Evidence map›Paper›PMID 42523343›Full record

ArticlebioRxiv : the preprint server for biology2026

Selective convergence and graded divergence of hippocampal and amygdala subregions using functional connectivity.

Doruk Yiğit Erigüç, Mylla Marsiglia, Alexandra John, Şeyma Bayrak, Bin Wan, Anton Jakovčić, Jordan DeKraker, Jessica Royer, Boris C Bernhardt, Sofie L Valk

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 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

10 authors.

Doruk Yiğit ErigüçMax Planck Institute for Human Cognitive and Brain Sciences, Leipzig, Germany.ORCID 0009-0003-8073-8135
Mylla MarsigliaMax Planck Institute for Human Cognitive and Brain Sciences, Leipzig, Germany.ORCID 0000-0001-9138-7359
Alexandra JohnMax Planck Institute for Human Cognitive and Brain Sciences, Leipzig, Germany.ORCID 0009-0007-1380-420X
Şeyma BayrakMax Planck Institute for Human Cognitive and Brain Sciences, Leipzig, Germany.ORCID 0000-0002-9108-323X
Bin WanMax Planck Institute for Human Cognitive and Brain Sciences, Leipzig, Germany.ORCID 0000-0001-9077-3354
Anton JakovčićMedical Faculty, University of Zagreb, Zagreb, Croatia.
Jordan DeKrakerCentre for Excellence in Epilepsy (CEEN) and McConnell Brain Imaging Centre (BIC), Montreal Neurological Institute and Hospital McGill University, Montreal, Canada.ORCID 0000-0002-4093-0582
Jessica RoyerMax Planck Institute for Human Cognitive and Brain Sciences, Leipzig, Germany.ORCID 0000-0002-4448-8998
Boris C BernhardtCentre for Excellence in Epilepsy (CEEN) and McConnell Brain Imaging Centre (BIC), Montreal Neurological Institute and Hospital McGill University, Montreal, Canada.ORCID 0000-0001-9256-6041
Sofie L ValkMax Planck Institute for Human Cognitive and Brain Sciences, Leipzig, Germany.ORCID 0000-0003-2998-6849

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The hippocampus and amygdala are neighboring medial temporal lobe structures linked to memory and affect, yet how their subregions are jointly embedded within distributed isocortical systems remains unclear. Using resting-state fMRI from 722 Human Connectome Project Young Adult participants, we mapped hippocampal and amygdalar subregions within a unified cortex-wide framework, quantifying subregion-to-cortex connectivity via Pearson correlation (broad co-fluctuation) and GLASSO partial correlation (relatively more direct functional association). We introduced two count-based metrics: dominance (relative hippocampal vs. amygdalar representation) and sharedness (balanced co-representation). Direct associations showed both structures sharing coupling with paralimbic areas and, more modestly, default mode regions, while broader co-fluctuations extended into somatomotor and paralimbic networks. Divergence patterns depended on the estimator: hippocampal subregions preferentially coupled with default-mode and visual networks under direct association, while amygdalar nuclei favored ventral attention and limbic networks; broader co-fluctuations additionally implicated somatomotor cortex for amygdala and visual cortex for hippocampus. These principles held at the subfield/nucleus level, varying along the hippocampal long axis and identifying the paralaminar nucleus as the most hippocampus-like amygdalar subregion. Data-driven connectivity gradients confirmed both systems' separation and fine-scale interdigitation. Hippocampal and amygdalar subregions are thus embedded in cortex not as discrete systems, but through structured, spatially organized co-representation.

Identifiers

PMID42523343
PMCPMC13405180

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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.