Yushi T Redhead

Developmental Biology, Down Syndrome

Jeremy Green	grad student	2016-2020	Kings College London (KCL)
Victor Tybulewicz	grad student	2016-2020

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Redhead Y, Gibbins D, Lana-Elola E, et al. (2023) Craniofacial dysmorphology in Down syndrome is caused by increased dosage of Dyrk1a and at least three other genes. Development (Cambridge, England). 150
Donovan APA, Rosko L, Ellegood J, et al. (2023) Pervasive cortical and white matter anomalies in a mouse model for CHARGE syndrome. Journal of Anatomy
Chern T, Achilleos A, Tong X, et al. (2022) Mutations in Hcfc1 and Ronin result in an inborn error of cobalamin metabolism and ribosomopathy. Nature Communications. 13: 134
Lin Z, Kim E, Ahmed M, et al. (2021) MRI-guided histology of TDP-43 knock-in mice implicates parvalbumin interneuron loss, impaired neurogenesis and aberrant neurodevelopment in amyotrophic lateral sclerosis-frontotemporal dementia. Brain Communications. 3: fcab114
Toussaint N, Redhead Y, Vidal-García M, et al. (2021) A landmark-free morphometrics pipeline for high-resolution phenotyping: application to a mouse model of Down syndrome. Development (Cambridge, England). 148