Robert F. Mueller

Identification of Microcephalin, a Protein Implicated in Determining the Size of the Human Brain

Andrew P. Jackson, Helen Eastwood, Sandra Bell et al. · The American Journal of Human Genetics · 2002 · 474 citations · Full text

Developmental Biology, Ependyma, Brain Structure +9

Mutations in COL11A2 cause non-syndromic hearing loss (DFNA13)

Wyman T. McGuirt, Sai Prasad, Andrew J. Griffith et al. · Nature Genetics · 1999 · 267 citations

Auditory Processing, Genetic Disorder, Genetics +4

Fraser syndrome and mouse blebbed phenotype caused by mutations in FRAS1/Fras1 encoding a putative extracellular matrix protein

Lesley McGregor, Ville Makela, S. M. Darling et al. · Nature Genetics · 2003 · 257 citations

Fraser Syndrome, Fibrosis, Developmental Biology +9

Mutations in a new gene encoding a protein of the hair bundle cause non-syndromic deafness at the DFNB16 locus

Elisabeth Verpy, Saber Masmoudi, Ingrid Zwaenepoel et al. · Nature Genetics · 2001 · 191 citations

Developmental Biology, Mendelian Disorder, Genetic Disorder +8

Primary Autosomal Recessive Microcephaly (MCPH1) Maps to Chromosome 8p22-pter

Andrew P. Jackson, Duncan P. McHale, David A. Campbell et al. · The American Journal of Human Genetics · 1998 · 168 citations · Full text

Developmental Biology, Mendelian Disorder, Genetic Disorder +4