Publications | Maryland Cochlear Implant Center of Excellence l Hearing and Speech Sciences Department l University of Maryland

Hertzano R and Elkon R. (2012) High throughput gene expression analysis of the inner ear. Hear Res. 288:77-88
Litovsky, R. Y., Goupell, M. J., et al. (2012). “Studies on bilateral cochlear implants at the University of Wisconsin’s Binaural Hearing and Speech Laboratory,” J. Am. Acad. Audiol. 23, 476-494.
Hertzano R, Elkon R, Kurima K, Morrisson A, Chan SL, Sallin M, Biedlingmaier A, Darling D, Griffith AJ, Eisenman DJ, Strome SE. Cell type-specific transcriptome analysis reveals a major role for Zeb1 and miR-200b in mouse inner ear morphogenesis. PLoS Genet. 2011 Sep;7(9):e1002309.
Kurima K, Hertzano R, Gavrilova O, Monahan K, Shpargel KB, Nadaraja G, Kawashima Y, Lee KY, Ito T, Higashi Y, Eisenman DJ, Strome SE, Griffith AJ. A Noncoding Point Mutation of Zeb1 Causes Multiple Developmental Malformations and Obesity in Twirler mice. PLoS Genet. 2011 Sep;7(9):e1002307
Majdak, P., Goupell, M. J., and Laback, B. (2011). “Two-dimensional localization of virtual sound sources in cochlear-implant listeners,” Ear Hear. 32, 198-208.
Todd, A., Edwards, J., Litovsky, R., (2011). Production of contrast between sibilant fricatives by children with cochlear implants. Journal of the Acoustical Society of America, 130, 3969-3979. [PMCID: PMC3253598]
Goupell, M. J., Majdak, P., and Laback, B. (2010). “Median-plane sound localization as a function of the number of spectral channels using a channel vocoder,” J. Acoust. Soc. Am. 127, 990-1001.
Choi BY, Stewart AK, Madeo AC, Pryor SP, Lenhard S, Kittles R, Eisenman D, Kim HJ, Niparko J, Thomsen J, Amos KS, Nance WE, King KA, Zalewski CK, Brewer CC, Shawker T, Reynolds JC, Butman JA, Karniski LP, Alper SA, Griffith AJ. (2009). Hypo-functional SLC26A4 variants associated with nonsyndromic hearing loss and enlargement of the vestibular aqueduct: genotype-phenotype correlation or coincidental polymorphism? Human Mutation, 30: 599-608.
Choi BY, Stewart AK, Madeo AC, Pryor SP, Lenhard S, Kittles R, Eisenman D, Kim HJ, Niparko J, Thomsen J, Amos KS, Nance WE, King KA, Zalewski CK, Brewer CC, Shawker T, Reynolds JC, Butman JA, Karniski LP, Alper SA, Griffith AJ. Hypo-functionalSLC26A4 variants associated with nonsyndromic hearing loss and enlargement of the vestibular aqueduct: genotype-phenotype correlation or coincidental polymorphism? Human Mutation 2009; 30: 599-608
Goupell, M. J., Laback, B., Majdak, P., and Baumgartner, W.-D. (2008). “Current-level discrimination and spectral profile analysis in multi-channel electrical stimulation,” J. Acoust. Soc. Am. 124, 3142-3157.
King KA., Choi BY, Zalewski C, Madeo AC, Manichaikul A, Pryor SP, Ferruggiaro A, Eisenman D, Kim HJ, Niparko J, Thomsen J, Butman JA, Griffith AJ, Brewer CC. SLC26A4 genotype, but not cochlear radiologic structure, is correlated with hearing loss in earswith an enlarged vestibular aqueduct (EVA). Laryngoscope 2009; 120: 384-389
King KA., Choi BY, Zalewski C, Madeo AC, Manichaikul A, Pryor SP, Ferruggiaro A, Eisenman D, Kim HJ, Niparko J, Thomsen J, Butman JA, Griffith AJ, Brewer CC. (2009). SLC26A4 genotype, but not cochlear radiologic structure, is correlated with hearing loss in ears with an enlarged vestibular aqueduct (EVA). Laryngoscope,120: 384-389.
Goupell, M. J., Laback, B., Majdak, P., and Baumgartner, W.-D. (2008). “Effects of upper-frequency boundary and spectral warping on speech intelligibility in electrical stimulation,” J. Acoust. Soc. Am. 123, 2295-2309.
Hertzano R, Shalit E, Rzadzinska AK, Dror AA, Song L, Ron U, Tan JT, Starovolsky Shitrit A, Fuchs A, Hasson T, Ben-Tal N, Sweeney HL, Hrabe de Angelis M, Steel KP and Avraham KB. (2008) A Myo6 mutation destroys coordination between the myosin heads,
Hertzano R, Shalit E, Rzadzinska AK, Dror AA, Song L, Ron U, Tan JT, Starovolsky Shitrit A, Fuchs A, Hasson T, Ben-Tal N, Sweeney HL, Hrabe de Angelis M, Steel KP and Avraham KB. (2008) A Myo6 mutation destroys coordination between the myosin heads, re
Hertzano R, Dror AA, Montcouquiol M, Ahmed Z, Ellsworth B, Camper S, Friedman TB, Kelley MW and Avraham KB. (2007) Lhx3, a LIM domain transcription factor, is regulated by Pou4f3 in the auditory, but not in the vestibular system. Eur J Neurosci. 25:999-10
Fiolka K, Hertzano R, Zeng H, Hermesh O, Avraham KB, Dührsen U and Möröy T. (2006) Gfi1 and Gfi1b act equivalently in haematopoiesis, but have distinct, non-overlapping functions in inner ear development. EMBO Reports. 7:326-33.
Clough RL, Sud R, Davis-Silberman N, Hertzano R, Avraham KB, Holley M, Dawson SJ. (2004) Brn-3c (POU4F3) regulates BDNF and NT-3 promoter activity. Biochem Biophys Res Commun. 5;324:372-81.
Hertzano R, Montcouquiol M, Rashi-Elkeles S, Elkon R, Yücel R, Frankel WN, Rechavi G, Möröy T, Friedman TB, Kelley MW and Avraham KB. (2004) Transcription profiling of inner ears from Pou4f3ddl/ddl identifies Gfi1 as a target of the Pou4f3 deafness gene.
Rhodes CR, Hertzano R, Fuchs H, Bell RE, Hrabé de Angelis M, Steel KP, Avraham KB. (2004) A Myo7a mutation co-segregates with stereocilia defects and low frequency hearing impairment. Mamm Genome. 15:686-97
Rhodes CR, Hertzano R, Fuchs H, Bell RE, Hrabé de Angelis M, Steel KP, Avraham KB. (2004) A Myo7a mutation co-segregates with stereocilia defects and low frequency hearing impairment. Mamm Genome. 15:686-97.
Eisenman DJ, Ashbaugh C, Zwolan T, Arts HA, Telian SA. (2001). Implantation of the malformed cochlea. Otol Neurotol, 22: 834-41.
Eisenman DJ, Ashbaugh C, Zwolan T, Arts HA, Telian SA. Implantation of the malformed cochlea. Otol Neurotol 2001;22: 834-41.
Eisenman DJ, Arts HA. (2000). Effectiveness of Treatment for Idiopathic Sudden Sensorineural Hearing Loss. Arch Otolaryngol Head Neck Surg, 126: 1161-4.
Eisenman DJ, Arts HA. Effectiveness of Treatment for Idiopathic Sudden Sensorineural Hearing Loss. Arch Otolaryngol Head Neck Surg 2000;126: 1161-4.