| 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 | 487 | 2015 |
| 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 | 466 | 2019 |
| 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 Bossé, N Shrine, MS Artigas, ... Nature genetics 49 (3), 426-432, 2017 | 398 | 2017 |
| 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 | 344 | 2019 |
| 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 | 319 | 2017 |
| 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 | 144 | 2015 |
| 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 | 141 | 2020 |
| 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 | 113 | 2020 |
| 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 | 106 | 2018 |
| 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 | 102 | 2020 |
| 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 | 92 | 2017 |
| 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 | 79 | 2020 |
| 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 | 77 | 2019 |
| 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 | 68 | 2013 |
| 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 | 59 | 2019 |
| 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 | 53 | 2017 |
| 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 | 52 | 2022 |
| Genetic aetiologies for childhood speech disorder: novel pathways co-expressed during brain development A Kaspi, MS Hildebrand, VE Jackson, R Braden, O Van Reyk, T Howell, ... Molecular psychiatry 28 (4), 1647-1663, 2023 | 41 | 2023 |
| 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, 4, 2018 | 39* | 2018 |
| 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 | 36 | 2021 |
