Claes Möller

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 et al. · Science · 1998 · 391 citations

Molecular Physiology, Developmental Biology, Markers Afm268zd1 +14

Clinical diagnosis of the Usher syndromes

Richard J. Smith, Charles I. Berlín, J. Fielding Hejtmancik et al. · American Journal of Medical Genetics · 1994 · 341 citations

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 et al. · The American Journal of Human Genetics · 2004 · 338 citations · Full text

Signal Transduction, Molecular Physiology, Signaling Pathway +6

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 et al. · International Journal of Pediatric Otorhinolaryngology · 2009 · 233 citations

Pediatric Otolaryngology, Audiology, Pediatrics +9

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 et al. · The American Journal of Human Genetics · 2002 · 230 citations · Full text

Mendelian Disorder, Genetic Disorder, Phenotype Heterogeneity +6