| Year |
Citation |
Score |
| 2023 |
Redhead Y, Gibbins D, Lana-Elola E, Watson-Scales S, Dobson L, Krause M, Liu KJ, Fisher EMC, Green JBA, Tybulewicz VLJ. Craniofacial dysmorphology in Down syndrome is caused by increased dosage of Dyrk1a and at least three other genes. Development (Cambridge, England). 150. PMID 37102702 DOI: 10.1242/dev.201077 |
0.513 |
|
| 2023 |
Donovan APA, Rosko L, Ellegood J, Redhead Y, Green JBA, Lerch JP, Huang JK, Basson MA. Pervasive cortical and white matter anomalies in a mouse model for CHARGE syndrome. Journal of Anatomy. PMID 36914558 DOI: 10.1111/joa.13856 |
0.503 |
|
| 2022 |
Chern T, Achilleos A, Tong X, Hill MC, Saltzman AB, Reineke LC, Chaudhury A, Dasgupta SK, Redhead Y, Watkins D, Neilson JR, Thiagarajan P, Green JBA, Malovannaya A, Martin JF, et al. Mutations in Hcfc1 and Ronin result in an inborn error of cobalamin metabolism and ribosomopathy. Nature Communications. 13: 134. PMID 35013307 DOI: 10.1038/s41467-021-27759-7 |
0.478 |
|
| 2021 |
Lin Z, Kim E, Ahmed M, Han G, Simmons C, Redhead Y, Bartlett J, Pena Altamira LE, Callaghan I, White MA, Singh N, Sawiak S, Spires-Jones T, Vernon AC, Coleman MP, et al. 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. PMID 34136812 DOI: 10.1093/braincomms/fcab114 |
0.483 |
|
| 2021 |
Toussaint N, Redhead Y, Vidal-García M, Lo Vercio L, Liu W, Fisher EMC, Hallgrímsson B, Tybulewicz VLJ, Schnabel JA, Green JBA. A landmark-free morphometrics pipeline for high-resolution phenotyping: application to a mouse model of Down syndrome. Development (Cambridge, England). 148. PMID 33712441 DOI: 10.1242/dev.188631 |
0.507 |
|
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