Sadeghzadeh, Sina
Stanford Medicine · Stanford University
2 papers on CoChatORCID 0000-0003-3360-1016
Most cited papers
- Verified
Loss-or gain-of-function mutations in ACOX1 cause axonal loss via different mechanisms
Chung, H.-L., Wangler, M. F., Marcogliese, P. C., Jo, J., Ravenscroft, T. A., Zuo, Z., Duraine, L., Sadeghzadeh, S., Li-Kroeger, D., Schmidt, R. E., et al. (2020) · Neuron
Hereditary Neurological DisordersMetabolism and Genetic Disorders
Cited by 154
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ConvNeXt-Driven Detection of Alzheimer’s Disease: A Benchmark Study on Expert-Annotated AlzaSet MRI Dataset Across Anatomical Planes
Basereh, M., Abikenari, M. A., Sadeghzadeh, S., Dunn, T., Freichel, R., Siddarth, P., Ghahremani, D., Lavretsky, H., & Buch, V. P. (2025) · Diagnostics
Dementia and Cognitive Impairment ResearchMedical Image Segmentation Techniques
Cited by 4
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