Michael Hoa

Single-cell RNA-Seq resolves cellular complexity in sensory organs from the neonatal inner ear.

mutation and cochlear autoinflammation cause syndromic and nonsyndromic hearing loss DFNA34 responsive to anakinra therapy.

Molecular architecture underlying fluid absorption by the developing inner ear.

CDC14A phosphatase is essential for hearing and male fertility in mouse and human.

Deafness and loss of cochlear hair cells in the absence of thyroid hormone transporters Slc16a2 (Mct8) and Slc16a10 (Mct10).

Mutational and phenotypic spectra of KCNE1 deficiency in Jervell and Lange-Nielsen Syndrome and Romano-Ward Syndrome.

Single Cell and Single Nucleus RNA-Seq Reveal Cellular Heterogeneity and Homeostatic Regulatory Networks in Adult Mouse Stria Vascularis.

Noncoding Microdeletion in Mouse Disrupts Neural Crest Migration into the Stria Vascularis, Reduces the Endocochlear Potential, and Suggests the Neuropathology for Human Nonsyndromic Deafness DFNB39.

Applications of single-cell sequencing for the field of otolaryngology: A contemporary review.

Mouse Models of Human Pathogenic Variants of Associated with Non-Syndromic Deafness DFNB86 and DFNA65 and Syndromes Involving Deafness.

Characterization of rare spindle and root cell transcriptional profiles in the stria vascularis of the adult mouse cochlea.

Identification of Potential Meniere's Disease Targets in the Adult Stria Vascularis.

New insights into Perrault syndrome, a clinically and genetically heterogeneous disorder.

Utilizing Single Cell RNA-Sequencing to Implicate Cell Types and Therapeutic Targets for SSNHL in the Adult Cochlea.

Single-Cell RNA-Seq of Cisplatin-Treated Adult Stria Vascularis Identifies Cell Type-Specific Regulatory Networks and Novel Therapeutic Gene Targets.

Repurposable Drugs That Interact with Steroid Responsive Gene Targets for Inner Ear Disease.

Editorial: Autoinflammation of the inner ear.

The role of the stria vascularis in neglected otologic disease.

Variants of LRP2, encoding a multifunctional cell-surface endocytic receptor, associated with hearing loss and retinal dystrophy.