William Whitehouse

Characterization of human disease phenotypes associated with mutations in <i>TREX1</i>, <i>RNASEH2A</i>, <i>RNASEH2B</i>, <i>RNASEH2C</i>, <i>SAMHD1</i>, <i>ADAR</i>, and <i>IFIH1</i>

Yanick J. Crow, Diana Chase, Johanna L. Schmidt et al. · American Journal of Medical Genetics Part A · 2015 · 613 citations · Full text

Life Sciences, Genetics, Molecular Genetics +9

Assessment of interferon-related biomarkers in Aicardi-Goutières syndrome associated with mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, and ADAR: a case-control study

Gillian Rice, Gabriella Forte, Marcin Szynkiewicz et al. · The Lancet Neurology · 2013 · 438 citations

Life Sciences, Genetics, Molecular Genetics +16

Safety and efficacy of buccal midazolam versus rectal diazepam for emergency treatment of seizures in children: a randomised controlled trial

John S. McIntyre, Sue Robertson, Elizabeth Norris et al. · The Lancet · 2005 · 438 citations

Medicine, Pediatrics, Pharmacotherapy +13

Melatonin for sleep problems in children with neurodevelopmental disorders: randomised double masked placebo controlled trial

Paul Gringras, Carrol Gamble, Ashley P Jones et al. · BMJ · 2012 · 214 citations · Full text

Life Sciences, Immunology, Physiology +17

Severe Myoclonic Epilepsy of Infancy: Extended Spectrum of GEFS⁺?

Rita Singh, E. Andermann, William Whitehouse et al. · Epilepsia · 2001 · 202 citations

Medicine, Genetics, Neurology +17