The Research Symposium is an annual event at ASHA's Convention where clinicians and researchers discuss current research in communication sciences and disorders (CSD). Each year's symposium has a specific research theme.
Find out more about the Research Symposium at the ASHA Convention and its associated travel award.
Symposium Topic: Genetics in CSD
Coordinated by Beate Peter, PhD, CCC-SLP (Arizona State University), the Symposium focused on the role of genetics in a diverse range of communication abilities and disabilities.
Symposium Presentations
Update on Phenotypes and Genotypes for Studies of Speech Sound Disorders
Speakers: Barbara A. Lewis, PhD, CCC-SLP and Sudha K. Iyengar, PhD (Case Western Reserve University)
Molecular and Neuronal Pathways Implicated by Stuttering Genetics and Their Broader Clinical Consequences
Speakers: Jennifer E. Below, PhD, (Vanderbilt University Medical Center) and Shelly Jo Kraft, PhD (Wayne State University)
Can Genetics Help Identify Specific Reading Disabilities?
Speaker: Elena L. Grigorenko, PhD (University of Houston and Baylor College of Medicine)
Using Genetics to Uncover the Biological Substrates of Spoken and Written Language
Speaker: Simon Fisher, DPhil (Max Planck Institute for Psycholinguistics & Donders Institute for Brain, Cognition and Behaviour)
Translating the Power of Precision Medicine into the World of Communication Disorders
Speaker: Beate Peter, PhD, CCC-SLP (Arizona State University)
The Research Symposium at ASHA Convention is funded, in part, by a grant from the National Institute on Deafness and Other Communication Disorders (NIDCD).
Symposium Publications
Papers based on the 2024 Research Symposium were published in a Forum in the November 2025 issue of Journal of Speech, Language, and Hearing Research (JSLHR) and are open access.
- Peter, B. (2025). Deciphering the language in our DNA and leveraging the discoveries toward improved outcomes: Introduction to the Forum. Journal of Speech, Language, and Hearing Research, 68(11), 5101-5103. https://doi.org/10.1044/2025_JSLHR-25-00681.
- Pruett, D.G., Scartozzi, A.C., Polikowsky, H.G., Highland, H.M., Doug M., Shaw, D.M., Petty, L.E., Petty, A.S., Kraft, S.J. and Below, J.E. (2025). Challenges and opportunities in characterizing the genetics of stuttering: from sample acquisition to functional interpretation of the genome. Journal of Speech, Language, and Hearing Research, 68(11), 5137-5157. https://doi.org/10.1044/2025_JSLHR-25-00093.
- Dobrynin, P., Zeng, Y., Norkina, M., Fedorova, A., Zhuk, A. and Grigorenko, E.L. (2025). Four decades of inquiry into the genetic bases of specific reading disability. Journal of Speech, Language, and Hearing Research, 68(11), 5158-5173. https://doi.org/10.1044/2025_JSLHR-25-00050.
- Fisher, S.E. (2025). Genomic investigations of spoken and written language abilities: A guide to advances in approaches, technologies, and discovery. Journal of Speech, Language, and Hearing Research, 68(11), 5104-5121. https://doi.org/10.1044/2025_JSLHR-25-00152.
- Lewis, B.A., Miller, G.J., Benchek, P., Stein, C., and Iyengar, S.K. (2025). The Cleveland Family Speech and Reading Study: A review of long-term outcomes linking phenotypes and genotypes for speech sound disorders. Journal of Speech, Language, and Hearing Research, 68(11), 5122-5136. https://doi.org/10.1044/2025_JSLHR-25-00052.
- Peter, B., Davis, J., Bruce, L., Finestack, L., Kornelis, M., Eng, L., Kim, Y., Scherer, N., Potter, N., VanDam, M., Thompson, L., Loveall, S., Stoel-Gammon, C., Raaz, C., Armstrong-Heimsoth, A. and Buckley, S. (2025). Translating the power of precision medicine into the world of communication disorders. Journal of Speech, Language, and Hearing Research, 68(11), 5174-5189. https://doi.org/10.1044/2025_JSLHR-25-00077.