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Victoria E Jackson
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Novel insights into the genetics of smoking behaviour, lung function, and chronic obstructive pulmonary disease (UK BiLEVE): a genetic association study in UK Biobank
LV Wain, N Shrine, S Miller, VE Jackson, I Ntalla, MS Artigas, ...
The Lancet Respiratory Medicine 3 (10), 769-781, 2015
4392015
New genetic signals for lung function highlight pathways and chronic obstructive pulmonary disease associations across multiple ancestries
N Shrine, AL Guyatt, AM Erzurumluoglu, VE Jackson, BD Hobbs, ...
Nature genetics 51 (3), 481-493, 2019
3652019
Genetic loci associated with chronic obstructive pulmonary disease overlap with loci for lung function and pulmonary fibrosis
BD Hobbs, K De Jong, M Lamontagne, Y Bossť, N Shrine, MS Artigas, ...
Nature genetics 49 (3), 426-432, 2017
3492017
Genome-wide association analyses for lung function and chronic obstructive pulmonary disease identify new loci and potential druggable targets
LV Wain, N Shrine, MS Artigas, AM Erzurumluoglu, B Noyvert, ...
Nature genetics 49 (3), 416-425, 2017
2892017
Genetic landscape of chronic obstructive pulmonary disease identifies heterogeneous cell-type and phenotype associations
P Sakornsakolpat, D Prokopenko, M Lamontagne, NF Reeve, AL Guyatt, ...
Nature genetics 51 (3), 494-505, 2019
2812019
Sixteen new lung function signals identified through 1000 Genomes Project reference panel imputation
MS Artigas, LV Wain, S Miller, AK Kheirallah, JE Huffman, I Ntalla, ...
Nature communications 6 (1), 8658, 2015
1282015
Meta-analysis of up to 622,409 individuals identifies 40 novel smoking behaviour associated genetic loci
AM Erzurumluoglu, M Liu, VE Jackson, DR Barnes, G Datta, ...
Molecular psychiatry 25 (10), 2392-2409, 2020
1202020
Multiethnic meta-analysis identifies ancestry-specific and cross-ancestry loci for pulmonary function
AB Wyss, T Sofer, MK Lee, N Terzikhan, JN Nguyen, L Lahousse, ...
Nature communications 9 (1), 2976, 2018
972018
Severe childhood speech disorder: Gene discovery highlights transcriptional dysregulation
MS Hildebrand, VE Jackson, TS Scerri, O Van Reyk, M Coleman, ...
Neurology 94 (20), e2148-e2167, 2020
852020
Chronic obstructive pulmonary disease and related phenotypes: polygenic risk scores in population-based and case-control cohorts
M Moll, P Sakornsakolpat, N Shrine, BD Hobbs, DL DeMeo, C John, ...
The Lancet Respiratory Medicine 8 (7), 696-708, 2020
792020
Phenotypic and pharmacogenetic evaluation of patients with thiazide-induced hyponatremia
JS Ware, LV Wain, SK Channavajjhala, VE Jackson, E Edwards, R Lu, ...
The Journal of clinical investigation 127 (9), 3367-3374, 2017
782017
Exome chip meta-analysis fine maps causal variants and elucidates the genetic architecture of rare coding variants in smoking and alcohol use
DM Brazel, Y Jiang, JM Hughey, V Turcot, X Zhan, J Gong, C Batini, ...
Biological psychiatry 85 (11), 946-955, 2019
682019
A missense mutation in the MLKL brace region promotes lethal neonatal inflammation and hematopoietic dysfunction
JM Hildebrand, M Kauppi, IJ Majewski, Z Liu, AJ Cox, S Miyake, EJ Petrie, ...
Nature communications 11 (1), 3150, 2020
672020
Causal and Synthetic Associations of Variants in the SERPINA Gene Cluster with Alpha1-antitrypsin Serum Levels
GA Thun, M Imboden, I Ferrarotti, A Kumar, M Obeidat, M Zorzetto, ...
PLoS genetics 9 (8), e1003585, 2013
642013
Inhibition of Upf2-dependent nonsense-mediated decay leads to behavioral and neurophysiological abnormalities by activating the immune response
JL Johnson, L Stoica, Y Liu, PJ Zhu, A Bhattacharya, SA Buffington, ...
Neuron 104 (4), 665-679. e8, 2019
482019
Evidence for large-scale gene-by-smoking interaction effects on pulmonary function
H Aschard, MD Tobin, DB Hancock, D Skurnik, A Sood, A James, ...
International journal of epidemiology 46 (3), 894-904, 2017
482017
Meta-analysis of exome array data identifies six novel genetic loci for lung function
VE Jackson, JC Latourelle, LV Wain, AV Smith, ML Grove, TM Bartz, ...
Wellcome open research 3, 2018
37*2018
Cell-specific cis-regulatory elements and mechanisms of non-coding genetic disease in human retina and retinal organoids
ED Thomas, AE Timms, S Giles, S Harkins-Perry, P Lyu, T Hoang, J Qian, ...
Developmental Cell 57 (6), 820-836. e6, 2022
342022
Exome-wide analysis of rare coding variation identifies novel associations with COPD and airflow limitation in MOCS3, IFIT3 and SERPINA12
VE Jackson, I Ntalla, I Sayers, R Morris, P Whincup, JP Casas, A Amuzu, ...
Thorax 71 (6), 501-509, 2016
312016
Identification of genetic factors influencing metabolic dysregulation and retinal support for MacTel, a retinal disorder
R Bonelli, VE Jackson, A Prasad, JE Munro, S Farashi, TFC Heeren, ...
Communications biology 4 (1), 274, 2021
292021
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