Smith G, Newton-Cheh C. Genome-wide association studies of late-onset cardiovascular disease. J Mol Cell Cardiol. 2015;83:131-41. doi:10.1016/j.yjmcc.2015.04.004
Jabbari J, Olesen MS, Yuan L, et al. Common and rare variants in SCN10A modulate the risk of atrial fibrillation. Circ Cardiovasc Genet. 2015;8(1):64-73. doi:10.1161/HCG.0000000000000022
Crosslin DR, Carrell DS, Burt A, et al. Genetic variation in the HLA region is associated with susceptibility to herpes zoster. Genes Immun. 2015;16(1):1-7. doi:10.1038/gene.2014.51
Minikel EV, Zerr I, Collins SJ, et al. Ascertainment bias causes false signal of anticipation in genetic prion disease. Am J Hum Genet. 2014;95(4):371-82. doi:10.1016/j.ajhg.2014.09.003
Brand H, Pillalamarri V, Collins RL, et al. Cryptic and complex chromosomal aberrations in early-onset neuropsychiatric disorders. Am J Hum Genet. 2014;95(4):454-61. doi:10.1016/j.ajhg.2014.09.005
Naj AC, Jun G, Reitz C, et al. Effects of multiple genetic loci on age at onset in late-onset Alzheimer disease: a genome-wide association study. JAMA Neurol. 2014;71(11):1394-404. doi:10.1001/jamaneurol.2014.1491
Traylor M, Mäkelä KM, Kilarski LL, et al. A novel MMP12 locus is associated with large artery atherosclerotic stroke using a genome-wide age-at-onset informed approach. PLoS Genet. 2014;10(7):e1004469. doi:10.1371/journal.pgen.1004469
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
Consortium STD 2, Estrada K, Aukrust I, et al. Association of a low-frequency variant in HNF1A with type 2 diabetes in a Latino population. JAMA. 2014;311(22):2305-14. doi:10.1001/jama.2014.6511
Bergen SE, O’Dushlaine CT, Lee PH, et al. Genetic modifiers and subtypes in schizophrenia: investigations of age at onset, severity, sex and family history. Schizophr Res. 2014;154(1-3):48-53. doi:10.1016/j.schres.2014.01.030