Author

Margaret L. Sutherland

National Institutes of HealthORCID 0000-0002-8262-4110Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Research Focus:cell type annotation· 1 Research Focus:cell-cell communication· 1 Assay:clinical cohort / trial· 1 Assay:CRISPR screen· 1 Research Focus:differential expression· 1 Assay:DNA methylation· 1 Research Focus:eQTL / molecular QTL mapping· 1 Approach:experimental assay· 1

Frequent Co-Authors

Mark CooksoniD· 2 shared Akbota M. AitkulovaiD· 1 shared Alastair John NoyceiD· 1 shared Alexis BriceiD· 1 shared Amber Keith· 1 shared Ana CámaraiD· 1 shared Andrew SingletoniD· 1 shared Angli XueiD· 1 shared

Activity by Year

2019-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 37 mutual co-author links

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2 shared papersNeuroscience

Mark CooksonORCID

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2 papers

Recent·Most cited

iPSC Neurodegenerative Disease Initiative isogenic CAG repeat iPSC line for Huntingtons disease

Lisa Salazar, Mara S. Burns, Jennifer T. Stocksdale, Keona Q. Wang, Gloria Cao, Ricardo Miramontes, Nicolette R. McClure, Leanne N. Ho, Amber Keith, Margaret L. Sutherland, Mark Cookson, Michael Emmerson Ward, William C. Skarnes, Leslie Michels Thompson

The paper generates isogenic iPSC lines with CAG repeats and HTT KO for Huntington's disease study, showing differentiation potential and altered gene expression in neurons and astrocytes.

Journal of Huntington s Disease · Oct 16, 2026Peer-reviewedNeuroscience

Expanding Parkinson’s disease genetics: novel risk loci, genomic context, causal insights and heritable risk

Mike A. Nalls, Cornelis Blauwendraat, Costanza Ludovica Vallerga, Karl Heilbron, Sara Bandrés‐Ciga, Diana Chang, Manuela M. X. Tan, Demis A. Kia, Alastair John Noyce, Angli Xue, José Brás, Emily Young, Rainer von Coelln, Javier Simón-Sánchez, Claudia Schulte, , Ciara García

Across 37,688 Parkinson's cases, 18,618 proxy-cases and 1.4M controls, 90 risk signals map to 78 loci (37 new); an 1805-variant polygenic score explains 26-36% of heritability.

The Lancet Neurology · Nov 6, 2019Peer-reviewedGenetics✦ In-depth digest