Claes Möller - Concepedia

Author

Claes Möller

Also Known As

C G Moller, C Möller, C. G. Möller, C.G. Moller, C.G. Möller, CLAES G. MÖLLER, Claes G. Möller, Claes Moller, Claes Möller, Möller, Claes

231

Publications

5.1K

Citations

H-Index

162

Concepts

All Affiliations

Örebro University Hospital Swedish Institute Örebro University University of Gothenburg Sahlgrenska University Hospital

About

Claes Möller is an author at Örebro University Hospital specializing in medicine, health sciences, and hearing loss.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	18	22	2.4K
2	Health Sciences	13	14	435
3	Arts	9	9	595
4	Public Health	2	2	44
5	Language Studies	1	1	17

Claes Möller

Publications

4.4K

Citations

H-Index

Page 1

	Year	Citations
Mutation of a Gene Encoding a Protein with Extracellular Matrix Motifs in Usher Syndrome Type IIa James D. Eudy, Michael D. Weston, Su-Fang Yao, Science Molecular PhysiologyDevelopmental BiologyMarkers Afm268zd1Genetic DisorderExtracellular Matrix Motifs	1998	391
Clinical diagnosis of the Usher syndromes Richard J. Smith, Charles I. Berlín, J. Fielding Hejtmancik, American Journal of Medical Genetics	1994	341
Mutations in the VLGR1 Gene Implicate G-Protein Signaling in the Pathogenesis of Usher Syndrome Type II Michael D. Weston, Mirjam W.J. Luijendijk, Kurt Humphrey, The American Journal of Human Genetics Signal TransductionMolecular PhysiologySignaling PathwayG Protein-coupled ReceptorGenetic Disorder	2004	338
The high prevalence of otitis media with effusion in children with cleft lip and palate as compared to children without clefts Traci Flynn, Claes Möller, Radoslava Jönsson, International Journal of Pediatric Otorhinolaryngology Pediatric OtolaryngologyAudiologyPediatricsOtolaryngologyOtorhinolaryngology	2009	233
CDH23 Mutation and Phenotype Heterogeneity: A Profile of 107 Diverse Families with Usher Syndrome and Nonsyndromic Deafness Lisa M. Astuto, Julie M. Bork, Michael D. Weston, The American Journal of Human Genetics Mendelian DisorderGenetic DisorderPhenotype HeterogeneityGeneticsGenetic Epidemiology	2002	230
Localization of Usher syndrome type II to chromosome 1q William J. Kimberling, Michael D. Weston, Claes Möller, Genomics MedicineMolecular GeneticsGeneticsGenetic Disorder	1990	217
Linkage of usher syndrome type I gene (USH1B) to the long arm of chromosome 11 William J. Kimberling, Claes Möller, Sandra L. H. Davenport, Genomics Usher Syndrome TypeDevelopmental BiologyGenetic DisorderGeneticsLong Arm	1992	182
Identification of p.A684V missense mutation in the <i>WFS1</i> gene as a frequent cause of autosomal dominant optic atrophy and hearing impairment Nanna Dahl Rendtorff, Marianne Lodahl, Houda Boulahbel, American Journal of Medical Genetics Part A Optic Atrophy-1 GeneMendelian DisorderGenetic DisorderGeneticsP.a684v Missense Mutation	2011	119
Spectrum of USH2A mutations in Scandinavian patients with Usher syndrome type II Bo Dreyer, Vigdis Brox, Lisbeth Tranebjærg, Human Mutation	2008	107
Clinical and molecular genetics of Usher syndrome. William J. Kimberling, Claes Möller PubMed Developmental AnomalyClinical DisordersMendelian DisorderUsher SyndromesMedicine	1995	104

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