Matthew R. Avenarius
Neuroscience · The Ohio State University
Publications
59
Citations
1,968
Est. group size
~11
Recurring co-author estimate
Active years
22
Publishing since 2005
Matthew R. Avenarius has worked across two related areas: the molecular biology of hearing, including how tiny hair-like structures in the inner ear (stereocilia) are built and maintained, and clinical genetics/genomics, particularly cancer cytogenetics and genetic testing for conditions like spinal muscular atrophy. His more recent work focuses heavily on clinical genetic diagnostics, including chromosome abnormalities in leukemia and improving genetic test accuracy. This research combines laboratory studies of gene function with applied clinical genetics aimed at improving diagnosis of genetic and blood-related diseases.
Publication output has grown steadily over the last decade, rising from about 2-3 papers per year around 2017-2019 to 6-8 per year by 2023-2025.
Generated by claude-sonnet-5 from public bibliographic data · Jul 20, 2026
- Novel Recurrent Cytogenetic Abnormalities Predict Overall Survival in Tetraploid/Near-Tetraploid Myelodysplastic Syndrome and Acute Myeloid Leukemia
Cancers · 2025
- 2: Artificial intelligence-assisted conventional chromosome analysis to explore clonal dynamics in chronic lymphocytic leukemia
Genetics in Medicine Open · 2025
- Addendum: Points to consider in the reevaluation and reanalysis of genomic test results: A statement of the American College of Medical Genetics and Genomics (ACMG)
Genetics in Medicine · 2024
- Clinical SMN1 and SMN2 Gene-Specific Sequencing to Enhance the Clinical Sensitivity of Spinal Muscular Atrophy Diagnostic Testing
Human Mutation · 2023
- P423: SMN1 SMN2 gene-specific sequencing enhances the clinical sensitivity of spinal muscular atrophy diagnostic testing
Genetics in Medicine Open · 2023
- The clinical utility of a risk‐modifying <scp>SNP</scp> to detect carriers for spinal muscular atrophy with increased sensitivity
Molecular Genetics & Genomic Medicine · 2022
- 52. Novel recurrent cytogenetic abnormalities predict overall survival in tetraploid/near-tetraploid MDS/AML
Cancer Genetics · 2022
- Somatic PIK3R1 variation as a cause of vascular malformations and overgrowth
Genetics in Medicine · 2021
- 6. Genetic characterization of tetraploid/near-tetraploid acute myeloid leukemia patients
Cancer Genetics · 2021
- Loss of <i>Baiap2l2</i> destabilizes the transducing stereocilia of cochlear hair cells and leads to deafness
The Journal of Physiology · 2020
- 30. Detection of gene fusions in sarcomas is improved by targeted anchored multiplex PCR based next generation sequencing
Cancer Genetics · 2019
- Grxcr2 is required for stereocilia morphogenesis in the cochlea
PLoS ONE · 2018
- TRPV6, TRPM6 and TRPM7 Do Not Contribute to Hair-Cell Mechanotransduction
Frontiers in Cellular Neuroscience · 2018
- Heterodimeric capping protein is required for stereocilia length and width regulation
The Journal of Cell Biology · 2017
- Correction: Corrigendum: Stereocilia-staircase spacing is influenced by myosin III motors and their cargos espin-1 and espin-like
Nature Communications · 2017
- Blood×5
- Genetics in Medicine Open×3
- Cancer Genetics×3
- Genetics in Medicine×2
- Nature Communications×2
- Eri Hashino
Neuroscience · Indiana University
- Benjamin J. Seicol
Neuroscience · The Ohio State University
- Bo Zhao
Neuroscience · Indiana University
- Amir M. Mafi
Neuroscience · The Ohio State University
- Eric C. Bielefeld
Neuroscience · The Ohio State University
This profile was generated automatically from public scholarly data (OpenAlex). Group size and activity levels are estimates derived from co-authorship patterns.
Last updated Jul 19, 2026.
Claim or correct this profile