive (Ludwig Maximilian University of Munich). 45(10). 569–76.3 indexed citations
19.
Maroteaux, P, et al.. (1977). Severe neonatal dwarfism resembling the Kniest and Rolland types of chondrodysplasia.. Munich Personal RePEc Archive (Ludwig Maximilian University of Munich). 30(2). 77–84.1 indexed citations
Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive
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