Year |
Citation |
Score |
2019 |
Iwaki H, Blauwendraat C, Leonard HL, Liu G, Maple-Grødem J, Corvol JC, Pihlstrøm L, van Nimwegen M, Hutten SJ, Nguyen KH, Rick J, Eberly S, Faghri F, Auinger P, Scott KM, ... ... Day-Williams AG, et al. Genetic risk of Parkinson disease and progression:: An analysis of 13 longitudinal cohorts. Neurology. Genetics. 5: e348. PMID 31404238 DOI: 10.1212/Nxg.0000000000000348 |
0.326 |
|
2018 |
Bodea CA, Mitchell AA, Bloemendal A, Day-Williams AG, Runz H, Sunyaev SR. PINES: phenotype-informed tissue weighting improves prediction of pathogenic noncoding variants. Genome Biology. 19: 173. PMID 30359302 DOI: 10.1186/S13059-018-1546-6 |
0.373 |
|
2018 |
Diogo D, Tian C, Franklin CS, Alanne-Kinnunen M, March M, Spencer CCA, Vangjeli C, Weale ME, Mattsson H, Kilpeläinen E, Sleiman PMA, Reilly DF, McElwee J, Maranville JC, Chatterjee AK, ... ... Day-Williams AG, et al. Phenome-wide association studies across large population cohorts support drug target validation. Nature Communications. 9: 4285. PMID 30327483 DOI: 10.1038/S41467-018-06540-3 |
0.397 |
|
2018 |
Estrada K, Whelan CW, Zhao F, Bronson P, Handsaker RE, Sun C, Carulli JP, Harris T, Ransohoff RM, McCarroll SA, Day-Williams AG, Greenberg BM, MacArthur DG. A whole-genome sequence study identifies genetic risk factors for neuromyelitis optica. Nature Communications. 9: 1929. PMID 29769526 DOI: 10.1038/S41467-018-04332-3 |
0.448 |
|
2018 |
Flannick J, Fuchsberger C, Mahajan A, Teslovich TM, Agarwala V, Gaulton KJ, Caulkins L, Koesterer R, Ma C, Moutsianas L, McCarthy DJ, Rivas MA, Perry JRB, Sim X, Blackwell TW, ... ... Day-Williams AG, et al. Erratum: Sequence data and association statistics from 12,940 type 2 diabetes cases and controls. Scientific Data. 5: 180002. PMID 29360107 DOI: 10.1038/sdata.2018.2 |
0.446 |
|
2017 |
Jason F, Fuchsberger C, Mahajan A, Teslovich TM, Agarwala V, Gaulton KJ, Caulkins L, Koesterer R, Ma C, Moutsianas L, McCarthy DJ, Rivas MA, Perry JRB, Sim X, Blackwell TW, ... ... Day-Williams AG, et al. Sequence data and association statistics from 12,940 type 2 diabetes cases and controls. Scientific Data. 4: 170179. PMID 29257133 DOI: 10.1038/Sdata.2017.179 |
0.577 |
|
2016 |
Panoutsopoulou K, Thiagarajah S, Zengini E, Day-Williams AG, Ramos YF, Meessen JM, Huetink K, Nelissen RG, Southam L, Rayner NW, Doherty M, Meulenbelt I, Zeggini E, Wilkinson JM. Radiographic endophenotyping in hip osteoarthritis improves the precision of genetic association analysis. Annals of the Rheumatic Diseases. PMID 27974301 DOI: 10.1136/Annrheumdis-2016-210373 |
0.409 |
|
2016 |
Fuchsberger C, Flannick J, Teslovich TM, Mahajan A, Agarwala V, Gaulton KJ, Ma C, Fontanillas P, Moutsianas L, McCarthy DJ, Rivas MA, Perry JR, Sim X, Blackwell TW, Robertson NR, ... ... Day-Williams AG, et al. The genetic architecture of type 2 diabetes. Nature. PMID 27398621 DOI: 10.1038/Nature18642 |
0.585 |
|
2015 |
Lindner C, Thiagarajah S, Wilkinson JM, Panoutsopoulou K, Day-Williams AG, Cootes TF, Wallis GA. Investigation of association between hip osteoarthritis susceptibility loci and radiographic proximal femur shape. Arthritis & Rheumatology (Hoboken, N.J.). PMID 25939412 DOI: 10.1002/Art.39186 |
0.393 |
|
2015 |
Panoutsopoulou K, Thiagarajah S, Day-Williams AG, Southam L, Doherty M, Zeggini E, Wilkinson J. Improved phenotype definitions of OA in genetic association studies highlight a structural role for a common variant in LRCH1 Osteoarthritis and Cartilage. 23. DOI: 10.1016/J.Joca.2015.02.143 |
0.406 |
|
2014 |
Evangelou E, Kerkhof HJ, Styrkarsdottir U, Ntzani EE, Bos SD, Esko T, Evans DS, Metrustry S, Panoutsopoulou K, Ramos YF, Thorleifsson G, Tsilidis KK, Arden N, Aslam N, ... ... Day-Williams AG, et al. A meta-analysis of genome-wide association studies identifies novel variants associated with osteoarthritis of the hip. Annals of the Rheumatic Diseases. 73: 2130-6. PMID 23989986 DOI: 10.1136/Annrheumdis-2012-203114 |
0.479 |
|
2013 |
Ma RC, Hu C, Tam CH, Zhang R, Kwan P, Leung TF, Thomas GN, Go MJ, Hara K, Sim X, Ho JS, Wang C, Li H, Lu L, Wang Y, ... ... Day-Williams AG, et al. Genome-wide association study in a Chinese population identifies a susceptibility locus for type 2 diabetes at 7q32 near PAX4. Diabetologia. 56: 1291-305. PMID 23532257 DOI: 10.1007/S00125-013-2874-4 |
0.406 |
|
2013 |
Elliott KS, Chapman K, Day-Williams A, Panoutsopoulou K, Southam L, Lindgren CM, Arden N, Aslam N, Birrell F, Carluke I, Carr A, Deloukas P, Doherty M, Loughlin J, McCaskie A, et al. Evaluation of the genetic overlap between osteoarthritis with body mass index and height using genome-wide association scan data. Annals of the Rheumatic Diseases. 72: 935-41. PMID 22956599 DOI: 10.1136/Annrheumdis-2012-202081 |
0.45 |
|
2012 |
Mägi R, Asimit JL, Day-Williams AG, Zeggini E, Morris AP. Genome-wide association analysis of imputed rare variants: application to seven common complex diseases. Genetic Epidemiology. 36: 785-96. PMID 22951892 DOI: 10.1002/Gepi.21675 |
0.507 |
|
2012 |
Zeggini E, Panoutsopoulou K, Southam L, Rayner NW, Day-Williams AG, Lopes MC, Boraska V, Esko T, Evangelou E, Hoffman A, Houwing-Duistermaat JJ, Ingvarsson T, Jonsdottir I, et al. Identification of new susceptibility loci for osteoarthritis (arcOGEN): a genome-wide association study. Lancet. 380: 815-23. PMID 22763110 DOI: 10.1016/S0140-6736(12)60681-3 |
0.396 |
|
2012 |
Boraska V, Day-Williams A, Franklin CS, Elliott KS, Panoutsopoulou K, Tachmazidou I, Albrecht E, Bandinelli S, Beilin LJ, Bochud M, Cadby G, Ernst F, Evans DM, Hayward C, Hicks AA, et al. Genome-wide association study to identify common variants associated with brachial circumference: a meta-analysis of 14 cohorts. Plos One. 7: e31369. PMID 22479309 DOI: 10.1371/Journal.Pone.0031369 |
0.434 |
|
2012 |
Asimit JL, Day-Williams AG, Morris AP, Zeggini E. ARIEL and AMELIA: testing for an accumulation of rare variants using next-generation sequencing data. Human Heredity. 73: 84-94. PMID 22441326 DOI: 10.1159/000336982 |
0.407 |
|
2012 |
Asimit J, Day-Williams A, Zgaga L, Rudan I, Boraska V, Zeggini E. An evaluation of different meta-analysis approaches in the presence of allelic heterogeneity European Journal of Human Genetics. 20: 709-712. PMID 22293689 DOI: 10.1038/Ejhg.2011.274 |
0.482 |
|
2011 |
Day-Williams AG, McLay K, Drury E, Edkins S, Coffey AJ, Palotie A, Zeggini E. An evaluation of different target enrichment methods in pooled sequencing designs for complex disease association studies Plos One. 6. PMID 22069447 DOI: 10.1371/Journal.Pone.0026279 |
0.414 |
|
2011 |
Day-Williams AG, Southam L, Panoutsopoulou K, Rayner NW, Esko T, Estrada K, Helgadottir HT, Hofman A, Ingvarsson T, Jonsson H, Keis A, Kerkhof HJ, Thorleifsson G, Arden NK, Carr A, et al. A variant in MCF2L is associated with osteoarthritis. American Journal of Human Genetics. 89: 446-50. PMID 21871595 DOI: 10.1016/J.Ajhg.2011.08.001 |
0.418 |
|
2011 |
Day-Williams AG, Blangero J, Dyer TD, Lange K, Sobel EM. Unifying ideas for non-parametric linkage analysis. Human Heredity. 71: 267-80. PMID 21822022 DOI: 10.1159/000323752 |
0.531 |
|
2011 |
Day-Williams AG, Blangero J, Dyer TD, Lange K, Sobel EM. Linkage analysis without defined pedigrees. Genetic Epidemiology. 35: 360-70. PMID 21465549 DOI: 10.1002/Gepi.20584 |
0.55 |
|
2011 |
Panoutsopoulou K, Southam L, Elliott KS, Wrayner N, Zhai G, Beazley C, Thorleifsson G, Arden NK, Carr A, Chapman K, Deloukas P, Doherty M, McCaskie A, Ollier WE, Ralston SH, ... ... Day-Williams AG, et al. Insights into the genetic architecture of osteoarthritis from stage 1 of the arcOGEN study. Annals of the Rheumatic Diseases. 70: 864-7. PMID 21177295 DOI: 10.1136/Ard.2010.141473 |
0.441 |
|
2011 |
Day-Williams AG, Zeggini E. The effect of next-generation sequencing technology on complex trait research. European Journal of Clinical Investigation. 41: 561-7. PMID 21155765 DOI: 10.1111/J.1365-2362.2010.02437.X |
0.407 |
|
2011 |
Day-Williams AG, Blangero J, Dyer TD, Lange K, Sobel EM, Hiekkalinna T, Schäffer AA, Lambert B, Norrgrann P, Göring HHH, Terwilliger JD, Basu S, Pan W, Oetting WS, Andrade Md, et al. Contents Vol. 71, 2011 Human Heredity. 71. DOI: 10.1159/000331865 |
0.434 |
|
2010 |
Lawrence R, Day-Williams AG, Elliott KS, Morris AP, Zeggini E. CCRaVAT and QuTie-enabling analysis of rare variants in large-scale case control and quantitative trait association studies. Bmc Bioinformatics. 11: 527. PMID 20964851 DOI: 10.1186/1471-2105-11-527 |
0.476 |
|
2010 |
Boraska V, Rayner NW, Groves CJ, Frayling TM, Diakite M, Rockett KA, Kwiatkowski DP, Day-Williams AG, McCarthy MI, Zeggini E. Large-scale association analysis of TNF/LTA gene region polymorphisms in type 2 diabetes. Bmc Medical Genetics. 11: 69. PMID 20459604 DOI: 10.1186/1471-2350-11-69 |
0.379 |
|
2010 |
Panoutsopoulou K, Southam L, Rayner W, Zhai G, Beazley C, Arden N, Carr A, Chapman K, Deloukas P, Doherty M, McCaskie A, Oilier W, Ralston S, Spector T, Valdes A, ... ... Day-Williams A, et al. 378 THE arcOGEN CONSORTIUM: STAGE 1 OF A GENOME-WIDE ASSOCIATION SCAN FOR OSTEOARTHRITIS Osteoarthritis and Cartilage. 18: S166-S167. DOI: 10.1016/S1063-4584(10)60405-0 |
0.382 |
|
2009 |
Lawrence R, Day-Williams AG, Mott R, Broxholme J, Cardon LR, Zeggini E. GLIDERS--a web-based search engine for genome-wide linkage disequilibrium between HapMap SNPs. Bmc Bioinformatics. 10: 367. PMID 19878600 DOI: 10.1186/1471-2105-10-367 |
0.418 |
|
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