The Cochlear Cleft

מאת Chadwell, Jon B., Halsted, Mark J., Choo, Daniel I., Greinwald, John H., Benton, Corning
הוצא לאור ב AJNR Am J Neuroradiol (2004)

Expression of Aquaporin 1 and 5 in the Developing Mouse Inner Ear and Audiovestibular Assessment of an Aqp5 Null Mutant

מאת Merves, Michele, Krane, Carissa M., Dou, Hongwei, Greinwald, John H., Menon, Anil G., Choo, Daniel
יצא לאור 2003

An Overview of Custom Array Sequencing

מאת Kothiyal, Prachi, Cox, Stephanie, Ebert, Jonathan, Aronow, Bruce J., Greinwald, John H., Rehm, Heidi L.
הוצא לאור ב Curr Protoc Hum Genet (2009)

High-throughput detection of mutations responsible for childhood hearing loss using resequencing microarrays

מאת Kothiyal, Prachi, Cox, Stephanie, Ebert, Jonathan, Husami, Ammar, Kenna, Margaret A, Greinwald, John H, Aronow, Bruce J, Rehm, Heidi L
יצא לאור 2010

Clinical and Molecular Characterization of a Chinese Patient With Auditory Neuropathy Associated With Mitochondrial 12S rRNA T1095C Mutation

מאת Wang, Qiuju, Li, Roughua, Zhao, Hui, Peters, Jennifer L., Liu, Qiong, Yang, Li, Han, Dongyi, Greinwald, John H., Young, Wie-Yen, Guan, Min-Xin
יצא לאור 2005

A rapid method for detection of five known mutations associated with aminoglycoside-induced deafness

מאת 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
יצא לאור 2009

Audiologic and Temporal Bone Imaging Findings in Patients With Sensorineural Hearing Loss and GJB2 Mutations

מאת 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.
הוצא לאור ב Laryngoscope (2009)

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 Nonsyndromi...

מאת 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
יצא לאור 2005

Molecular genetics of MARVELD2 and clinical phenotype in Pakistani and Slovak families segregating DFNB49 hearing loss

מאת 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
הוצא לאור ב Hum Genet (2015)

Genetic Analysis through OtoSeq of Pakistani Families Segregating Prelingual Hearing Loss

מאת 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.
יצא לאור 2013

Maternally inherited aminoglycoside-induced and nonsyndromic hearing loss is associated with the 12S rRNA C1494T mutation in three Han Chinese pedigrees

מאת Chen, Jianfu, Yang, Li, Yang, Aifeng, Zhu, Yi, Zhao, Jianyue, Sun, Dongmei, Tao, Zhihua, Tang, Xiaowen, Wang, Jindan, Wang, Xinjian, Lan, Jinshan, Li, Weixing, Wu, Fangli, Yuan, Qian, Feng, Jinbao, Wu, Chunli, Liao, Zhisu, Li, Zhiyuan, Greinwald, John H., Lu, Jianxin, Guan, Min-Xin
יצא לאור 2007