Alterations in white matter tract myelination in carriers of copy number variations at the 16p11.2 locus

Motivation: Individuals with 16p11.2 copy number variations (CNVs) have a heightened risk for neurodevelopmental disorders. Diffusion MRI studies have identified white matter alterations in 16p11.2 carriers; however, the exact neurobiological differences underlying these alterations remain unclear. Goal(s): To investigate white matter tract caliber and myelination in 16p11.2 CNV carriers. Approach: We analyzed 3T multi-modal quantitative MRI using tract-specific methods to minimize partial volume effects from crossing tracts. We used linear models to compare tract microstructural features between 16p11.2 CNV carriers and neurotypical controls. Results: Preliminary data indicate that gene dosage influences the g-ratio, increasing in 16p11.2 deletion carriers and decreasing in duplication carriers. Impact: This quantitative MRI study demonstrates for the first time that 16p11.2 CNV carriers exhibit altered myelination of their white matter tracts. Future work will investigate the association between network myelination and brain function.

Authors

Publication Details

Journal
Proceedings on CD-ROM - International Society for Magnetic Resonance in Medicine. Scientific Meeting and Exhibition/Proceedings of the International Society for Magnetic Resonance in Medicine, Scientific Meeting and Exhibition
Published
2025-09-16
DOI
https://doi.org/10.58530/2025/0632
Primary Topic
RNA regulation and disease
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Alterations in white matter tract myelination in carriers of copy number variations at the 16p11.2 locus

Khadijé Jizi, Christine Tardif, Sébastien Jacquemont, Wen Da Lu et al.
Proceedings on CD-ROM - International Society for Magnetic Resonance in Medicine. Scientific Meeting and Exhibition/Proceedings of the International Society for Magnetic Resonance in Medicine, Scientific Meeting and Exhibition
RNA regulation and disease
article

Alterations in white matter tract myelination in carriers of copy number variations at the 16p11.2 locus

Khadijé Jizi, Christine Tardif, Sébastien Jacquemont, Wen Da Lu, Mark C. Nelson, Charles-Olivier Martin
article en

Abstract

Motivation: Individuals with 16p11.2 copy number variations (CNVs) have a heightened risk for neurodevelopmental disorders. Diffusion MRI studies have identified white matter alterations in 16p11.2 carriers; however, the exact neurobiological differences underlying these alterations remain unclear. Goal(s): To investigate white matter tract caliber and myelination in 16p11.2 CNV carriers. Approach: We analyzed 3T multi-modal quantitative MRI using tract-specific methods to minimize partial volume effects from crossing tracts. We used linear models to compare tract microstructural features between 16p11.2 CNV carriers and neurotypical controls. Results: Preliminary data indicate that gene dosage influences the g-ratio, increasing in 16p11.2 deletion carriers and decreasing in duplication carriers. Impact: This quantitative MRI study demonstrates for the first time that 16p11.2 CNV carriers exhibit altered myelination of their white matter tracts. Future work will investigate the association between network myelination and brain function.

Proceedings on CD-ROM - International Society for Magnetic Resonance in Medicine. Scientific Meeting and Exhibition/Proceedings of the International Society for Magnetic Resonance in Medicine, Scientific Meeting and Exhibition
Openalex Percentile: Top 78%
RNA regulation and disease
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.