Evidence map›Paper›PMID 42276070›Full record

ArticleCell reports methods2026

A hybrid micro-ECoG for functionally targeted multi-site and multi-scale investigation.

Patrick Jendritza, Rickard Liljemalm, Thomas Stieglitz, Pascal Fries, Christopher Murphy Lewis

Abstract read
In one paragraph

Article in Cell reports methods, 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

5 · Who and what money

Authors and funding

5 authors.

Patrick JendritzaErnst Strüngmann Institute (ESI) for Neuroscience in Cooperation with Max Planck Society, Deutschordenstraße 46, 60528 Frankfurt, Germany; International Max Planck Research School for Neural Circuits, Max-von-Laue-Straße 4, 60438 Frankfurt, Germany; Else Kröner Fresenius Center for Optogenetic Therapies, University Medical Center Göttingen, Göttingen, Germany; Institute for Auditory Neuroscience, University Medical Center Göttingen, Göttingen, Germany; Visual Circuits & Interfaces group, German Primate Center, Göttingen, Germany. Electronic address: pjendritza@dpz.eu.
Rickard LiljemalmLaboratory for Biomedical Microtechnology, Department of Microsystems Engineering (IMTEK), BrainLinks-BrainTools Center and the Bernstein Center Freiburg, Albert-Ludwigs-Universität Freiburg, 79110 Freiburg, Germany.
Thomas StieglitzMax Planck Institute for Biological Cybernetics, Max-Planck-Ring 8, 72076 Tübingen, Germany.
Pascal FriesErnst Strüngmann Institute (ESI) for Neuroscience in Cooperation with Max Planck Society, Deutschordenstraße 46, 60528 Frankfurt, Germany; International Max Planck Research School for Neural Circuits, Max-von-Laue-Straße 4, 60438 Frankfurt, Germany; Max Planck Institute for Biological Cybernetics, Max-Planck-Ring 8, 72076 Tübingen, Germany.
Christopher Murphy LewisErnst Strüngmann Institute (ESI) for Neuroscience in Cooperation with Max Planck Society, Deutschordenstraße 46, 60528 Frankfurt, Germany; Brain Research Institute, University of Zurich, Winterthurerstrasse 190, 8057 Zurich, Switzerland. Electronic address: lewis@hifo.uzh.ch.

Funding

Mapping the Human Connectome: Structure, Function, and HeritabilityU54MH091657 · NIMH · WASHINGTON UNIVERSITY · PI UGURBIL, KAMIL, VAN ESSEN, DAVID C · 2010 to 2014
$34.7M
NIMH NIH HHS U54 MH091657
6 · The paper itself

Abstract

Brain function relies on coordinated activity across spatial and temporal scales. Single neurons integrate local and long-range connectivity and reflect activity across brain-wide networks. Understanding integrated brain function requires tools capable of recording from anatomically connected populations in distributed brain areas to bridge local and global dynamics. Here, we present high-density, micro-electrocorticography arrays that facilitate multi-scale studies of brain activity. The hybrid arrays integrate the desirable features of silicone elastomers and polyimide films: silicone provides optical transparency and permits repeated penetration with intracortical arrays, while polyimide enables fine photolithographic feature definition. This combination facilitates high-throughput functional mapping to identify targets and insertion of intracortical arrays for dense local sampling. We demonstrate functional mapping in rats, cats, and marmosets, showing how functional maps guide multi-area laminar recordings. Finally, we demonstrate local and feedforward optogenetic stimulation to investigate cortico-cortical interactions. These capabilities establish the hybrid μECoG as a compelling tool for systems neuroscience.

Indexed as

BrainBrain MappingElectrocorticographyAnimalsCallithrixCatsNeuronsOptogeneticsRatsbrainCP: biotechnologyCP: neuroscienceECoGelectrocorticographyLFPmultimodalneuroscienceoptogeneticsprimatesensory codingtopography

Identifiers

PMID42276070
PMCPMC13494546

What OpenQuestion holds

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LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

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.