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Combined hearing screening and genetic screening of deafness among Hakka newborns in China.

• Authors : Zeng X; Laboratory of Medical Genetics, Heyuan Women and Children's Hospital, Heyuan, Guangdong, China; Department of Clinical Laboratory, Heyuan Women and Children's Hospital, Heyuan, Guangdong, China. Electronic address: .

Subjects: Genetic Testing/Genetic Testing/Genetic Testing/*methods ; Hearing Loss/Hearing Loss/Hearing Loss/*diagnosis ; Hearing Tests/Hearing Tests/Hearing Tests/*methods

• Source: International journal of pediatric otorhinolaryngology [Int J Pediatr Otorhinolaryngol] 2020 Sep; Vol. 136, pp. 110120. Date of Electronic Publication: 2020 Jun 17.Publisher: Elsevier Scientific Publishers Country of Publication: Ireland NLM ID: 8003603 Publication Model: Print-Electronic Cited Medium: Internet

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Deafness induces complete crossmodal plasticity in a belt region of dorsal auditory cortex.

• Authors : Merrikhi, Yaser (AUTHOR); Mirzaei, Ali (AUTHOR); Kok, Melanie A. (AUTHOR)

Subjects: DEAFNESS; AUDITORY cortex; VISUAL perception

• Source: European Journal of Neuroscience. Aug2023, Vol. 58 Issue 4, p3058-3073. 16p. 1 Color Photograph, 1 Diagram, 5 Charts, 5 Graphs.

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Screening Consanguineous Families for Hearing Loss Using the MiamiOtoGenes Panel.

• Authors : Kannan-Sundhari A; Department of Otolaryngology, University of Miami Miller School of Medicine, Miami, Florida, USA.; Dr. John T. Macdonald Foundation, Department of Human Genetics, University of Miami Miller School of Medicine, Miami, Florida, USA.

Subjects: Genetic Testing/Genetic Testing/Genetic Testing/*methods ; Hearing Loss/Hearing Loss/Hearing Loss/*diagnosis; Adult

• Source: Genetic testing and molecular biomarkers [Genet Test Mol Biomarkers] 2020 Oct; Vol. 24 (10), pp. 674-680. Date of Electronic Publication: 2020 Sep Publisher: Mary Ann Liebert, Inc Country of Publication: United States NLM ID: 101494210 Publication Model: Print-Electronic Cited Medium: Internet

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Genetic testing in the acute setting: a round table discussion.

• Authors : McDermott JH; Manchester Centre for Genomic, Manchester University NHS Foundation Trust, Manchester, UK .

Subjects: Hearing Loss*/Hearing Loss*/Hearing Loss*/chemically induced ; Hearing Loss*/Hearing Loss*/Hearing Loss*/genetics ; Point-of-Care Testing*

• Source: Journal of medical ethics [J Med Ethics] 2020 Aug; Vol. 46 (8), pp. 531-532. Date of Electronic Publication: 2020 Jul 10.Publisher: BMJ Publishing Group Country of Publication: England NLM ID: 7513619 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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ClinGen expert clinical validity curation of 164 hearing loss gene-disease pairs.

• Authors : DiStefano MT; ClinGen Hearing Loss Clinical Domain Working Group

Subjects: Deafness/Deafness/Deafness/*genetics ; Genetic Testing/Genetic Testing/Genetic Testing/*methods ; Hearing Loss/Hearing Loss/Hearing Loss/*genetics

• Source: Genetics in medicine : official journal of the American College of Medical Genetics [Genet Med] 2019 Oct; Vol. 21 (10), pp. 2239-2247. Date of Electronic Publication: 2019 Mar 21.Publisher: Elsevier Country of Publication: United States NLM ID: 9815831 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Nationwide population genetic screening improves outcomes of newborn screening for hearing loss in China.

• Authors : Wang Q; Department of Otolaryngology-Head and Neck Surgery, Chinese PLA Institute of Otolaryngology, Chinese PLA General Hospital, Beijing, China.; Xiang J

Subjects: Genetic Testing/Genetic Testing/Genetic Testing/*methods ; Hearing Loss/Hearing Loss/Hearing Loss/*genetics ; Neonatal Screening/Neonatal Screening/Neonatal Screening/*methods

• Source: Genetics in medicine : official journal of the American College of Medical Genetics [Genet Med] 2019 Oct; Vol. 21 (10), pp. 2231-2238. Date of Electronic Publication: 2019 Mar 20.Publisher: Elsevier Country of Publication: United States NLM ID: 9815831 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Detection of hereditary hearing loss gene by DNA microarray.

• Authors : Han GY; Xuzhou Institute of Medical Sciences, Xuzhou, Jiangsu, China. .; Xu Z

Subjects: Oligonucleotide Array Sequence Analysis*; Connexins/Connexins/Connexins/*genetics ; Genetic Testing/Genetic Testing/Genetic Testing/*methods

• Source: European review for medical and pharmacological sciences [Eur Rev Med Pharmacol Sci] 2017 Aug; Vol. 21 (16), pp. 3538-3542.Publisher: Verduci Country of Publication: Italy NLM ID: 9717360 Publication Model: Print Cited Medium: Internet ISSN: 2284-0729 (Electronic)

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Prospective mutation screening of three common deafness genes in a large Taiwanese Cohort with idiopathic bilateral sensorineural hearing impairment reveals a difference in the results between families from hospitals and those from rehabilitation facilities.

• Authors : Wu CC; Department of Otolaryngology, National Taiwan University Hospital, Taipei, Taiwan.; Chen PJ

Subjects: Genetic Testing*; Deafness/Deafness/Deafness/*genetics ; Deafness/Deafness/Deafness/*rehabilitation

• Source: Audiology & neuro-otology [Audiol Neurootol] 2008; Vol. 13 (3), pp. 172-81. Date of Electronic Publication: 2007 Dec 13.Publisher: Karger Country of Publication: Switzerland NLM ID: 9606930 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1421-9700

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New Research on Hearing Loss from National Institute on Deafness and Other Communication Disorders Summarized (Pathophysiology of human hearing loss associated with variants in myosins).

• Source: Health & Medicine Week. 2024, pages. 3943

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Hereditary deafness carrier screening in 9,993 Chinese individuals.

• Authors : Yanqiu Liu; Lei Wang; Lanlai Yuan

Subjects: MEDICAL screening; DEAFNESS; GENETIC testingCHINA

• Source: Frontiers in Genetics; 2024, p1-7, 7p

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Genetic screening of common genetic deafness in 60,391 women of childbearing age and intervention of birth defects.

• Authors : Linyuan Niu; Liqin Liu; Jinjun Tian

Subjects: GENETIC testing; CHILDBEARING age; DEAFNESS

• Source: Archives of Medical Science; Jan2024, Vol. 20 Issue 1, p113-123, 11p

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Retrospective Analysis of the Outcomes of Genetic Testing in Patients Suspected to Have Hereditary Hearing Loss or Deafness.

• Authors : Bowden, Acacia; Hubbel, Alexandra; Smith, Lindsay

Subjects: GENETICS of deafness; COCHLEAR implants; SEQUENCE analysis

• Source: American Journal of Audiology. Mar2024, Vol. 33 Issue 1, p233-241. 9p.

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Genetic testing involving 100 common mutations for antenatal diagnosis of hereditary hearing loss in Chongqing, China.

• Authors : Hu H; Second Affiliated Hospital, Army Military Medical University, Chongqing.; Zhou P

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

• Source: Medicine [Medicine (Baltimore)] 2021 Apr 30; Vol. 100 (17), pp. e25647.Publisher: Lippincott Williams & Wilkins Country of Publication: United States NLM ID: 2985248R Publication Model: Print Cited Medium: Internet ISSN:

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Assessing variants of uncertain significance implicated in hearing loss using a comprehensive deafness proteome.

• Authors : Tollefson, Mallory R.; Gogal, Rose A.; Weaver, A. Monique

• Source: Human Genetics. June, 2023, Vol. 142 Issue 6, p819, 16 p.

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New Research on Hearing Loss from National Institute on Deafness and Other Communication Disorders Summarized (Pathophysiology of human hearing loss associated with variants in myosins)

• Source: Health & Medicine Week. April 5, 2024, 3943

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Hearing loss in patients with chronic kidney disease undergoing haemodialysis.

• Authors : T. D., Thimmappa¹ ; K. S., Gangadhar¹; S., Ramesh¹

Subjects: *CHRONIC kidney failure; *DEAFNESS; *HEMODIALYSIS

• Source: Al Ameen Journal of Medical Sciences. Jan-Mar2024, Vol. 17 Issue 1, p81-84. 4p.

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Factors influencing parental decision about genetics evaluation for their deaf or hard-of-hearing child.

• Authors : Palmer CG; Department of Psychiatry and Biobehavioral Sciences, University of California, Los Angeles, California, USA. ; Lueddeke JT

Subjects: Surveys and Questionnaires*; Deafness/Deafness/Deafness/*diagnosis ; Genetic Testing/Genetic Testing/Genetic Testing/*psychology

• Source: Genetics in medicine : official journal of the American College of Medical Genetics [Genet Med] 2009 Apr; Vol. 11 (4), pp. 248-55.Publisher: Elsevier Country of Publication: United States NLM ID: 9815831 Publication Model: Print Cited Medium: Internet ISSN: 1530-0366

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Attitudes of deaf and hard of hearing subjects towards genetic testing and prenatal diagnosis of hearing loss.

• Authors : Stern SJ; Arnos KS; Murrelle L

Subjects: Deafness/Deafness/Deafness/*psychology ; Genetic Testing/Genetic Testing/Genetic Testing/*psychology ; Hearing Loss/Hearing Loss/Hearing Loss/*psychology

• Source: Journal of medical genetics [J Med Genet] 2002 Jun; Vol. 39 (6), pp. 449-53.Publisher: British Medical Association Country of Publication: England NLM ID: 2985087R Publication Model: Print Cited Medium: Internet ISSN:

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A CDH23 missense variant in Beauceron dogs with non‐syndromic deafness.

• Authors : Abitbol, Marie^1,2 (AUTHOR) ‐sup.fr; Jagannathan, Vidhya³ (AUTHOR); Lopez, Marie⁴ (AUTHOR)

Subjects: *HAIR cells; *DEAFNESS; *HOMOZYGOSITYFRANCE

• Source: Animal Genetics. Feb2023, Vol. 54 Issue 1, p73-77. 5p.

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[The effects of newborn genetic screening for GJB2 and hearing follow-ups].

• Authors : Gao R; Chen X; Li D

Subjects: Genetic Testing* ; Mutation* ; Neonatal Screening*

• Source: Lin chuang er bi yan hou tou jing wai ke za zhi = Journal of clinical otorhinolaryngology, head, and neck surgery [Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi] 2015 Feb; Vol. 29 (4), Publisher: Lin chuang er bi yan hou tou jing wai ke za zhi bain ji bu Country of Publication: China NLM ID: 101303164 Publication Model: Print Cited Medium:

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New Sensorineural Hearing Loss Research from Chinese People's Liberation Army (PLA) Medical School Discussed (MPZL2-a common autosomal recessive deafness gene related to moderate sensorineural hearing loss in the Chinese population).

• Source: Health & Medicine Week. 2024, pages. 3803

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The responsible genes in Japanese deafness patients and clinical application using Invader assay.

• Authors : Usami, Shin-Ichi (AUTHOR); Wagatsuma, Michio (AUTHOR); Fukuoka, Hisakuni (AUTHOR)

Subjects: GENETICS of deafness; DEAFNESS; DEAF people

• Source: Acta Oto-Laryngologica. Apr2008, Vol. 128 Issue 4, p446-454. 9p. 3 Diagrams, 1 Chart.

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Inclusion Programmes for Students Who are Deaf and Hard of Hearing in Saudsi Arabia: Issues and Recommendations.

• Authors : Alasim, Khalid

Subjects: EDUCATION of the deaf; DEAFNESS; HEARING disordersSAUDI Arabia

• Source: International Journal of Disability, Development & Education. Nov2020, Vol. 67 Issue 6, p571-591. 21p. 5 Charts.

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GJB2, SLC26A4 and mitochondrial DNA A1555G mutations in prelingual deafness in Northern Chinese subjects.

• Authors : Guo, Yu-Fen (AUTHOR); Liu, Xiao-Wen (AUTHOR); Guan, Jing (AUTHOR)

Subjects: DEAFNESS; GENES; HUMAN chromosome abnormality diagnosisCHINA

• Source: Acta Oto-Laryngologica. Mar2008, Vol. 128 Issue 3, p297-303. 7p. 3 Charts, 2 Graphs.

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Exome sequencing in infants with congenital hearing impairment: a population-based cohort study.

• Authors : Downie L; Melbourne Genomics Health Alliance

Subjects: Genetic Testing/Genetic Testing/Genetic Testing/*standards ; Hearing Loss/Hearing Loss/Hearing Loss/*genetics ; Neonatal Screening/Neonatal Screening/Neonatal Screening/*standards

• Source: European journal of human genetics : EJHG [Eur J Hum Genet] 2020 May; Vol. 28 (5), pp. 587-596. Date of Electronic Publication: 2019 Dec 12.Publisher: Nature Publishing Group Country of Publication: England NLM ID: 9302235 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Concurrent Hearing and Genetic Screening of 180,469 Neonates with Follow-up in Beijing, China.

• Authors : Dai P; Department of Otolaryngology Head and Neck Surgery, Chinese People's Liberation Army (PLA) General Hospital, Beijing, 100853, P. R. China.; Huang LH

Subjects: Genetic Testing/Genetic Testing/Genetic Testing/*methods ; Hearing Loss/Hearing Loss/Hearing Loss/*diagnosis; Beijing

• Source: American journal of human genetics [Am J Hum Genet] 2019 Oct 03; Vol. 105 (4), pp. 803-812. Date of Electronic Publication: 2019 Sep 26.Publisher: Cell Press Country of Publication: United States NLM ID: 0370475 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Case report: Prenatal diagnosis in the fetus of a couple with both thalassemia and deafness genes.

• Authors : Youqiong Li; Liang Liang; Jinping Bai

Subjects: PRENATAL diagnosis; DEAFNESS; FETUS

• Source: Frontiers in Genetics; 2023, p1-5, 5p

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Reports Outline Hearing Loss Study Results from National Institute of Deafness and Other Communication Disorders (Chd7 Variants Associated With Hearing Loss and Enlargement of the Vestibular Aqueduct).

• Source: Health & Medicine Week. 2023, pages. 4288

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Newborn genetic screening for hearing impairment: a preliminary study at a tertiary center.

• Authors : Wu CC; Department of Otolaryngology, National Taiwan University Hospital, Taipei, Taiwan.; Hung CC

Subjects: Hospitals*; Genetic Testing/Genetic Testing/Genetic Testing/*methods ; Hearing Loss/Hearing Loss/Hearing Loss/*diagnosis

• Source: PloS one [PLoS One] 2011; Vol. 6 (7), pp. e22314. Date of Electronic Publication: 2011 Jul 19.Publisher: Public Library of Science Country of Publication: United States NLM ID: 101285081 Publication Model: Print-Electronic Cited Medium: Internet

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The clinical and genetic characteristics of maternally inherited diabetes and deafness (MIDD) with mitochondrial m.3243A > G mutation: A 10‐year follow‐up observation study and literature review.

• Authors : Zheng, Shasha; Wang, Juanjuan; Sun, Minxian

Subjects: LITERATURE reviews; DEAFNESS; MITOCHONDRIAL DNA

• Source: Clinical Case Reports; Feb2024, Vol. 12 Issue 2, p1-9, 9p

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The Inheritance of Hearing Loss and Deafness: A Historical Perspective.

• Authors : Martini, Alessandro; Cozza, Andrea; Di Pasquale Fiasca, Valerio Maria

Subjects: HEARING disorders; DEAFNESS; HEREDITYMENDEL, Gregor, 1822-1884

• Source: Audiology Research; Feb2024, Vol. 14 Issue 1, p116-128, 13p

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Deafness alters auditory nerve fibre responses to cochlear implant stimulation.

• Authors : Sly, David J. (AUTHOR); Heffer, Leon F. (AUTHOR); White, Mark W. (AUTHOR)

Subjects: DEAFNESS; EAR diseases; ELECTRIC stimulation

• Source: European Journal of Neuroscience. Jul2007, Vol. 26 Issue 2, p510-522. 13p. 2 Charts, 8 Graphs.

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Easy, rapid, and cost-effective methods for identifying carriers of recurrent GJB2 mutations causing nonsyndromic hearing impairment in the Greek population.

• Authors : Kokotas H; Department of Genetics, Institute of Child Health, Aghia Sophia Children's Hospital, Athens, Greece. ; Grigoriadou M

Subjects: Mutation*; Connexins/Connexins/Connexins/*genetics ; Genetic Carrier Screening/Genetic Carrier Screening/Genetic Carrier Screening/*methods

• Source: Genetic testing and molecular biomarkers [Genet Test Mol Biomarkers] 2010 Apr; Vol. 14 (2), pp. 189-92.Publisher: Mary Ann Liebert, Inc Country of Publication: United States NLM ID: 101494210 Publication Model: Print Cited Medium: Internet ISSN:

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New Sensorineural Hearing Loss Research from Chinese People's Liberation Army (PLA) Medical School Discussed (MPZL2-a common autosomal recessive deafness gene related to moderate sensorineural hearing loss in the Chinese population)

• Source: Health & Medicine Week. March 22, 2024, 3803

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Impact of genetic advances and testing for hearing loss: results from a national consumer survey.

• Authors : Withrow KA; Department of Human and Molecular Genetics, Virginia Commonwealth University, Richmond, VA 23298-0033, USA.; Tracy KA

Subjects: Attitude to Health* ; Motivation*; Deafness/Deafness/Deafness/*genetics

• Source: American journal of medical genetics. Part A [Am J Med Genet A] 2009 Jun; Vol. 149A (6), pp. 1159-68.Publisher: Wiley-Blackwell Country of Publication: United States NLM ID: 101235741 Publication Model: Print Cited Medium: Internet ISSN:

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Research from National Institute on Deafness and Other Communication Disorders Broadens Understanding of Noise-Induced Hearing Loss (Metformin Protects Against Noise-Induced Hearing Loss in Male Mice).

• Source: Health & Medicine Week. 2023, pages. 5047

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Deafness Gene Mutations in Newborns in the Foshan Area of South China With Bloodspot-Based Genetic Screening Tests

• Authors : Cao, Shunwang; Sha, Yanhua; Ke, Peifeng

• Source: American Journal of Audiology. June, 2020, Vol. 29 Issue 2, p165, 5 p.

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Comparison of treatment modalities for single-sided deafness in paediatric patients.

• Authors : Kubina, M; Fornwalt, B; Patel, S

Subjects: TREATMENT of hearing disorders; COCHLEAR implants; DEAFNESS

• Source: Journal of Laryngology & Otology; Jul2023, Vol. 137 Issue 7, p725-731, 7p

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Health-related quality of life in hearing-impaired adolescents and children.

• Authors : Niemensivu, Riina; Roine, Risto Paavo; Sintonen, Harri

Subjects: ACADEMIC medical centers; DEAFNESS; HEARING impaired childrenFINLAND

• Source: Acta Oto-Laryngologica. Jul2018, Vol. 138 Issue 7, p652-658. 7p.

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Otolaryngologists’ role in improving cognitive decline.

• Authors : Blebea, Cristina Maria¹; Ujvary, Laszlo Peter¹ ; George Dindelegan, Maximilian¹

Subjects: *DEAFNESS; *DEMENTIAWORLD Health Organization

• Source: ORL.ro. 2021, Issue 52, p18-20. 3p.

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Reports Outline Hearing Loss Study Results from National Institute of Deafness and Other Communication Disorders (Chd7 Variants Associated With Hearing Loss and Enlargement of the Vestibular Aqueduct)

• Source: Health & Medicine Week. October 20, 2023, p4288

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