Akbari A, Vitti JJ, Iranmehr A, et al. Identifying the favored mutation in a positive selective sweep. Nat Methods. 2018;15(4):279-282. doi:10.1038/nmeth.4606
Denson LA, Jurickova I, Karns R, et al. Clinical and Genomic Correlates of Neutrophil Reactive Oxygen Species Production in Pediatric Patients With Crohn’s Disease. Gastroenterology. 2018;154(8):2097-2110. doi:10.1053/j.gastro.2018.02.016
Pardiñas AF, Holmans P, Pocklington AJ, et al. Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection. Nat Genet. 2018;50(3):381-389. doi:10.1038/s41588-018-0059-2
Zhang JY, Wang M, Tian L, et al. modifies -induced kidney disease risk. Proc Natl Acad Sci U S A. 2018;115(13):3446-3451. doi:10.1073/pnas.1716113115
Hu R, Morley MP, Brandimarto J, et al. Genetic Reduction in Left Ventricular Protein Kinase C-α and Adverse Ventricular Remodeling in Human Subjects. Circ Genom Precis Med. 2018;11(3):e001901. doi:10.1161/CIRCGEN.117.001901
Özbek U, Lin HM, Lin Y, et al. Statistics for X-chromosome associations. Genet Epidemiol. 2018;42(6):539-550. doi:10.1002/gepi.22132
Genereux DP, Laird CD. At what rate do new premutation alleles arise at the fragile X locus? Hum Genet. 2013;132(6):715-7. doi:10.1007/s00439-013-1291-6
Di Gioia SA, Shaaban S, Tuysuz B, et al. Recessive MYF5 Mutations Cause External Ophthalmoplegia, Rib, and Vertebral Anomalies. Am J Hum Genet. 2018;103(1):115-124. doi:10.1016/j.ajhg.2018.05.003
Hindy G, Wiberg F, Almgren P, Melander O, Orho-Melander M. Polygenic Risk Score for Coronary Heart Disease Modifies the Elevated Risk by Cigarette Smoking for Disease Incidence. Circ Genom Precis Med. 2018;11(1):e001856. doi:10.1161/CIRCGEN.117.001856
Kelly RS, Chawes BL, Blighe K, et al. An Integrative Transcriptomic and Metabolomic Study of Lung Function in Children With Asthma. Chest. 2018;154(2):335-348. doi:10.1016/j.chest.2018.05.038