Bird, Adrian

Gene expression analysis exposes mitochondrial abnormalities in a mouse model of Rett syndrome

Kriaucionis, S., Paterson, A., Curtis, J., Guy, J., MacLeod, N., & Bird, A. (2006) · Molecular and Cellular Biology

Genetics and Neurodevelopmental DisordersMitochondrial Function and Pathology

Cited by 219

Morphological and functional reversal of phenotypes in a mouse model of Rett syndrome

Robinson, L., Guy, J., McKay, L., Brockett, E., Spike, R. C., Selfridge, J., De Sousa, D., Merusi, C., Riedel, G., Bird, A., et al. (2012) · Brain

Genetics and Neurodevelopmental DisordersNeuroscience and Neuropharmacology Research

Cited by 157

Radically truncated MeCP2 rescues Rett syndrome-like neurological defects

Tillotson, R., Selfridge, J., Koerner, M. V., Gadalla, K. K. E., Guy, J., De Sousa, D., Hector, R. D., Cobb, S. R., & Bird, A. (2017) · Nature

Genetics and Neurodevelopmental DisordersEpigenetics and DNA Methylation

Cited by 155

Rett Syndrome: Crossing the Threshold to Clinical Translation

Katz, D. M., Bird, A., Coenraads, M., Gray, S. J., Menon, D. U., Philpot, B. D., & Tarquinio, D. C. (2016) · Trends in Neurosciences

Genetics and Neurodevelopmental DisordersAutism Spectrum Disorder Research

Cited by 150

Structure of the MeCP2–TBLR1 complex reveals a molecular basis for Rett syndrome and related disorders

Kruusvee, V., Lyst, M. J., Taylor, C., Tarnauskaitė, Ž., Bird, A. P., & Cook, A. G. (2017) · Proceedings of the National Academy of Sciences

Genetics and Neurodevelopmental DisordersGenomics and Rare Diseases

Cited by 82

Reversibility of functional deficits in experimental models of Rett syndrome

Cobb, S., Guy, J., & Bird, A. (2010) · Biochemical Society Transactions

Genetics and Neurodevelopmental DisordersNeuroscience and Neuropharmacology Research

Cited by 67

SALL4 controls cell fate in response to DNA base composition

Pantier, R., Chhatbar, K., Quante, T., Skourti-Stathaki, K., Cholewa-Waclaw, J., Alston, G., Alexander-Howden, B., Lee, H. Y., Cook, A. G., Spruijt, C. G., et al. (2021) · Molecular Cell

Genomics and Chromatin DynamicsPluripotent Stem Cells Research

Cited by 45

Do short, frequent DNA sequence motifs mould the epigenome

Quante, T., & Bird, A. (2016) · Nature Reviews Molecular Cell Biology

Genomics and Chromatin DynamicsEpigenetics and DNA Methylation

Cited by 40

Structure of SALL4 zinc finger domain reveals link between AT-rich DNA binding and Okihiro syndrome

Watson, J. A., Pantier, R., Jayachandran, U., Chhatbar, K., Alexander-Howden, B., Kruusvee, V., Prendecki, M., Bird, A., & Cook, A. G. (2023) · Life Science Alliance

Genomics and Chromatin DynamicsProtein Structure and Dynamics

Cited by 14

Dysfunction of a SET3-like complex underlies a family of related neurological disorders

Paton, K. M., Alexander-Howden, B., Hare, J. I., Guy, J., Chhatbar, K., Yudina, M., Morris, S. T., Walls, R., Mathieson, T., Spanos, C., et al. (2026) · Nature Communications

Genetics and Neurodevelopmental DisordersGenomics and Rare Diseases

Cited by 0

Tetramerisation governs SALL transcription factor function in development and disease

Giuliani, S., Chhatbar, K., Wear, M., Guy, J., Mathieson, T., Burdett, H., George, L., Alston, G., Spanos, C., McHugh, T., et al. (2025) · bioRxiv

Genomics and Chromatin DynamicsDevelopmental Biology and Gene Regulation

Cited by 0