Linda S. Weaving

Mutations of CDKL5 Cause a Severe Neurodevelopmental Disorder with Infantile Spasms and Mental Retardation

Linda S. Weaving, John Christodoulou, Sarah Williamson et al. · The American Journal of Human Genetics · 2004 · 500 citations · Full text

Medicine, Genetics, Molecular Genetics +14

Effects of<i>MECP2</i>mutation type, location and X‐inactivation in modulating Rett syndrome phenotype

Linda S. Weaving, Sarah Williamson, Bruce Bennetts et al. · American Journal of Medical Genetics Part A · 2002 · 115 citations

Life Sciences, Genetics, Molecular Genetics +14

Impact of primary kidney disease on the effects of empagliflozin in patients with chronic kidney disease: secondary analyses of the EMPA-KIDNEY trial

PK Judge, Natalie Staplin, KJ Mayne et al. · The Lancet Diabetes & Endocrinology · 2023 · 108 citations · Full text

Medicine, Nephrology, Pharmacotherapy +11

Arts Syndrome Is Caused by Loss-of-Function Mutations in PRPS1

Arjan P.M. de Brouwer, Kelly L. Williams, John A. Duley et al. · The American Journal of Human Genetics · 2007 · 105 citations · Full text

Life Sciences, Neurology, Neuroscience +12

Effects of empagliflozin on progression of chronic kidney disease: a prespecified secondary analysis from the empa-kidney trial

Natalie Staplin, Richard Haynes, PK Judge et al. · The Lancet Diabetes & Endocrinology · 2023 · 90 citations · Full text

Medicine, Pharmacology, Pharmacotherapy +14