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Fast pairwise IBD association testing in genome-wide association studies.

Han B, Kang EY, Raychaudhuri S, de Bakker PIW, Eskin E. Fast pairwise IBD association testing in genome-wide association studies. Bioinformatics. 2014;30(2):206-13. doi:10.1093/bioinformatics/btt609

Maximizing the power of principal-component analysis of correlated phenotypes in genome-wide association studies.

Aschard H, Vilhjálmsson BJ, Greliche N, Morange PE, Trégouët DA, Kraft P. Maximizing the power of principal-component analysis of correlated phenotypes in genome-wide association studies. Am J Hum Genet. 2014;94(5):662-76. doi:10.1016/j.ajhg.2014.03.016

Whole-exome imputation of sequence variants identified two novel alleles associated with adult body height in African Americans.

Du M, Auer PL, Jiao S, et al. Whole-exome imputation of sequence variants identified two novel alleles associated with adult body height in African Americans. Hum Mol Genet. 2014;23(24):6607-15. doi:10.1093/hmg/ddu361

Describing the genetic architecture of epilepsy through heritability analysis.

Speed D, O’Brien TJ, Palotie A, et al. Describing the genetic architecture of epilepsy through heritability analysis. Brain. 2014;137(Pt 10):2680-9. doi:10.1093/brain/awu206

A simple repeat polymorphism in the MITF-M promoter is a key regulator of white spotting in dogs.

Körberg IB, Sundström E, Meadows JRS, et al. A simple repeat polymorphism in the MITF-M promoter is a key regulator of white spotting in dogs. PLoS One. 2014;9(8):e104363. doi:10.1371/journal.pone.0104363

A novel common variant in DCST2 is associated with length in early life and height in adulthood.

van der Valk RJP, Kreiner-Møller E, Kooijman MN, et al. A novel common variant in DCST2 is associated with length in early life and height in adulthood. Hum Mol Genet. 2015;24(4):1155-68. doi:10.1093/hmg/ddu510