Gregory M. Palmer

Optimal methods for fluorescence and diffuse reflectance measurements of tissue biopsy samples.

Steady-state fluorescence imaging of neoplasia.

Comparison of multiexcitation fluorescence and diffuse reflectance spectroscopy for the diagnosis of breast cancer (March 2003).

Autofluorescence spectroscopy of normal and malignant human breast cell lines.

Autofluorescence and diffuse reflectance properties of malignant and benign breast tissues.

Investigation of fiber-optic probe designs for optical spectroscopic diagnosis of epithelial pre-cancers.

Use of a multiseparation fiber optic probe for the optical diagnosis of breast cancer.

Monte Carlo-based inverse model for calculating tissue optical properties. Part I: Theory and validation on synthetic phantoms.

Monte Carlo-based inverse model for calculating tissue optical properties. Part II: Application to breast cancer diagnosis.

Diagnosis of breast cancer using diffuse reflectance spectroscopy: Comparison of a Monte Carlo versus partial least squares analysis based feature extraction technique.

Effect of optical clearing agents on the in vivo optical properties of squamous epithelial tissue.

Use of genetic algorithms to optimize fiber optic probe design for the extraction of tissue optical properties.

Comparison of a physical model and principal component analysis for the diagnosis of epithelial neoplasias in vivo using diffuse reflectance spectroscopy.

Monte-Carlo-based model for the extraction of intrinsic fluorescence from turbid media.

Diagnosis of breast cancer using fluorescence and diffuse reflectance spectroscopy: a Monte-Carlo-model-based approach.

Electromagnetic spectroscopy of normal breast tissue specimens obtained from reduction surgeries: comparison of optical and microwave properties.

Cost-effective diffuse reflectance spectroscopy device for quantifying tissue absorption and scattering in vivo.

A strategy for quantitative spectral imaging of tissue absorption and scattering using light emitting diodes and photodiodes.

Advances in quantitative UV-visible spectroscopy for clinical and pre-clinical application in cancer.

Quantitative optical spectroscopy: a robust tool for direct measurement of breast cancer vascular oxygenation and total hemoglobin content in vivo.

Quantitative diffuse reflectance and fluorescence spectroscopy: tool to monitor tumor physiology in vivo.

A robust Monte Carlo model for the extraction of biological absorption and scattering in vivo.

A dual-emissive-materials design concept enables tumour hypoxia imaging.

Non-invasive monitoring of intra-tumor drug concentration and therapeutic response using optical spectroscopy.

Stereocomplexed poly(lactic acid)-poly(ethylene glycol) nanoparticles with dual-emissive boron dyes for tumor accumulation.

Optical imaging of tumor hypoxia dynamics.

Molecular imaging of hypoxia.

In vivo optical molecular imaging and analysis in mice using dorsal window chamber models applied to hypoxia, vasculature and fluorescent reporters.

Application of optical imaging and spectroscopy to radiation biology.

High-resolution in vivo imaging of fluorescent proteins using window chamber models.

Experimental validation of an inverse fluorescence Monte Carlo model to extract concentrations of metabolically relevant fluorophores from turbid phantoms and a murine tumor model.

Measuring tumor cycling hypoxia and angiogenesis using a side-firing fiber optic probe.

A diffuse reflectance spectral imaging system for tumor margin assessment using custom annular photodiode arrays.

Wavelength optimization for quantitative spectral imaging of breast tumor margins.

18F-EF5 PET imaging as an early response biomarker for the hypoxia-activated prodrug SN30000 combined with radiation treatment in a non-small cell lung cancer xenograft model.

Quantitative mapping of hemodynamics in the lung, brain, and dorsal window chamber-grown tumors using a novel, automated algorithm.

Hypoxia in melanoma: using optical spectroscopy and EF5 to assess tumor oxygenation before and during regional chemotherapy for melanoma.

Plasmonics-enhanced and optically modulated delivery of gold nanostars into brain tumor.

Biomimetic engineered muscle with capacity for vascular integration and functional maturation in vivo.

Cellular migration and invasion uncoupled: increased migration is not an inexorable consequence of epithelial-to-mesenchymal transition.

Systemic anti-tumour effects of local thermally sensitive liposome therapy.