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Kinney, H. C.

Publications and source records attributed to Kinney, H. C..

3 recordsLinked to original sources

Cortical reconstruction and anatomical parcellation of high-resolution multi-modal postmortem ex vivo MRI of the human infant brain

High-resolutionpostmortemmagneticresonanceimagingen- ables detailed examination of brain anatomy at spatial scales not achiev- able in vivo and provides a unique opportunity to link morphomet- ric measurements with the underlying pathology. Despite these advan- tages, robust computational tools for automated anatomical segmen- tation and cortical surface reconstruction remain limited, particularly in postmortem infant brains. Incomplete myelination, thinner cortical ribbons, small-scale neuroanatomy, evolving tissue contrast, fixation- induced signal alterations, and variability in postmortem preparation make standard neuroimaging pipelines unsuitable for postmortem in- fant MRI. In this work, we introduce a unique high-resolution multi- sequence postmortem infant MRI dataset and a unified computational framework that combines deep learning-based volumetric segmentation with surface-based cortical reconstruction and anatomical parcellation in native subject-space resolution. The framework is designed to general- ize across diverse postmortem MRI acquisition protocols, spatial resolu- tions, tissue preparation conditions, and specimen characteristics while remaining robust to substantial variability in image contrast, tissue de- formation, fixation-induced intensity changes, background signal char- acteristics, and anatomical variability encountered in postmortem in- fant MRI. We benchmark our framework against widely used contrast- agnostic and foundational brain segmentation models, demonstrating improved anatomical consistency and segmentation performance across heterogeneous high-resolution postmortem infant datasets. Our method enables morphometric analysis in native postmortem space, providing the same downstream quantitative analyses routinely available for in vivo developmental neuroimaging. The complete framework is released as open-source software with command-line workflows, containers, and comprehensive documentation to facilitate reproducible postmortem in- fant MRI analysis as part of the purple-mri package: https://purple-mri.readthedocs.io

neuroscience↗

Functional fractionation of large-scale brain networks in the human subcortex

Brain network mapping plays a crucial role in advancing our understanding of human brain organization and the neuroanatomic foundations of cognition. Historically, the identification of large-scale brain networks has focused on the cerebral cortex. Some cortical networks have been fractionated into subnetworks, yielding valuable insights into their domain-specific cognitive functions. In contrast, functional mapping of large-scale brain networks within subcortical regions remains an emerging and challenging field, hindered by a low signal-to-noise ratio in subcortical functional MRI data and an inability to distinguish networks with substantial spatiotemporal overlap. In this study, we fractionated and identified fifteen spatially overlapped and temporally correlated subnetworks, which can be categorized into four large-scale brain networks. The subcortical functional connectivity patterns of these subnetworks exhibited distinct, yet overlapping, spatial configurations, with widely connected hub nodes identified in the caudate, putamen, hippocampus, and thalamus. These subnetworks are highly reproducible across healthy human brains and provide normative functional atlases, which we release here as a resource for the academic community. As a proof-of-principle demonstration of how the atlases can be used to elucidate the pathophysiology of neuropsychiatric disorders, we show that the spatial patterns of the subnetworks predict the level of consciousness in patients with severe traumatic brain injury. These observations indicate a highly conserved and spatially overlapped subcortical functional architecture in the human brain, providing opportunities to elucidate pathophysiologic mechanisms and develop new neuromodulatory therapies for a broad spectrum of neuropsychiatric diseases.

neuroscience↗

Sustaining wakefulness: Brainstem connectivity in human consciousness

Consciousness is comprised of arousal (i.e., wakefulness) and awareness. Substantial progress has been made in mapping the cortical networks that modulate awareness in the human brain, but knowledge about the subcortical networks that sustain arousal is lacking. We integrated data from ex vivo diffusion MRI, immunohistochemistry, and in vivo 7 Tesla functional MRI to map the connectivity of a subcortical arousal network that we postulate sustains wakefulness in the resting, conscious human brain, analogous to the cortical default mode network (DMN) that is believed to sustain self-awareness. We identified nodes of the proposed default ascending arousal network (dAAN) in the brainstem, hypothalamus, thalamus, and basal forebrain by correlating ex vivo diffusion MRI with immunohistochemistry in three human brain specimens from neurologically normal individuals scanned at 600-750 {micro}m resolution. We performed deterministic and probabilistic tractography analyses of the diffusion MRI data to map dAAN intra-network connections and dAAN-DMN internetwork connections. Using a newly developed network-based autopsy of the human brain that integrates ex vivo MRI and histopathology, we identified projection, association, and commissural pathways linking dAAN nodes with one another and with cortical DMN nodes, providing a structural architecture for the integration of arousal and awareness in human consciousness. We release the ex vivo diffusion MRI data, corresponding immunohistochemistry data, network-based autopsy methods, and a new brainstem dAAN atlas to support efforts to map the connectivity of human consciousness. One sentence summaryWe performed ex vivo diffusion MRI, immunohistochemistry, and in vivo 7 Tesla functional MRI to map brainstem connections that sustain wakefulness in human consciousness.

neuroscience↗