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Ronna Hertzano - Publications

Affiliations: 
University of Maryland School of Medicine, Baltimore, MD, United States 
Area:
cochlear deveopment
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36 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2021 Milon B, Shulman ED, So KS, Cederroth CR, Lipford EL, Sperber M, Sellon JB, Sarlus H, Pregernig G, Shuster B, Song Y, Mitra S, Orvis J, Margulies Z, Ogawa Y, ... ... Hertzano R, et al. A cell-type-specific atlas of the inner ear transcriptional response to acoustic trauma. Cell Reports. 36: 109758. PMID 34592158 DOI: 10.1016/j.celrep.2021.109758  0.315
2020 Brownstein Z, Gulsuner S, Walsh T, Martins FTA, Taiber S, Isakov O, Lee MK, Bordeynik-Cohen M, Birkan M, Chang W, Casadei S, Danial-Farran N, Abu-Rayyan A, Carlson R, Kamal L, ... ... Hertzano R, et al. Spectrum of genes for inherited hearing loss in the Israeli Jewish population, including the novel human deafness gene ATOH1. Clinical Genetics. 98: 353-364. PMID 33111345 DOI: 10.1111/Cge.13817  0.393
2020 Kalra G, Milon B, Casella AM, Herb BR, Humphries E, Song Y, Rose KP, Hertzano R, Ament SA. Biological insights from multi-omic analysis of 31 genomic risk loci for adult hearing difficulty. Plos Genetics. 16: e1009025. PMID 32986727 DOI: 10.1371/journal.pgen.1009025  0.32
2020 Matern MS, Milon B, Lipford EL, McMurray M, Ogawa Y, Tkaczuk A, Song Y, Elkon R, Hertzano R. GFI1 functions to repress neuronal gene expression in the developing inner ear hair cells. Development (Cambridge, England). 147. PMID 32917668 DOI: 10.1242/Dev.186015  0.421
2020 Hertzano R, Gwilliam K, Rose K, Milon B, Matern MS. Cell Type-Specific Expression Analysis of the Inner Ear: A Technical Report. The Laryngoscope. PMID 32579737 DOI: 10.1002/Lary.28765  0.415
2020 Sadler E, Ryals MM, May LA, Martin D, Welsh N, Boger ET, Morell RJ, Hertzano R, Cunningham LL. Cell-Specific Transcriptional Responses to Heat Shock in the Mouse Utricle Epithelium. Frontiers in Cellular Neuroscience. 14: 123. PMID 32528249 DOI: 10.3389/Fncel.2020.00123  0.306
2020 Kolla L, Kelly MC, Mann ZF, Anaya-Rocha A, Ellis K, Lemons A, Palermo AT, So KS, Mays JC, Orvis J, Burns JC, Hertzano R, Driver EC, Kelley MW. Characterization of the development of the mouse cochlear epithelium at the single cell level. Nature Communications. 11: 2389. PMID 32404924 DOI: 10.1038/S41467-020-16113-Y  0.407
2020 Engeln M, Song Y, Chandra R, La A, Fox ME, Evans B, Turner MD, Thomas S, Francis TC, Hertzano R, Lobo MK. Individual differences in stereotypy and neuron subtype translatome with TrkB deletion. Molecular Psychiatry. PMID 32366954 DOI: 10.1038/S41380-020-0746-0  0.31
2020 Hertzano R, Lipford EL, Depireux D. Noise: Acoustic Trauma to the Inner Ear. Otolaryngologic Clinics of North America. 53: 531-542. PMID 32362563 DOI: 10.1016/J.Otc.2020.03.008  0.389
2020 Brooks PM, Rose KP, Macrae ML, Rangoussis KM, Gurjar M, Hertzano R, Coate TM. Pou3f4-Expressing Otic Mesenchyme Cells Promote Spiral Ganglion Neuron Survival in the Postnatal Mouse Cochlea. The Journal of Comparative Neurology. PMID 31994726 DOI: 10.1002/Cne.24867  0.42
2019 Clifford RE, Hertzano R, Ohlemiller KK. Untangling the genomics of noise-induced hearing loss and tinnitus: Contributions of Mus musculus and Homo sapiens. The Journal of the Acoustical Society of America. 146: 4007. PMID 31795683 DOI: 10.1121/1.5132552  0.368
2019 Dunbar LA, Patni P, Aguilar C, Mburu P, Corns L, Wells HR, Delmaghani S, Parker A, Johnson S, Williams D, Esapa CT, Simon MM, Chessum L, Newton S, Dorning J, ... ... Hertzano R, et al. Clarin-2 is essential for hearing by maintaining stereocilia integrity and function. Embo Molecular Medicine. e10288. PMID 31448880 DOI: 10.15252/Emmm.201910288  0.45
2019 Shuster BZ, Depireux DA, Mong JA, Hertzano R. Sex differences in hearing: Probing the role of estrogen signaling. The Journal of the Acoustical Society of America. 145: 3656. PMID 31255106 DOI: 10.1121/1.5111870  0.376
2019 Nesmith JE, Hostelley TL, Leitch CC, Matern MS, Sethna S, McFarland R, Lodh S, Westlake CJ, Hertzano R, Ahmed ZM, Zaghloul NA. Genomic knockout of alms1 in zebrafish recapitulates Alström syndrome and provides insight into metabolic phenotypes. Human Molecular Genetics. 28: 2212-2223. PMID 31220269 DOI: 10.1093/Hmg/Ddz053  0.322
2019 Jung JS, Zhang KD, Wang Z, McMurray M, Tkaczuk A, Ogawa Y, Hertzano R, Coate TM. Semaphorin-5B Controls Spiral Ganglion Neuron Branch Refinement During Development. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. PMID 31209173 DOI: 10.1523/Jneurosci.0113-19.2019  0.374
2019 So EC, Khaladj-Ghom A, Ji Y, Amin J, Song Y, Burch E, Zhou H, Sun H, Chen S, Bentzen S, Hertzano R, Zhang X, Strome SE. NK cell expression of Tim-3: First impressions matter. Immunobiology. PMID 30876792 DOI: 10.1016/J.Imbio.2019.03.001  0.313
2018 Hertzano R, Tomlinson JA, Mackowiak PA. Goya's Lost Hearing: A Twenty-First Century Perspective on Its Cause, Effects and Possible Treatment. The American Journal of the Medical Sciences. PMID 30711190 DOI: 10.1016/J.Amjms.2018.12.009  0.331
2018 Chessum L, Matern MS, Kelly MC, Johnson SL, Ogawa Y, Milon B, McMurray M, Driver EC, Parker A, Song Y, Codner G, Esapa CT, Prescott J, Trent G, Wells S, ... ... Hertzano R, et al. Helios is a key transcriptional regulator of outer hair cell maturation. Nature. PMID 30464345 DOI: 10.1038/S41586-018-0728-4  0.489
2018 Matern MS, Beirl A, Ogawa Y, Song Y, Paladugu N, Kindt KS, Hertzano R. Corrigendum: Transcriptomic Profiling of Zebrafish Hair Cells Using RiboTag. Frontiers in Cell and Developmental Biology. 6: 84. PMID 30191151 DOI: 10.3389/Fcell.2018.00084  0.31
2018 Matern MS, Beirl A, Ogawa Y, Song Y, Paladugu N, Kindt KS, Hertzano R. Transcriptomic Profiling of Zebrafish Hair Cells Using RiboTag. Frontiers in Cell and Developmental Biology. 6: 47. PMID 29765956 DOI: 10.3389/Fcell.2018.00047  0.424
2018 Milon B, Mitra S, Song Y, Margulies Z, Casserly R, Drake V, Mong JA, Depireux DA, Hertzano R. The impact of biological sex on the response to noise and otoprotective therapies against acoustic injury in mice. Biology of Sex Differences. 9: 12. PMID 29530094 DOI: 10.1186/S13293-018-0171-0  0.344
2017 Crowson MG, Hertzano R, Tucci DL. Emerging Therapies for Sensorineural Hearing Loss Otology & Neurotology. 38: 792-803. PMID 28383465 DOI: 10.1097/Mao.0000000000001427  0.307
2017 Matern M, Vijayakumar S, Margulies Z, Milon B, Song Y, Elkon R, Zhang X, Jones SM, Hertzano R. Gfi1(Cre) mice have early onset progressive hearing loss and induce recombination in numerous inner ear non-hair cells. Scientific Reports. 7: 42079. PMID 28181545 DOI: 10.1038/Srep42079  0.457
2015 Elkon R, Milon B, Morrison L, Shah M, Vijayakumar S, Racherla M, Leitch CC, Silipino L, Hadi S, Weiss-Gayet M, Barras E, Schmid CD, Ait-Lounis A, Barnes A, Song Y, ... ... Hertzano R, et al. RFX transcription factors are essential for hearing in mice. Nature Communications. 6: 8549. PMID 26469318 DOI: 10.1038/Ncomms9549  0.462
2012 Hertzano R, Elkon R. High throughput gene expression analysis of the inner ear. Hearing Research. 288: 77-88. PMID 22710153 DOI: 10.1016/J.Heares.2012.01.002  0.387
2011 Hertzano R, Elkon R, Kurima K, Morrisson A, Chan SL, Sallin M, Biedlingmaier A, Darling DS, 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 Genetics. 7: e1002309. PMID 21980309 DOI: 10.1371/Journal.Pgen.1002309  0.414
2011 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 Genetics. 7: e1002307. PMID 21980308 DOI: 10.1371/Journal.Pgen.1002307  0.41
2010 Hertzano R, Puligilla C, Chan SL, Timothy C, Depireux DA, Ahmed Z, Wolf J, Eisenman DJ, Friedman TB, Riazuddin S, Kelley MW, Strome SE. CD44 is a marker for the outer pillar cells in the early postnatal mouse inner ear. Journal of the Association For Research in Otolaryngology : Jaro. 11: 407-18. PMID 20386946 DOI: 10.1007/S10162-010-0211-X  0.346
2008 Hertzano R, Shalit E, Rzadzinska AK, Dror AA, Song L, Ron U, Tan JT, Shitrit AS, Fuchs H, Hasson T, Ben-Tal N, Sweeney HL, de Angelis MH, Steel KP, Avraham KB. A Myo6 mutation destroys coordination between the myosin heads, revealing new functions of myosin VI in the stereocilia of mammalian inner ear hair cells. Plos Genetics. 4: e1000207. PMID 18833301 DOI: 10.1371/Journal.Pgen.1000207  0.356
2007 Hertzano R, Dror AA, Montcouquiol M, Ahmed ZM, Ellsworth B, Camper S, Friedman TB, Kelley MW, Avraham KB. Lhx3, a LIM domain transcription factor, is regulated by Pou4f3 in the auditory but not in the vestibular system. The European Journal of Neuroscience. 25: 999-1005. PMID 17331196 DOI: 10.1111/J.1460-9568.2007.05332.X  0.462
2006 Fiolka K, Hertzano R, Vassen L, Zeng H, Hermesh O, Avraham KB, Dührsen U, Möröy T. Gfi1 and Gfi1b act equivalently in haematopoiesis, but have distinct, non-overlapping functions in inner ear development. Embo Reports. 7: 326-33. PMID 16397623 DOI: 10.1038/Sj.Embor.7400618  0.341
2004 Clough RL, Sud R, Davis-Silberman N, Hertzano R, Avraham KB, Holley M, Dawson SJ. Brn-3c (POU4F3) regulates BDNF and NT-3 promoter activity. Biochemical and Biophysical Research Communications. 324: 372-81. PMID 15465029 DOI: 10.1016/J.Bbrc.2004.09.074  0.374
2004 Rhodes CR, Hertzano R, Fuchs H, Bell RE, de Angelis MH, Steel KP, Avraham KB. A Myo7a mutation cosegregates with stereocilia defects and low-frequency hearing impairment. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 15: 686-97. PMID 15389316 DOI: 10.1007/S00335-004-2344-X  0.399
2004 Hertzano R, Montcouquiol M, Rashi-Elkeles S, Elkon R, Yücel R, Frankel WN, Rechavi G, Möröy T, Friedman TB, Kelley MW, Avraham KB. Transcription profiling of inner ears from Pou4f3(ddl/ddl) identifies Gfi1 as a target of the Pou4f3 deafness gene. Human Molecular Genetics. 13: 2143-53. PMID 15254021 DOI: 10.1093/Hmg/Ddh218  0.467
2003 Donaudy F, Ferrara A, Esposito L, Hertzano R, Ben-David O, Bell RE, Melchionda S, Zelante L, Avraham KB, Gasparini P. Multiple mutations of MYO1A, a cochlear-expressed gene, in sensorineural hearing loss. American Journal of Human Genetics. 72: 1571-7. PMID 12736868 DOI: 10.1086/375654  0.382
2002 Walsh T, Walsh V, Vreugde S, Hertzano R, Shahin H, Haika S, Lee MK, Kanaan M, King MC, Avraham KB. From flies' eyes to our ears: mutations in a human class III myosin cause progressive nonsyndromic hearing loss DFNB30. Proceedings of the National Academy of Sciences of the United States of America. 99: 7518-23. PMID 12032315 DOI: 10.1073/Pnas.102091699  0.349
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