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Human Molecular Genetics|December 4, 2020
A Neurexin2aa deficiency results in axon pathfinding defects and increased anxiety in zebrafishAngela Koh, Shijie Tao, Yun Jing Goh, et al.Journal of Clinical Medicine|July 2, 2021
Whole-Exome Sequencing to Identify Potential Genetic Risk in Substance Use Disorders: A Pilot Feasibility StudyP V AshaRani, Syidda Amron, Noor Azizah Bte Zainuldin, et al.Human Molecular Genetics|July 24, 2021
A novel zebrafish model for intermediate type spinal muscular atrophy demonstrates importance of Smn for maintenance of mature motor neuronsShermaine Huiping Tay, Erna Nur Ellieyana, Yao Le, et al.Elife|April 2, 2020
Application of optogenetic Amyloid-β distinguishes between metabolic and physical damages in neurodegenerationChu Hsien Lim, Prameet Kaur, Emelyne Teo, et al.Cells|January 21, 2022
Wnt Signaling Rescues Amyloid Beta-Induced Gut Stem Cell LossPrameet Kaur, Ellora Hui Zhen Chua, Wen Kin Lim, et al.Scientific Reports|May 10, 2022
A non-canonical Raf function is required for dorsal-ventral patterning during Drosophila embryogenesisJay B Lusk, Ellora Hui Zhen Chua, Prameet Kaur, et al.American Journal of Human Genetics|May 26, 2021
Loss of C2orf69 defines a fatal autoinflammatory syndrome in humans and zebrafish that evokes a glycogen-storage-associated mitochondriopathyHui Hui Wong, Sze Hwee Seet, Michael Maier, et al.Nature Communications|February 1, 2020
Loss-of-function mutations in UDP-Glucose 6-Dehydrogenase cause recessive developmental epileptic encephalopathyHolger Hengel, Célia Bosso-Lefèvre, George Grady, et al.Pageof 3