Nishant Mohan, PhD

Nishant Mohan, PhD

Raleigh, North Carolina, United States
4K followers 500+ connections

About

Dr. Mohan is an award-winning, goal-centric professional who has made significant…

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Experience

  • Notal Vision Graphic
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    Raleigh-Durham, North Carolina Area

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    Raleigh-Durham, North Carolina Area

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    Raleigh-Durham, North Carolina Area

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    Rochester, New York Area

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Education

  • Harvard Medical School

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Licenses & Certifications

Publications

  • Quantitative optical inspection of contact lenses immersed in wet cell using swept source OCT

    Optics Letter

    We demonstrate swept source optical coherence tomography (OCT) imaging of contact lenses (CLs) in a wet cell and comprehensive quantitative characterization of CLs from volumetric OCT datasets. The approach is based on a technique developed for lens autopositioning and autoleveling enabled by lateral capillary interactions between the wet cell wall and the lens floating on the liquid surface. The demonstrated OCT imaging has enhanced contrast due to the application of a scattering medium and it…

    We demonstrate swept source optical coherence tomography (OCT) imaging of contact lenses (CLs) in a wet cell and comprehensive quantitative characterization of CLs from volumetric OCT datasets. The approach is based on a technique developed for lens autopositioning and autoleveling enabled by lateral capillary interactions between the wet cell wall and the lens floating on the liquid surface. The demonstrated OCT imaging has enhanced contrast due to the application of a scattering medium and it improves visualization of both CL interfaces and edges. We also present precise and accurate three-dimensional metrology of soft and rigid CLs based on the OCT data. The accuracy and precision of the extracted lens parameters are compared with the manufacturer’s specifications. The presented methodology facilitates industrial inspection methods of the CLs.

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  • Targeting Placental Growth Factor/Neuropilin 1 Pathway Inhibits Growth and Spread of Medulloblastoma

    Cell

    Medulloblastoma is the most common pediatric malignant brain tumor. Although current therapies improve survival, these regimens are highly toxic and are associated with significant morbidity. Here, we report that placental growth factor (PlGF) is expressed in the majority of medulloblastomas, independent of their subtype. Moreover, high expression of PlGF receptor neuropilin 1 (Nrp1) correlates with poor overall survival in patients. We demonstrate that PlGF and Nrp1 are required for the growth…

    Medulloblastoma is the most common pediatric malignant brain tumor. Although current therapies improve survival, these regimens are highly toxic and are associated with significant morbidity. Here, we report that placental growth factor (PlGF) is expressed in the majority of medulloblastomas, independent of their subtype. Moreover, high expression of PlGF receptor neuropilin 1 (Nrp1) correlates with poor overall survival in patients. We demonstrate that PlGF and Nrp1 are required for the growth and spread of medulloblastoma: PlGF/Nrp1 blockade results in direct antitumor effects in vivo, resulting in medulloblastoma regression, decreased metastasis, and increased mouse survival. We reveal that PlGF is produced in the cerebellar stroma via tumor-derived Sonic hedgehog (Shh) and show that PlGF acts through Nrp1—and not vascular endothelial growth factor receptor 1—to promote tumor cell survival. This critical tumor-stroma interaction—mediated by Shh, PlGF, and Nrp1 across medulloblastoma subtypes—supports the development of therapies targeting PlGF/Nrp1 pathway.

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  • Principal-component-analysis-based estimation of blood flow velocities using optical coherence tomography intensity signals

    Optics Letters

    The intensity signal in optical coherence tomography contains information about the translational velocity of scatterers, and can be used to quantify blood flow. We apply principal component analysis to efficiently extract this information. We also study use of nonuniform temporal sampling of the intensity signal to increase the range of quantifiable flow velocities. We demonstrate this technique in simulation, phantom and in vivo blood flow measurements, and highlight its potential to enable…

    The intensity signal in optical coherence tomography contains information about the translational velocity of scatterers, and can be used to quantify blood flow. We apply principal component analysis to efficiently extract this information. We also study use of nonuniform temporal sampling of the intensity signal to increase the range of quantifiable flow velocities. We demonstrate this technique in simulation, phantom and in vivo blood flow measurements, and highlight its potential to enable three-dimensional wide-field mapping of blood flow using OCT.

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  • Fast angiographic OCT imaging using sparse representations over learned dictionaries

    IEEE

    Recent developments in optical coherence tomography (OCT) have enabled wide-field and high-resolution angiographic imaging. However, generation of vascular contrast inherently requires long imaging times. In this work, we demonstrate a reconstruction technique based on sparse and redundant representations over trained dictionaries that can be used to reduce acquisition times and accurately reconstruct angiographic OCT projection images with full vascular detail from a smaller number of B-scans…

    Recent developments in optical coherence tomography (OCT) have enabled wide-field and high-resolution angiographic imaging. However, generation of vascular contrast inherently requires long imaging times. In this work, we demonstrate a reconstruction technique based on sparse and redundant representations over trained dictionaries that can be used to reduce acquisition times and accurately reconstruct angiographic OCT projection images with full vascular detail from a smaller number of B-scans than conventionally required. Our technique for fast angiographic imaging through reconstruction (FAIR), shows excellent reconstruction quality while using only half of the number of B-scans and graceful quality degradation with further undersampling.

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  • Compressed sensing in optical coherence tomography

    SPIE

    Optical coherence tomography (OCT) is a valuable technique for non-invasive imaging in medicine and biology. In some applications, conventional time-domain OCT (TD-OCT) has been supplanted by spectral-domain OCT (SD-OCT); the latter uses an apparatus that contains no moving parts and can achieve orders of magnitude faster imaging. This enhancement comes at a cost, however: the CCD array detectors required for SD-OCT are more expensive than the simple photodiodes used in TD-OCT. We explore the…

    Optical coherence tomography (OCT) is a valuable technique for non-invasive imaging in medicine and biology. In some applications, conventional time-domain OCT (TD-OCT) has been supplanted by spectral-domain OCT (SD-OCT); the latter uses an apparatus that contains no moving parts and can achieve orders of magnitude faster imaging. This enhancement comes at a cost, however: the CCD array detectors required for SD-OCT are more expensive than the simple photodiodes used in TD-OCT. We explore the possibility of extending the notion of compressed sensing (CS) to SD-OCT, potentially allowing the use of smaller detector arrays. CS techniques can yield accurate signal reconstructions from highly undersampled measurements, i.e., data sampled significantly below the Nyquist rate. The Fourier relationship between the measurements and the desired signal in SD-OCT makes it a good candidate for compressed sensing. Fourier measurements represent good linear projections for the compressed sensing of sparse point-like signals by random under-sampling of frequency-domain data, and axial scans in OCT are generally sparse in nature. This sparsity property has recently been used for the reduction of speckle in OCT images. We have carried out simulations to demonstrate the usefulness of compressed sensing for simplifying detection schemes in SD-OCT. In particular, we demonstrate the reconstruction of a sparse axial scan by using fewer than 10 percent of the measurements required by standard SD-OCT.

  • Ultrabroadband coherence-domain imaging using parametric downconversion and superconducting single-photon detectors at 1064 nm

    Applied Optics

    Coherence-domain imaging systems can be operated in a single-photon-counting mode, offering low detector noise; this in turn leads to increased sensitivity for weak light sources and weakly reflecting samples. We have demonstrated that excellent axial resolution can be obtained in a photon-counting coherence-domain imaging (CDI) system that uses light generated via spontaneous parametric downconversion (SPDC) in a chirped periodically poled stoichiometric lithium tantalate (chirped-PPSLT)…

    Coherence-domain imaging systems can be operated in a single-photon-counting mode, offering low detector noise; this in turn leads to increased sensitivity for weak light sources and weakly reflecting samples. We have demonstrated that excellent axial resolution can be obtained in a photon-counting coherence-domain imaging (CDI) system that uses light generated via spontaneous parametric downconversion (SPDC) in a chirped periodically poled stoichiometric lithium tantalate (chirped-PPSLT) structure, in conjunction with a niobium nitride superconducting single-photon detector (SSPD). The bandwidth of the light generated via SPDC, as well as the bandwidth over which the SSPD is sensitive, can extend over a wavelength region that stretches from 700 to 1500 nm . This ultrabroad wavelength band offers a near-ideal combination of deep penetration and ultrahigh axial resolution for the imaging of biological tissue. The generation of SPDC light of adjustable bandwidth in the vicinity of 1064 nm , via the use of chirped-PPSLT structures, had not been previously achieved. To demonstrate the usefulness of this technique, we construct images for a hierarchy of samples of increasing complexity: a mirror, a nitrocellulose membrane, and a biological sample comprising onion-skin cells

  • Photon-counting optical coherence-domain reflectometry using superconducting single-photon detectors

    Optics Express

    We consider the use of single-photon counting detectors in coherence-domain imaging. Detectors operated in this mode exhibit reduced noise, which leads to increased sensitivity for weak light sources and weakly reflecting samples. In particular, we experimentally demonstrate the possibility of using superconducting single-photon detectors (SSPDs) for optical coherence-domain reflectometry (OCDR). These detectors are sensitive over the full spectral range that is useful for carrying out such…

    We consider the use of single-photon counting detectors in coherence-domain imaging. Detectors operated in this mode exhibit reduced noise, which leads to increased sensitivity for weak light sources and weakly reflecting samples. In particular, we experimentally demonstrate the possibility of using superconducting single-photon detectors (SSPDs) for optical coherence-domain reflectometry (OCDR). These detectors are sensitive over the full spectral range that is useful for carrying out such imaging in biological samples. With counting rates as high as 100 MHz, SSPDs also offer a high rate of data acquisition if the light flux is sufficient.

Patents

Organizations

  • SPIE

    Future Leaders Committee Member

    - Present
  • New England Section of Optical Society of America

    President

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  • SPIE - Boston University Student Chapter

    President and Founder

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