Haiyan Zhou - Concepedia

Author

Haiyan Zhou

Also Known As

H. -Y. Zhou, H. Zhou, H.-Y. Zhou, H.Y. Zhou, Hai-Yan Zhou, Hai-yan Zhou, Haiyan Zhou, Hongyan Zhou, Zhou, H, Zhou, Haiyan

127

Publications

3.8K

Citations

H-Index

Concepts

All Affiliations

University College London St Thomas' Hospital Great Ormond Street Hospital University Hospital of Basel King's College London

About

Haiyan Zhou is an author at University College London specializing in medicine, cell biology, and genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	21	27	1.7K
2	Social Sciences	4	4	205
3	Engineering	2	2	130
4	Natural Sciences	2	2	84
5	Health Sciences	1	1	88

Haiyan Zhou

Publications

3.4K

Citations

H-Index

Page 1

	Year	Citations
<i>RYR1</i> mutations are a common cause of congenital myopathies with central nuclei Jo M. Wilmshurst, Suzanne Lillis, Haiyan Zhou, Annals of Neurology	2010	261
Systemic peptide-mediated oligonucleotide therapy improves long-term survival in spinal muscular atrophy Suzan M. Hammond, Gareth Hazell, Fazel Shabanpoor, Proceedings of the National Academy of Sciences	2016	192
Molecular mechanisms and phenotypic variation in RYR1-related congenital myopathies Haiyan Zhou, Heinz Jungbluth, C. Sewry, Brain Mendelian DisorderRyr1-related Congenital MyopathiesSkeletal MuscleMalignant Hyperthermia SusceptibilityGenetics	2007	173
Clinical and genetic findings in a large cohort of patients with ryanodine receptor 1 gene-associated myopathies Andrea Klein, Suzanne Lillis, Iulia Munteanu, Human Mutation GeneticsGenetic EpidemiologyPathologyMolecular GeneticsDisease Gene Identification	2012	166
Minicore myopathy with ophthalmoplegia caused by mutations in the ryanodine receptor type 1 gene Heinz Jungbluth, Haiyan Zhou, Louise Hartley, Neurology	2005	152
Epigenetic Allele Silencing Unveils Recessive RYR1 Mutations in Core Myopathies Haiyan Zhou, Martin Brockington, Heinz Jungbluth, The American Journal of Human Genetics Mendelian DisorderGenetic DisorderGeneticsMolecular BiologyMolecular Genetics	2006	131
A Novel Morpholino Oligomer Targeting ISS-N1 Improves Rescue of Severe Spinal Muscular Atrophy Transgenic Mice Haiyan Zhou, Narinder Janghra, Chalermchai Mitrpant, Human Gene Therapy Knockout MouseTranslational MedicineNeuroregenerationMolecular NeuroscienceGene Therapies	2013	121
Centronuclear myopathy due to a de novo dominant mutation in the skeletal muscle ryanodine receptor (RYR1) gene Heinz Jungbluth, Haiyan Zhou, Caroline A. Sewry, Neuromuscular Disorders Muscle FunctionSkeletal MuscleMedicineGeneticsMolecular Biology	2007	115
Characterization of recessive RYR1 mutations in core myopathies Haiyan Zhou Human Molecular Genetics Muscle FunctionMolecular PhysiologySignal TransductionMendelian DisorderGenetic Disorder	2006	112
In Vivo Translatome Profiling in Spinal Muscular Atrophy Reveals a Role for SMN Protein in Ribosome Biology Paola Bernabò, Toma Tebaldi, Ewout J. N. Groen, Cell Reports	2017	112

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