Jonathan Gershenson

Dr. Jonathan Gershenson

orcid

Research Focus & Metrics

Academic Career Length

7Years (2020-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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10 March 2023 in Sensors
Verified
Journal Article
Open access
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MGMeir Gershenson
Meir Gershenson
JGJonathan Gershenson
Jonathan Gershenson
Mammography is considered the gold standard for breast cancer screening and diagnostic imaging; however, there is an unmet clinical need for complementary methods to detect lesions not characterized by mammography. Far-infrared ‘thermogram’ breast imaging can map the skin temperature, and signal inversion with components analysis can be used to identify the mechanisms of thermal image generation of the vasculature using dynamic thermal data. This work focuses on using dynamic infrared breast imaging to identify the thermal response of the stationary vascular system and the physiologic vascular response to a temperature stimulus affected by vasomodulation. The recorded data are analyzed by converting the diffusive heat propagation into a virtual wave and identifying the reflection using component analysis. Clear images of passive thermal reflection and thermal response to vasomodulation were obtained. In our limited data, the magnitude of vasoconstriction appears to depend on the presence of cancer. The authors propose future studies with supporting diagnostic and clinical data that may provide validation of the proposed paradigm.

16 February 2023 in Preprints.org
Verified
Preprint
Open access
PDF file
MGMeir Gershenson
Meir Gershenson
JGJonathan Gershenson
Jonathan Gershenson
Mammography is the gold standard for breast cancer screening and diagnostic imaging; however, there is an unmet clinical need for complementary methods to detect lesions not characterized by mammography. Far-infrared 'thermogram' breast imaging can map the skin temperature, and signal inversion with components analysis can be used to identify the mechanisms of thermal image generation of the vasculature using dynamic thermal data. This work focuses on using dynamic infrared breast imaging to identify the thermal response of the stationary vascular system and the physiologic vascular response to a temperature stimulus affected by vasomodulation. The recorded data is analyzed by converting the diffusive heat propagation into a virtual wave and identifying the reflection using component analysis. Clear images of passive thermal reflection and thermal response to vasomodulation were obtained. Validation of this proposed paradigm through further clinical exploration may demonstrate clinical utility for the IR modality in diagnostic imaging, offering a potential solution to the current unmet clinical need.

16 March 2020
Verified
Conference Paper
Closed access
PDF file
JGJonathan Gershenson
Jonathan Gershenson
MGMeir Gershenson
Meir Gershenson
The purpose of this work is to introduce a new analytical inversion method for three-dimensional (3D) sub-surface imaging beneath the skin from time sequenced infrared (IR) thermography images. The work was motivated by advances in transient thermal nondestructive evaluation methods. Using relationships between wave propagation and thermal diffusive propagation, transformation from diffusive propagation into an equivalent wave field is performed. This transformation results in well-defined reflections with time delay proportional to the distance. We apply the algorithm to a dynamic thermogram of the breasts obtained from the Brazilian breast thermal imaging set. Inversion of the raw data reveals intensities that correspond to heat conduction. Equivalent wave field transform (EWFT) serves as a computationally efficient method of extracting depth resolved anatomical and physiological information from skin surface thermogram data.

28 September 2021 in Journal of Nuclear Medicine Technology
Verified
Journal Article
Open access
PDF file
YLYuxin Li
Yuxin Li
ECEsther Choi
Esther Choi
AHArtineh Hayrapetian
Artineh Hayrapetian
EAEmmanuel Appiah-Kubi
Emmanuel Appiah-Kubi
JGJonathan Gershenson
Jonathan Gershenson
GBGholam Berenji
Gholam Berenji
123I thyroid scintigraphy can be performed with either a low energy or medium energy collimator. The high-energy photon emissions from 123I cause septal penetration with scattered photons, which deteriorate image quality. The aim of this study is to evaluate the impact of collimator choice on 123I thyroid scintigraphy in clinical practice. Methods: Forty seven patients who received thyroid planar scintigraphy with both a low energy high resolution (LEHR) collimator and a medium energy (ME) collimator were prospectively recruited using the same imaging protocol. Image quality, collimator sensitivity, and estimation of thyroid size were assessed between LEHR and ME collimators, and were compared with thyroid ultrasonography as the gold standard. Results: Images acquired with the ME collimator demonstrate less scattered background noise, improved thyroid to background contrast, and increased sensitivity in the thyroid gland compared to images acquired by the LEHR collimator. Manual measurement of the thyroid length is more accurate by using the ME collimator. Automatic estimation of the thyroid area size by using the same thyroid cutoff threshold is larger in ME collimator images than in LEHR collimator images. Conclusion:123I thyroid scintigraphy using the ME collimator generates cleaner images with less background noise and has higher collimator sensitivity for thyroid imaging compared to the LEHR collimator. Different thyroid cutoff threshold should be used to estimate the thyroid area size and volume between low and medium energy collimators.