Evidence map›Paper›PMID 41427309›Full record

ArticlebioRxiv : the preprint server for biology2025

CURVATURE-BASED MACHINE LEARNING METHOD FOR AUTOMATED SEGMENTATION OF DENDRITIC SPINES.

Abdel Kader A Geraldo, Michael A Chirillo, Kristen M Harris, Thomas G Fai

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2025. 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

4 authors.

Abdel Kader A GeraldoDepartment of Mathematics, Brandeis University, Waltham, MA, USA.ORCID 0000-0001-8066-1308
Michael A ChirilloDepartment of Biological Sciences, University of Rhode Island, Kingston, RI, USA.ORCID 0000-0003-0667-8050
Kristen M HarrisDepartment of Neuroscience, University of Texas at Austin, Austin, TX, USA.ORCID 0000-0002-1943-4744
Thomas G FaiDepartment of Mathematics and Volen Center for Complex Systems, Brandeis University, Waltham, MA, USA.ORCID 0000-0003-0383-5217

Funding

Quantitative Neuroscience: Tools for Bridging Levels of AnalysisT32NS007292 · NINDS · BRANDEIS UNIVERSITY · PI GINA G TURRIGIANO · 1986 to 2026
$12.7M
Synaptic plasticity across the lifespanR01MH095980 · NIMH · UNIVERSITY OF TEXAS AT AUSTIN · PI KRISTEN M HARRIS · 2012 to 2026
$5.0M
Synaptic plasticity mechanisms that protect and refine local circuitsR56MH139176 · NIMH · UNIVERSITY OF TEXAS AT AUSTIN · PI HARRIS, KRISTEN M, ZITO, KAREN · 2024 to 2024
$467k
NIMH NIH HHS R01 MH095980NIMH NIH HHS R56 MH139176NINDS NIH HHS T32 NS007292
6 · The paper itself

Abstract

Recent advances in connectomics have been led by high-resolution reconstruction of large volumes of neural tissues using electron microscopy (EM), providing unprecedented insights into brain structure and function. Dendritic spines-dynamic protrusions on neuronal dendrites-play crucial roles in synaptic plasticity, influencing learning, memory, and various neurological disorders. However, current spine analysis methods often rely on manual annotation of subcellular features, limiting their ability to handle the complexity of spines in dense dendritic networks. This paper introduces a novel automated computational framework that integrates discrete differential geometry, machine learning, and 3D image processing to analyze dendritic spines in these intricate environments. By generating distributions of spine morphology from high resolution images including many thousands of spines, our approach captures subtle variations in spine shapes, offering a nuanced understanding of their roles in synaptic function. This framework is tested on multiple EM datasets, with the aim of enhancing our understanding of synaptic plasticity and its alterations in disease states. The proposed method is poised to accelerate neuroscience research by providing a scalable, objective, and comprehensive solution for spine analysis, uncovering insights into the role of spine geometry for neural function.

Identifiers

PMID41427309
PMCPMC12713589

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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.