Andrea Haworth

<i>C9orf72</i> expansions are the most common genetic cause of Huntington disease phenocopies

Davina J. Hensman Moss, Mark Poulter, Jon Beck et al. · Neurology · 2013 · 203 citations · Full text

Life Sciences, Genetics, Molecular Genetics +16

Prevalence study of genetically defined skeletal muscle channelopathies in England

Alejandro Horga, D.L. Raja Rayan, Emma Matthews et al. · Neurology · 2013 · 138 citations · Full text

Life Sciences, Genetics, Neurology +16

Refined exercise testing can aid dna‐based diagnosis in muscle channelopathies

S. Veronica Tan, Emma Matthews, Melissa Barber et al. · Annals of Neurology · 2011 · 105 citations · Full text

Life Sciences, Genetics, Molecular Genetics +16

SSCP analysis: A blind sensitivity trial

Albena Jordanova, Luba Kalaydjieva, Alexey Savov et al. · Human Mutation · 1997 · 74 citations

Life Sciences, Genetics, Molecular Genetics +9

Cystic fibrosis mutation analysis: Report from 22 U.K. regional genetics laboratories

Martin Schwarz, Geraldine Malone, Andrea Haworth et al. · Human Mutation · 1995 · 37 citations

Life Sciences, Genetics, Molecular Genetics +11