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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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High-resolution optical coherence tomographic imaging using a mode-locked Ti:Al(2)O(3) laser source.

TL;DR: A Kerr-lens mode-locked Ti:Al(2)O(3) oscillator, optimized for minimal coherence length, is demonstrated as a high-power source for high-resolution optical coherence tomographic imaging.
Patent

Fiber optic imaging endoscope interferometer with at least one faraday rotator

TL;DR: In this article, an endoscopic system for performing optical coherence tomography includes an optical radiation source; a reference optical reflector; a first optical path leading to the reference optical reflectedor; and a second optical path coupled to an endoscopy unit.
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Assessing atherosclerotic plaque morphology: comparison of optical coherence tomography and high frequency intravascular ultrasound.

TL;DR: In this paper, the authors compared OCT and intravascular ultrasound (IVUS) imaging of in vitro atherosclerotic plaques and found that OCT yielded superior structural information in all plaques examined.
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Interferometric synthetic aperture microscopy

Abstract: State-of-the-art methods in high-resolution three-dimensional optical microscopy require that the focus be scanned through the entire region of interest. However, an analysis of the physics of the light–sample interaction reveals that the Fourier-space coverage is independent of depth. Here we show that, by solving the inverse scattering problem for interference microscopy, computed reconstruction yields volumes with a resolution in all planes that is equivalent to the resolution achieved only at the focal plane for conventional high-resolution microscopy. In short, the entire illuminated volume has spatially invariant resolution, thus eliminating the compromise between resolution and depth of field. We describe and demonstrate a novel computational image-formation technique called interferometric synthetic aperture microscopy (ISAM). ISAM has the potential to broadly impact real-time three-dimensional microscopy and analysis in the fields of cell and tumour biology, as well as in clinical diagnosis where in vivo imaging is preferable to biopsy.
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High resolution in vivo intra-arterial imaging with optical coherence tomography

TL;DR: In this paper, the abdominal aorta of New Zealand white rabbits was demonstrated at a source resolution of 10 µm, but required the displacement of blood with saline during imaging.