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An integrated map of genetic variation from 1,092 human genomes 1000 Genomes Project Consortium Nature 491 (7422), 56, 2012 | 8310 | 2012 |
A flexible and accurate genotype imputation method for the next generation of genome-wide association studies BN Howie, P Donnelly, J Marchini PLoS genetics 5 (6), e1000529, 2009 | 4584 | 2009 |
A new multipoint method for genome-wide association studies by imputation of genotypes J Marchini, B Howie, S Myers, G McVean, P Donnelly Nature genetics 39 (7), 906-913, 2007 | 3103 | 2007 |
Fast and accurate genotype imputation in genome-wide association studies through pre-phasing B Howie, C Fuchsberger, M Stephens, J Marchini, GR Abecasis Nature genetics 44 (8), 955-959, 2012 | 2005 | 2012 |
Genotype imputation for genome-wide association studies J Marchini, B Howie Nature Reviews Genetics 11 (7), 499-511, 2010 | 1994 | 2010 |
Identification of loci associated with schizophrenia by genome-wide association and follow-up MC O'donovan, N Craddock, N Norton, H Williams, T Peirce, V Moskvina, ... Nature genetics 40 (9), 1053-1055, 2008 | 1312 | 2008 |
Genotype imputation with thousands of genomes B Howie, J Marchini, M Stephens G3: Genes| Genomes| Genetics 1 (6), 457-470, 2011 | 1170 | 2011 |
Genome-wide and fine-resolution association analysis of malaria in West Africa M Jallow, YY Teo, KS Small, KA Rockett, P Deloukas, TG Clark, K Kivinen, ... Nature genetics 41 (6), 657-665, 2009 | 463 | 2009 |
Haplotype estimation using sequencing reads O Delaneau, B Howie, AJ Cox, JF Zagury, J Marchini The American Journal of Human Genetics 93 (4), 687-696, 2013 | 421 | 2013 |
Improved imputation of low-frequency and rare variants using the UK10K haplotype reference panel J Huang, B Howie, S McCarthy, Y Memari, K Walter, JL Min, P Danecek, ... Nature communications 6 (1), 8111, 2015 | 417 | 2015 |
Landscape of immunogenic tumor antigens in successful immunotherapy of virally induced epithelial cancer S Stevanović, A Pasetto, SR Helman, JJ Gartner, TD Prickett, B Howie, ... Science 356 (6334), 200-205, 2017 | 387 | 2017 |
The origin, evolution, and functional impact of short insertion–deletion variants identified in 179 human genomes SB Montgomery, DL Goode, E Kvikstad, CA Albers, ZD Zhang, XJ Mu, ... Genome research 23 (5), 749-761, 2013 | 275 | 2013 |
High-throughput pairing of T cell receptor α and β sequences B Howie, AM Sherwood, AD Berkebile, J Berka, RO Emerson, ... Science translational medicine 7 (301), 301ra131-301ra131, 2015 | 242 | 2015 |
A statin-dependent QTL for GATM expression is associated with statin-induced myopathy LM Mangravite, BE Engelhardt, MW Medina, JD Smith, CD Brown, ... Nature 502 (7471), 377-380, 2013 | 234 | 2013 |
Tumor-and neoantigen-reactive T-cell receptors can be identified based on their frequency in fresh tumor A Pasetto, A Gros, PF Robbins, DC Deniger, TD Prickett, ... Cancer immunology research 4 (9), 734-743, 2016 | 195 | 2016 |
Rare variants in PPARG with decreased activity in adipocyte differentiation are associated with increased risk of type 2 diabetes AR Majithia, J Flannick, P Shahinian, M Guo, MA Bray, P Fontanillas, ... Proceedings of the National Academy of Sciences 111 (36), 13127-13132, 2014 | 178 | 2014 |
1000 Genomes-based imputation identifies novel and refined associations for the Wellcome Trust Case Control Consortium phase 1 Data J Huang, D Ellinghaus, A Franke, B Howie, Y Li European Journal of Human Genetics 20 (7), 801-805, 2012 | 165 | 2012 |
Detection of Minimal Residual Disease in B Lymphoblastic Leukemia by High-Throughput Sequencing of IGH D Wu, RO Emerson, A Sherwood, ML Loh, A Angiolillo, B Howie, J Vogt, ... Clinical Cancer Research 20 (17), 4540-4548, 2014 | 157 | 2014 |