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Genetics of atrial fibrillation: from families to genomes.

Christophersen IE, Ellinor PT. Genetics of atrial fibrillation: from families to genomes. J Hum Genet. 2016;61(1):61-70. doi:10.1038/jhg.2015.44

Loss of PCLO function underlies pontocerebellar hypoplasia type III.

Ahmed MY, Chioza BA, Rajab A, et al. Loss of PCLO function underlies pontocerebellar hypoplasia type III. Neurology. 2015;84(17):1745-50. doi:10.1212/WNL.0000000000001523

High-density mapping of the MHC identifies a shared role for HLA-DRB1*01:03 in inflammatory bowel diseases and heterozygous advantage in ulcerative colitis.

Goyette P, Boucher G, Mallon D, et al. High-density mapping of the MHC identifies a shared role for HLA-DRB1*01:03 in inflammatory bowel diseases and heterozygous advantage in ulcerative colitis. Nat Genet. 2015;47(2):172-9. doi:10.1038/ng.3176

Biallelic truncating mutations in FMN2, encoding the actin-regulatory protein Formin 2, cause nonsyndromic autosomal-recessive intellectual disability.

Law R, Dixon-Salazar T, Jerber J, et al. Biallelic truncating mutations in FMN2, encoding the actin-regulatory protein Formin 2, cause nonsyndromic autosomal-recessive intellectual disability. Am J Hum Genet. 2014;95(6):721-8. doi:10.1016/j.ajhg.2014.10.016

Evaluating empirical bounds on complex disease genetic architecture.

Agarwala V, Flannick J, Sunyaev S, GoT2D Consortium, Altshuler D. Evaluating empirical bounds on complex disease genetic architecture. Nat Genet. 2013;45(12):1418-27. doi:10.1038/ng.2804

Genetic surveillance detects both clonal and epidemic transmission of malaria following enhanced intervention in Senegal.

Daniels R, Chang HH, Séne PD, et al. Genetic surveillance detects both clonal and epidemic transmission of malaria following enhanced intervention in Senegal. PLoS One. 2013;8(4):e60780. doi:10.1371/journal.pone.0060780

Mutations causing medullary cystic kidney disease type 1 lie in a large VNTR in MUC1 missed by massively parallel sequencing.

Kirby A, Gnirke A, Jaffe DB, et al. Mutations causing medullary cystic kidney disease type 1 lie in a large VNTR in MUC1 missed by massively parallel sequencing. Nat Genet. 2013;45(3):299-303. doi:10.1038/ng.2543

Fine-scale mapping of the Nasonia genome to chromosomes using a high-density genotyping microarray.

Desjardins CA, Gadau J, Lopez JA, et al. Fine-scale mapping of the Nasonia genome to chromosomes using a high-density genotyping microarray. G3 (Bethesda). 2013;3(2):205-15. doi:10.1534/g3.112.004739

Linkage to the mating-type locus across the genus Microbotryum: insights into nonrecombining chromosomes.

Petit E, Giraud T, de Vienne DM, et al. Linkage to the mating-type locus across the genus Microbotryum: insights into nonrecombining chromosomes. Evolution. 2012;66(11):3519-33. doi:10.1111/j.1558-5646.2012.01703.x

Comparison of Heritability Estimation and Linkage Analysis for Multiple Traits Using Principal Component Analyses.

Liang J, Cade BE, Wang H, et al. Comparison of Heritability Estimation and Linkage Analysis for Multiple Traits Using Principal Component Analyses. Genet Epidemiol. 2016;40(3):222-32. doi:10.1002/gepi.21957