Kyle, Stephanie M

A suppressor screen in Mecp2 mutant mice implicates cholesterol metabolism in Rett syndrome

Buchovecky, C. M., Turley, S. D., Brown, H. M., Kyle, S. M., McDonald, J. G., Liu, B., Pieper, A. A., Huang, W., Katz, D. M., Russell, D. W., et al. (2013) · Nature Genetics

Genetics and Neurodevelopmental DisordersAutism Spectrum Disorder Research

Cited by 234

Rett syndrome: a neurological disorder with metabolic components

Kyle, S. M., Vashi, N., & Justice, M. J. (2018) · Open Biology

Genetics and Neurodevelopmental DisordersHereditary Neurological Disorders

Cited by 213

MeCP2 co-ordinates liver lipid metabolism with the NCoR1/HDAC3 corepressor complex

Kyle, S. M., Saha, P. K., Brown, H. M., Chan, L. C., & Justice, M. J. (2016) · Human Molecular Genetics

Genetics and Neurodevelopmental DisordersCancer, Lipids, and Metabolism

Cited by 84

A role for metabolism in Rett syndrome pathogenesis: New clinical findings and potential treatment targets

Justice, M. J., Buchovecky, C. M., Kyle, S. M., & Djukic, A. (2013) · Rare Diseases

Genetics and Neurodevelopmental DisordersGenetic Neurodegenerative Diseases

Cited by 61