| A comprehensive 1000 Genomes–based genome-wide association meta-analysis of coronary artery disease Nature genetics 47 (10), 1121-1130, 2015 | 2344 | 2015 |
| Genomic risk prediction of coronary artery disease in 480,000 adults: implications for primary prevention M Inouye, G Abraham, CP Nelson, AM Wood, MJ Sweeting, F Dudbridge, ... Journal of the American College of Cardiology 72 (16), 1883-1893, 2018 | 644 | 2018 |
| Association analyses based on false discovery rate implicate new loci for coronary artery disease CP Nelson, A Goel, AS Butterworth, S Kanoni, TR Webb, E Marouli, ... Nature genetics 49 (9), 1385-1391, 2017 | 619* | 2017 |
| Coding Variation in ANGPTL4, LPL, and SVEP1 and the Risk of Coronary Disease Myocardial Infarction Genetics and CARDIoGRAM Exome Consortia Investigators New England Journal of Medicine 374 (12), 1134-1144, 2016 | 398 | 2016 |
| Systematic evaluation of pleiotropy identifies 6 further loci associated with coronary artery disease TR Webb, J Erdmann, KE Stirrups, NO Stitziel, NGD Masca, H Jansen, ... Journal of the American College of Cardiology 69 (7), 823-836, 2017 | 259* | 2017 |
| MRAP and MRAP2 are bidirectional regulators of the melanocortin receptor family LF Chan, TR Webb, TT Chung, E Meimaridou, SN Cooray, L Guasti, ... Proceedings of the National Academy of Sciences 106 (15), 6146-6151, 2009 | 259 | 2009 |
| Discovery and systematic characterization of risk variants and genes for coronary artery disease in over a million participants KG Aragam, T Jiang, A Goel, S Kanoni, BN Wolford, DS Atri, EM Weeks, ... Nature genetics 54 (12), 1803-1815, 2022 | 206 | 2022 |
| The ataxia protein sacsin is a functional co-chaperone that protects against polyglutamine-expanded ataxin-1 DA Parfitt, GJ Michael, EGM Vermeulen, NV Prodromou, TR Webb, ... Human molecular genetics 18 (9), 1556-1565, 2009 | 189 | 2009 |
| Association of the PHACTR1/EDN1 Genetic Locus With Spontaneous Coronary Artery Dissection D Adlam, TM Olson, N Combaret, JC Kovacic, SE Iismaa, A Al-Hussaini, ... Journal of the American College of Cardiology 73 (1), 58-66, 2019 | 178 | 2019 |
| Meta-analysis of genome-wide association studies for abdominal aortic aneurysm identifies four new disease-specific risk loci GT Jones, G Tromp, H Kuivaniemi, S Gretarsdottir, AF Baas, B Giusti, ... Circulation research 120 (2), 341-353, 2017 | 178 | 2017 |
| Deep intronic mutation in OFD1, identified by targeted genomic next-generation sequencing, causes a severe form of X-linked retinitis pigmentosa (RP23) TR Webb, DA Parfitt, JC Gardner, A Martinez, D Bevilacqua, AE Davidson, ... Human molecular genetics 21 (16), 3647-3654, 2012 | 170 | 2012 |
| Minireview: the melanocortin 2 receptor accessory proteins TR Webb, AJL Clark Molecular endocrinology 24 (3), 475-484, 2010 | 137 | 2010 |
| Prediction of causal candidate genes in coronary artery disease loci I Brænne, M Civelek, B Vilne, A Di Narzo, AD Johnson, Y Zhao, B Reiz, ... Arteriosclerosis, thrombosis, and vascular biology 35 (10), 2207-2217, 2015 | 120 | 2015 |
| Long noncoding RNA NEXN-AS1 mitigates atherosclerosis by regulating the actin-binding protein NEXN YW Hu, FX Guo, YJ Xu, P Li, ZF Lu, DG McVey, L Zheng, Q Wang, ... The Journal of clinical investigation 129 (3), 1115-1128, 2019 | 115 | 2019 |
| The melanocortin 2 receptor accessory protein exists as a homodimer and is essential for the function of the melanocortin 2 receptor in the mouse y1 cell line SN Cooray, I Almiro Do Vale, KY Leung, TR Webb, JP Chapple, ... Endocrinology 149 (4), 1935-1941, 2008 | 102 | 2008 |
| The majority of adrenocorticotropin receptor (melanocortin 2 receptor) mutations found in familial glucocorticoid deficiency type 1 lead to defective trafficking of the … TT Chung, TR Webb, LF Chan, SN Cooray, LA Metherell, PJ King, ... The Journal of Clinical Endocrinology & Metabolism 93 (12), 4948-4954, 2008 | 92* | 2008 |
| Distinct melanocortin 2 receptor accessory protein domains are required for melanocortin 2 receptor interaction and promotion of receptor trafficking TR Webb, L Chan, SN Cooray, ME Cheetham, JP Chapple, AJL Clark Endocrinology 150 (2), 720-726, 2009 | 85 | 2009 |
| Diphthamide modification of eEF2 requires a J-domain protein and is essential for normal development TR Webb, SH Cross, L McKie, R Edgar, L Vizor, J Harrison, J Peters, ... Journal of cell science 121 (19), 3140-3145, 2008 | 78 | 2008 |
| X-linked megalocornea caused by mutations in CHRDL1 identifies an essential role for ventroptin in anterior segment development TR Webb, M Matarin, JC Gardner, D Kelberman, H Hassan, W Ang, ... The American Journal of Human Genetics 90 (2), 247-259, 2012 | 71 | 2012 |
| X-linked cataract and Nance-Horan syndrome are allelic disorders M Coccia, SP Brooks, TR Webb, K Christodoulou, IO Wozniak, V Murday, ... Human molecular genetics 18 (14), 2643-2655, 2009 | 68 | 2009 |
