| Joint genome-wide association study of progressive supranuclear palsy identifies novel susceptibility loci and genetic correlation to neurodegenerative diseases JA Chen, Z Chen, H Won, AY Huang, JK Lowe, K Wojta, JS Yokoyama, ... Molecular neurodegeneration 13 (1), 1-11, 2018 | 62 | 2018 |
| Meta‐analysis of symptomatic response attributable to the pacing component of cardiac resynchronization therapy SMA Sohaib, Z Chen, ZI Whinnett, S Bouri, K Dickstein, C Linde, ... European journal of heart failure 15 (12), 1419-1428, 2013 | 49 | 2013 |
| Neuronal intranuclear inclusion disease is genetically heterogeneous Z Chen, W Yan Yau, Z Jaunmuktane, A Tucci, P Sivakumar, ... Annals of clinical and translational neurology 7 (9), 1716-1725, 2020 | 32 | 2020 |
| Rare genetic variation in UNC13A may modify survival in amyotrophic lateral sclerosis B Gaastra, A Shatunov, S Pulit, AR Jones, W Sproviero, A Gillett, Z Chen, ... Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration 17 (7-8), 593-599, 2016 | 30 | 2016 |
| Metal-on-metal hip resurfacings—a radiological perspective Z Chen, H Pandit, A Taylor, H Gill, D Murray, S Ostlere European radiology 21, 485-491, 2011 | 27 | 2011 |
| Genome‐wide survey of copy number variants finds MAPT duplications in progressive supranuclear palsy Z Chen, JA Chen, A Shatunov, AR Jones, SN Kravitz, AY Huang, ... Movement Disorders 34 (7), 1049-1059, 2019 | 24 | 2019 |
| The internet for self-diagnosis and prognostication in ALS Z Chen, MR Turner Amyotrophic Lateral Sclerosis 11 (6), 565-567, 2010 | 23 | 2010 |
| Low Prevalence of NOTCH2NLC GGC Repeat Expansion in White Patients with Movement Disorders WY Yau, J Vandrovcova, R Sullivan, Z Chen, A Zecchinelli, R Cilia, ... Movement Disorders 36 (1), 251-255, 2021 | 22 | 2021 |
| Concordance of CSF measures of Alzheimer's pathology with amyloid PET status in a preclinical cohort: A comparison of Lumipulse and established immunoassays A Keshavan, H Wellington, Z Chen, A Khatun, M Chapman, M Hart, ... Alzheimer's & Dementia: Diagnosis, Assessment & Disease Monitoring 13 (1 …, 2021 | 16 | 2021 |
| GGC repeat expansion in NOTCH2NLC is rare in European leukoencephalopathy WY Yau, R Sullivan, Z Chen, DS Lynch, J Vandrovcova, NW Wood, ... Annals of neurology 88 (3), 641-642, 2020 | 14 | 2020 |
| GGC repeat expansion in NOTCH2NLC is rare in European patients with essential tremor WY Yau, E O’Connor, Z Chen, J Vandrovcova, NW Wood, H Houlden Brain 143 (7), e57-e57, 2020 | 13 | 2020 |
| Deep Intronic FGF14 GAA Repeat Expansion in Late-Onset Cerebellar Ataxia D Pellerin, MC Danzi, C Wilke, M Renaud, S Fazal, MJ Dicaire, CK Scriba, ... New England Journal of Medicine 388 (2), 128-141, 2023 | 12 | 2023 |
| Mitochondrial-nuclear cross-talk in the human brain is modulated by cell type and perturbed in neurodegenerative disease A Fairbrother-Browne, AT Ali, RH Reynolds, S Garcia-Ruiz, D Zhang, ... Communications Biology 4 (1), 1262, 2021 | 8 | 2021 |
| Proposed association between the hexanucleotide repeat of C9orf72 and opposability index of the thumb Z Chen, K Lin, JD Macklis, A Al-Chalabi Amyotrophic lateral sclerosis and frontotemporal degeneration 18 (3-4), 175-181, 2017 | 6 | 2017 |
| Human-lineage-specific genomic elements are associated with neurodegenerative disease and APOE transcript usage Z Chen, D Zhang, RH Reynolds, EK Gustavsson, S García-Ruiz, K D’Sa, ... Nature communications 12 (1), 2076, 2021 | 5 | 2021 |
| Novel variants broaden the phenotypic spectrum of PLEKHG5‐associated neuropathies Z Chen, R Maroofian, AN Başak, L Shingavi, M Karakaya, S Efthymiou, ... European journal of neurology 28 (4), 1344-1355, 2021 | 5 | 2021 |
| Sneddon's syndrome: it is all in the ectoderm Z Rutter-Locher, Z Chen, L Flores, T Basu, D Creamer, R Weeks, R Arya, ... Practical Neurology 16 (4), 300-303, 2016 | 5 | 2016 |
| PhenoExam: an R package and Web application for the examination of phenotypes linked to genes and gene sets A Cisterna, A González-Vidal, D Ruiz, J Ortiz, A Gómez-Pascual, Z Chen, ... bioRxiv, 2021.06. 29.450324, 2021 | 3 | 2021 |
| IntroVerse: a comprehensive database of introns across human tissues S García-Ruiz, EK Gustavsson, D Zhang, RH Reynolds, Z Chen, ... Nucleic Acids Research 51 (D1), D167-D178, 2023 | 2 | 2023 |
| The annotation and function of the Parkinson’s and Gaucher disease-linked gene GBA1 has been concealed by its protein-coding pseudogene GBAP1 EK Gustavsson, S Sethi, Y Gao, JW Brenton, S García-Ruiz, D Zhang, ... BioRxiv, 2022.10. 21.513169, 2022 | 2 | 2022 |
