Yi, Fei
Stanford Medicine · Stanford University
3 papers on CoChatORCID 0000-0002-2464-3655
Most cited papers
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A Werner syndrome stem cell model unveils heterochromatin alterations as a driver of human aging
Zhang, W., Li, J., Suzuki, K., Qu, J., Wang, P., Zhou, J., Liu, X., Ren, R., Xu, X., Ocampo, A., et al. (2015) · Science
Telomeres, Telomerase, and SenescenceNuclear Structure and Function
Cited by 551
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Progressive degeneration of human neural stem cells caused by pathogenic LRRK2
Liu, G.-H., Qu, J., Suzuki, K., Nivet, E., Li, M., Montserrat, N., Yi, F., Xu, X., Ruiz, S., Zhang, W., et al. (2012) · Nature
Parkinson's Disease Mechanisms and TreatmentsNuclear Receptors and Signaling
Cited by 339
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Autism-associated SHANK3 haploinsufficiency causes I h channelopathy in human neurons
Yi, F., Danko, T., Botelho, S. C., Patzke, C., Pak, C., Wernig, M., & Südhof, T. C. (2016) · Science
Genetics and Neurodevelopmental DisordersIon channel regulation and function
Cited by 313
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