C Oudet - Concepedia

Author

C Oudet

Also Known As

C L Oudet, C Oudet, C. (a) Oudet, C. L. Oudet, C. Oudet, Claudine L Oudet, Claudine L. Oudet, Claudine OUDET, Claudine Oudet, Oudet, C

Publications

2.7K

Citations

H-Index

Concepts

All Affiliations

Inserm Centre National de la Recherche Scientifique University College London Institut de génétique et de biologie moléculaire et cellulaire North Middlesex Hospital

About

C Oudet is an author at Inserm specializing in medicine, genetics, and molecular genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	12	12	2K
2	Biology	3	3	201
3	Health Sciences	2	2	72
4	Natural Sciences	2	2	196
5	Anatomy	1	1	22

C Oudet

Publications

2.5K

Citations

H-Index

Page 1

	Year	Citations
A gene (PEX) with homologies to endopeptidases is mutated in patients with X–linked hypophosphatemic rickets Fiona Francis, Steffen Hennig, Bernd Korn, Nature Genetics Genetic DisorderGeneticsX–linked Hypophosphatemic RicketsMolecular BiologyMolecular Genetics	1995	1.1K
MEPE, a New Gene Expressed in Bone Marrow and Tumors Causing Osteomalacia Peter Rowe, P A de Zoysa, Rong Dong, Genomics Bone DiseaseBone Morphogenic ProteinNew GeneTumors Causing OsteomalaciaPathology	2000	364
Genomic Organization of the Human <i>PEX</i> Gene Mutated in X-Linked Dominant Hypophosphatemic Rickets Fiona Francis, Tim M. Strom, Steffen Hennig, Genome Research GeneticsGenomic MechanismMolecular BiologyMolecular GeneticsDisease Gene Identification	1997	162
Linkage disequilibrium between the fragile X mutation and two closely linked CA repeats suggests that fragile X chromosomes are derived from a small number of founder chromosomes. C Oudet, Étienne Mornet, J.L. Serre, PubMed	1993	130
Two hot spots of recombination in the DMD gene correlate with the deletion prone regions C Oudet, André Hanauer, Paula R. Clemens, Human Molecular Genetics	1992	123
Non-random distribution of mutations in the PHEX gene, and under-detected missense mutations at non-conserved residues Denis Filisetti, Georg Ostermann, M. von Bredow, European Journal of Human Genetics Genetic DisorderGeneticsPhex GeneMolecular BiologyNon-random Distribution	1999	68
Nonradioactive assay for new microsatellite polymorphisms at the 5' end of the dystrophin gene, and estimation of intragenic recombination. C Oudet, Roland Heilig, André Hanauer, PubMed	1991	62
Striking Founder Effect for the Fragile X Syndrome in Finland C Oudet, Harriet von Koskull, Ann‐Marie Nordström, European Journal of Human Genetics Family MedicineGenetic DisorderDisabilityFragile X SpectrumAbnormal Development	1993	59
A PHEX Gene Mutation Is Responsible for Adult-Onset Vitamin D-Resistant Hypophosphatemic Osteomalacia: Evidence That the Disorder Is Not a Distinct Entity from X-Linked Hypophosphatemic Rickets1 Michael J. Econs, Nancy Friedman, Peter Rowe, The Journal of Clinical Endocrinology & Metabolism GeneticsMolecular BiologyPathologyOsteogenesisMolecular Genetics	1998	50
An informative polymorphism detectable by polymerase chain reaction at the 3? end of the dystrophin gene C Oudet, Roland Heilig, Jean‐Louis Mandel Human Genetics Polymerase Chain ReactionGenetic AnalysisInformative PolymorphismDystrophin GeneGenetic Disorder	1990	45

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