Lal D, Reinthaler EM, Dejanovic B, et al. Evaluation of Presumably Disease Causing SCN1A Variants in a Cohort of Common Epilepsy Syndromes. PLoS One. 2016;11(3):e0150426. doi:10.1371/journal.pone.0150426
Daly MJ, Pearce AV, Farwell L, et al. Association of DLG5 R30Q variant with inflammatory bowel disease. Eur J Hum Genet. 2005;13(7):835-9. doi:10.1038/sj.ejhg.5201403
Zaitlen N, Lindström S, Pasaniuc B, et al. Informed conditioning on clinical covariates increases power in case-control association studies. PLoS Genet. 2012;8(11):e1003032. doi:10.1371/journal.pgen.1003032
Lemaitre RN, Johnson CO, Hesselson S, et al. Common variation in fatty acid metabolic genes and risk of incident sudden cardiac arrest. Heart Rhythm. 2014;11(3):471-7. doi:10.1016/j.hrthm.2014.01.008
Georgieva L, Rees E, Moran JL, et al. De novo CNVs in bipolar affective disorder and schizophrenia. Hum Mol Genet. 2014;23(24):6677-83. doi:10.1093/hmg/ddu379
Betz RC, Petukhova L, Ripke S, et al. Genome-wide meta-analysis in alopecia areata resolves HLA associations and reveals two new susceptibility loci. Nat Commun. 2015;6:5966. doi:10.1038/ncomms6966
Pocklington AJ, Rees E, Walters JTR, et al. Novel Findings from CNVs Implicate Inhibitory and Excitatory Signaling Complexes in Schizophrenia. Neuron. 2015;86(5):1203-14. doi:10.1016/j.neuron.2015.04.022
Yu Y, Yao R, Wang L, et al. De novo mutations in ARID1B associated with both syndromic and non-syndromic short stature. BMC Genomics. 2015;16:701. doi:10.1186/s12864-015-1898-1
Lu HF, Hung KS, Hsu YW, et al. Association Study between the FTCDNL1 (FONG) and Susceptibility to Osteoporosis. PLoS One. 2015;10(10):e0140549. doi:10.1371/journal.pone.0140549
Smith G, Melander O, Lövkvist H, et al. Common genetic variants on chromosome 9p21 confers risk of ischemic stroke: a large-scale genetic association study. Circ Cardiovasc Genet. 2009;2(2):159-64. doi:10.1161/CIRCGENETICS.108.835173