Haiyan Zhou

<i>RYR1</i> mutations are a common cause of congenital myopathies with central nuclei

Jo M. Wilmshurst, Suzanne Lillis, Haiyan Zhou et al. · Annals of Neurology · 2010 · 266 citations · Full text

Life Sciences, Genetics, Molecular Genetics +12

Systemic peptide-mediated oligonucleotide therapy improves long-term survival in spinal muscular atrophy

Suzan M. Hammond, Gareth Hazell, Fazel Shabanpoor et al. · Proceedings of the National Academy of Sciences · 2016 · 193 citations · Full text

Pharmacy, Neuroscience, Pharmacology +16

Molecular mechanisms and phenotypic variation in RYR1-related congenital myopathies

Haiyan Zhou, Heinz Jungbluth, C. Sewry et al. · Brain · 2007 · 177 citations · Full text

Life Sciences, Genetics, Molecular Genetics +15

Clinical and genetic findings in a large cohort of patients with ryanodine receptor 1 gene-associated myopathies

Andrea Klein, Suzanne Lillis, Iulia Munteanu et al. · Human Mutation · 2012 · 168 citations

Life Sciences, Molecular Biology, Molecular Genetics +16

Minicore myopathy with ophthalmoplegia caused by mutations in the ryanodine receptor type 1 gene

Heinz Jungbluth, Haiyan Zhou, Louise Hartley et al. · Neurology · 2005 · 156 citations

Medicine, Genetics, Ophthalmology +15