Evidence map›Paper›PMID 40617381›Full record

Trial reportBiological psychiatry2026

Mapping Cerebellar Connectivity to Cognition in Psychosis: Convergent Evidence From Functional Magnetic Resonance Imaging and Transcranial Magnetic Stimulation.

Hengyi Cao, Miklos Argyelan, Joanna Yan, Halil Aziz Velioglu, Franky Fang, Andrea Joanlanne, Simran Kang, Lara Prizgint, Jenna Schugart, Kadeem Brown and 8 more

Abstract readRandomized Controlled Trial
In one paragraph

Trial report in Biological psychiatry, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed, 1 pooled it
–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

5 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Cerebellar Connectivity Addresses Gaps in Cognitive Deficits and Negative Symptoms in Psychosis.Biological psychiatry. Cognitive neuroscience and neuroimaging · 2026
    Article
  4. Cerebellar-Prefrontal Connectivity Predicts Negative Symptom Severity Across the Psychosis Spectrum.Biological psychiatry. Cognitive neuroscience and neuroimaging · 2026
    Article
  5. Article
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

18 authors.

Hengyi CaoInstitute of Behavioral Science, Feinstein Institutes for Medical Research, Manhasset, New York; Division of Psychiatry Research, Zucker Hillside Hospital, Glen Oaks, New York; Department of Psychiatry, Zucker School of Medicine at Hofstra/Northwell, Hempstead, New York. Electronic address: hcao2@northwell.edu.
Miklos ArgyelanInstitute of Behavioral Science, Feinstein Institutes for Medical Research, Manhasset, New York; Division of Psychiatry Research, Zucker Hillside Hospital, Glen Oaks, New York; Division of Psychiatry Research, Zucker Hillside Hospital, Glen Oaks, New York.
Joanna YanInstitute of Behavioral Science, Feinstein Institutes for Medical Research, Manhasset, New York; Division of Psychiatry Research, Zucker Hillside Hospital, Glen Oaks, New York; Department of Psychiatry, Zucker School of Medicine at Hofstra/Northwell, Hempstead, New York.
Halil Aziz VeliogluInstitute of Behavioral Science, Feinstein Institutes for Medical Research, Manhasset, New York; Division of Psychiatry Research, Zucker Hillside Hospital, Glen Oaks, New York; Department of Psychiatry, Zucker School of Medicine at Hofstra/Northwell, Hempstead, New York.
Franky FangInstitute of Behavioral Science, Feinstein Institutes for Medical Research, Manhasset, New York; Division of Psychiatry Research, Zucker Hillside Hospital, Glen Oaks, New York; Department of Psychiatry, Zucker School of Medicine at Hofstra/Northwell, Hempstead, New York.
Andrea JoanlanneInstitute of Behavioral Science, Feinstein Institutes for Medical Research, Manhasset, New York; Division of Psychiatry Research, Zucker Hillside Hospital, Glen Oaks, New York; Department of Psychiatry, Zucker School of Medicine at Hofstra/Northwell, Hempstead, New York.
Simran KangInstitute of Behavioral Science, Feinstein Institutes for Medical Research, Manhasset, New York; Division of Psychiatry Research, Zucker Hillside Hospital, Glen Oaks, New York; Department of Psychiatry, Zucker School of Medicine at Hofstra/Northwell, Hempstead, New York.
Lara PrizgintInstitute of Behavioral Science, Feinstein Institutes for Medical Research, Manhasset, New York; Division of Psychiatry Research, Zucker Hillside Hospital, Glen Oaks, New York; Department of Psychiatry, Zucker School of Medicine at Hofstra/Northwell, Hempstead, New York.
Jenna SchugartInstitute of Behavioral Science, Feinstein Institutes for Medical Research, Manhasset, New York; Division of Psychiatry Research, Zucker Hillside Hospital, Glen Oaks, New York; Department of Psychiatry, Zucker School of Medicine at Hofstra/Northwell, Hempstead, New York.
Kadeem BrownInstitute of Behavioral Science, Feinstein Institutes for Medical Research, Manhasset, New York; Division of Psychiatry Research, Zucker Hillside Hospital, Glen Oaks, New York; Department of Psychiatry, Zucker School of Medicine at Hofstra/Northwell, Hempstead, New York.
John CholewaInstitute of Behavioral Science, Feinstein Institutes for Medical Research, Manhasset, New York; Division of Psychiatry Research, Zucker Hillside Hospital, Glen Oaks, New York; Department of Psychiatry, Zucker School of Medicine at Hofstra/Northwell, Hempstead, New York.
Philip WatsonInstitute of Behavioral Science, Feinstein Institutes for Medical Research, Manhasset, New York; Division of Psychiatry Research, Zucker Hillside Hospital, Glen Oaks, New York; Department of Psychiatry, Zucker School of Medicine at Hofstra/Northwell, Hempstead, New York.
Sunny X TangInstitute of Behavioral Science, Feinstein Institutes for Medical Research, Manhasset, New York; Division of Psychiatry Research, Zucker Hillside Hospital, Glen Oaks, New York; Department of Psychiatry, Zucker School of Medicine at Hofstra/Northwell, Hempstead, New York.
Ricardo CarrionInstitute of Behavioral Science, Feinstein Institutes for Medical Research, Manhasset, New York; Division of Psychiatry Research, Zucker Hillside Hospital, Glen Oaks, New York; Department of Psychiatry, Zucker School of Medicine at Hofstra/Northwell, Hempstead, New York.
Jose RubioInstitute of Behavioral Science, Feinstein Institutes for Medical Research, Manhasset, New York; Division of Psychiatry Research, Zucker Hillside Hospital, Glen Oaks, New York; Department of Psychiatry, Zucker School of Medicine at Hofstra/Northwell, Hempstead, New York.
Moein ForoughiDepartment of Psychiatry, Zucker Hillside Hospital, Glen Oaks, New York.
Todd LenczInstitute of Behavioral Science, Feinstein Institutes for Medical Research, Manhasset, New York; Division of Psychiatry Research, Zucker Hillside Hospital, Glen Oaks, New York; Department of Psychiatry, Zucker School of Medicine at Hofstra/Northwell, Hempstead, New York.
Anil K MalhotraInstitute of Behavioral Science, Feinstein Institutes for Medical Research, Manhasset, New York; Division of Psychiatry Research, Zucker Hillside Hospital, Glen Oaks, New York; Department of Psychiatry, Zucker School of Medicine at Hofstra/Northwell, Hempstead, New York.

Funding

Human Connectome Project for Early PsychosisU01MH109977 · NIMH · BRIGHAM AND WOMEN'S HOSPITAL · PI BREIER, ALAN, SHENTON, MARTHA E. · 2016 to 2020
$5.5M
Cerebellar-Cortical Circuitry and Treatment Response in Early PsychosisR01MH137501 · NIMH · FEINSTEIN INSTITUTE FOR MEDICAL RESEARCH · PI Hengyi Cao · 2025 to 2026
$980k
Development of Cerebellar-Cortical Functional Connectivity in Youth and Its Prediction of PsychosisR01MH138682 · NIMH · FEINSTEIN INSTITUTE FOR MEDICAL RESEARCH · PI Hengyi Cao · 2025 to 2026
$854k
NIMH NIH HHS R01 MH137501NIMH NIH HHS R01 MH138682NIMH NIH HHS U01 MH109977
6 · The paper itself

Abstract

backgroundCerebellar dysfunction is strongly implicated in both cognitive impairments and psychosis, and the cognitive dysmetria hypothesis posits cognition as the intermediary in the pathway from cerebellar dysfunction to psychopathology. However, the nuanced cerebellum-behavior relationships in psychosis remain unclear. Establishing such a link is crucial to understand cerebellar mechanisms and to identify treatment targets for cognitive deficits in patients.

methodsWe studied 100 patients with early psychosis from the Human Connectome Project for Early Psychosis study. Connectome-based predictive modeling was conducted to probe cognitive functions most strongly predicted by cerebellar connectivity. Mediation analysis was performed to test for a possible mediating role of cognition between cerebellar connectivity and symptoms. To further support the causality of the findings, we also recruited 16 patients with psychosis for a 2-week randomized, sham-controlled cerebellar transcranial magnetic stimulation (TMS) trial.

resultsCerebellar connectivity significantly predicted 3 cognitive functions, namely verbal ability, working memory, and cognitive flexibility. Verbal ability fully mediated the relationship between cerebellar connectivity and negative symptoms, in particular alogia. While each cognitive function was predicted by a distinct cerebellar connectivity pattern, the left crus I/II appeared to be a common area with connectivity that consistently predicted all 3 functions. Stimulating this region via TMS was associated with significantly improved cognitive composite score and medium-to-large effects on scores for memory, verbal, and executive functions.

conclusionsThese findings suggest a potential causal pathway from cerebellar connectivity to domain-specific cognitive deficits and psychopathology in schizophrenia. They also point to the cerebellum as a potential target for the treatment of cognitive dysfunction in psychotic disorders.

Indexed as

CerebellumCognitionPsychotic DisordersAdolescentAdultConnectomeFemaleHumansMagnetic Resonance ImagingMaleMemory, Short-TermNeural PathwaysTranscranial Magnetic StimulationYoung AdultCerebellumCognitionFunctional connectivityNeuroimagingSchizophreniaTranscranial Magnetic Stimulation

Identifiers

PMID40617381
PMCPMC12351477

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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.