Evidence map›Paper›PMID 42358667›Full record

ArticleFrontiers in neural circuits2026

A modular and flexible pipeline for intraoperative electrode reconstruction and localization in patients with brain lesions.

Haziq Rabbani, Ipsita Das, Ayan S Mandal, Thomas Nelson, Peter Hadar, Brian Hsueh, Roberto Ciordia, Brian F Coughlin, Emory Peng, Daniel R Cleary and 15 more

Abstract read
In one paragraph

Article in Frontiers in neural circuits, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

25 authors.

Haziq Rabbani *College of Medicine, Northeast Ohio Medical University, Rootstown, OH, United States.
Ipsita Das *Department of Neurology, Mass General Brigham, Boston, MA, United States.
Ayan S MandalDepartment of Neurology, Mass General Brigham, Boston, MA, United States.
Thomas NelsonDivision of Neuro-Oncology, Department of Neurosurgery, University of California, San Francisco, San Francisco, CA, United States.
Peter HadarDepartment of Neurology, Mass General Brigham, Boston, MA, United States.
Brian HsuehDepartment of Neurology, Mass General Brigham, Boston, MA, United States.
Roberto CiordiaDepartment of Neurology, Mass General Brigham, Boston, MA, United States.
Brian F CoughlinDepartment of Neurology, Mass General Brigham, Boston, MA, United States.
Emory PengDepartment of Neurology, Mass General Brigham, Boston, MA, United States.
Daniel R ClearyDepartment of Neurosurgery, Oregon Health State University, Portland, OR, United States.
Kelly L CollinsDepartment of Neurosurgery, Oregon Health State University, Portland, OR, United States.
Ahmed M T RaslanDepartment of Neurosurgery, Oregon Health State University, Portland, OR, United States.
Ziv M WilliamsDepartment of Neurosurgery, Mass General Brigham, Boston, MA, United States.
Bryan D ChoiDepartment of Neurosurgery, Mass General Brigham, Boston, MA, United States.
Garth Rees CosgroveDepartment of Neurosurgery, Mass General Brigham, Boston, MA, United States.
Shadi A DayehDepartment of Neurosurgery, University of California, San Diego, La Jolla, CA, United States.
Pamela S JonesDepartment of Neurosurgery, Mass General Brigham, Boston, MA, United States.
Harmanpreet K TiwanaDepartment of Neurology, Mass General Brigham, Boston, MA, United States.
Gavin P DunnDepartment of Neurosurgery, Mass General Brigham, Boston, MA, United States.
R Mark RichardsonDepartment of Neurosurgery, Mass General Brigham, Boston, MA, United States.
Wenya Linda BiDepartment of Neurosurgery, Mass General Brigham, Boston, MA, United States.
Steven TobochnikCenter for Neuro-Oncology, Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, United States.
Sydney S CashDepartment of Neurology, Mass General Brigham, Boston, MA, United States.
Daniel P CahillDepartment of Neurosurgery, Mass General Brigham, Boston, MA, United States.
Angelique C PaulkDepartment of Neurology, Mass General Brigham, Boston, MA, United States.

Funding

Thin, High-Density, High-Performance, Depth and Surface Microelectrodes for Diagnosis and Treatment of EpilepsyUG3NS123723 · NINDS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI DAYEH, SHADI · 2021 to 2025
$9.5M
Bringing Light to Functional Mapping in Resective NeurosurgeryDP2EB029757 · NIBIB · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI DAYEH, SHADI · 2019 to 2019
$2.4M
Integration of High Definition Display Technologies with Platinum Nanorod Microelectrodes for Large Scale in-vivo Recording and StimulationR01NS123655 · NINDS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI DAYEH, SHADI · 2021 to 2021
$2.0M
Neural Activity Signatures of Tumor Infiltration in the Human BrainR01NS134410 · NINDS · MASSACHUSETTS GENERAL HOSPITAL · PI ANGELIQUE C PAULK · 2024 to 2026
$1.8M
Seizure focus delineation using spontaneous and stimulus evoked EEG featuresK24NS088568 · NINDS · MASSACHUSETTS GENERAL HOSPITAL · PI CASH, SYDNEY S · 2015 to 2019
$923k
High-density microgrid development for human neural interface devicesF32MH120886 · NIMH · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI CLEARY, DANIEL R · 2019 to 2019
$73k
NIBIB NIH HHS DP2 EB029757NIMH NIH HHS F32 MH120886NINDS NIH HHS K24 NS088568NINDS NIH HHS R01 NS123655NINDS NIH HHS R01 NS134410NINDS NIH HHS UG3 NS123723
6 · The paper itself

Abstract

Intraoperative intracranial electrophysiological recordings provide unique access to human cortical dynamics but remain difficult to translate across patients due to inconsistent localization of transient surface electrodes. Unlike chronic implantations, intraoperative electrodes are placed transiently, rarely visible on imaging, and often inconsistently documented. We present an open-source imaging pipeline, ALIGNER (Advanced Localization and Imaging Guidance for Neurosurgical Electrode Recording), designed to reconstruct intraoperative surface electrode array placements and quantitatively map neural activity to individualized anatomical and pathological substrates. By enabling anatomical localization of these electrodes, this framework supports systematic analysis of spatial gradients in neural activity relative to pathological tissue. We developed a multimodal reconstruction framework integrating pre- and postoperative MRI and CT, cortical surface modeling, semi-automated pathology segmentation, intraoperative photographs or videos when available, and physics-based electrode modeling. To improve robustness in cases with distorted anatomy, artificial intelligence tools such as SynthSR were used to enable reliable cortical surface reconstruction prior to FreeSurfer processing. A monocular depth-estimation network was incorporated to constrain electrode placement in conjunction with Blender cloth-physics simulation when photographic images were available, while atlas- and note-guided inference supported reconstruction otherwise. The pipeline was applied to 38 neurosurgical patients across drug-resistant epilepsy resection (

Indexed as

BrainBrain MappingElectrocorticographyElectrodes, ImplantedImage Processing, Computer-AssistedIntraoperative Neurophysiological MonitoringBrain NeoplasmsFemaleHumansMagnetic Resonance Imagingelectrophysiologyepilepsyhumanimagingintraoperativeparcellationtumor

Identifiers

PMID42358667
PMCPMC13290761

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.