Author

Christopher Kobylecki

Manchester Academic Health Science CentreORCID 0000-0002-7797-0756Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 1 Genetics· 1

Signature Assays, Organisms & Methods

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Research Focus:GWAS / association mapping· 2 Assay:GWAS summary statistics· 2 Organism:human· 2 Approach:statistical model· 2

Frequent Co-Authors

Dennis W. DicksoniD· 2 shared Huw R. MorrisiD· 2 shared James Benedict RoweiD· 2 shared John HardyiD· 2 shared Kin Ying MokiD· 2 shared Maryam ShoaiiD· 2 shared Owen A. RossiD· 2 shared Rebecca R. ValentinoiD· 2 shared

Activity by Year

2020-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 44 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Dennis W. DicksonORCID

Mutual co-authors in cluster

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2 papers

Recent·Most cited

Identification of common variants influencing risk of the three-repeat tauopathy Pick's disease: a genome wide association study.

William J. Scotton, Rebecca R. Valentino, Alejandro Martínez-Carrasco, Raquel Real, Hannah L. Macpherson, Nicole Tamvaka, Kin Ying Mok, Michael G. Heckman, Christopher Kobylecki, Valentina Escott‐Price, James Benedict Rowe, Huw R. Morris, Rosa Rademakers, Shanu Faerch Roemer, Tammaryn Lashley, , Maryam Shoai

This study conducts a GWAS on Pick's disease and identifies two SNPs associated with risk, though not at genome-wide significance, suggesting potential genetic factors beyond MAPT mutations.

medRxiv · Dec 27, 2025 · PreprintGenetic & Genomic Medicine

Common variation at the LRRK2 locus is associated with survival in the primary tauopathy progressive supranuclear palsy

Edwin Jabbari, Manuela M. X. Tan, Regina Hertfelder Reynolds, Kin Ying Mok, Raffaele Ferrari, David P. Murphy, Rebecca R. Valentino, Owen A. Ross, Dennis W. Dickson, Safa Al‐Sarraj, Steve Gentleman, Kieren S. J. Allinson, Zane Jaunmuktane, Janice L. Holton, Tamás Révész, , Huw R. Morris

The paper identifies common LRRK2 locus variation associated with survival in progressive supranuclear palsy, linking it to gene expression regulation and suggesting therapeutic implications for tauopathies.

bioRxiv · Feb 4, 2020 · PreprintGenetics