Functional imaging of the human brain is an increasingly important technique for clinical and cognitive neuroscience research, with functional MRI (fMRI) of the blood oxygen level-dependent (BOLD) response and electroencephalography or magnetoencephalography (MEG) recordings of neural oscillations being 2 of the most popular approaches. However, the neural and physiological mechanisms that generate these responses are only partially understood and sources of interparticipant variability in these measures are rarely investigated. Here, we test the hypothesis that the properties of these neuroimaging metrics are related to individual levels of cortical inhibition by combining magnetic resonance spectroscopy to quantify resting GABA concentration in the visual cortex, MEG to measure stimulus-induced visual gamma oscillations and fMRI to measure the BOLD response to a simple visual grating stimulus. Our results demonstrate that across individuals gamma oscillation frequency is positively correlated with resting GABA concentration in visual cortex (R ؍ 0.68; P < 0.02), BOLD magnitude is inversely correlated with resting GABA (R ؍ ؊0.64; P < 0.05) and that gamma oscillation frequency is strongly inversely correlated with the magnitude of the BOLD response (R ؍ ؊0.88; P < 0.001). Our results are therefore supportive of recent theories suggesting that these functional neuroimaging metrics are dependent on the excitation/inhibition balance in an individual's cortex and have important implications for the interpretation of functional imaging results, particularly when making between-group comparisons in clinical research.functional magnetic resonance imaging ͉ magnetic resonance spectroscopy ͉ magnetoencephalography ͉ oscillations T he high spatial resolution and noninvasive nature of blood oxygen level-dependent (BOLD) functional MRI (fMRI) (1) have led to it becoming one of the most popular tools for measuring brain function in human neuroscience. However, fMRI provides only an indirect measure of neural activity by measuring task-related changes in cerebral haemodynamics that are coupled by a complex and only partially understood mechanism to changes in underlying neural activity. Recent evidence suggests that oscillations in the gamma frequency range, loosely defined as approximately 30-100 Hz, are well correlated temporally, spatially, and functionally with haemodynamic changes in cortex, suggesting a close relationship with the BOLD response (2-6). There is also increasing evidence that the most plausible mechanism for the generation of gamma oscillations is a neuronal network containing a mixture of interconnected pyramidal cells and GABAergic inhibitory interneurons (7-10) with the balance of excitation-inhibition setting the peak gamma oscillation frequency of the network (11). Similarly, it has recently been argued that the magnitude of the BOLD response is also sensitive to this excitation-inhibition balance (12, 13).In the current study, we tested the hypothesis that the local level of inhibition in an i...