Evidence map›Paper›PMID 41667872›Full record

ArticleCerebellum (London, England)2026

A Multi-parametric MRI and Machine Learning Study of Cerebellar Structure in Youth with Neurofibromatosis Type 1.

Sara K Pardej, Julia R Plank, Mira M Raman, Tamar Green

Abstract read
In one paragraph

Article in Cerebellum (London, England), 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

4 authors.

Sara K PardejDivision of Interdisciplinary Brain Sciences, Department of Psychiatry and Behavioral Sciences, Stanford University, 1520 Page Mill Road, Palo Alto, CA, 94304, United States. spardej@stanford.edu.ORCID http://orcid.org/0000-0003-0299-3651
Julia R PlankDivision of Interdisciplinary Brain Sciences, Department of Psychiatry and Behavioral Sciences, Stanford University, 1520 Page Mill Road, Palo Alto, CA, 94304, United States.ORCID http://orcid.org/0009-0008-5929-0651
Mira M RamanDivision of Interdisciplinary Brain Sciences, Department of Psychiatry and Behavioral Sciences, Stanford University, 1520 Page Mill Road, Palo Alto, CA, 94304, United States.
Tamar GreenDivision of Interdisciplinary Brain Sciences, Department of Psychiatry and Behavioral Sciences, Stanford University, 1520 Page Mill Road, Palo Alto, CA, 94304, United States.ORCID http://orcid.org/0000-0001-5661-8297

Funding

TRAINING FOR CHILD PSYCHIATRY AND CHILD DEVELOPMENTT32MH019908 · NIMH · STANFORD UNIVERSITY · PI IAN H GOTLIB, DAVID S HONG · 1993 to 2026
$6.3M
Gaining insights: the effects of the RMK gain-of-function mutations on brain development and neurodevelopmental disordersR01HD108684 · NICHD · STANFORD UNIVERSITY · PI Tamar Green · 2022 to 2026
$3.0M
Ras/MAPK Mutations Effects on the Developing BrainK23HD090209 · NICHD · STANFORD UNIVERSITY · PI GREEN, TAMAR · 2018 to 2022
$837k
Eunice Kennedy Shriver National Institute of Child Health and Human Development K23123752NICHD NIH HHS K23 HD090209NICHD NIH HHS R01 HD108684NIMH NIH HHS T32 MH019908
6 · The paper itself

Abstract

backgroundNeurofibromatosis type 1 (NF1) is a genetic condition caused by pathogenic variants of the NF1 gene. While alterations in cerebral structural and microstructural differences have been reported in NF1, the cerebellum remains largely unexplored. Since individuals with NF1 are at risk for cognitive difficulties, which are in turn associated with cerebellar processes, understanding the underlying neural mechanisms is critical for intervention development.

methodsYouth (5-16 years) with NF1 (n = 30) and unaffected youth (n = 40) participated in neuropsychological (i.e., neurocognitive, parent report of motor abilities) testing and MRI to ascertain structural cerebellar metrics, including volume and white matter mean diffusivity (MD), fractional anisotropy (FA), neurite density (NDI), and orientation dispersion (ODI). We used ANCOVAs to compare between-groups and support vector modeling to investigate which variables (imaging, neurocognitive, motor) contribute the most to NF1 and unaffected participants distinction.

resultsAfter controlling for total brain volume, white matter volume was larger in the NF1 versus unaffected group with a large effect (partial η²=0.57). Cerebellar MD was higher in the NF1 group, while FA, NDI and ODI were lower in the NF1 group (p's < 0.05). Support vector modeling correctly classified 90.20% of participants as being in the NF1 or unaffected group. Top three weights were white matter volume, mobility ratings, and NDI.

conclusionsDifferences in cerebellar white matter microstructure (compared to unaffected youth) were identified in NF1. Cerebellar white matter volume, NDI, and MD were particularly useful differentiators between NF1 and unaffected youth and may be underlying mechanisms of cerebellum-mediated neurocognitive deficits in NF1.

Indexed as

CerebellumMachine LearningMagnetic Resonance ImagingNeurofibromatosis 1AdolescentChildChild, PreschoolFemaleHumansMaleNeuropsychological TestsWhite MatterCerebellumMachine learningNeurofibromatosisRASopathiesStructural neuroimagingWhite matter

Identifiers

PMID41667872
PMCPMC13271018

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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.