David W. Webb

机构：West Virginia School of Osteopathic Medicine, Children's Health Ireland at Crumlin · ORCID：0000-0002-0762-8277

发表论文 140 篇 · 总被引 5499 次 · h-index 36

代表论文

• De novo mutations in ATP1A3 cause alternating hemiplegia of childhood (2012 · Nature Genetics · 被引 427)
• Glucose transporter-1 deficiency syndrome: the expanding clinical and genetic spectrum of a treatable disorder (2010 · Brain · 被引 423)
• Multiorgan involvement and management in children with Down syndrome (2020 · Acta Paediatrica · 被引 100)
• A novel locus for episodic ataxia:UBR4 the likely candidate (2013 · European Journal of Human Genetics · 被引 98)
• The European/International Fibromuscular Dysplasia Registry and Initiative (FEIRI)—clinical phenotypes and their predictors based on a cohort of 1000 patients (2020 · Cardiovascular Research · 被引 80)
• Towards the identification of a genetic basis for L andau‐ K leffner s yndrome (2014 · Epilepsia · 被引 58)