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Editorial to the Special Issue on "The molecular genetics of hearing and deafness".

• Authors : Booth, Kevin T.; Shearer, A. Eliot

Subjects: MOLECULAR genetics; HUMAN genetics; GENETIC testing

• Source: Human Genetics; Apr2022, Vol. 141 Issue 3/4, p305-306, 2p

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Concurrent hearing and genetic screening in a general newborn population.

• Authors : Guo L; Jining Maternal and Child Health Care Service Center, Jining, 272000, China.; Xiang J

Subjects: Genetic Testing* ; Hearing Loss*/Hearing Loss*/Hearing Loss*/diagnosis ; Hearing Loss*/Hearing Loss*/Hearing Loss*/genetics

• Source: Human genetics [Hum Genet] 2020 Apr; Vol. 139 (4), pp. 521-530. Date of Electronic Publication: 2020 Jan 30.Publisher: Springer Verlag Country of Publication: Germany NLM ID: 7613873 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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A common variant in CLDN14 causes precipitous, prelingual sensorineural hearing loss in multiple families due to founder effect.

• Authors : Pater, Justin A.; Benteau, Tammy; Griffin, Anne

• Source: Human Genetics. January, 2017, Vol. 136 Issue 1, p107, 12 p.

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Comprehensive genetic testing in the clinical evaluation of 1119 patients with hearing loss.

• Authors : Sloan-Heggen CM; Molecular Otolaryngology and Renal Research Laboratories, Department of Otolaryngology-Head and Neck Surgery, University of Iowa Carver College of Medicine, 200 Hawkins Drive, Iowa City, IA, 52242, USA.; Department of Molecular Physiology and Biophysics, University of Iowa Carver College of Medicine, Iowa City, 52242, IA, USA.

Subjects: Genetic Testing*; Hearing Loss/Hearing Loss/Hearing Loss/*genetics; Adolescent

• Source: Human genetics [Hum Genet] 2016 Apr; Vol. 135 (4), pp. 441-450. Date of Electronic Publication: 2016 Mar 11.Publisher: Springer Verlag Country of Publication: Germany NLM ID: 7613873 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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The genetic etiology of hearing loss in Japan revealed by the social health insurance-based genetic testing of 10K patients.

• Authors : Usami, Shin-ichi; Nishio, Shin-ya

Subjects: GENETIC testing; HEARING disorders; SENSORINEURAL hearing lossJAPAN

• Source: Human Genetics; Apr2022, Vol. 141 Issue 3/4, p665-681, 17p

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Molecular and genetic characterization of a large Brazilian cohort presenting hearing loss.

• Authors : Batissoco, Ana Carla; Pedroso-Campos, Vinicius; Pardono, Eliete

Subjects: HEARING disorders; GENETIC testing; MEDICAL screening

• Source: Human Genetics; Apr2022, Vol. 141 Issue 3/4, p519-538, 20p

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Genetic testing for pediatric hearing loss: no time to waste.

• Authors : Kenna, Margaret A.

Subjects: GENETIC testing; HEARING disorders; HUMAN genes

• Source: Human Genetics; Apr2022, Vol. 141 Issue 3/4, p315-317, 3p

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Racial and ethnic disparities in genetic testing for hearing loss: a systematic review and synthesis.

• Authors : Rouse, Stephanie L.; Florentine, Michelle M.; Taketa, Emily

Subjects: HEARING disorders; GENETIC testing; RACIAL inequality

• Source: Human Genetics; Apr2022, Vol. 141 Issue 3/4, p485-494, 10p

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The PMEL gene and merle (dapple) in the dachshund: cryptic, hidden, and mosaic variants demonstrate the need for genetic testing prior to breeding.

• Authors : Ballif BC; Paw Print Genetics, Genetic Veterinary Sciences, Inc., 220 E Rowan, Suite 220, Spokane, WA, 99207, USA. .; Emerson LJ

Subjects: Animal Fur/Animal Fur/Animal Fur/*anatomy & histology ; Dogs/Dogs/Dogs/*genetics ; Genetic Testing/Genetic Testing/Genetic Testing/*veterinary

• Source: Human genetics [Hum Genet] 2021 Nov; Vol. 140 (11), pp. 1581-1591. Date of Electronic Publication: 2021 Aug 09.Publisher: Springer Verlag Country of Publication: Germany NLM ID: 7613873 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Genome-first approach to rare EYA4 variants and cardio-auditory phenotypes in adults.

• Authors : Ahmadmehrabi, Shadi; Li, Binglan; Park, Joseph

Subjects: GENETIC testing; PHENOTYPES; ADULTS

• Source: Human Genetics; Jun2021, Vol. 140 Issue 6, p957-967, 11p

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