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pubmedKB: an interactive web server for exploring biomedical entity relations in the biomedical literature.
- Published in:
- Nucleic Acids Research, 2022, v. 50, n. W1, p. W616, doi. 10.1093/nar/gkac310
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- Publication type:
- Article
Integrated machine learning with semantic web for open government data recommendation based on cloud computing.
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- Software: Practice & Experience, 2020, v. 50, n. 12, p. 2293, doi. 10.1002/spe.2892
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- Publication type:
- Article
An integrative approach for pediatric auditory neuropathy spectrum disorders: revisiting etiologies and exploring the prognostic utility of auditory steady-state response.
- Published in:
- Scientific Reports, 2020, v. 10, n. 1, p. 1, doi. 10.1038/s41598-020-66877-y
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- Article
Genetic Epidemiology and Clinical Features of Hereditary Hearing Impairment in the Taiwanese Population.
- Published in:
- Genes, 2019, v. 10, n. 10, p. 772, doi. 10.3390/genes10100772
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- Publication type:
- Article
Unique spectra of deafness-associated mutations in Mongolians provide insights into the genetic relationships among Eurasian populations.
- Published in:
- PLoS ONE, 2018, v. 13, n. 12, p. 1, doi. 10.1371/journal.pone.0209797
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- Publication type:
- Article
ABO genotyping with next-generation sequencing to resolve heterogeneity in donors with serology discrepancies.
- Published in:
- 2018
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- Publication type:
- journal article
Etiologic and Audiologic Characteristics of Patients With Pediatric-Onset Unilateral and Asymmetric Sensorineural Hearing Loss.
- Published in:
- 2017
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- Publication type:
- journal article
Long-Term Cochlear Implant Outcomes in Children with GJB2 and SLC26A4 Mutations.
- Published in:
- PLoS ONE, 2015, v. 10, n. 9, p. 1, doi. 10.1371/journal.pone.0138575
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- Publication type:
- Article
Differences in the Pathogenicity of the p.H723R Mutation of the Common Deafness-Associated <i>SLC26A4</i> Gene in Humans and Mice.
- Published in:
- PLoS ONE, 2013, v. 8, n. 6, p. 1, doi. 10.1371/journal.pone.0064906
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- Publication type:
- Article
Application of Massively Parallel Sequencing to Genetic Diagnosis in Multiplex Families with Idiopathic Sensorineural Hearing Impairment.
- Published in:
- PLoS ONE, 2013, v. 8, n. 2, p. 1, doi. 10.1371/journal.pone.0057369
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- Publication type:
- Article
Mutation screening of the EYA1, SIX1, and SIX5 genes in an east asian cohort with branchio-oto-renal syndrome.
- Published in:
- Laryngoscope, 2012, v. 122, n. 5, p. 1130, doi. 10.1002/lary.23217
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- Publication type:
- Article