Michael D. Weston

Defective myosin VIIA gene responsible for Usher syndrome type IB

Dominique Well, Stéphane Blanchard, Josseline Kaplan et al. · Nature · 1995 · 1.1K citations

Mendelian Disorder, Genetic Disorder, Genetics +3

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

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

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

Localization of Usher syndrome type II to chromosome 1q

William J. Kimberling, Michael D. Weston, Claes Möller et al. · Genomics · 1990 · 217 citations

Medicine, Molecular Genetics, Genetics +1