متابعة
David Zhang
David Zhang
بريد إلكتروني تم التحقق منه على ucl.ac.uk
عنوان
عدد مرات الاقتباسات
عدد مرات الاقتباسات
السنة
ggtranscript: an R package for the visualization and interpretation of transcript isoforms using ggplot2
EK Gustavsson, D Zhang, RH Reynolds, S Garcia-Ruiz, M Ryten
Bioinformatics 38 (15), 3844-3846, 2022
2122022
recount3: summaries and queries for large-scale RNA-seq expression and splicing
C Wilks, SC Zheng, FY Chen, R Charles, B Solomon, JP Ling, EL Imada, ...
Genome biology 22, 1-40, 2021
1872021
Identification of candidate Parkinson disease genes by integrating genome-wide association study, expression, and epigenetic data sets
DA Kia, D Zhang, S Guelfi, C Manzoni, L Hubbard, RH Reynolds, J Botía, ...
JAMA neurology 78 (4), 464-472, 2021
1502021
Developmental consequences of defective ATG7-mediated autophagy in humans
JJ Collier, C Guissart, M Oláhová, S Sasorith, F Piron-Prunier, F Suomi, ...
New England Journal of Medicine 384 (25), 2406-2417, 2021
1392021
Mitochondria function associated genes contribute to Parkinson’s Disease risk and later age at onset
KJ Billingsley, IA Barbosa, S Bandrés-Ciga, JP Quinn, VJ Bubb, ...
npj Parkinson's Disease 5 (1), 8, 2019
1172019
Cognitive markers of preclinical and prodromal Alzheimer's disease in Down syndrome
CM Startin, S Hamburg, R Hithersay, T Al-Janabi, KY Mok, J Hardy, ...
Alzheimer's & Dementia 15 (2), 245-257, 2019
902019
Genetic variability in response to amyloid beta deposition influences Alzheimer’s disease risk
DA Salih, S Bayram, S Guelfi, RH Reynolds, M Shoai, M Ryten, ...
Brain communications 1 (1), fcz022, 2019
882019
Variation at the TRIM11 locus modifies progressive supranuclear palsy phenotype
E Jabbari, J Woodside, MMX Tan, M Shoai, A Pittman, R Ferrari, KY Mok, ...
Annals of neurology 84 (4), 485-496, 2018
582018
Incomplete annotation has a disproportionate impact on our understanding of Mendelian and complex neurogenetic disorders
D Zhang, S Guelfi, S Garcia-Ruiz, B Costa, RH Reynolds, K D’Sa, W Liu, ...
Science Advances 6 (24), eaay8299, 2020
572020
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
542020
Megadepth: efficient coverage quantification for BigWigs and BAMs
C Wilks, O Ahmed, DN Baker, D Zhang, L Collado-Torres, B Langmead
Bioinformatics 37 (18), 3014-3016, 2021
292021
Regulatory sites for splicing in human basal ganglia are enriched for disease-relevant information
S Guelfi, K D’sa, JA Botía, J Vandrovcova, RH Reynolds, D Zhang, ...
Nature communications 11 (1), 1041, 2020
262020
Duplication of 10q24 locus: broadening the clinical and radiological spectrum
M Holder-Espinasse, A Jamsheer, F Escande, J Andrieux, F Petit, ...
European Journal of Human Genetics 27 (4), 525-534, 2019
242019
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
112021
Regulation of mitophagy by the NSL complex underlies genetic risk for Parkinson’s disease at Chr16q11. 2 and on the MAPT H1 allele
MPM Soutar, D Melandri, B O’Callaghan, E Annuario, AE Monaghan, ...
BioRxiv, 2020.01. 06.896241, 2020
112020
Integration of eQTL and Parkinson’s disease GWAS data implicates 11 disease genes
DA Kia, D Zhang, S Guelfi, C Manzoni, L Hubbard, ...
BioRxiv, 627216, 2019
112019
G2P: Using machine learning to understand and predict genes causing rare neurological disorders
JA Botía, S Guelfi, D Zhang, K D’Sa, R Reynolds, D Onah, EM McDonagh, ...
bioRxiv, 288845, 2018
102018
Leveraging omic features with F3UTER enables identification of unannotated 3’UTRs for synaptic genes
S Sethi, D Zhang, S Guelfi, Z Chen, S Garcia-Ruiz, EO Olagbaju, M Ryten, ...
Nature Communications 13 (1), 2270, 2022
42022
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مقالات 1–18