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Improving accuracy of rare variant imputation with a two-step imputation approach.

Kreiner-Møller E, Medina-Gomez C, Uitterlinden AG, Rivadeneira F, Estrada K. Improving accuracy of rare variant imputation with a two-step imputation approach. Eur J Hum Genet. 2015;23(3):395-400. doi:10.1038/ejhg.2014.91

Construction and application of a Korean reference panel for imputing classical alleles and amino acids of human leukocyte antigen genes.

Kim K, Bang SY, Lee HS, Bae SC. Construction and application of a Korean reference panel for imputing classical alleles and amino acids of human leukocyte antigen genes. PLoS One. 2014;9(11):e112546. doi:10.1371/journal.pone.0112546

Rare genetic variants in the CFI gene are associated with advanced age-related macular degeneration and commonly result in reduced serum factor I levels.

Kavanagh D, Yu Y, Schramm EC, et al. Rare genetic variants in the CFI gene are associated with advanced age-related macular degeneration and commonly result in reduced serum factor I levels. Hum Mol Genet. 2015;24(13):3861-70. doi:10.1093/hmg/ddv091

Disentangling the Effects of Colocalizing Genomic Annotations to Functionally Prioritize Non-coding Variants within Complex-Trait Loci.

Trynka G, Westra HJ, Slowikowski K, et al. Disentangling the Effects of Colocalizing Genomic Annotations to Functionally Prioritize Non-coding Variants within Complex-Trait Loci. Am J Hum Genet. 2015;97(1):139-52. doi:10.1016/j.ajhg.2015.05.016

Reply to Lee: Downward bias in heritability estimation is not due to simplified linkage equilibrium SNP simulation.

Golan D, Rosset S, Lander ES. Reply to Lee: Downward bias in heritability estimation is not due to simplified linkage equilibrium SNP simulation. Proc Natl Acad Sci U S A. 2015;112(40):E5452-3. doi:10.1073/pnas.1511370112

HaploReg v4: systematic mining of putative causal variants, cell types, regulators and target genes for human complex traits and disease.

Ward LD, Kellis M. HaploReg v4: systematic mining of putative causal variants, cell types, regulators and target genes for human complex traits and disease. Nucleic Acids Res. 2016;44(D1):D877-81. doi:10.1093/nar/gkv1340

Functional Implications of Human-Specific Changes in Great Ape microRNAs.

Gallego A, Melé M, Balcells I, et al. Functional Implications of Human-Specific Changes in Great Ape microRNAs. PLoS One. 2016;11(4):e0154194. doi:10.1371/journal.pone.0154194

Association of a Genetic Risk Score With Body Mass Index Across Different Birth Cohorts.

Walter S, Mejía-Guevara I, Estrada K, Liu SY, Glymour M. Association of a Genetic Risk Score With Body Mass Index Across Different Birth Cohorts. JAMA. 2016;316(1):63-9. doi:10.1001/jama.2016.8729

Large-scale identification, mapping, and genotyping of single-nucleotide polymorphisms in the human genome.

Wang DG, Fan JB, Siao CJ, et al. Large-scale identification, mapping, and genotyping of single-nucleotide polymorphisms in the human genome. Science. 1998;280(5366):1077-82.