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Identifying genetic variants associated with cerebellar volume in 33,265 individuals from the UK-Biobank

Tom Chambers, Valentina Escott-Price, View ORCID ProfileSophie Legge, Emily Baker, Krish D. Singh, James TR Walters, Xavier Caseras, View ORCID ProfileRichard JL Anney
doi: https://doi.org/10.1101/2020.11.24.393249
Tom Chambers
1MRC Centre for Neuropsychiatric Genetics and Genomics, School of Medicine, Cardiff University, Cardiff, UK
2Cardiff University Brain Research Imaging Centre (CUBRIC), School of Psychology, Cardiff University, Cardiff, UK
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Valentina Escott-Price
1MRC Centre for Neuropsychiatric Genetics and Genomics, School of Medicine, Cardiff University, Cardiff, UK
3UK Dementia Research Institute, Cardiff University, Cardiff, UK
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Sophie Legge
1MRC Centre for Neuropsychiatric Genetics and Genomics, School of Medicine, Cardiff University, Cardiff, UK
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  • ORCID record for Sophie Legge
Emily Baker
3UK Dementia Research Institute, Cardiff University, Cardiff, UK
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Krish D. Singh
2Cardiff University Brain Research Imaging Centre (CUBRIC), School of Psychology, Cardiff University, Cardiff, UK
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James TR Walters
1MRC Centre for Neuropsychiatric Genetics and Genomics, School of Medicine, Cardiff University, Cardiff, UK
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Xavier Caseras
1MRC Centre for Neuropsychiatric Genetics and Genomics, School of Medicine, Cardiff University, Cardiff, UK
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  • For correspondence: CaserasX@cardiff.ac.uk
Richard JL Anney
1MRC Centre for Neuropsychiatric Genetics and Genomics, School of Medicine, Cardiff University, Cardiff, UK
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  • ORCID record for Richard JL Anney
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Abstract

There is expanding interest in researching the cerebellum given accumulating evidence of its important contributions to cognitive and emotional functions, in addition to more established sensorimotor roles. While large genome-wide association studies (GWAS) have shed light on the common allele architecture of cortical and subcortical brain structures, the cerebellum remains under investigated. We conducted a meta-GWAS of cerebellar volume in 33,265 UK-Biobank European participants. Results show cerebellar volume to be moderately heritable (h2SNP=50.6%). We identified 33 independent genome-wide associated SNPs with total cerebellar volume, with 6 of these SNPs mapped to protein-coding genes and 5 more shown to alter cerebellar gene expression. We highlight 21 unique candidate genes for follow-up analysis. Cerebellar volume showed significant genetic correlation with brainstem, pallidum and thalamus volumes, but no significant correlations with neuropsychiatric phenotypes. Our results provide important new knowledge of the genetic architecture of cerebellar volume and its relationship with other brain phenotypes.

Competing Interest Statement

JTRW has received grant funding from Takeda Pharmaceutical Company for research unrelated to this work. All other authors declare no competing interests.

Copyright 
The copyright holder for this preprint is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under a CC-BY-NC-ND 4.0 International license.
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Posted November 24, 2020.
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Identifying genetic variants associated with cerebellar volume in 33,265 individuals from the UK-Biobank
Tom Chambers, Valentina Escott-Price, Sophie Legge, Emily Baker, Krish D. Singh, James TR Walters, Xavier Caseras, Richard JL Anney
bioRxiv 2020.11.24.393249; doi: https://doi.org/10.1101/2020.11.24.393249
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Identifying genetic variants associated with cerebellar volume in 33,265 individuals from the UK-Biobank
Tom Chambers, Valentina Escott-Price, Sophie Legge, Emily Baker, Krish D. Singh, James TR Walters, Xavier Caseras, Richard JL Anney
bioRxiv 2020.11.24.393249; doi: https://doi.org/10.1101/2020.11.24.393249

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