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Bryan Howie
Bryan Howie
Postdoctoral Scholar, University of Chicago
Bestätigte E-Mail-Adresse bei uchicago.edu
Titel
Zitiert von
Zitiert von
Jahr
Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls
1958 Birth Cohort Controls Jones Richard W. 18 McArdle Wendy L. 18 Ring ...
Nature 447 (7145), 661-678, 2007
93362007
A map of human genome variation from population scale sequencing
DM Altshuler, ES Lander, L Ambrogio, T Bloom, K Cibulskis, TJ Fennell, ...
Nature 467 (7319), 1061-1073, 2010
8727*2010
An integrated map of genetic variation from 1,092 human genomes
1000 Genomes Project Consortium
Nature 491 (7422), 56, 2012
82382012
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
45202009
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
30722007
Genotype imputation for genome-wide association studies
J Marchini, B Howie
Nature Reviews Genetics 11 (7), 499-511, 2010
19692010
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
19642012
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
13042008
Genotype imputation with thousands of genomes
B Howie, J Marchini, M Stephens
G3: Genes| Genomes| Genetics 1 (6), 457-470, 2011
11432011
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
4592009
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
4102013
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
4002015
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
3752017
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
2652013
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
2382015
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
2292013
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
1892016
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
1772014
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
1662012
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
1572014
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