Christina M. Sloan
Publications by Year
Research Areas
Hearing, Cochlea, Tinnitus, Genetics, Hearing Loss and Rehabilitation, Cellular transport and secretion, Ear Surgery and Otitis Media, Genomics and Phylogenetic Studies
Most-Cited Works
- → Copy number variants are a common cause of non-syndromic hearing loss(2014)194 cited
- → Advancing genetic testing for deafness with genomic technology(2013)125 cited
- → Deafness in the genomics era(2011)80 cited
- → Cone photoreceptor mosaic disruption associated with Cys203Arg mutation in the M-cone opsin(2009)74 cited
- → PDZD7 and hearing loss: More than just a modifier(2015)59 cited
- → Comprehensive genetic testing with ethnic‐specific filtering by allele frequency in a Japanese hearing‐loss population(2015)45 cited
- → AudioGene: Predicting Hearing Loss Genotypes from Phenotypes to Guide Genetic Screening(2012)40 cited
- → Hearing Loss Caused by a P2RX2 Mutation Identified in a MELAS Family With a Coexisting Mitochondrial 3243AG Mutation(2015)24 cited
- → De Novo Mutation in X-Linked Hearing Loss–Associated POU3F4 in a Sporadic Case of Congenital Hearing Loss(2015)22 cited
- → Novel PTPRQ Mutations Identified in Three Congenital Hearing Loss Patients With Various Types of Hearing Loss(2015)21 cited