Author

Asha L. Bayliss

University of Oxford

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Genetic & Genomic Medicine· 1 Genetics· 1 Genomics· 1

Signature Assays, Organisms & Methods

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Organism:human· 2 Approach:statistical model· 2 Research Focus:differential expression· 1 Approach:experimental assay· 1 Research Focus:GWAS / association mapping· 1 Assay:GWAS summary statistics· 1 Organism:mouse· 1

Frequent Co-Authors

Rajesh V. ThakkeriD· 3 shared Fadil M. HannaniD· 2 shared Kreepa G. KooblalliD· 2 shared Mark StevensoniD· 2 shared Victoria J. StokesiD· 2 shared Abigail TurnwaldiD· 1 shared Adeline JacquinetiD· 1 shared Akira WibergiD· 1 shared

Activity by Year

2019-2024 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 37 mutual co-author links

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3 shared papersGenetic & Genomic Medicine

Rajesh V. ThakkerORCID

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Author profile →

3 papers

Recent·Most cited

Adaptor protein 2 sigma subunit (AP2S1) variants associated with neurodevelopmental disorders

Mark Stevenson, Asha L. Bayliss, Victoria J. Stokes, Katherine A. English, Kreepa G. Kooblall, Roman Fischer, Raphael Heilig, Iolanda Vendrell, Maria E. W. A. Albers, Meghan N. Bartos, Amber Hogart Begtrup, Alexia Bourgois, Rebecca Buchert, David J. Carey, Deanna Alexis Carere, , Rajesh V. Thakker

The paper identifies AP2S1 variants linked to neurodevelopmental disorders by showing they impair clathrin-mediated endocytosis and disrupt protein interactions.

medRxiv · Jul 22, 2024 · PreprintGenetic & Genomic Medicine

Ap2s1 mutation in mice causes familial hypocalciuric hypercalcemia type 3

Fadil M. Hannan, Mark Stevenson, Asha L. Bayliss, Victoria J. Stokes, Michelle E. Stewart, Kreepa G. Kooblall, Caroline M. Gorvin, Gemma F. Codner, Lydia Teboul, Sara E. Wells, Rajesh V. Thakker

This study creates a mouse model with an AP2S1 mutation causing FHH3, showing hypercalcemia and demonstrating cinacalcet's effect on calcium levels.

bioRxiv · Aug 10, 2020 · PreprintGenetics

Genetic variants of calcium and vitamin D metabolism in kidney stone disease

Sarah Howles, Akira Wiberg, Michelle E. Goldsworthy, Asha L. Bayliss, Anna Gluck, Michael Ng, Emily Grout, Chizu Tanikawa, Yoichiro Kamatani, Chikashi C. Terao, Atsushi Takahashi, Michiaki Kubo, Koichi Matsuda, Rajesh V. Thakker, Benjamin W. Turney, Dominic Furniss

This study identifies 20 genetic loci associated with kidney stone disease, including novel variants in CYP24A1 and DGKD, which influence vitamin D metabolism and calcium-sensing receptor signaling.

Nature Communications · Nov 15, 2019Peer-reviewedGenomics