The Girl With the Bleeding Earlobe Mass.
Nistel, M; Lee, SH; Born, H; Greinwald, JH; Abdaljaleel, M; Sobolewski, B.
Pediatric Emergency Care.
2021;
37:e1718-e1720.
Disease-specific ACMG/AMP guidelines improve sequence variant interpretation for hearing loss.
Patel, MJ; DiStefano, MT; Oza, AM; Hughes, MY; Wilcox, EH; Hemphill, SE; Cushman, BJ; Grant, AR; Siegert, RK; Shen, J; et al.
Genetics in Medicine.
2021;
23:2208-2212.
Cortical processing of location and frequency changes of sounds in normal hearing listeners.
Zhang, F; McGuire, K; Firestone, G; Dalrymple, K; Greinwald, J; Fu, QJ.
Hearing Research.
2021;
400.
Socioeconomic Disparities in Pediatric Single-Sided Deafness.
Lipschitz, N; Kohlberg, GD; Scott, M; Smith, MM; Jr, GJ H.
Otolaryngology - Head and Neck Surgery.
2020;
163:829-834.
How Strong Is the Duty to Treat in a Pandemic? Ethics in Practice: Point-Counterpoint.
Redmann, AJ; Manning, A; Kennedy, A; Greinwald, JH; deAlarcon, A.
Otolaryngology - Head and Neck Surgery.
2020;
163:325-327.
Imaging findings in pediatric single-sided deafness and asymmetric hearing loss.
Lipschitz, N; Kohlberg, GD; Scott, M; Jr, GJ H.
Laryngoscope.
2020;
130:1007-1010.
International Pediatric Otolaryngology Group (IPOG) Consensus Recommendations: Congenital Cholesteatoma.
Denoyelle, F; Simon, F; Chang, KW; Chan, KH; Cheng, AG; Cheng, AT; Choo, DI; Daniel, SJ; Farinetti, A; Garabedian, E; et al.
Otology and Neurotology.
2020;
41:345-351.
The Clinical Journey of Patients with Riboflavin Transporter Deficiency Type 2.
Amir, F; Atzinger, C; Massey, K; Greinwald, J; Hunter, LL; Ulm, E; Kettler, M.
Journal of Child Neurology.
2020;
35:283-290.
Consensus interpretation of the p.Met34Thr and p.Val37Ile variants in GJB2 by the ClinGen Hearing Loss Expert Panel.
Shen, J; Oza, AM; del Castillo, I; Duzkale, H; Matsunaga, T; Pandya, A; Kang, HP; Mar-Heyming, R; Guha, S; Moyer, K; et al.
Genetics in Medicine.
2019;
21:2442-2452.
ClinGen expert clinical validity curation of 164 hearing loss gene-disease pairs.
DiStefano, MT; Hemphill, SE; Oza, AM; Siegert, RK; Grant, AR; Hughes, MY; Cushman, BJ; Azaiez, H; Booth, KT; Chapin, A; et al.
Genetics in Medicine.
2019;
21:2239-2247.