C Oudet

2.7k total citations
43 papers, 1.2k citations indexed

About

C Oudet is a scholar working on Molecular Biology, Genetics and Anatomy. According to data from OpenAlex, C Oudet has authored 43 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Molecular Biology, 13 papers in Genetics and 9 papers in Anatomy. Recurrent topics in C Oudet's work include Medical and Biological Sciences (9 papers), Temporomandibular Joint Disorders (6 papers) and Genetics and Neurodevelopmental Disorders (5 papers). C Oudet is often cited by papers focused on Medical and Biological Sciences (9 papers), Temporomandibular Joint Disorders (6 papers) and Genetics and Neurodevelopmental Disorders (5 papers). C Oudet collaborates with scholars based in France, United States and United Kingdom. C Oudet's co-authors include Peter Rowe, Jean‐Louis Mandel, Michael J. Econs, André Hanauer, A. Petrović, Kenneth E. White, P A de Zoysa, Rong Dong, Roland Heilig and J Stutzmann and has published in prestigious journals such as Nature Genetics, The Journal of Clinical Endocrinology & Metabolism and Genome Research.

In The Last Decade

C Oudet

43 papers receiving 1.2k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
C Oudet France	18	563	472	390	183	171	43	1.2k
Katsuhiko Amano Japan	14	636 1.1×	208 0.4×	76 0.2×	129 0.7×	288 1.7×	35	1.0k
Dieter Kotzot Austria	29	1.3k 2.4×	1.9k 4.1×	99 0.3×	123 0.7×	167 1.0×	100	2.9k
Imranul Alam United States	13	956 1.7×	285 0.6×	55 0.1×	368 2.0×	126 0.7×	37	1.6k
Yoko Kurotaki Japan	13	856 1.5×	603 1.3×	429 1.1×	90 0.5×	103 0.6×	16	1.5k
J. Morris-Wiman United States	15	315 0.6×	285 0.6×	6 0.0×	43 0.2×	98 0.6×	28	675
Toshitaka Akisaka Japan	16	418 0.7×	51 0.1×	12 0.0×	106 0.6×	157 0.9×	52	791
Philip Catalá-Lehnen Germany	16	502 0.9×	109 0.2×	32 0.1×	200 1.1×	128 0.7×	34	1.1k
Henny H. Lemmink Netherlands	24	1.3k 2.4×	383 0.8×	393 1.0×	45 0.2×	58 0.3×	55	2.4k
Jennifer A. Lawson United States	10	1.4k 2.5×	193 0.4×	76 0.2×	41 0.2×	42 0.2×	14	1.7k
Hervé Kempf France	16	673 1.2×	237 0.5×	87 0.2×	73 0.4×	217 1.3×	33	1.1k

Countries citing papers authored by C Oudet

Since Specialization

Citations

This map shows the geographic impact of C Oudet'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 C Oudet with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites C Oudet more than expected).

Fields of papers citing papers by C Oudet

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by C Oudet. 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 C Oudet. The network helps show where C Oudet may publish in the future.

Co-authorship network of co-authors of C Oudet

This figure shows the co-authorship network connecting the top 25 collaborators of C Oudet. A scholar is included among the top collaborators of C Oudet 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 C Oudet. C Oudet 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

Bianchetti, Laurent, C Oudet, & Olivier Poch. (2002). M13 endopeptidases: New conserved motifs correlated with structure, and simultaneous phylogenetic occurrence of PHEX and the bony fish. Proteins Structure Function and Bioinformatics. 47(4). 481–488. 29 indexed citations

Rowe, Peter, P A de Zoysa, Rong Dong, et al.. (2000). MEPE, a New Gene Expressed in Bone Marrow and Tumors Causing Osteomalacia. Genomics. 67(1). 54–68. 266 indexed citations

Filisetti, Denis, Georg Ostermann, Tim M. Strom, et al.. (1999). Non-random distribution of mutations in the PHEX gene, and under-detected missense mutations at non-conserved residues. European Journal of Human Genetics. 7(5). 615–619. 54 indexed citations

Francis, Fiona, Tim M. Strom, Steffen Hennig, et al.. (1997). Genomic Organization of the Human PEX Gene Mutated in X-Linked Dominant Hypophosphatemic Rickets. Genome Research. 7(6). 573–585. 129 indexed citations

Oudet, C, et al.. (1997). A second family with XLRH displays the mutation S244L in the CLCN5 gene. Human Genetics. 99(6). 781–784. 24 indexed citations

Richards, Robert I., K. Holman, K. Friend, et al.. (1994). FRAXAC2 instability. Nature Genetics. 7(2). 122–122. 1 indexed citations

Rowe, Peter, J.N. Goulding, Andrew Read, et al.. (1994). Refining the genetic map for the region flanking the X-linked hypophosphataemic rickets locus (Xp22.1?22.2). Human Genetics. 93(3). 291–294. 18 indexed citations

Biancalana, Valérie, Elisabeth Trivier, C. R. Weber, et al.. (1994). Construction of a High-Resolution Linkage Map for Xp22.1-p22.2 and Refinement of the Genetic Localization of the Coffin-Lowry Syndrome Gene. Genomics. 22(3). 617–625. 32 indexed citations

Oudet, C, et al.. (1993). Striking Founder Effect for the Fragile X Syndrome in Finland. European Journal of Human Genetics. 1(3). 181–189. 48 indexed citations

10.

Rowe, Peter, J.N. Goulding, Andrew Read, et al.. (1993). New markers for linkage analysis of X-linked hypophosphataemic rickets. Human Genetics. 91(6). 571–5. 14 indexed citations

11.

Oudet, C, André Hanauer, Paula R. Clemens, T. Caskey, & Jean‐Louis Mandel. (1992). Two hot spots of recombination in the DMD gene correlate with the deletion prone regions. Human Molecular Genetics. 1(8). 599–603. 97 indexed citations

12.

Oudet, C, Roland Heilig, André Hanauer, & Jean‐Louis Mandel. (1991). Nonradioactive assay for new microsatellite polymorphisms at the 5' end of the dystrophin gene, and estimation of intragenic recombination.. PubMed. 49(2). 311–9. 52 indexed citations

13.

Oudet, C, Roland Heilig, & Jean‐Louis Mandel. (1990). An informative polymorphism detectable by polymerase chain reaction at the 3? end of the dystrophin gene. Human Genetics. 84(3). 283–5. 38 indexed citations

14.

Petrović, A., C Oudet, & J Stutzmann. (1989). Ultradian Mitotic Rhythms in Culture of Human Sarcomatous Bone Cells Originating from the Patient Before and After Chemotherapy. Chronobiology International. 6(2). 173–183. 1 indexed citations

15.

Oudet, C, A. Petrović, M Champy, & Jean-Luc Kahn. (1989). Is the myosin type altered in the ageing platysma?. Journal of Cranio-Maxillofacial Surgery. 17(4). 190–194. 1 indexed citations

16.

Oudet, C, et al.. (1988). An experimental orthopedic treatment of the rat mandible using a functional appliance alters the fibre and myosin types in masticatory muscles. annales de biologie animale biochimie biophysique. 28(3B). 795–803. 13 indexed citations

17.

Petrović, A, J Stutzmann, & C Oudet. (1986). Procesos de control en el crecimiento postnatal del cartílago condilar de la mandíbula. 6(1). 11–58. 1 indexed citations

18.

Oudet, C, A. Petrović, & J Stutzmann. (1984). Time-Dependent Effects of a Functional'-Type Orthopedic Appliance on the Rat Mandible Growth. Chronobiology International. 1(1). 51–57. 15 indexed citations

19.

Oudet, C & A. Petrović. (1981). Tages- und jahresperiodische Schwankungen der Reaktion des Kondylenknorpels bei der kieferorthopädischen Behandlung. Journal of Orofacial Orthopedics / Fortschritte der Kieferorthopädie. 42(1). 1–9. 4 indexed citations

20.

Petrović, A, et al.. (1973). [Effect of devices for mandibular propulsion and retropulsion on the number of serial sarcomeres of the external pterygoid muscle and on the growth of condylar cartilage in young rats].. PubMed. 44(1). 191–212. 8 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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