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FEBS Letters|August 31, 2014
A commonly used Drosophila model of Alzheimer's disease generates an aberrant species of amyloid-β with an additional N-terminal glutamine residueKirsten Allan, Keyla A Perez, Kevin J Barnham, et al.Disease Models & Mechanisms|January 18, 2013
In Drosophila, RhoGEF2 cooperates with activated Ras in tumorigenesis through a pathway involving Rho1-Rok-Myosin-II and JNK signallingPeytee Khoo, Kirsten Allan, Lee Willoughby, et al.International Journal of Molecular Sciences|December 10, 2021
PTP61F Mediates Cell Competition and Mitigates TumorigenesisJohn E La Marca, Lee F Willoughby, Kirsten Allan, et al.The FEBS Journal|May 26, 2017
Differential regulation of protein tyrosine kinase signalling by Dock and the PTP61F variantsLee F Willoughby, Jan Manent, Kirsten Allan, et al.American Journal of Medical Genetics. Part A|October 22, 2025
Functional Characterization of a Novel GPC3 Missense Variant in Simpson-Golabi-Behmel SyndromeTeresa Zhao, Kirsten Allan, Juliet Taylor, et al.Plos One|January 20, 2010
Control of Alzheimer's amyloid beta toxicity by the high molecular weight immunophilin FKBP52 and copper homeostasis in DrosophilaReiko Sanokawa-Akakura, Weihuan Cao, Kirsten Allan, et al.Medrxiv : the Preprint Server for Health Sciences|May 25, 2026
A genome-wide deletion map in 125,730 individuals for novel rare disease gene and variant discoveryAnthony McGuigan, Alistair T Pagnamenta, Laura E Covill, et al.Medrxiv : the Preprint Server for Health Sciences|July 3, 2026
Structural variant discovery and diagnostic impact in rare diseases from short-read and long-read sequencingAlba Sanchis-Juan, Yulia Mostovoy, Sarah L Stenton, et al.Medrxiv : the Preprint Server for Health Sciences|April 22, 2024
<i>De novo</i> variants in the non-coding spliceosomal snRNA gene <i>RNU4-2</i> are a frequent cause of syndromic neurodevelopmental disordersYuyang Chen, Ruebena Dawes, Hyung Chul Kim, et al.Nature|July 11, 2024
De novo variants in the RNU4-2 snRNA cause a frequent neurodevelopmental syndromeYuyang Chen, Ruebena Dawes, Hyung Chul Kim, et al.Pageof 1