Victor Tybulewicz
Affiliations: | The Francis Crick Institute, London, England, United Kingdom |
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Collaborators
Sign in to add collaborator| Annette Karmiloff-Smith | collaborator | Francis Crick Institute | ||
| Elizabeth Mary Claire Fisher | collaborator | 1991- | UCL Institute of Neurology, Queen Square | |
| (Source: https://iris.ucl.ac.uk/iris/browse/profile?upi=EMCFI97) | ||||
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Publications
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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 |
| Sloan K, Thomas J, Blackwell M, et al. (2023) Genetic dissection of triplicated Hsa21 orthologs produces differential skeletal phenotypes in Down syndrome mouse models. Disease Models & Mechanisms |
| Muza PM, Bush D, Pérez-González M, et al. (2023) Cognitive impairments in a Down syndrome model with abnormal hippocampal and prefrontal dynamics and cytoarchitecture. Iscience. 26: 106073 |
| Mumford P, Tosh J, Anderle S, et al. (2022) Genetic mapping of APP and amyloid-β biology modulation by trisomy 21. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience |
| Tosh J, Tybulewicz V, Fisher EMC. (2021) Mouse models of aneuploidy to understand chromosome disorders. Mammalian Genome : Official Journal of the International Mammalian Genome Society |
| Lana-Elola E, Cater H, Watson-Scales S, et al. (2021) Comprehensive phenotypic analysis of the Dp1Tyb mouse strain reveals a broad range of down syndrome-related phenotypes. Disease Models & Mechanisms |
| 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 |
| 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 |
| Tosh JL, Rhymes ER, Mumford P, et al. (2021) Genetic dissection of down syndrome-associated alterations in APP/amyloid-β biology using mouse models. Scientific Reports. 11: 5736 |
| Lana-Elola E, Watson-Scales S, Slender A, et al. (2020) Correction: Genetic dissection of Down syndrome-associated congenital heart defects using a new mouse mapping panel. Elife. 9 |