Detalhe da pesquisa
1.
Otitis media susceptibility and shifts in the head and neck microbiome due to SPINK5 variants.
J Med Genet
; 58(7): 442-452, 2021 07.
Artigo
Inglês
| MEDLINE | ID: mdl-32709676
2.
FUT2 Variants Confer Susceptibility to Familial Otitis Media.
Am J Hum Genet
; 103(5): 679-690, 2018 11 01.
Artigo
Inglês
| MEDLINE | ID: mdl-30401457
3.
A2ML1 and otitis media: novel variants, differential expression, and relevant pathways.
Hum Mutat
; 40(8): 1156-1171, 2019 08.
Artigo
Inglês
| MEDLINE | ID: mdl-31009165
4.
Audiologic Measures in an Indigenous Community with A2ML1- and FUT2-Related Otitis Media.
Genet Test Mol Biomarkers
; 27(1): 12-17, 2023 Jan.
Artigo
Inglês
| MEDLINE | ID: mdl-36719978
5.
Lack of Methylation Changes in GJB2 and RB1 Non-coding Regions of Cochlear Implant Patients with Sensorineural Hearing Loss.
Acta Med Philipp
; 57(9): 116-120, 2023 Sep 28.
Artigo
Inglês
| MEDLINE | ID: mdl-37990697
6.
Microbiota Associated With Cholesteatoma Tissue in Chronic Suppurative Otitis Media.
Front Cell Infect Microbiol
; 12: 746428, 2022.
Artigo
Inglês
| MEDLINE | ID: mdl-35521215
7.
Identification of Novel Candidate Genes and Variants for Hearing Loss and Temporal Bone Anomalies.
Genes (Basel)
; 12(4)2021 04 13.
Artigo
Inglês
| MEDLINE | ID: mdl-33924653
8.
Genetic counseling in an indigenous Filipino community with a high prevalence of A2ML1-related otitis media.
J Community Genet
; 10(1): 143-151, 2019 Jan.
Artigo
Inglês
| MEDLINE | ID: mdl-29949068
9.
The SLC26A4 c.706C>G (p.Leu236Val) Variant is a Frequent Cause of Hearing Impairment in Filipino Cochlear Implantees.
Otol Neurotol
; 39(8): e726-e730, 2018 09.
Artigo
Inglês
| MEDLINE | ID: mdl-30113565