Cohen's lab develops genetically encoded fluorescent voltage indicators and all-optical electrophysiology ('Optopatch') to simultaneously stimulate and image membrane voltage in individual neurons and cardiomyocytes at the single-cell and network level, combining protein engineering, optics, and theory to push the temporal and spatial resolution of bioelectrical imaging well past conventional patch-clamp limits.
Deisseroth co-invented optogenetics (light-gated ion channels for millisecond-scale neural control) and CLARITY-type hydrogel tissue-clearing methods that render intact brains optically transparent for whole-organ, cellular-resolution light-sheet and confocal imaging, together forming a foundational toolkit for causal, high-resolution circuit neuroscience.
Garrido is a computational cognitive neuroscientist — predictive coding, Bayesian brain models, neuroimaging biomarkers for mental health — who was appointed a chief investigator of the ARC Centre of Excellence in Quantum Biotechnology specifically to work with the Melbourne and UQ physics groups on non-invasive quantum-sensor recording of human brain magnetic fields. She is the human-subject and source-reconstruction end of the QUBIC portable-brain-imager programme: her lab supplies the paradigms, the clinical cohorts and the inverse-problem modelling that a diamond- or OPM-based MEG system has to serve. Positioned against the established body of NV-ensemble quantum sensing work — DEER, nanoscale NMR and T1 relaxometry protocols operating at pT/sqrt(Hz) field sensitivity — she is not a sensor developer, but she is the reason the pT/sqrt(Hz)-class magnetometers being built at Melbourne have a human-trials pathway at all. Preferred attributes present in strength: bioelectromagnetism and human trials with novel quantum technologies. Included as a deliberate borderline case — a sensing postdoc would be the physics half of a collaboration with this lab, not a member of it.
Gruetter leads the Laboratory for Functional and Metabolic Imaging (LFMI) at EPFL and co-directs the CIBM (Centre for Biomedical Imaging). Research directions: (1) Ultra-high-field in vivo MR spectroscopy — developing 1H, 13C, 31P, 23Na MRS at 14.1T animal and 7T human systems to measure metabolite concentrations (glutamate, GABA, lactate) in brain with unprecedented sensitivity; (2) Quantum coherence effects in NMR — exploiting J-coupling evolution and JPRESS sequences for quantum-selective metabolite editing; (3) Hyperpolarization — DNP-enhanced metabolite sensing in vivo for tracking metabolic flux in real time; (4) Neuroimaging — quantitative BOLD fMRI calibration and cerebral blood flow mapping. The 14.1T magnet is among the world's most powerful for biological NMR spectroscopy.
Prof. Kozorovitskiy (Neurobiology) studies neuromodulation and plasticity in the striatum and basal ganglia, with a distinctive emphasis on developing and applying advanced optical imaging methods. Imaging technique innovations: (1) Oblique plane illumination (OPI / scanned oblique plane illumination, SOPi) microscopy — a single-objective light-sheet technique achieving tilt-invariant volumetric imaging for rapid 3D capture of fluorescently labeled neural structures without mechanical tilting; (2) Two-photon fluorescence imaging and two-photon glutamate/neuromodulator photorelease for single-synapse resolution in live tissue; (3) Near-infrared genetically-encoded calcium indicators (with Verkhusha group) for in vivo multi-color neural recording with reduced photobleaching. The lab's technical contributions are centered on extending the spatial and volumetric resolution of live-tissue fluorescence imaging. Irving M. Klotz Research Professor of Neurobiology; Beckman Young Investigator 2015.
Leifer develops closed-loop optical instrumentation that simultaneously records brain-wide calcium activity and delivers single-neuron optogenetic perturbations in freely moving C. elegans, building functional atlases of signal propagation and studying how whole-brain neural dynamics generate behavior. His group's whole-brain, cellular-resolution imaging in unrestrained animals is a benchmark advanced-microscopy approach for linking neural dynamics to behavior.
Lichtman invented the multicolor 'Brainbow' fluorescent labeling method and pioneered large-scale, automated serial-section electron microscopy to reconstruct complete synaptic wiring diagrams (connectomes) of neural tissue, pushing spatial resolution and scale together to map circuit-level brain structure.
Uses information theory and statistical physics to study neural circuit sensing. Directions: (1) multi-electrode array recording from salamander and mouse retina to map how retinal ganglion cells encode and predict natural visual scenes; (2) information-theoretic quantification of predictive coding strategies in sensory neurons; (3) developing statistical models of population neural codes. Technique focus: high-density multi-electrode arrays as a sensing platform for neural population dynamics. Joint appointment Organismal Biology and Anatomy.
Schnitzer's lab invents miniaturized and fiber-based two-photon microscopes and voltage/calcium imaging methods that allow single-cell-resolution recording of neural activity in freely behaving animals, including recent wide-field fluorescence-lifetime voltage imaging developed with the Kasevich group for high-throughput readout of neuronal spiking.
Tank is a pioneer of two-photon laser-scanning microscopy for imaging calcium dynamics in dendrites and neural circuits in vivo, and co-directs the Bezos Center for Neural Circuit Dynamics, which develops large-scale optical recording instrumentation combined with rodent virtual-reality systems to study persistent neural activity and short-term memory. His group's methodological contributions to cellular-resolution optical imaging underpin much of modern systems neuroscience.