Robert F. Mueller
Publications by Year
Research Areas
Hearing, Cochlea, Tinnitus, Genetics, Connexins and lens biology, Congenital heart defects research, Prenatal Screening and Diagnostics, Hearing Loss and Rehabilitation
Most-Cited Works
- → Identification of Microcephalin, a Protein Implicated in Determining the Size of the Human Brain(2002)474 cited
- → Mutations in COL11A2 cause non-syndromic hearing loss (DFNA13)(1999)269 cited
- → Fraser syndrome and mouse blebbed phenotype caused by mutations in FRAS1/Fras1 encoding a putative extracellular matrix protein(2003)257 cited
- → Mutations in a new gene encoding a protein of the hair bundle cause non-syndromic deafness at the DFNB16 locus(2001)191 cited
- → Primary Autosomal Recessive Microcephaly (MCPH1) Maps to Chromosome 8p22-pter(1998)168 cited
- → Mitochondrial DNA mutations in patients with postlingual, nonsyndromic hearing impairment(2004)132 cited
- → Connexin-26 mutations in sporadic non-syndromal sensorineural deafness(1998)117 cited
- → A Third Novel Locus for Primary Autosomal Recessive Microcephaly Maps to Chromosome 9q34(2000)107 cited
- → Characterization of initial events in bacterial surface colonization by two Pseudomonas species using image analysis(1992)96 cited
- → Evaluation of a Protocol for Post-Mortem Examination of Stillbirths(1983)93 cited