On the public citation graph

NeuroRoots, a bio-inspired, seamless Brain Machine Interface device for long-term recording

https://doi.org/10.1101/460949
0 signed · 69 inferred · view as graph

Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.

Is this your work? Sign in with ORCID and put your name on the claims that are yours.
Claim with ORCID
Reference health. See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.
See reference health

What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1001/archneurol.2010.260openalex-snapshot
Deep Brain Stimulation for Parkinson Disease
inferredcites →https://doi.org/10.1002/adma.200600195openalex-snapshot
Soft Deposition of Large‐Area Metal Contacts for Molecular Electronics
inferredcites →https://doi.org/10.1002/adma.201500218openalex-snapshot
Localized Neuron Stimulation with Organic Electrochemical Transistors on Delaminating Depth Probes
inferredcites →https://doi.org/10.1002/mrm.27236openalex-snapshot
Revealing sub‐voxel motions of brain tissue using phase‐based amplified MRI (aMRI)
inferredcites →https://doi.org/10.1007/s00422-014-0626-2openalex-snapshot
Distribution of axon diameters in cortical white matter: an electron-microscopic study on three human brains and a macaque
inferredcites →https://doi.org/10.1016/j.actbio.2017.02.010openalex-snapshot
Ultrasoft microwire neural electrodes improve chronic tissue integration
inferredcites →https://doi.org/10.1016/j.conb.2017.11.007openalex-snapshot
Mesh electronics: a new paradigm for tissue-like brain probes
inferredcites →https://doi.org/10.1016/j.jneumeth.2005.08.015openalex-snapshot
Response of brain tissue to chronically implanted neural electrodes
inferredcites →https://doi.org/10.1016/j.neuron.2005.02.014openalex-snapshot
Deep brain stimulation for treatment-resistant depression.
inferredcites →https://doi.org/10.1016/j.neuron.2014.12.035openalex-snapshot
Soft Materials in Neuroengineering for Hard Problems in Neuroscience
inferredcites →https://doi.org/10.1038/551172aopenalex-snapshot
Neurons recorded en masse
inferredcites →https://doi.org/10.1038/natrevmats.2016.93openalex-snapshot
Neural recording and modulation technologies
inferredcites →https://doi.org/10.1038/nature04968openalex-snapshot
A high-performance brain–computer interface
inferredcites →https://doi.org/10.1038/nature04970openalex-snapshot
Neuronal ensemble control of prosthetic devices by a human with tetraplegia
inferredcites →https://doi.org/10.1038/nature21004openalex-snapshot
The rise of plastic bioelectronics
inferredcites →https://doi.org/10.1038/nature24636openalex-snapshot
Fully integrated silicon probes for high-density recording of neural activity
inferredcites →https://doi.org/10.1038/ncomms3133openalex-snapshot
High transconductance organic electrochemical transistors
inferredcites →https://doi.org/10.1038/nmat3468openalex-snapshot
Ultrasmall implantable composite microelectrodes with bioactive surfaces for chronic neural interfaces
inferredcites →https://doi.org/10.1038/nmeth.3969openalex-snapshot
Stable long-term chronic brain mapping at the single-neuron level
inferredcites →https://doi.org/10.1038/nn.3905openalex-snapshot
NeuroGrid: recording action potentials from the surface of the brain
inferredcites →https://doi.org/10.1038/s41551-017-0154-1openalex-snapshot
Glial responses to implanted electrodes in the brain
inferredcites →https://doi.org/10.1073/pnas.1717695114openalex-snapshot
Highly scalable multichannel mesh electronics for stable chronic brain electrophysiology
inferredcites →https://doi.org/10.1088/0960-1317/25/12/125003openalex-snapshot
Silk and PEG as means to stiffen a parylene probe for insertion in the brain: toward a double time-scale tool for local drug delivery
inferredcites →https://doi.org/10.1088/1741-2552/aadc1dopenalex-snapshot
A bilayered PVA/PLGA-bioresorbable shuttle to improve the implantation of flexible neural probes
inferredcites →https://doi.org/10.1088/1741-2560/10/6/066014openalex-snapshot
Failure mode analysis of silicon-based intracortical microelectrode arrays in non-human primates
inferredcites →https://doi.org/10.1088/1741-2560/13/2/026003openalex-snapshot
Scanning electron microscopy of chronically implanted intracortical microelectrode arrays in non-human primates
inferredcites →https://doi.org/10.1088/1741-2560/4/1/s09openalex-snapshot
Optoelectronic retinal prosthesis: system design and performance
inferredcites →https://doi.org/10.1101/370080openalex-snapshot
Recording from the same neuron with high-density CMOS probes and patch-clamp: a ground-truth dataset and an experiment in collaboration
inferredcites →https://doi.org/10.1101/454520openalex-snapshot
Ultra-sensitive measurement of brain penetration with microscale probes for brain machine interface considerations
inferredcites →https://doi.org/10.1111/j.1749-6632.2010.05568.xopenalex-snapshot
Stress, sex, and neural adaptation to a changing environment: mechanisms of neuronal remodeling
inferredcites →https://doi.org/10.1126/sciadv.1601027openalex-snapshot
Organic electronics for high-resolution electrocorticography of the human brain
inferredcites →https://doi.org/10.1126/sciadv.1601649openalex-snapshot
Next-generation probes, particles, and proteins for neural interfacing
inferredcites →https://doi.org/10.1126/sciadv.1601966openalex-snapshot
Ultraflexible nanoelectronic probes form reliable, glial scar–free neural integration
inferredcites →https://doi.org/10.1126/science.1260318openalex-snapshot
Electronic dura mater for long-term multimodal neural interfaces
inferredcites →https://doi.org/10.1152/jn.00493.2017openalex-snapshot
Stable long-term BCI-enabled communication in ALS and locked-in syndrome using LFP signals
inferredcites →https://doi.org/10.1152/jn.2000.84.1.401openalex-snapshot
Accuracy of Tetrode Spike Separation as Determined by Simultaneous Intracellular and Extracellular Measurements
inferredcites →https://doi.org/10.1186/1754-1611-7-21openalex-snapshot
Contribution of cytoskeletal elements to the axonal mechanical properties
inferredcites →https://doi.org/10.3390/ma3031803openalex-snapshot
Surface Engineering and Patterning Using Parylene for Biological Applications
inferredcites →https://doi.org/10.3390/s17102388openalex-snapshot
Time Multiplexed Active Neural Probe with 1356 Parallel Recording Sites

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.1002/adma.202207847openalex-snapshot
3D Bioelectronics with a Remodellable Matrix for Long‐Term Tissue Integration and Recording
inferred← citeshttps://doi.org/10.1002/advs.202505100openalex-snapshot
Stiffness‐Tunable Neurotentacles for Minimally Invasive Implantation and Long‐Term Neural Activity Recordings
inferred← citeshttps://doi.org/10.1007/s10544-024-00700-7openalex-snapshot
A self-stiffening compliant intracortical microprobe
inferred← citeshttps://doi.org/10.1016/j.bioactmat.2024.08.034openalex-snapshot
Enhancing biocompatibility of the brain-machine interface: A review
inferred← citeshttps://doi.org/10.1016/j.biomaterials.2020.120559openalex-snapshot
How is flexible electronics advancing neuroscience research?
inferred← citeshttps://doi.org/10.1016/j.biomaterials.2022.121905openalex-snapshot
Longitudinal neural and vascular recovery following ultraflexible neural electrode implantation in aged mice
inferred← citeshttps://doi.org/10.1016/j.copbio.2021.07.020openalex-snapshot
Learning from the brain’s architecture: bioinspired strategies towards implantable neural interfaces
inferred← citeshttps://doi.org/10.1016/j.isci.2020.101387openalex-snapshot
Ultraflexible Neural Electrodes for Long-Lasting Intracortical Recording
inferred← citeshttps://doi.org/10.1016/j.jneumeth.2021.109388openalex-snapshot
Neural tissue-microelectrode interaction: Brain micromotion, electrical impedance, and flexible microelectrode insertion
inferred← citeshttps://doi.org/10.1016/j.matt.2020.08.002openalex-snapshot
Bioinspired Materials for In Vivo Bioelectronic Neural Interfaces
inferred← citeshttps://doi.org/10.1016/j.mser.2023.100726openalex-snapshot
Organic microelectrode arrays for bioelectronic applications
inferred← citeshttps://doi.org/10.1016/j.neuron.2019.08.011openalex-snapshot
Can One Concurrently Record Electrical Spikes from Every Neuron in a Mammalian Brain?
inferred← citeshttps://doi.org/10.1021/acs.nanolett.0c00467openalex-snapshot
Switchless Multiplexing of Graphene Active Sensor Arrays for Brain Mapping
inferred← citeshttps://doi.org/10.1038/s41378-022-00451-6openalex-snapshot
Implantable intracortical microelectrodes: reviewing the present with a focus on the future
inferred← citeshttps://doi.org/10.1038/s41467-024-49226-9openalex-snapshot
Months-long tracking of neuronal ensembles spanning multiple brain areas with Ultra-Flexible Tentacle Electrodes
inferred← citeshttps://doi.org/10.1038/s41551-023-01021-5openalex-snapshot
Translational opportunities and challenges of invasive electrodes for neural interfaces
inferred← citeshttps://doi.org/10.1088/1741-2552/ab965copenalex-snapshot
Sputtered porous Pt for wafer-scale manufacture of low-impedance flexible microelectrodes
inferred← citeshttps://doi.org/10.1088/1741-2552/abebc2openalex-snapshot
Long-term in vivo monitoring of gliotic sheathing of ultrathin entropic coated brain microprobes with fiber-based optical coherence tomography
inferred← citeshttps://doi.org/10.1088/1741-2552/ac514fopenalex-snapshot
jULIEs: nanostructured polytrodes for low traumatic extracellular recordings and stimulation in the mammalian brain
inferred← citeshttps://doi.org/10.1093/nsr/nwae333openalex-snapshot
Flexible multimaterial fibers in modern biomedical applications
inferred← citeshttps://doi.org/10.1101/2024.04.25.591141openalex-snapshot
Self-Assembled Origami Neural Probes for Scalable, Multifunctional, Three-Dimensional Neural Interface
inferred← citeshttps://doi.org/10.1101/721548openalex-snapshot
jULIEs: extracellular probes for recordings and stimulation in the structurally and functionally intact mouse brain
inferred← citeshttps://doi.org/10.1109/compe49325.2020.9200106openalex-snapshot
Brain Automation, Panacea for Physical Disabilities
inferred← citeshttps://doi.org/10.1109/jssc.2022.3141688openalex-snapshot
A Light-Tolerant Wireless Neural Recording IC for Motor Prediction With Near-Infrared-Based Power and Data Telemetry
inferred← citeshttps://doi.org/10.1186/s42234-025-00168-7openalex-snapshot
Overcoming failure: improving acceptance and success of implanted neural interfaces
inferred← citeshttps://doi.org/10.1371/journal.pbio.3002884openalex-snapshot
The future of transcranial ultrasound as a precision brain interface
inferred← citeshttps://doi.org/10.1557/adv.2019.424openalex-snapshot
Materials and Devices for Micro-invasive Neural Interfacing
inferred← citeshttps://doi.org/10.2196/16194openalex-snapshot
An Integrated Brain-Machine Interface Platform With Thousands of Channels
inferred← citeshttps://doi.org/10.3390/coatings11020204openalex-snapshot
Implantable Thin Film Devices as Brain-Computer Interfaces: Recent Advances in Design and Fabrication Approaches
inferred← citeshttps://doi.org/10.54254/2753-8818/45/20240588openalex-snapshot
A review of recent developments and challenges in the brain-machine interface
Editorial review for independent work. ICSAC — the Institute for Complexity Science and Advanced Computing — runs a structured editorial panel for researchers publishing outside journals, and publishes on CiteStamp rails. Submission is free and goes through ORCID: icsacinstitute.org/submit.