Abstract:Magnetoencephalography (MEG) represents a sophisticated, non-invasive functional neuroimaging modality that resolves neuronal activity with millisecond temporal precision. Unlike Electroencephalography (EEG), MEG detects magnetic fields that permeate the skull and scalp with negligible distortion, offering superior source localization accuracy, particularly for tangential currents originating in cortical sulci. A pivotal evolution in this field is the technological transition from traditional Superconducting Quantum Interference Device (SQUID) systems—which are bulky, stationary, and reliant on cryogenic liquid helium—to next-generation Optically Pumped Magnetometer (OPM) sensors. OPMs operate at room temperature and can be placed directly on the scalp, significantly enhancing signal-to-noise ratios while enabling wearable, motion-tolerant designs that revolutionize pediatric and naturalistic neuroscience. In clinical epileptology, MEG has become indispensable for the presurgical evaluation of drug-resistant epilepsy, particularly in MRI-negative cases. It effectively localizes epileptogenic zones (EZs) often obscured in scalp EEG and guides the strategic implantation of stereoelectroencephalography (SEEG) electrodes. Crucially, MEG is uniquely capable of non-invasively detecting High-Frequency Oscillations (HFOs), a highly specific biomarker for the seizure onset zone, thereby refining resection boundaries and improving postoperative seizure-free outcomes. In neuro-oncology, MEG addresses a critical limitation of functional MRI: Neurovascular Uncoupling (NVU). In patients with high-grade gliomas, tumor-induced vascular dysregulation often compromises the BOLD signal, leading to false-negative activation maps. MEG, by directly measuring neuronal magnetic fields independent of hemodynamics, accurately delineates eloquent motor and language cortices even in areas of compromised vascular reactivity. This precision facilitates "maximal safe resection," a key prognostic factor for extending overall survival while preserving quality of life. Furthermore, MEG provides unique insights into neurodegenerative and neurodevelopmental disorders. In Alzheimer’s Disease (AD), MEG detects synaptic dysfunction manifested as spectral slowing (increased delta/theta power) and functional network fragmentation, which often precede structural atrophy, offering a window for early diagnosis and therapeutic monitoring. In Parkinson’s Disease (PD), MEG characterizes the dynamics of pathological beta bursts within basal ganglia-cortical loops. These neural signatures correlate with motor severity and are increasingly utilized to optimize Deep Brain Stimulation (DBS) targeting and programming, paving the way for adaptive, closed-loop neuromodulation. Finally, regarding Autism Spectrum Disorder (ASD), the silent, open, and motion-tolerant nature of OPM-MEG overcomes the compliance challenges inherent in examining sensory-sensitive and pediatric populations. It enables the precise quantification of rapid neural dynamics, such as Gamma oscillation abnormalities and Excitation/Inhibition (E/I) imbalance, supporting a paradigm shift from subjective behavioral assessment to objective neurophysiological phenotyping. In summary, with the advent of wearable OPM technology, MEG is evolving from a research instrument into a cornerstone of precision neurology, playing a critical role in localization, surgical guidance, and the development of network-based biomarkers.