Bryan Howie to Polymorphism, Single Nucleotide
This is a "connection" page, showing publications Bryan Howie has written about Polymorphism, Single Nucleotide.
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0.750
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Comparing algorithms for genotype imputation. Am J Hum Genet. 2008 Oct; 83(4):535-9; author reply 539-40.
Score: 0.182
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Efficient selection of tagging single-nucleotide polymorphisms in multiple populations. Hum Genet. 2006 Aug; 120(1):58-68.
Score: 0.154
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1000 Genomes-based imputation identifies novel and refined associations for the Wellcome Trust Case Control Consortium phase 1 Data. Eur J Hum Genet. 2012 Jul; 20(7):801-5.
Score: 0.057
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Genotype imputation for genome-wide association studies. Nat Rev Genet. 2010 Jul; 11(7):499-511.
Score: 0.051
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A flexible and accurate genotype imputation method for the next generation of genome-wide association studies. PLoS Genet. 2009 Jun; 5(6):e1000529.
Score: 0.048
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Genome-wide and fine-resolution association analysis of malaria in West Africa. Nat Genet. 2009 Jun; 41(6):657-65.
Score: 0.048
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Analysis of 10 independent samples provides evidence for association between schizophrenia and a SNP flanking fibroblast growth factor receptor 2. Mol Psychiatry. 2009 Jan; 14(1):30-6.
Score: 0.046
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Association scan of 14,500 nonsynonymous SNPs in four diseases identifies autoimmunity variants. Nat Genet. 2007 Nov; 39(11):1329-37.
Score: 0.043
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Estimating the Ages of Selection Signals from Different Epochs in Human History. Mol Biol Evol. 2016 Mar; 33(3):657-69.
Score: 0.019
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Improved imputation of low-frequency and rare variants using the UK10K haplotype reference panel. Nat Commun. 2015 Sep 14; 6:8111.
Score: 0.018
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Haplotype estimation using sequencing reads. Am J Hum Genet. 2013 Oct 03; 93(4):687-96.
Score: 0.016
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A statin-dependent QTL for GATM expression is associated with statin-induced myopathy. Nature. 2013 Oct 17; 502(7471):377-80.
Score: 0.016
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The origin, evolution, and functional impact of short insertion-deletion variants identified in 179 human genomes. Genome Res. 2013 May; 23(5):749-61.
Score: 0.016
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Multiple common susceptibility variants near BMP pathway loci GREM1, BMP4, and BMP2 explain part of the missing heritability of colorectal cancer. PLoS Genet. 2011 Jun; 7(6):e1002105.
Score: 0.014
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Identification of loci associated with schizophrenia by genome-wide association and follow-up. Nat Genet. 2008 Sep; 40(9):1053-5.
Score: 0.011
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A new multipoint method for genome-wide association studies by imputation of genotypes. Nat Genet. 2007 Jul; 39(7):906-13.
Score: 0.010