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Stephen A. Boppart

Researcher at University of Illinois at Urbana–Champaign

Publications -  684
Citations -  33772

Stephen A. Boppart is an academic researcher from University of Illinois at Urbana–Champaign. The author has contributed to research in topics: Optical coherence tomography & Laser. The author has an hindex of 90, co-authored 631 publications receiving 31497 citations. Previous affiliations of Stephen A. Boppart include Harvard University & Boston University.

Papers
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Book ChapterDOI

Imaging and Tracking of Bone Marrow-Derived Immune and Stem Cells

TL;DR: Methods and algorithms for nonrigid registration of time-lapse images are introduced, which allows for long-term tracking of cell dynamics over several months, in in vivo three-dimensional tissue environments with an integrated optical microscope.
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Intraoperative optical coherence tomography of the human thyroid: Feasibility for surgical assessment.

TL;DR: In this paper, the authors demonstrate optical coherence tomography (OCT) imaging of the human thyroid as a potential intraoperative imaging tool for providing tissue assessment in real time during surgical procedures.
Journal ArticleDOI

Depixelation and enhancement of fiber bundle images by bundle rotation

TL;DR: This approach combines digital filtering and spatial resampling to reconstruct higher-quality images, enhancing the utility of images acquired using fiber bundles and removal of honeycomb-like artifacts.
Journal ArticleDOI

Comparison of a MEMS-Based Handheld OCT Scanner With a Commercial Desktop OCT System for Retinal Evaluation

TL;DR: The authors' handheld OCT system can be used to identify relevant anatomical structures and pathologies in the eye, potentially enabling earlier screening, disease detection, and treatment and enabling patients to be referred to a specialist for treatment.
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Label-free characterization of single extracellular vesicles using two-photon fluorescence lifetime imaging microscopy of NAD(P)H

TL;DR: In this paper, the authors used two-photon fluorescence lifetime imaging microscopy (FLIM) to image and characterize NAD(P)H in single isolated extracellular vesicles (EVs).