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

Medicine, Neurobiology, Neuroscience +7

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

Wyman T. McGuirt, Sai Prasad, Andrew J. Griffith et al. · Nature Genetics · 1999 · 270 citations

Medicine, Genetics, Molecular Genetics +11

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 · 258 citations

Life Sciences, Genetics, Molecular Genetics +14

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 · 195 citations

Life Sciences, Genetics, Molecular Genetics +11

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

Life Sciences, Genetics, Molecular Genetics +6