Bio


Hoda S. Hashemi is a postdoctoral scholar at the Ultrasound Imaging & Instrumentation Lab at Stanford University. She received her PhD in Electrical and Computer Engineering from the University of British Columbia (UBC) in 2023. She was also an ultrasound research intern in research and innovation team at DarkVision Technologies Inc. from 2021 to 2023. She holds a M.A.Sc. from Concordia University and a B.Sc. from Sharif University of Technology. Her research interests are ultrasound molecular imaging, elastography and AI in medical image processing. Her research has been funded by the NIH T32 Fellowship at Stanford, the Canadian NSERC Postdoctoral Fellowship, and the Ultrasound Imaging & Instrumentation Lab at Stanford University.

Honors & Awards


  • NIH T32 (SCIT) Fellowship, Stanford University (2024-2025)
  • NSERC Postdoctoral Fellowship, Natural Sciences and Engineering Research Council of Canada (2024-2025)
  • President’s Academic Excellence Award, The University of British Columbia (2020-2023)
  • Faculty of Applied Science Graduate Award, The University of British Columbia (2017-2023)
  • Four Year Fellowship (4YF) Award, The University of British Columbia (2017-2021)
  • ECE MASc. Convocation Award (Best MSc. student), Concordia University (2018)
  • Power Corporation Of Canada Scholarship, Concordia University (2016-2017)
  • The Clara Strozyk Scholarship, Concordia University (2015-2016)

Professional Education


  • Doctor of Philosophy, University of British Columbia, Electrical and Computer Engineering (2023)
  • Master of Applied Science, Concordia University, Electrical and Computer Engineering (2017)
  • Bachelor of Science, Sharif University of Technology, Electrical and Computer Engineering (2014)

Stanford Advisors


All Publications


  • Enhancing Ultrasound Molecular Imaging: Toward Real-Time RPCA-Based Filtering to Differentiate Bound and Free Microbubbles. IEEE transactions on ultrasonics Hashemi, H. S., Hyun, D., Nguyen, N., Baek, J., Natarajan, A., Tabesh, F., Andrzejek, A., Paulmurugan, R., Dahl, J. J. 2025

    Abstract

    Ultrasound molecular imaging (UMI) is an advanced imaging modality that shows promise in detecting cancer at early stages. It uses microbubbles as contrast agents, which are functionalized to bind to cancer biomarkers overexpressed on endothelial cells. A major challenge in UMI is isolating bound microbubble signal, which represents the molecular imaging signal, from that of free-floating microbubbles, which is considered background noise. In this work, we propose a fast GPU-based method using robust principal component analysis (RPCA) to distinguish bound microbubbles from free-floating ones. We explore the method using simulations and measure the accuracy using the Dice coefficient and RMS error as functions of the number of frames used in RPCA reconstruction. Experiments using stationary and flowing microbubbles in tissue-mimicking phantoms were used to validate the method. Additionally, the method was applied to data from ten transgenic mouse models of breast cancer development, injected with B7-H3 targeted microbubbles, and two mice injected with non-targeted microbubbles. The results showed that RPCA using 20 frames achieved a Dice score of 0.95 and a computation time of 0.2 seconds, indicating that 20 frames is potentially suitable for real-time implementation. On in vivo data, RPCA using 20 frames achieved a Dice score of 0.82 with DTE, indicating good agreement between the two, given the limitations of each method.

    View details for DOI 10.1109/tuson.2025.3647590

    View details for PubMedID 42078652

    View details for PubMedCentralID PMC13132560

  • UltraFlex: Iterative Model-Based Ultrasonic Flexible-Array Shape Calibration IEEE TRANSACTIONS ON ULTRASONICS FERROELECTRICS AND FREQUENCY CONTROL Frey, B. N., Hyun, D., Simson, W., Zhuang, L., Hashemi, H. S., Schneider, M., Dahl, J. J. 2025; 72 (11): 1462-1475

    Abstract

    UltraFlex is an iterative model-based ultrasonic flexible-array shape calibration framework that uses automatic differentiation. This work evaluates array shape calibration model performance while examining multiple image quality metrics: speckle brightness, envelope entropy, coherence factor, lag-one coherence, common-midpoint correlation coefficient (CMCC), and common-midpoint phase error (CMPE). The accuracy of these image quality metrics was evaluated on simulated phantoms using a variety of array shapes. Experimental phantom and in vivo liver datasets were also investigated using transducers with known geometries. While speckle brightness, envelope entropy, and coherence factor enable model convergence under many conditions, lag-one coherence, CMCC, and CMPE enable more accurate element position estimations and improved visual ultrasound image focusing quality. Furthermore, the models based on the CMCC and phase-error quality metrics are the most robust against additive white noise while achieving median mean Euclidean errors (MEEs) of 3.7 μm for simulation, 29.7 μm for phantom, and 69.0 μm for in vivo liver data. These array shape calibration results show promise for future development of experimental flexible- and wearableultrasonic arrays.

    View details for DOI 10.1109/TUFFC.2025.3627525

    View details for Web of Science ID 001629793500002

    View details for PubMedID 41171672