Follow
Haiyan Zhou
Haiyan Zhou
Verified email at ucl.ac.uk
Title
Cited by
Cited by
Year
RYR1 mutations are a common cause of congenital myopathies with central nuclei
JM Wilmshurst, S Lillis, H Zhou, K Pillay, H Henderson, W Kress, ...
Annals of neurology 68 (5), 717-726, 2010
2822010
Molecular mechanisms and phenotypic variation in RYR1-related congenital myopathies
H Zhou, H Jungbluth, CA Sewry, L Feng, E Bertini, K Bushby, V Straub, ...
Brain 130 (8), 2024-2036, 2007
1942007
Systemic peptide-mediated oligonucleotide therapy improves long-term survival in spinal muscular atrophy
SM Hammond, G Hazell, F Shabanpoor, AF Saleh, M Bowerman, ...
Proceedings of the National Academy of Sciences 113 (39), 10962-10967, 2016
1912016
Oxidative stress in SEPN1‐related myopathy: From pathophysiology to treatment
S Arbogast, M Beuvin, B Fraysse, H Zhou, F Muntoni, A Ferreiro
Annals of Neurology: Official Journal of the American Neurological …, 2009
1752009
Clinical and genetic findings in a large cohort of patients with ryanodine receptor 1 gene‐associated myopathies
A Klein, S Lillis, I Munteanu, M Scoto, H Zhou, R Quinlivan, V Straub, ...
Human mutation 33 (6), 981-988, 2012
1712012
Minicore myopathy with ophthalmoplegia caused by mutations in the ryanodine receptor type 1 gene
H Jungbluth, H Zhou, L Hartley, B Halliger-Keller, S Messina, C Longman, ...
Neurology 65 (12), 1930-1935, 2005
1582005
Centronuclear myopathy due to a de novo dominant mutation in the skeletal muscle ryanodine receptor (RYR1) gene
H Jungbluth, H Zhou, CA Sewry, S Robb, S Treves, M Bitoun, ...
Neuromuscular Disorders 17 (4), 338-345, 2007
1312007
Epigenetic allele silencing unveils recessive RYR1 mutations in core myopathies
H Zhou, M Brockington, H Jungbluth, D Monk, P Stanier, CA Sewry, ...
The American Journal of Human Genetics 79 (5), 859-868, 2006
1312006
A novel morpholino oligomer targeting ISS-N1 improves rescue of severe spinal muscular atrophy transgenic mice
H Zhou, N Janghra, C Mitrpant, RL Dickinson, K Anthony, L Price, ...
Human gene therapy 24 (3), 331-342, 2013
1302013
King–Denborough syndrome with and without mutations in the skeletal muscle ryanodine receptor (RYR1) gene
JJ Dowling, S Lillis, K Amburgey, H Zhou, S Al-Sarraj, SJA Buk, E Wraige, ...
Neuromuscular disorders 21 (6), 420-427, 2011
1232011
Characterization of recessive RYR1 mutations in core myopathies
H Zhou, N Yamaguchi, L Xu, Y Wang, C Sewry, H Jungbluth, F Zorzato, ...
Human molecular genetics 15 (18), 2791-2803, 2006
1182006
In vivo translatome profiling in spinal muscular atrophy reveals a role for SMN protein in ribosome biology
P Bernabo, T Tebaldi, EJN Groen, FM Lane, E Perenthaler, F Mattedi, ...
Cell reports 21 (4), 953-965, 2017
1112017
Multi-minicore disease and atypical periodic paralysis associated with novel mutations in the skeletal muscle ryanodine receptor (RYR1) gene
H Zhou, S Lillis, RE Loy, F Ghassemi, MR Rose, F Norwood, K Mills, ...
Neuromuscular Disorders 20 (3), 166-173, 2010
1042010
Antisense oligonucleotide-based therapy for neuromuscular disease
V Sardone, H Zhou, F Muntoni, A Ferlini, MS Falzarano
Molecules 22 (4), 563, 2017
1022017
Improved antisense oligonucleotide design to suppress aberrant SMN2 gene transcript processing: towards a treatment for spinal muscular atrophy
C Mitrpant, P Porensky, H Zhou, L Price, F Muntoni, S Fletcher, SD Wilton, ...
PloS one 8 (4), e62114, 2013
922013
Vascular D efects and S pinal C ord H ypoxia in S pinal M uscular A trophy
E Somers, RD Lees, K Hoban, JN Sleigh, H Zhou, F Muntoni, K Talbot, ...
Annals of neurology 79 (2), 217-230, 2016
912016
Survival Motor Neuron (SMN) protein is required for normal mouse liver development
E Szunyogova, H Zhou, GK Maxwell, RA Powis, F Muntoni, ...
Scientific reports 6 (1), 34635, 2016
832016
Deletion of δ-opioid receptor in mice alters skin differentiation and delays wound healing
M Bigliardi-Qi, C Gaveriaux-Ruff, H Zhou, C Hell, P Bady, T Rufli, B Kieffer, ...
Differentiation 74 (4), 174-185, 2006
742006
Altered levels of MicroRNA-9,-206, and-132 in spinal muscular atrophy and their response to antisense oligonucleotide therapy
F Catapano, I Zaharieva, M Scoto, E Marrosu, J Morgan, F Muntoni, ...
Molecular Therapy-Nucleic Acids 5, 2016
682016
Epigenetic changes as a common trigger of muscle weakness in congenital myopathies
O Rokach, M Sekulic-Jablanovic, N Voermans, J Wilmshurst, K Pillay, ...
Human molecular genetics 24 (16), 4636-4647, 2015
582015
The system can't perform the operation now. Try again later.
Articles 1–20