Comparing algorithms for genotype imputation. per Marchini, J, Howie, B

Genotype imputation for genome-wide association studies. per Marchini, J, Howie, B

Genotype imputation with thousands of genomes. per Howie, B, Marchini, J, Stephens, M

A flexible and accurate genotype imputation method for the next generation of genome-wide association studies. per Howie, B, Donnelly, P, Marchini, J

A flexible and accurate genotype imputation method for the next generation of genome-wide association studies per Howie, B, Donnelly, P, Marchini, J

Fast and accurate genotype imputation in genome-wide association studies through pre-phasing. per Howie, B, Fuchsberger, C, Stephens, M, Marchini, J, Abecasis, G

A new multipoint method for genome-wide association studies by imputation of genotypes. per Marchini, J, Howie, B, Myers, S, McVean, G, Donnelly, P

Haplotype estimation using sequencing reads. per Delaneau, O, Howie, B, Cox, A, Zagury, J, Marchini, J

Improved imputation of low-frequency and rare variants using the UK10K haplotype reference panel per Huang, J, Howie, B, McCarthy, S, Memari, Y, Walter, K, Min, J, Danecek, P, Malerba, G, Trabetti, E, Zheng, H, Gambaro, G, Richards, J, Durbin, R, Timpson, N, Marchini, J, Soranzo, N

The origin, evolution, and functional impact of short insertion-deletion variants identified in 179 human genomes. per Montgomery, S, Goode, D, Kvikstad, E, Albers, C, Zhang, Z, Mu, X, Ananda, G, Howie, B, Karczewski, K, Smith, K, Anaya, V, Richardson, R, Davis, J, MacArthur, D, Sidow, A, Duret, L, Gerstein, M, Makova, K, Marchini, J, McVean, G, Lunter, G

A statin-dependent QTL for GATM expression is associated with statin-induced myopathy. per Mangravite, L, Engelhardt, B, Medina, M, Smith, J, Brown, C, Chasman, D, Mecham, B, Howie, B, Shim, H, Naidoo, D, Feng, Q, Rieder, M, Chen, Y, Rotter, J, Ridker, P, Hopewell, J, Parish, S, Armitage, J, Collins, R, Wilke, R, Nickerson, D, Stephens, M, Krauss, R

A statin-dependent QTL for GATM expression is associated with statin-induced myopathy per Mangravite, L, Engelhardt, B, Medina, M, Smith, J, Brown, C, Chasman, D, Mecham, B, Howie, B, Shim, H, Naidoo, D, Feng, Q, Rieder, M, Chen, Y, Rotter, J, Ridker, P, Hopewell, J, Parish, S, Armitage, J, Collins, R, Wilke, R, Nickerson, D, Stephens, M, Krauss, R

Analysis of 10 independent samples provides evidence for association between schizophrenia and a SNP flanking fibroblast growth factor receptor 2. per O'Donovan, M, Norton, N, Williams, H, Peirce, T, Moskvina, V, Nikolov, I, Hamshere, M, Carroll, L, Georgieva, L, Dwyer, S, Holmans, P, Marchini, J, Spencer, C, Howie, B, Leung, H, Giegling, I, Hartmann, A, Möller, H, Morris, D, Shi, Y, Feng, G, Hoffmann, P, Propping, P, Vasilescu, C, Maier, W

Identification of loci associated with schizophrenia by genome-wide association and follow-up per O'Donovan, M, Craddock, N, Norton, N, Williams, H, Peirce, T, Moskvina, V, Nikolov, I, Hamshere, M, Carroll, L, Georgieva, L, Dwyer, S, Holmans, P, Marchini, J, Spencer, C, Howie, B, Leung, H, Hartmann, A, Möller, H, Morris, D, Shi, Y, Feng, G, Hoffmann, P, Propping, P, Vasilescu, C, Maier, W

Identification of loci associated with schizophrenia by genome-wide association and follow-up. per O'Donovan, M, Craddock, N, Norton, N, Williams, H, Peirce, T, Moskvina, V, Nikolov, I, Hamshere, M, Carroll, L, Georgieva, L, Dwyer, S, Holmans, P, Marchini, J, Spencer, C, Howie, B, Leung, H, Hartmann, A, Möller, H, Morris, D, Shi, Y, Feng, G, Hoffmann, P, Propping, P, Vasilescu, C, Maier, W

Analysis of 10 independent samples provides evidence for association between schizophrenia and a SNP flanking fibroblast growth factor receptor 2 per O'Donovan, M, Norton, N, Williams, H, Peirce, T, Moskvina, V, Nikolov, I, Hamshere, M, Carroll, L, Georgieva, L, Dwyer, S, Holmans, P, Marchini, J, Spencer, C, Howie, B, Leung, H, Giegling, I, Hartmann, A, Möller, H, Morris, D, Shi, Y, Feng, G, Hoffmann, P, Propping, P, Vasilescu, C, Maier, W

Multiple common susceptibility variants near BMP pathway loci GREM1, BMP4, and BMP2 explain part of the missing heritability of colorectal cancer. per Tomlinson, I, Carvajal-Carmona, L, Dobbins, SE, Tenesa, A, Jones, A, Howarth, K, Palles, C, Broderick, P, Jaeger, E, Farrington, S, Lewis, A, Prendergast, J, Pittman, A, Theodoratou, E, Olver, B, Walker, M, Penegar, S, Barclay, E, Whiffin, N, Martin, L, Ballereau, S, Lloyd, A, Gorman, M, Lubbe, S, Howie, B, Marchini, J, Ruiz-Ponte, C, Fernandez-Rozadilla, C, Castells, A, Carracedo, A, Castellvi-Bel, S, Duggan, D, Conti, D, Cazier, J, Campbell, H, Sieber, O, Lipton, L, Gibbs, P, Martin, N, Montgomery, G, Young, J, Baird, P, Gallinger, S, Newcomb, P, Hopper, J, Jenkins, M, Aaltonen, L, Kerr, D, Cheadle, J, Pharoah, P, Casey, G, Houlston, R, Dunlop, MG