Publications

2025

1. seqLens: optimizing language models for genomic predictions. Baghbanzadeh, M., Mann, B., Crandall, K. A., & Rahnavard, A. bioRxiv, 2025.

2024

1. Estimating rare disease prevalence and costs in the USA: a cohort study approach using the Healthcare Cost Institute claims data. Cutillo, C. M., Tisdale, A., Baghbanzadeh, M., et al.
2. Discovering genotype–phenotype relationships with machine learning and the Visual Physiology Opsin Database (VPOD). Frazer, S. A., Baghbanzadeh, M., et al.

2023

1. DeepBreaks: A machine learning tool for identifying and prioritizing genotype-phenotype associations. Baghbanzadeh, M., Dawson, T., Sayoldin, B., et al.

Earlier years

• 2022, 2021, 2020, 2014 entries (see Google Scholar for full details)