Items where authors include "Brown, A.E.X."

Article

O’Brien, T.J., Navarro, E.P., Barroso, C. et al. (4 more authors) (2025) High-throughput behavioural phenotyping of 25 C. elegans disease models including patient-specific mutations. BMC Biology, 23. 281. ISSN 1741-7007

Maroofian, R., Sarraf, P., O'Brien, T.J. et al. (30 more authors) (2024) RTN2 deficiency results in an autosomal recessive distal motor neuropathy with lower limb spasticity. Brain, 147 (7). pp. 2334-2343. ISSN 0006-8950

Maroofian, R. orcid.org/0000-0001-6763-1542, Sarraf, P., O’Brien, T.J. et al. (29 more authors) (2024) RTN2 deficiency results in an autosomal recessive distal motor neuropathy with lower limb spasticity. Brain, 147 (7). pp. 2334-2343. ISSN 0006-8950

Catalano, F., O'Brien, T.J., Mekhova, A.A. et al. (18 more authors) (2024) A new Caenorhabditis elegans model to study copper toxicity in Wilson disease. Traffic, 25 (1). e12920. ISSN 1398-9219

Saida, K., Maroofian, R., Sengoku, T. et al. (84 more authors) (2023) Brain monoamine vesicular transport disease caused by homozygous SLC18A2 variants: A study in 42 affected individuals. Genetics in Medicine, 25 (1). pp. 90-102. ISSN 1098-3600

Rosenhahn, E., O’Brien, T.J., Zaki, M.S. et al. (44 more authors) (2022) Bi-allelic loss-of-function variants in PPFIBP1 cause a neurodevelopmental disorder with microcephaly, epilepsy, and periventricular calcifications. American Journal of Human Genetics, 109 (8). pp. 1421-1435. ISSN 0002-9297

Barlow, I.L., Feriani, L., Minga, E. et al. (8 more authors) (2022) Megapixel camera arrays enable high-resolution animal tracking in multiwell plates. Communications Biology, 5. 253. ISSN 2399-3642