Author

Cynthia Sandor

Cardiff UniversityORCID 0000-0002-8905-1052Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetics· 2 Neuroscience· 2

Signature Assays, Organisms & Methods

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Organism:human· 4 Approach:statistical model· 3 Research Focus:GWAS / association mapping· 2 Assay:GWAS summary statistics· 2 Approach:Bayesian inference· 1 Approach:benchmark study· 1 Research Focus:cell type annotation· 1 Research Focus:clustering· 1

Frequent Co-Authors

Caleb WebberiD· 4 shared Amy FergusoniD· 1 shared Anastasia IllarionovaiD· 1 shared Andrew DahliD· 1 shared Andrew SingletoniD· 1 shared Artur Francisco Schumacher SchuhiD· 1 shared Ashley HalliD· 1 shared Bobby Bojovic· 1 shared

Activity by Year

2019-2021 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 21 mutual co-author links

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4 shared papersNeuroscience

Caleb WebberORCID

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4 papers

Recent·Most cited

Universal latent axes capturing Parkinson's patient deep phenotypic variation reveals patients with a high genetic risk for Alzheimer's disease are more likely to develop a more aggressive form of Parkinson's.

Cynthia Sandor, Stephanie Millin, Andrew Dahl, Michael Lawton, Leon Hubbard, Bobby Bojovic, Marine Peyret Guzzon, Hannah Matten, Christine Blancher, Nigel M. Williams, Yoav Ben‐Shlomo, Michele T. Hu, Donald G. Grosset, Jonathan Marchini, Caleb Webber

bioRxiv · Feb 18, 2021 · PreprintNeuroscience

The Parkinson's Disease GWAS Locus Browser

Francis P. Grenn, Jonggeol Jeffrey Kim, Mary B. Makarious, Hirotaka Iwaki, Anastasia Illarionova, Kajsa Atterling Brolin, Jillian H. Kluss, Artur Francisco Schumacher Schuh, Hampton L. Leonard, Faraz Faghri, Kimberley J. Billingsley, Lynne Krohn, Ashley Hall, Mónica Díez-Fairén, María Teresa Periñán, , Cornelis Blauwendraat

The paper presents a GWAS locus browser for Parkinson's disease that helps prioritize genes associated with risk variants from multiple GWAS studies.

Movement Disorders · Aug 31, 2020Peer-reviewedGenetics

A human single-cell atlas of the Substantia nigra reveals novel cell-specific pathways associated with the genetic risk of Parkinson's disease and neuropsychiatric disorders.

Devika Agarwal, Cynthia Sandor, Viola Volpato, Tara M. Caffrey, Jimena Monzón‐Sandoval, Rory J. Bowden, Javier Alegre‐Abarrategui, Richard Wade‐Martins, Caleb Webber

The paper constructs a single-cell atlas of the Substantia nigra and identifies cell-specific gene expression patterns linked to Parkinson's disease and neuropsychiatric disorders.

Nature Communications · Aug 21, 2020Peer-reviewedNeuroscience

The genomic basis of mood instability: identification of 46 loci in 363,705 UK Biobank participants, genetic correlation with psychiatric disorders, and association with gene expression and function.

Joey Ward, Elizabeth M. Tunbridge, Cynthia Sandor, Laura M. Lyall, Amy Ferguson, Rona J. Strawbridge, Donald M. Lyall, Breda Cullen, Nicholas Graham, Keira J.A. Johnston, Caleb Webber, Valentina Escott‐Price, Michael C. O’Donovan, Jill P. Pell, Mark E.S. Bailey, , Daniel J. Smıth

This paper conducts a GWAS of mood instability in 363,705 UK Biobank participants, identifies 46 loci, and finds genetic correlations with psychiatric disorders and brain-specific gene expression.

Molecular Psychiatry · Jun 5, 2019Peer-reviewedGenetics