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Precision Health Database


Precision Health Database|Search|PHGKB

Reproductive and Child Health

Last data update: Jun 02, 2023. (Total: 60071 Documents since 2012)
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Query Trace: Hearing Loss Or Hearing Screening Or Congenital Deafness[original query]>>Original Studies[Product Type]
The qualitative experiences of otolaryngologists with genetic services in pediatric hearing loss evaluation.
Aaliyah Heyward et al. J Community Genet 2023
Optimized concurrent hearing and genetic screening in Beijing, China: A cross-sectional study.
Cheng Wen et al. Biosci Trends 2023
The Enigmatic Genetic Landscape of Hereditary Hearing Loss: A Multistep Diagnostic Strategy in the Italian Population.
Beatrice Spedicati et al. Biomedicines 2023 11(3)
Single Versus Multigene Testing for Hereditary Hearing Loss: Use and Costs in a Commercially Insured Cohort.
Peter K Moon et al. Otolaryngology--head and neck surgery : official journal of American Academy of Otolaryngology-Head and Neck Surgery 2023
Targeted Next-Generation Sequencing in Children With Bilateral Sensorineural Hearing Loss: Diagnostic Yield and Predictors of a Genetic Cause.
An Boudewyns et al. Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology 2023
Artificial Neural Network-Assisted Classification of Hearing Prognosis of Sudden Sensorineural Hearing Loss With Vertigo.
Sheng-Chiao Lin et al. IEEE journal of translational engineering in health and medicine 2023 11170-181
Parental Consanguinity and Risk for Childhood Hearing Loss: A Retrospective Cohort Study.
Bárbara Leal et al. Acta medica portuguesa 2023
[Analysis of genotypes on 850 newborns with SLC26A4 single-allele mutation and the phenotypes of those with second variant].
L H Huang et al. Zhonghua er bi yan hou tou jing wai ke za zhi = Chinese journal of otorhinolaryngology head and neck surgery 2023 58(2) 117-125
Rare-variant association analysis reveals known and new age-related hearing loss genes
DMC Sanchez et al, EJHG, February 15, 2023
Machine Learning Prediction of Objective Hearing Loss With Demographics, Clinical Factors, and Subjective Hearing Status.
Tyler J Gathman et al. Otolaryngology--head and neck surgery : official journal of American Academy of Otolaryngology-Head and Neck Surgery 2023
Views of healthcare professionals on the inclusion of genes associated with non-syndromic hearing loss in reproductive genetic carrier screening.
Lucinda Freeman et al. European journal of human genetics : EJHG 2023
Hereditary etiology of non-syndromic sensorineural hearing loss in the Republic of North Ossetia-Alania.
Nika Petrova et al. PeerJ 2023 11e14514
BCKDK deficiency: a treatable neurodevelopmental disease amenable to newborn screening.
Trine Tangeraas et al. Brain : a journal of neurology 2023
Views of healthcare professionals on the inclusion of genes associated with non-syndromic hearing loss in reproductive genetic carrier screening
L Freeman et al, EJHG, February 9, 2023
Association of Polygenic Risk Scores for Hearing Difficulty in Older Adults With Hearing Loss in Mid-Childhood and Midlife: A Population-Based Cross-sectional Study Within the Longitudinal Study of Australian Children.
Jing Wang et al. JAMA otolaryngology-- head & neck surgery 2023
Gene burden analysis identifies genes associated with increased risk and severity of adult-onset hearing loss in a diverse hospital-based cohort.
Hui Daniel et al. PLoS genetics 2023 19(1) e1010584
Non-Syndromic Hearing Loss in a Romanian Population: Carrier Status and Frequent Variants in the GJB2 Gene.
Riza Anca-Lelia et al. Genes 2023 14(1)
Association of Genetic Diagnoses of Childhood-Onset Hearing Loss With Cochlear Implant Outcomes.
Carlson Ryan J et al. JAMA otolaryngology-- head & neck surgery 2023
Offering and Returning Secondary Findings in the Context of Exome Sequencing for Hearing Loss: Clinicians' Views and Experiences.
Notini Lauren et al. AJOB empirical bioethics 2023 1-10
Genetic screening of a Chinese cohort of children with hearing loss using a next-generation sequencing panel.
Ma Jing et al. Human genomics 2023 17(1) 1
Audiological Evidence of Frequent Hereditary Mild, Moderate and Moderate-to-Severe Hearing Loss.
Markova Tatiana et al. Journal of personalized medicine 2022 12(11)
Detecting mitochondrial mutations associated with aminoglycoside ototoxicity by noninvasive prenatal testing.
Huang Quanfei et al. Journal of clinical laboratory analysis 2022 e24827
Aminoglycoside induced ototoxicity risk in the cystic fibrosis population: The utility of large-scale screening.
Lopes Jaime et al. Pediatric pulmonology 2022
Concurrent newborn hearing and genetic screening of common hearing loss variants with bloodspot-based targeted next generation sequencing in Jiangxi province.
Luo Haiyan et al. Frontiers in pediatrics 2022 101020519
Audiological Evidence of Frequent Hereditary Mild, Moderate and Moderate-to-Severe Hearing Loss
T Markova et al, J Per Med, November 4, 2022
Views of reproductive genetic carrier screening participants regarding screening for genes associated with non-syndromic hearing loss.
Freeman Lucinda et al. Prenatal diagnosis 2022
Effect of Health Education on Knowledge and Behaviour Towards Consanguineous Marriage and Infantile Hearing Loss.
Thingujam Sonee et al. Indian journal of otolaryngology and head and neck surgery : official publication of the Association of Otolaryngologists of India 2022 74(3) 343-349
De novo variants are a common cause of genetic hearing loss.
Klimara Miles J et al. Genetics in medicine : official journal of the American College of Medical Genetics 2022
Outcomes of Gene Panel Testing for Sensorineural Hearing Loss in a Diverse Patient Cohort.
Liao Elizabeth N et al. JAMA network open 2022 5(9) e2233441
Impact of Genetic Testing on Hearing Interventions.
Brodie Kara D et al. The Laryngoscope 2022
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