Marianne M. Van Den Bree

Cardiff, WLS, United Kingdom

Last Updated: 09/26/2026

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Found 116 publications

The Hidden Architecture of Brain Structural Variability in 22q11.2 Deletion Syndrome: A Multi-site Study.

The Hidden Architecture of Brain Structural Variability in 22q11.2 Deletion Syndrome: A Multi-site Study.

Journal: medRxiv : the preprint server for health sciences

Published: June 04, 2026

The Hidden Architecture of Brain Structural Variability in 22q11.2 Deletion Syndrome: A Multi-site Study.

The Hidden Architecture of Brain Structural Variability in 22q11.2 Deletion Syndrome: A Multi-site Study.

Journal: medRxiv : the preprint server for health sciences

Published: June 04, 2026

Recurrent Copy Number Variants and Psychiatric Outcomes in the Context of Polygenic Scores.

Recurrent Copy Number Variants and Psychiatric Outcomes in the Context of Polygenic Scores.

Journal: JAMA psychiatry

Published: May 27, 2026

Family functioning and psychiatric outcomes in children and young people with intellectual and developmental disabilities caused by rare genetic mutations.

Family functioning and psychiatric outcomes in children and young people with intellectual and developmental disabilities caused by rare genetic mutations.

Journal: medRxiv : the preprint server for health sciences

Published: May 25, 2026

Copy number variants reveal divergent genetic and diagnostic cortical signatures across psychiatric disorders.

Copy number variants reveal divergent genetic and diagnostic cortical signatures across psychiatric disorders.

Journal: Research square

Published: May 18, 2026

Synaptic and Circuit Mechanisms Shaping Neurodevelopmental and Psychiatric Outcomes Associated with 16p11.2 Copy Number Variation.

Synaptic and Circuit Mechanisms Shaping Neurodevelopmental and Psychiatric Outcomes Associated with 16p11.2 Copy Number Variation.

Journal: Genes

Published: May 15, 2026

Combinatorial effects of gene dosage, polygenic background and environment on complex traits.

Combinatorial effects of gene dosage, polygenic background and environment on complex traits.

Journal: medRxiv : the preprint server for health sciences

Published: May 07, 2026

Deletion size and background genetic variation shape congenital heart disease phenotypes in 3,016 individuals with 22q11.2 deletion syndrome.

Deletion size and background genetic variation shape congenital heart disease phenotypes in 3,016 individuals with 22q11.2 deletion syndrome.

Journal: medRxiv : the preprint server for health sciences

Published: March 27, 2026

Deletion size and background genetic variation shape congenital heart disease phenotypes in 3,016 individuals with 22q11.2 deletion syndrome.

Deletion size and background genetic variation shape congenital heart disease phenotypes in 3,016 individuals with 22q11.2 deletion syndrome.

Journal: medRxiv : the preprint server for health sciences

Published: March 27, 2026

Public involvement and co-design of longitudinal studies of sleep health alongside young people with rare genetic conditions.

Public involvement and co-design of longitudinal studies of sleep health alongside young people with rare genetic conditions.

Journal: Research involvement and engagement

Published: March 20, 2026

Genetic and sociodemographic factors associated with trajectories of physical and mental health multimorbidity in a South Asian cohort in the UK: A multistate modelling analysis.

Genetic and sociodemographic factors associated with trajectories of physical and mental health multimorbidity in a South Asian cohort in the UK: A multistate modelling analysis.

Journal: PLoS medicine

Published: November 11, 2025

Combining polygenic risk scores to understand genetic liability to physical-mental health multimorbidity in UK Biobank.

Combining polygenic risk scores to understand genetic liability to physical-mental health multimorbidity in UK Biobank.

Journal: Human molecular genetics

Published: October 09, 2025

Showing 1-12 of 116

Last Updated: 09/26/2026