Lack of Methylation Changes in GJB2 and RB1 Non-coding Regions of Cochlear Implant Patients with Sensorineural Hearing Loss.

Autor: Sumalde AAM; College of Medicine, University of the Philippines Manila, Manila, Philippines.; Department of Otolaryngology - Head and Neck Surgery, School of Medicine, University of Colorado Anschutz Medical Campus (CU-AMC), Aurora, Colorado, USA.; Department of Otolaryngology-Head and Neck Surgery, Philippine General Hospital, University of the Philippines Manila, Manila, Philippines., Yang IV; Department of Medicine, School of Medicine, University of Colorado Anschutz Medical Campus (CU-AMC), Aurora, Colorado, USA., Yarza TKL; Philippine National Ear Institute, National Institutes of Health, University of the Philippines Manila, Manila, Philippines.; Newborn Hearing Screening Reference Center, National Institutes of Health, University of the Philippines Manila, Manila, Philippines., Tobias-Grasso CAM; MED-EL, Innsbruck, Austria., Tantoco MLC; Department of Otolaryngology-Head and Neck Surgery, Philippine General Hospital, University of the Philippines Manila, Manila, Philippines.; Philippine National Ear Institute, National Institutes of Health, University of the Philippines Manila, Manila, Philippines.; Newborn Hearing Screening Reference Center, National Institutes of Health, University of the Philippines Manila, Manila, Philippines., Davidson E; Department of Medicine, School of Medicine, University of Colorado Anschutz Medical Campus (CU-AMC), Aurora, Colorado, USA., Chan AL; College of Medicine, University of the Philippines Manila, Manila, Philippines.; Department of Otolaryngology-Head and Neck Surgery, Philippine General Hospital, University of the Philippines Manila, Manila, Philippines., Azamian MS; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, USA., Cruz TLG; College of Medicine, University of the Philippines Manila, Manila, Philippines.; Department of Otolaryngology-Head and Neck Surgery, Philippine General Hospital, University of the Philippines Manila, Manila, Philippines., Lalani SR; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, USA., Reyes-Quintos MRT; Department of Otolaryngology-Head and Neck Surgery, Philippine General Hospital, University of the Philippines Manila, Manila, Philippines.; Philippine National Ear Institute, National Institutes of Health, University of the Philippines Manila, Manila, Philippines.; Newborn Hearing Screening Reference Center, National Institutes of Health, University of the Philippines Manila, Manila, Philippines., Cutiongco-de la Paz EM; National Institutes of Health, University of the Philippines Manila, Manila, Philippines.; Philippine Genome Center, UP Diliman Campus, Quezon City, Philippines., Santos-Cortez RLP; Department of Otolaryngology - Head and Neck Surgery, School of Medicine, University of Colorado Anschutz Medical Campus (CU-AMC), Aurora, Colorado, USA., Chiong CM; College of Medicine, University of the Philippines Manila, Manila, Philippines.; Department of Otolaryngology-Head and Neck Surgery, Philippine General Hospital, University of the Philippines Manila, Manila, Philippines.; Philippine National Ear Institute, National Institutes of Health, University of the Philippines Manila, Manila, Philippines.; Newborn Hearing Screening Reference Center, National Institutes of Health, University of the Philippines Manila, Manila, Philippines.

Publikováno v: Acta medica Philippina [Acta Med Philipp] 2023 Sep 28; Vol. 57 (9), pp. 116-120.

Exome sequencing reveals novel variants and unique allelic spectrum for hearing impairment in Filipino cochlear implantees.

Autor: Truong BT; Human Medical Genetics and Genomics Program, University of Colorado School of Medicine, Aurora, Colorado., Yarza TKL; Philippine National Ear Institute, University of the Philippines (UP) Manila-National Institutes of Health (NIH), Manila, Philippines.; Newborn Hearing Screening Reference Center, UP Manila-NIH, Manila, Philippines., Bootpetch Roberts T; Department of Otolaryngology, University of Colorado School of Medicine, Aurora, Colorado., Roberts S; Department of Otolaryngology, University of Colorado School of Medicine, Aurora, Colorado., Xu J; Department of Otolaryngology, University of Colorado School of Medicine, Aurora, Colorado., Steritz MJ; Department of Otolaryngology, University of Colorado School of Medicine, Aurora, Colorado., Tobias-Grasso CAM; MED-EL, Innsbruck, Austria., Azamian M; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas., Lalani SR; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas., Mohlke KL; Department of Genetics, University of North Carolina, Chapel Hill, North Carolina., Lee NR; Office of Population Studies Foundation and Department of Anthropology, Sociology and History, University of San Carlos, Cebu, Philippines., Cutiongco-de la Paz EM; UP Manila-NIH, Manila 1000, Philippines.; Philippine Genome Center, Quezon City, Philippines., Reyes-Quintos MRT; Philippine National Ear Institute, University of the Philippines (UP) Manila-National Institutes of Health (NIH), Manila, Philippines.; Newborn Hearing Screening Reference Center, UP Manila-NIH, Manila, Philippines.; UP Manila-NIH, Manila 1000, Philippines.; Department of Otorhinolaryngology, UP Manila College of Medicine-Philippine General Hospital, Manila, Philippines., Santos-Cortez RLP; Human Medical Genetics and Genomics Program, University of Colorado School of Medicine, Aurora, Colorado.; Philippine National Ear Institute, University of the Philippines (UP) Manila-National Institutes of Health (NIH), Manila, Philippines.; Department of Otolaryngology, University of Colorado School of Medicine, Aurora, Colorado., Chiong CM; Philippine National Ear Institute, University of the Philippines (UP) Manila-National Institutes of Health (NIH), Manila, Philippines.; Newborn Hearing Screening Reference Center, UP Manila-NIH, Manila, Philippines.; Department of Otorhinolaryngology, UP Manila College of Medicine-Philippine General Hospital, Manila, Philippines.

Publikováno v: Clinical genetics [Clin Genet] 2019 May; Vol. 95 (5), pp. 634-636. Date of Electronic Publication: 2019 Mar 04.