| The NHGRI-EBI GWAS Catalog of published genome-wide association studies, targeted arrays and summary statistics 2019 A Buniello, JAL MacArthur, M Cerezo, LW Harris, J Hayhurst, ... Nucleic acids research 47 (D1), D1005-D1012, 2019 | 3773 | 2019 |
| Shared genetic origin of asthma, hay fever and eczema elucidates allergic disease biology MA Ferreira, JM Vonk, H Baurecht, I Marenholz, C Tian, JD Hoffman, ... Nature genetics 49 (12), 1752-1757, 2017 | 526 | 2017 |
| Open Targets Genetics: systematic identification of trait-associated genes using large-scale genetics and functional genomics M Ghoussaini, E Mountjoy, M Carmona, G Peat, EM Schmidt, A Hercules, ... Nucleic acids research 49 (D1), D1311-D1320, 2021 | 349 | 2021 |
| Open Targets Platform: supporting systematic drug–target identification and prioritisation D Ochoa, A Hercules, M Carmona, D Suveges, A Gonzalez-Uriarte, ... Nucleic acids research 49 (D1), D1302-D1310, 2021 | 320 | 2021 |
| Education and myopia: assessing the direction of causality by mendelian randomisation E Mountjoy, NM Davies, D Plotnikov, GD Smith, S Rodriguez, CE Williams, ... bmj 361, 2018 | 294 | 2018 |
| An open approach to systematically prioritize causal variants and genes at all published human GWAS trait-associated loci E Mountjoy, EM Schmidt, M Carmona, J Schwartzentruber, G Peat, ... Nature genetics 53 (11), 1527-1533, 2021 | 267 | 2021 |
| Population-scale single-cell RNA-seq profiling across dopaminergic neuron differentiation J Jerber, DD Seaton, ASE Cuomo, N Kumasaka, J Haldane, J Steer, ... Nature genetics 53 (3), 304-312, 2021 | 180 | 2021 |
| A map of transcriptional heterogeneity and regulatory variation in human microglia AMH Young, N Kumasaka, F Calvert, TR Hammond, A Knights, ... Nature genetics 53 (6), 861-868, 2021 | 148 | 2021 |
| Network expansion of genetic associations defines a pleiotropy map of human cell biology I Barrio-Hernandez, J Schwartzentruber, A Shrivastava, N Del-Toro, ... Nature Genetics 55 (3), 389-398, 2023 | 40 | 2023 |
| Accurate sample assignment in a multiplexed, ultrasensitive, high-throughput sequencing assay for minimal residual disease J Bartram, E Mountjoy, T Brooks, J Hancock, H Williamson, G Wright, ... The Journal of Molecular Diagnostics 18 (4), 494-506, 2016 | 39 | 2016 |
| Reprogramming pig fetal fibroblasts reveals a functional LIF signaling pathway AJ Thomson, H Pierart, S Meek, A Bogerman, L Sutherland, H Murray, ... Cellular Reprogramming (Formerly" Cloning and Stem Cells") 14 (2), 112-122, 2012 | 37 | 2012 |
| A role for NPY-NPY2R signaling in albuminuric kidney disease AC Lay, AF Barrington, JA Hurcombe, RD Ramnath, M Graham, PA Lewis, ... Proceedings of the National Academy of Sciences 117 (27), 15862-15873, 2020 | 22 | 2020 |
| A comparative analysis of rod bipolar cell transcriptomes identifies novel genes implicated in night vision SM Woods, E Mountjoy, D Muir, SE Ross, D Atan Scientific Reports 8 (1), 5506, 2018 | 12 | 2018 |
| High‐throughput sequencing of peripheral blood for minimal residual disease monitoring in childhood precursor B‐cell acute lymphoblastic leukemia: a prospective feasibility study J Bartram, G Wright, S Adams, P Archer, T Brooks, D Edwards, J Hancock, ... Pediatric Blood & Cancer 69 (3), e29513, 2022 | 3 | 2022 |
| Full p-value summary statistics in the GWAS Catalog JAL MacArthur, A Buniello, M Cerezo, J Hayhurst, P Hall, L Harris, ... EUROPEAN JOURNAL OF HUMAN GENETICS 27, 1702-1702, 2019 | | 2019 |
