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John H. Greinwald, MD

Professor

Director, Genetics of Division of Pediatric Otolaryngology

Otolaryngology, Head & Neck Surgery | College of Medicine

Education/Credentials
  • Fellowship: University of Iowa (Pediatric Otolaryngology)
  • Residency: Naval Medical Center (Otolaryngology)
  • Medical Degree: University of South Carolina
Contact Information

Peer Reviewed Publications

Denoyelle, Françoise; Simon, François; Chang, Kay W; Chan, Kenny H; Cheng, Alan G; Cheng, Alan T; Choo, Daniel I; Daniel, Sam J; Farinetti, Anne; Garabedian, Erea-Noël; Greinwald, John H; Hoff, Stephen R; Hone, Stephen; Licameli, Greg R; Papsin, Blake C; Poe, Dennis S; Pransky, Seth; Smith, Richard J H; Triglia, Jean-Michel; Walton, Joanna; Zalzal, George; Leboulanger, Nicolas 2020. International Pediatric Otolaryngology Group (IPOG) Consensus Recommendations: Congenital Cholesteatoma. Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology, 41 3, 345-351

Lipschitz, Noga; Kohlberg, Gavriel D; Scott, Michael; Smith, Matthew M; Greinwald, John H 2020. Socioeconomic Disparities in Pediatric Single-Sided Deafness. Otolaryngology--head and neck surgery : official journal of American Academy of Otolaryngology-Head and Neck Surgery, 163 4, 829-834

Redmann, Andrew J; Manning, Amy; Kennedy, Aimee; Greinwald, John H; deAlarcon, Alessandro 2020. How Strong Is the Duty to Treat in a Pandemic? Ethics in Practice: Point-Counterpoint. Otolaryngology--head and neck surgery : official journal of American Academy of Otolaryngology-Head and Neck Surgery, 163 2, 325-327

Lipschitz, Noga; Kohlberg, Gavriel D; Scott, Michael; Greinwald, John H 2019. Imaging findings in pediatric single-sided deafness and asymmetric hearing loss. The Laryngoscope, ,

Nistel, Mason; Lee, Sang Hoon; Born, Hayley; Greinwald, John H; Abdaljaleel, Maram; Sobolewski, Brad 2019. The Girl With the Bleeding Earlobe Mass. Pediatric emergency care, ,

Kuhn, Jeffery J; Lavender, Violette H; Hunter, Lisa L; McGuire, Stephanie E; Meinzen-Derr, Jareen; Keith, Robert W; Greinwald, John H 2018. Ocular Vestibular Evoked Myogenic Potentials: Normative Findings in Children. Journal of the American Academy of Audiology, 29 5, 443-450

Yang, Christina J; Lavender, Violette; Meinzen-Derr, Jareen K; Cohen, Aliza P; Youssif, Mostafa; Castiglione, Micheal; Manickam, Vairavan; Bachmann, Katheryn R; Greinwald, John H 2016. Vestibular pathology in children with enlarged vestibular aqueduct. The Laryngoscope, 126 10, 2344-50

Johnson, Kaalan; Tabangin, Meredith; Meinzen-Derr, Jareen; Cohen, Aliza P; Greinwald, John H 2015. High-frequency sensorineural hearing loss in children. The Laryngoscope, ,

Nayak, Gowri; Varga, Lukas; Trincot, Claire; Shahzad, Mohsin; Friedman, Penelope L; Klimes, Iwar; Greinwald, John H; Riazuddin, S Amer; Masindova, Ivica; Profant, Milan; Khan, Shaheen N; Friedman, Thomas B; Ahmed, Zubair M; Gasperikova, Daniela; Riazuddin, Sheikh; Riazuddin, Saima 2015. Molecular genetics of MARVELD2 and clinical phenotype in Pakistani and Slovak families segregating DFNB49 hearing loss. Human genetics, 134 4, 423-37

Prosser, John Drew; Cohen, Aliza P; Greinwald, John H 2015. Diagnostic Evaluation of Children with Sensorineural Hearing Loss. Otolaryngologic clinics of North America, 48 6, 975-82

Prows, Cynthia A; Zhang, Xue; Huth, Myra M; Zhang, Kejian; Saldaña, Shannon N; Daraiseh, Nancy M; Esslinger, Hope R; Freeman, Edita; Greinwald, John H; Martin, Lisa J; Sadhasivam, Senthilkumar 2014. Codeine-related adverse drug reactions in children following tonsillectomy: a prospective study. The Laryngoscope, 124 5, 1242-50

Shahzad, Mohsin; Sivakumaran, Theru A; Qaiser, Tanveer A; Schultz, Julie M; Hussain, Zawar; Flanagan, Megan; Bhinder, Munir A; Kissell, Diane; Greinwald, John H; Khan, Shaheen N; Friedman, Thomas B; Zhang, Kejian; Riazuddin, Saima; Riazuddin, Sheikh; Ahmed, Zubair M 2013. Genetic analysis through OtoSeq of Pakistani families segregating prelingual hearing loss. Otolaryngology--head and neck surgery : official journal of American Academy of Otolaryngology-Head and Neck Surgery, 149 3, 478-87

Sivakumaran, Theru A; Husami, Ammar; Kissell, Diane; Zhang, Wenying; Keddache, Mehdi; Black, Angela P; Tinkle, Brad T; Greinwald, John H; Zhang, Kejian 2013. Performance evaluation of the next-generation sequencing approach for molecular diagnosis of hereditary hearing loss. Otolaryngology--head and neck surgery : official journal of American Academy of Otolaryngology-Head and Neck Surgery, 148 6, 1007-16

Prager, Jeremy D; Neidich, Marci J; Perkins, Jonathan N; Meinzen-Derr, Jareen; Greinwald, John H 2012. Minimal access and standard cochlear implantation: a comparative study. International journal of pediatric otorhinolaryngology, 76 8, 1102-6

Sun, Gordon H; Harmych, Brian M; Dickson, J Matthew; Gonzalez del Rey, Javier A; Myer, Charles M; Greinwald, John H 2011. Characteristics of children diagnosed as having coagulopathies following posttonsillectomy bleeding. Archives of otolaryngology--head & neck surgery, 137 1, 65-8

Hopkins, Brandon S; Johnson, Kaalan E; Ksiazek, Jeff M; Sun, Gordon; Greinwald, John H; Rutter, Michael 2010. H1N1 influenza A presenting as bacterial tracheitis. Otolaryngology--head and neck surgery : official journal of American Academy of Otolaryngology-Head and Neck Surgery, 142 4, 612-4

Johnson, Romaine F; Cohen, Aliza P; Guo, Yingshi; Schibler, Kurt; Greinwald, John H 2010. Genetic mutations and aminoglycoside-induced ototoxicity in neonates. Otolaryngology--head and neck surgery : official journal of American Academy of Otolaryngology-Head and Neck Surgery, 142 5, 704-7

Kothiyal, Prachi; Cox, Stephanie; Ebert, Jonathan; Husami, Ammar; Kenna, Margaret A; Greinwald, John H; Aronow, Bruce J; Rehm, Heidi L 2010. High-throughput detection of mutations responsible for childhood hearing loss using resequencing microarrays. BMC biotechnology, 10 , 10

Propst, Evan J; Greinwald, John H; Schmithorst, Vincent 2010. Neuroanatomic differences in children with unilateral sensorineural hearing loss detected using functional magnetic resonance imaging. Archives of otolaryngology--head & neck surgery, 136 1, 22-6

Bardien, Soraya; Human, Hannique; Harris, Tashneem; Hefke, Gwynneth; Veikondis, Rene; Schaaf, H Simon; van der Merwe, Lize; Greinwald, John H; Fagan, Johan; de Jong, Greetje 2009. A rapid method for detection of five known mutations associated with aminoglycoside-induced deafness. BMC medical genetics, 10 , 2

Kothiyal, Prachi; Cox, Stephanie; Ebert, Jonathan; Aronow, Bruce J; Greinwald, John H; Rehm, Heidi L 2009. An overview of custom array sequencing. Current protocols in human genetics / editorial board, Jonathan L. Haines ... [et al.], Chapter 7 , Unit 7.17

Lee, Kenneth H; Larson, Daniel A; Shott, Gordon; Rasmussen, Brian; Cohen, Aliza P; Benton, Corning; Halsted, Mark; Choo, Daniel; Meinzen-Derr, Jareen; Greinwald, John H 2009. Audiologic and temporal bone imaging findings in patients with sensorineural hearing loss and GJB2 mutations. The Laryngoscope, 119 3, 554-8

Saunders, James E; Greinwald, John H; Vaz, Sharon; Guo, Yinshi 2009. Aminoglycoside ototoxicity in Nicaraguan children: patient risk factors and mitochondrial DNA results. Otolaryngology--head and neck surgery : official journal of American Academy of Otolaryngology-Head and Neck Surgery, 140 1, 103-7

Chen, Jianfu; Yang, Li; Yang, Aifen; Zhu, Yi; Zhao, Jianyue; Sun, Dongmei; Tao, Zhihua; Tang, Xiaowen; Wang, Jindan; Wang, Xinjian; Tsushima, Asami; Lan, Jinshan; Li, Weixing; Wu, Fangli; Yuan, Qian; Ji, Jingzhang; Feng, Jinbao; Wu, Chunli; Liao, Zhisu; Li, Zhiyuan; Greinwald, John H; Lu, Jianxin; Guan, Min-Xin 2007. Maternally inherited aminoglycoside-induced and nonsyndromic hearing loss is associated with the 12S rRNA C1494T mutation in three Han Chinese pedigrees. Gene, 401 1-2, 4-11

Putcha, Girish V; Bejjani, Bassem A; Bleoo, Stacey; Booker, Jessica K; Carey, John C; Carson, Nancy; Das, Soma; Dempsey, Melissa A; Gastier-Foster, Julie M; Greinwald, John H; Hoffmann, Marcy L; Jeng, Linda Jo Bone; Kenna, Margaret A; Khababa, Ishrag; Lilley, Margaret; Mao, Rong; Muralidharan, Kasinathan; Otani, Iris M; Rehm, Heidi L; Schaefer, Fred; Seltzer, William K; Spector, Elaine B; Springer, Michelle A; Weck, Karen E; Wenstrup, Richard J; Withrow, Stacey; Wu, Bai-Lin; Zariwala, Maimoona A; Schrijver, Iris 2007. A multicenter study of the frequency and distribution of GJB2 and GJB6 mutations in a large North American cohort. Genetics in medicine : official journal of the American College of Medical Genetics, 9 7, 413-26

Saunders, James E; Vaz, Sharon; Greinwald, John H; Lai, James; Morin, Leonor; Mojica, Karen 2007. Prevalence and etiology of hearing loss in rural Nicaraguan children. The Laryngoscope, 117 3, 387-98

Schraff, Scott A; Brown, David K; Schleiss, Mark R; Meinzen-Derr, Jareen; Greinwald, John H; Choo, Daniel I 2007. The role of CMV inflammatory genes in hearing loss. Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology, 28 7, 964-9

Schraff, Scott A; Schleiss, Mark R; Brown, David K; Meinzen-Derr, Jareen; Choi, K Yeon; Greinwald, John H; Choo, Daniel I 2007. Macrophage inflammatory proteins in cytomegalovirus-related inner ear injury. Otolaryngology--head and neck surgery : official journal of American Academy of Otolaryngology-Head and Neck Surgery, 137 4, 612-8

Preciado, Diego A; Lawson, Louise; Madden, Colm; Myer, David; Ngo, Chris; Bradshaw, John K; Choo, Daniel I; Greinwald, John H 2005. Improved diagnostic effectiveness with a sequential diagnostic paradigm in idiopathic pediatric sensorineural hearing loss. Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology, 26 4, 610-5

Wang, Qiuju; Li, Roughua; Zhao, Hui; Peters, Jennifer L; Liu, Qiong; Yang, Li; Han, Dongyi; Greinwald, John H; Young, Wie-Yen; Guan, Min-Xin 2005. Clinical and molecular characterization of a Chinese patient with auditory neuropathy associated with mitochondrial 12S rRNA T1095C mutation. American journal of medical genetics. Part A, 133A 1, 27-30

Young, Wie-Yen; Zhao, Lidong; Qian, Yaping; Wang, Qiuju; Li, Ning; Greinwald, John H; Guan, Min-Xin 2005. Extremely low penetrance of hearing loss in four Chinese families with the mitochondrial 12S rRNA A1555G mutation. Biochemical and biophysical research communications, 328 4, 1244-51

Yuan, Huijun; Qian, Yaping; Xu, Yanjun; Cao, Juyang; Bai, Linna; Shen, Weidong; Ji, Fei; Zhang, Xin; Kang, Dongyang; Mo, Jun Qin; Greinwald, John H; Han, Dongyi; Zhai, Suoqiang; Young, Wie-Yen; Guan, Min-Xin 2005. Cosegregation of the G7444A mutation in the mitochondrial COI/tRNA(Ser(UCN)) genes with the 12S rRNA A1555G mutation in a Chinese family with aminoglycoside-induced and nonsyndromic hearing loss. American journal of medical genetics. Part A, 138A 2, 133-40

Chadwell, Jon B; Halsted, Mark J; Choo, Daniel I; Greinwald, John H; Benton, Corning 2004. The cochlear cleft. AJNR. American journal of neuroradiology, 25 1, 21-4

Dou, Hongwei; Xu, Jie; Wang, Zhaohui; Smith, Annabel N; Soleimani, Manoocher; Karet, Fiona E; Greinwald, John H; Choo, Daniel 2004. Co-expression of pendrin, vacuolar H+-ATPase alpha4-subunit and carbonic anhydrase II in epithelial cells of the murine endolymphatic sac. The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society, 52 10, 1377-84

Guo, Yingshi; Pilipenko, Valentina; Lim, Lynne H Y; Dou, Hongwei; Johnson, Liane; Srisailapathy, C R Srikumari; Ramesh, Arabandi; Choo, Daniel I; Smith, Richard J H; Greinwald, John H 2004. Refining the DFNB17 interval in consanguineous Indian families. Molecular biology reports, 31 2, 97-105

Li, R; Greinwald, J H; Yang, L; Choo, D I; Wenstrup, R J; Guan, M-X 2004. Molecular analysis of the mitochondrial 12S rRNA and tRNASer(UCN) genes in paediatric subjects with non-syndromic hearing loss. Journal of medical genetics, 41 8, 615-20

Pilipenko, Valentina V; Reece, Alisa; Choo, Daniel I; Greinwald, John H 2004. Genomic organization and expression analysis of the murine Fam3c gene. Gene, 335 , 159-68

Preciado, Diego A; Lim, Lynne H Y; Cohen, Aliza P; Madden, Colm; Myer, David; Ngo, Chris; Bradshaw, John K; Lawson, Louise; Choo, Daniel I; Greinwald, John H 2004. A diagnostic paradigm for childhood idiopathic sensorineural hearing loss. Otolaryngology--head and neck surgery : official journal of American Academy of Otolaryngology-Head and Neck Surgery, 131 6, 804-9

Salamone, Frank N; Bobbitt, D Bradley; Myer, Charles M; Rutter, Michael J; Greinwald, John H 2004. Bacterial tracheitis reexamined: is there a less severe manifestation? Otolaryngology--head and neck surgery : official journal of American Academy of Otolaryngology-Head and Neck Surgery, 131 6, 871-6

Lim, Lynne H Y; Bradshaw, John K; Guo, Yingshi; Pilipenko, Valentina; Madden, Colm; Ingala, David; Keddache, Mehdi; Choo, Daniel I; Wenstrup, Richard; Greinwald, John H 2003. Genotypic and phenotypic correlations of DFNB1-related hearing impairment in the Midwestern United States. Archives of otolaryngology--head & neck surgery, 129 8, 836-40

Madden, Colm; Halsted, Mark J; Hopkin, Robert J; Choo, Daniel I; Benton, Corning; Greinwald, John H 2003. Temporal bone abnormalities associated with hearing loss in Waardenburg syndrome. The Laryngoscope, 113 11, 2035-41

Merves, Michele; Krane, Carissa M; Dou, Hongwei; Greinwald, John H; Menon, Anil G; Choo, Daniel 2003. Expression of aquaporin 1 and 5 in the developing mouse inner ear and audiovestibular assessment of an Aqp5 null mutant. Journal of the Association for Research in Otolaryngology : JARO, 4 2, 264-75

Giguère, Chantal M; Bauman, Nancy M; Sato, Yutaka; Burke, Diane K; Greinwald, John H; Pransky, Seth; Kelley, Peggy; Georgeson, Keith; Smith, Richard J H 2002. Treatment of lymphangiomas with OK-432 (Picibanil) sclerotherapy: a prospective multi-institutional trial. Archives of otolaryngology--head & neck surgery, 128 10, 1137-44

Greinwald, John H; Hartnick, Christopher J 2002. The evaluation of children with sensorineural hearing loss. Archives of otolaryngology--head & neck surgery, 128 1, 84-7

Madden, Colm; Rutter, Michael; Hilbert, Lisa; Greinwald, John H; Choo, Daniel I 2002. Clinical and audiological features in auditory neuropathy. Archives of otolaryngology--head & neck surgery, 128 9, 1026-30

Scott, Kirby J; Schroeder, Ashley A; Greinwald, John H 2002. Ectopic cervical thymus: an uncommon diagnosis in the evaluation of pediatric neck masses. Archives of otolaryngology--head & neck surgery, 128 6, 714-7

Carron, J D; Greinwald, J H; Oberman, J P; Werner, A L; Derkay, C S 2001. Simulated reflux and laryngotracheal reconstruction: a rabbit model. Archives of otolaryngology--head & neck surgery, 127 5, 576-80

Gessler, E M; Hart, A K; Dunlevy, T M; Greinwald, J H 2001. Optimal concentration of epinephrine for vasoconstriction in ear surgery. The Laryngoscope, 111 10, 1687-90

Holcomb, J D; Jaffe, D M; Greinwald, J H; Bauman, N M; Smith, R J 2001. Nontraumatic atlantoaxial rotary subluxation in the pediatric otolaryngology patient. A report of four cases. The Annals of otology, rhinology, and laryngology, 110 12, 1137-40

Scott, K J; Greinwald, J H; Darrow, D; Smith, R J 2001. Endobronchial tumors in children: an uncommon clinical entity. The Annals of otology, rhinology, and laryngology, 110 1, 63-9

Lim, A A; Washington, A P; Greinwald, J H; Lassen, L F; Holtel, M R 2000. Effect of pentoxifylline on the healing of guinea pig tympanic membrane. The Annals of otology, rhinology, and laryngology, 109 3, 262-6

Greinwald, J H; Bauman, N M 1999. Larsen's syndrome. Otolaryngology--head and neck surgery : official journal of American Academy of Otolaryngology-Head and Neck Surgery, 121 6, 845

Greinwald, J H; Burke, D K; Bonthius, D J; Bauman, N M; Smith, R J 1999. An update on the treatment of hemangiomas in children with interferon alfa-2a. Archives of otolaryngology--head & neck surgery, 125 1, 21-7

Greinwald, J H; Burke, D K; Sato, Y; Poust, R I; Kimura, K; Bauman, N M; Smith, R J 1999. Treatment of lymphangiomas in children: an update of Picibanil (OK-432) sclerotherapy. Otolaryngology--head and neck surgery : official journal of American Academy of Otolaryngology-Head and Neck Surgery, 121 4, 381-7

Lim, A A; Wall, M P; Greinwald, J H 1999. Effects of dimethylthiourea, melatonin, and hyperbaric oxygen therapy on the survival of reimplanted rabbit auricular composite grafts. Otolaryngology--head and neck surgery : official journal of American Academy of Otolaryngology-Head and Neck Surgery, 121 3, 231-7

Olney, D R; Greinwald, J H; Smith, R J; Bauman, N M 1999. Laryngomalacia and its treatment. The Laryngoscope, 109 11, 1770-5

Chen, A H; Mueller, R F; Prasad, S D; Greinwald, J H; Manaligod, J; Muilenburg, A C; Verhoeven, K; Van Camp, G; Smith, R J 1998. Presymptomatic diagnosis of nonsyndromic hearing loss by genotyping. Archives of otolaryngology--head & neck surgery, 124 1, 20-4

Greinwald, J H; Simko, E J 1998. Diagnosis and management of middle ear osteomas: a case report and literature review. Ear, nose, & throat journal, 77 2, 134-6, 138-9

Greinwald, J H; Wayne, S; Chen, A H; Scott, D A; Zbar, R I; Kraft, M L; Prasad, S; Ramesh, A; Coucke, P; Srisailapathy, C R; Lovett, M; Van Camp, G; Smith, R J 1998. Localization of a novel gene for nonsyndromic hearing loss (DFNB17) to chromosome region 7q31. American journal of medical genetics, 78 2, 107-13

Hart, A K; Greinwald, J H; Shaffrey, C I; Postma, G N 1998. Thoracic duct injury during anterior cervical discectomy: a rare complication. Case report. Journal of neurosurgery, 88 1, 151-4

Scott, D A; Greinwald, J H; Marietta, J R; Drury, S; Swiderski, R E; Viñas, A; DeAngelis, M M; Carmi, R; Ramesh, A; Kraft, M L; Elbedour, K; Skworak, A B; Friedman, R A; Srikumari Srisailapathy, C R; Verhoeven, K; Van Gamp, G; Lovett, M; Deininger, P L; Batzer, M A; Morton, C C; Keats, B J; Smith, R J; Sheffield, V C 1998. Identification and mutation analysis of a cochlear-expressed, zinc finger protein gene at the DFNB7/11 and dn hearing-loss loci on human chromosome 9q and mouse chromosome 19. Gene, 215 2, 461-9

Dunlevy, T M; Washington, A P; Greinwald, J H 1997. Pathologic quiz case 2. Congenital cartilaginous rests of the neck (CCRNs) (wattles). Archives of otolaryngology--head & neck surgery, 123 6, 655, 657

Gnuechtel, M M; Keyser, J S; Greinwald, J H; Postma, G N 1997. Electrocautery versus carbon dioxide laser for uvulopalatoplasty in the treatment of snoring. The Laryngoscope, 107 7, 848-54

Greinwald, J H; Lassen, L F 1997. Lipomas of the internal auditory canal. The Laryngoscope, 107 3, 364-8

Greinwald, J H; Scott, D A; Marietta, J R; Carmi, R; Manaligod, J; Ramesh, A; Zbar, R I; Kraft, M L; Elbedour, K; Yairi, Y; Musy, M; Skvorak, A B; Van Camp, G; Srisailapathy, C R; Lovett, M; Morton, C C; Sheffield, V C; Smith, R J 1997. Construction of P1-derived artificial chromosome and yeast artificial chromosome contigs encompassing the DFNB7 and DFNB11 region of chromosome 9q13-21. Genome research, 7 9, 879-86

Greinwald, J H; Holtel, M R 1996. Absorption of topical cocaine in rhinologic procedures. The Laryngoscope, 106 10, 1223-5

Greinwald, J H; Leichtman, L G; Simko, E J 1996. Hereditary thyroglossal duct cysts. Archives of otolaryngology--head & neck surgery, 122 10, 1094-6

Greinwald, J H; Wilson, J F; Haggerty, P G 1995. Peritonsillar abscess: an unlikely cause of necrotizing fasciitis. The Annals of otology, rhinology, and laryngology, 104 2, 133-7

Greinwald J.;Kelly K.;Tami T. 12-01-2005. Temporal Bone and Skull Base Trauma Neurotology, , 1070-1088

Lim L.;Greinwald J. 12-01-2002. Current status of genetics in the evaluation and management of sensorineural hearing loss Current Opinion in Otolaryngology and Head and Neck Surgery, 10 6, 435-439

Greinwald J.;Holtel M. 12-01-1997. Absorption of topical cocaine in rhinologic procedures American Journal of Rhinology, 11 1, 94

Shen J.;Oza A.M.;del Castillo I.;Duzkale H.;Matsunaga T.;Pandya A.;Kang H.P.;Mar-Heyming R.;Guha S.;Moyer K.;Lo C.;Kenna M.;Alexander J.J.;Zhang Y.;Hirsch Y.;Luo M.;Cao Y.;Wai Choy K.;Cheng Y.F.;Avraham K.B.;Hu X.;Garrido G.;Moreno-Pelayo M.A.;Greinwald J.;Zhang K.;Zeng Y.;Brownstein Z.;Basel-Salmon L.;Davidov B.;Frydman M.;Weiden T.;Nagan N.;Willis A.;Hemphill S.E.;Grant A.R.;Siegert R.K.;DiStefano M.T.;Amr S.S.;Rehm H.L.;Abou Tayoun A.N.;Azaiez H.;Booth K.T.;Smith R.J.;Giersch A.B.;Morton C.C.;Liu X.Z.;Tekin M.;Lu Y.;Yuan H.;Mutai H.;Schimmenti L. 11-01-2019. Consensus interpretation of the p.Met34Thr and p.Val37Ile variants in GJB2 by the ClinGen Hearing Lo Genetics in Medicine, 21 11, 2442-2452

DiStefano M.T.;Hemphill S.E.;Oza A.M.;Siegert R.K.;Grant A.R.;Hughes M.Y.;Cushman B.J.;Azaiez H.;Booth K.T.;Chapin A.;Duzkale H.;Matsunaga T.;Shen J.;Zhang W.;Kenna M.;Schimmenti L.A.;Tekin M.;Rehm H.L.;Tayoun A.N.A.;Amr S.S.;Abdelhak S.;Alexander J.;Avraham K.;Bhatia N.;Bai D.;Boczek N.;Brownstein Z.;Burt R.;Bylstra Y.;del Castillo I.;Choi B.Y.;Downie L.;Friedman T.;Giersch A.;Goh J.;Greinwald J.;Griffith A.J.;Hernandez A.;Holt J.;Hosoya M.;Ying L.J.;Jain K.;Kim U.K.;Kremer H.;Krantz I.;Leal S.;Lewis M.;Liu X.Z.;Low W.;Lu Y.;Luo M.;Masmoudi S.;Ming T.Y.;Moreno-Pelayo M.A.;Morín M.;Morton C.;Murray J.;Mutai H.;Nara K.;Pandya A.;Pei-Rong S.K.;Smith R.J.H.;Jamuar S.S.;Suer F.E.;Usami S.I.;Van Camp G.;Yamazawa K.;Yuan H.J.;Black-Zeigelbein E.;Zhang K. 10-01-2019. Correction: ClinGen expert clinical validity curation of 164 hearing loss gene–disease pairs (Geneti Genetics in Medicine, 21 10, 2409

DiStefano M.T.;Hemphill S.E.;Oza A.M.;Siegert R.K.;Grant A.R.;Hughes M.Y.;Cushman B.J.;Azaiez H.;Booth K.T.;Chapin A.;Duzkale H.;Matsunaga T.;Shen J.;Zhang W.;Kenna M.;Schimmenti L.A.;Tekin M.;Rehm H.L.;Tayoun A.N.A.;Amr S.S.;Abdelhak S.;Alexander J.;Avraham K.;Bhatia N.;Bai D.;Boczek N.;Brownstein Z.;Burt R.;Bylstra Y.;del Castillo I.;Choi B.Y.;Downie L.;Friedman T.;Giersch A.;Goh J.;Greinwald J.;Griffith A.J.;Hernandez A.;Holt J.;Hosoya M.;Ying L.J.;Jain K.;Kim U.K.;Kremer H.;Krantz I.;Leal S.;Lewis M.;Liu X.Z.;Low W.;Lu Y.;Luo M.;Masmoudi S.;Ming T.Y.;Moreno-Pelayo M.A.;Morín M.;Morton C.;Murray J.;Mutai H.;Nara K.;Pandya A.;Pei-Rong S.K.;Smith R.J.H.;Jamuar S.S.;Suer F.E.;Usami S.I.;Van Camp G.;Yamazawa K.;Yuan H.J.;Black-Zeigelbein E.;Zhang K. 10-01-2019. ClinGen expert clinical validity curation of 164 hearing loss gene–disease pairs Genetics in Medicine, 21 10, 2239-2247

Smith N.;Greinwald J. 10-01-2011. To tube or not to tube: Indications for myringotomy with tube placement Current Opinion in Otolaryngology and Head and Neck Surgery, 19 5, 363-366

Greinwald J.;Taggart R. 10-01-2002. Environmentally induced hearing impairment: The impact of genetics Current Opinion in Otolaryngology and Head and Neck Surgery, 10 5, 346-349

Greinwald J.;Dealarcon A.;Cohen A.;Uwiera T.;Zhang K.;Benton C.;Halstead M.;Meinzen-Derr J. 06-01-2013. Significance of unilateral enlarged vestibular aqueduct Laryngoscope, 123 6, 1537-1546

Boston M.;Halsted M.;Meinzen-Derr J.;Bean J.;Vijayasekaran S.;Arjmand E.;Choo D.;Benton C.;Greinwald J. 06-01-2007. The large vestibular aqueduct: A new definition based on audiologic and computed tomography correlat Otolaryngology - Head and Neck Surgery, 136 6, 972-977

Vijayasekaran S.;Halsted M.;Boston M.;Meinzen-Derr J.;Bardo D.;Greinwald J.;Benton C. 06-01-2007. When is the vestibular aqueduct enlarged? A statistical analysis of the normative distribution of ve American Journal of Neuroradiology, 28 6, 1133-1138

Dyer L.;Wang X.;Zhang K.;Greinwald J.;Valencia C.A. 05-15-2017. Erratum to: Application of next-generation sequencing to hearing loss. [Next Generation Sequencing B Next Generation Sequencing Based Clinical Molecular Diagnosis of Human Genetic Disorders, , E1

Valencia C.A.;Dyer L.;Wang X.;Zhang K.;Greinwald J. 05-15-2017. Application of next-generation sequencing to hearing loss Next Generation Sequencing Based Clinical Molecular Diagnosis of Human Genetic Disorders, , 71-87

Epperson M.V.;Born H.L.;Greinwald J. 05-01-2019. Radiologic recognition of cochlear implant magnet displacement International Journal of Pediatric Otorhinolaryngology, 120 , 64-67

Schmithorst V.;Holland S.;Ret J.;Duggins A.;Arjmand E.;Greinwald J. 04-04-2005. Cortical reorganization in children with unilateral sensorineural hearing loss NeuroReport, 16 5, 463-467

Greinwald J.;Cohen A.;Hemanackah S.;Azizkhan R. 04-01-2008. Massive lymphatic malformations of the head, neck, and chest Journal of Otolaryngology - Head and Neck Surgery, 37 2, 169-173

Amir F.;Atzinger C.;Massey K.;Greinwald J.;Hunter L.L.;Ulm E.;Kettler M. 03-01-2020. The Clinical Journey of Patients with Riboflavin Transporter Deficiency Type 2 Journal of Child Neurology, 35 4, 283-290

Propst E.;Prager J.;Shott S.;Koch B.;Mortensen J.;Greinwald J. 03-01-2011. Resolution of hypoglossal nerve palsy associated with retropharyngeal abscess after prompt medical a International Journal of Pediatric Otorhinolaryngology Extra, 6 2, 74-77

Madden C.;Halsted M.;Meinzen-Derr J.;Bardo D.;Boston M.;Arjmand E.;Nishimura C.;Yang T.;Benton C.;Das V.;Smith R.;Choo D.;Greinwald J. 02-01-2007. The influence of mutations in the SLC26A4 gene on the temporal bone in a population with enlarged ve Archives of Otolaryngology - Head and Neck Surgery, 133 2, 162-168

Choo D.;Ward J.;Reece A.;Dou H.;Lin Z.;Greinwald J. 01-15-2006. Molecular mechanisms underlying inner ear patterning defects in kreisler mutants Developmental Biology, 289 2, 308-317

Pique L.;Brennan M.;Davidson C.;Schaefer F.;Greinwald J.;Schrijver I. 01-01-2014. Mutation analysis of the SLC26A4, FOXI1 and KCNJ10 genes in individuals with congenital hearing loss PeerJ, 2014 1,

Uwiera T.C.;Dealarcon A.;Meinzen-Derr J.;Cohen A.P.;Rasmussen B.;Shott G.;Greinwald J. 01-01-2010. Hearing Loss Progression and Contralateral Involvement in Children with Unilateral Sensorineural Hea Annals of Otology, Rhinology & Laryngology, 119 11, 781-785

Uwiera T.;DeAlarcon A.;Meinzen-Derr J.;Cohen A.;Rasmussen B.;Shott G.;Greinwald J. 01-01-2009. Hearing loss progression and contralateral involvement in children with unilateral sensorineural hea Annals of Otology, Rhinology and Laryngology, 118 11, 781-785

Wiley S.;Choo D.;Meinzen-Derr J.;Hilbert L.;Greinwald J. 01-01-2006. GJB2 mutations and additional disabilities in a pediatric cochlear implant population International Journal of Pediatric Otorhinolaryngology, 70 3, 493-500

Madden C.;Wiley S.;Schleiss M.;Benton C.;Meinzen-Derr J.;Greinwald J.;Choo D. 01-01-2005. Audiometric, clinical and educational outcomes in a pediatric symptomatic congenital cytomegalovirus International Journal of Pediatric Otorhinolaryngology, 69 9, 1191-1198

Salamone F.;Bobbitt D.;Myer C.;Rutter M.;Greinwald J. 01-01-2004. Bacterial tracheitis reexamined: Is there a less severe manifestation? Otolaryngology - Head and Neck Surgery, 131 6, 871-876

Madden C.;Halsted M.;Benton C.;Greinwald J.;Choo D. 01-01-2003. Enlarged vestibular aqueduct syndrome in the pediatric population Otology and Neurotology, 24 4, 625-632

Salamone F.;Myer C.;Rutter M.;Bobbitt D.;Greinwald J. 01-01-2003. Bacterial Tracheitis Otolaryngology- Head and Neck Surgery, 129 2, P83-P83

Madden C.;Hilbert L.;Rutter M.;Greinwald J.;Choo D. 01-01-2002. Pediatric cochlear implantation in auditory neuropathy Otology and Neurotology, 23 2, 163-168

Gessler, Eric M; Simko, Eric J; Greinwald, John H . Adult laryngomalacia: an uncommon clinical entity. American journal of otolaryngology, 23 6, 386-9

Van Laer, L; Van Camp, G; van Zuijlen, D; Green, E D; Verstreken, M; Schatteman, I; Van de Heyning, P; Balemans, W; Coucke, P; Greinwald, J H; Smith, R J; Huizing, E; Willems, P . Refined mapping of a gene for autosomal dominant progressive sensorineural hearing loss (DFNA5) to a 2-cM region, and exclusion of a candidate gene that is expressed in the cochlea. European journal of human genetics : EJHG, 5 6, 397-405