Richards AL, Leonenko G, Walters JT, et al. Exome arrays capture polygenic rare variant contributions to schizophrenia. Hum Mol Genet. 2016;25(5):1001-7. doi:10.1093/hmg/ddv620
Publications
Salihovic S, Ganna A, Fall T, et al. The metabolic fingerprint of p,p’-DDE and HCB exposure in humans. Environ Int. 2016;88:60-6. doi:10.1016/j.envint.2015.12.015
Logan DJ, Shan J, Bhatia SN, Carpenter AE. Quantifying co-cultured cell phenotypes in high-throughput using pixel-based classification. Methods. 2016;96:6-11. doi:10.1016/j.ymeth.2015.12.002
Hogarth MW, Garton FC, Houweling PJ, et al. Analysis of the ACTN3 heterozygous genotype suggests that α-actinin-3 controls sarcomeric composition and muscle function in a dose-dependent fashion. Hum Mol Genet. 2016;25(5):866-77. doi:10.1093/hmg/ddv613
Bigdeli TB, Ripke S, Bacanu SA, et al. Genome-wide association study reveals greater polygenic loading for schizophrenia in cases with a family history of illness. Am J Med Genet B Neuropsychiatr Genet. 2016;171B(2):276-89. doi:10.1002/ajmg.b.32402
Conde J, Oliva N, Atilano M, Song HS, Artzi N. Self-assembled RNA-triple-helix hydrogel scaffold for microRNA modulation in the tumour microenvironment. Nat Mater. 2016;15(3):353-63. doi:10.1038/nmat4497
Kenttä TV, Nearing BD, Porthan K, et al. Prediction of sudden cardiac death with automated high-throughput analysis of heterogeneity in standard resting 12-lead electrocardiograms. Heart Rhythm. 2016;13(3):713-20. doi:10.1016/j.hrthm.2015.11.035
Wakabayashi A, Sankaran VG. Society for Pediatric Research 2015 Young Investigator Award: genetics of human hematopoiesis-what patients can teach us about blood cell production. Pediatr Res. 2016;79(3):366-70. doi:10.1038/pr.2015.245
Kevans D, Tyler AD, Holm K, et al. Characterization of Intestinal Microbiota in Ulcerative Colitis Patients with and without Primary Sclerosing Cholangitis. J Crohns Colitis. 2016;10(3):330-7. doi:10.1093/ecco-jcc/jjv204
Payton A, Dawes P, Platt H, et al. A role for HLA-DRB1*1101 and DRB1*0801 in cognitive ability and its decline with age. Am J Med Genet B Neuropsychiatr Genet. 2016;171B(2):209-14. doi:10.1002/ajmg.b.32393