Trynka G, Sandor C, Han B, et al. Chromatin marks identify critical cell types for fine mapping complex trait variants. Nat Genet. 2013;45(2):124-30. doi:10.1038/ng.2504
Choudhury AD, Eeles R, Freedland SJ, et al. The role of genetic markers in the management of prostate cancer. Eur Urol. 2012;62(4):577-87. doi:10.1016/j.eururo.2012.05.054
Smith JG, Almgren P, Engström G, et al. Genetic polymorphisms for estimating risk of atrial fibrillation: a literature-based meta-analysis. J Intern Med. 2012;272(6):573-82. doi:10.1111/j.1365-2796.2012.02563.x
Bergen SE, Petryshen TL. Genome-wide association studies of schizophrenia: does bigger lead to better results? Curr Opin Psychiatry. 2012;25(2):76-82. doi:10.1097/YCO.0b013e32835035dd
Baxt LA, Xavier RJ. Role of Autophagy in the Maintenance of Intestinal Homeostasis. Gastroenterology. 2015;149(3):553-62. doi:10.1053/j.gastro.2015.06.046
Patterson N, Hattangadi N, Lane B, et al. Methods for high-density admixture mapping of disease genes. Am J Hum Genet. 2004;74(5):979-1000. doi:10.1086/420871
Sawcer SJ, Maranian M, Singlehurst S, et al. Enhancing linkage analysis of complex disorders: an evaluation of high-density genotyping. Hum Mol Genet. 2004;13(17):1943-9. doi:10.1093/hmg/ddh202
Altshuler D, Clark AG. Genetics. Harvesting medical information from the human family tree. Science. 2005;307(5712):1052-3. doi:10.1126/science.1109682
Sawcer S, Ban M, Maranian M, et al. A high-density screen for linkage in multiple sclerosis. Am J Hum Genet. 2005;77(3):454-67. doi:10.1086/444547
Scolnick EM, Petryshen T, Sklar P. Schizophrenia: do the genetics and neurobiology of neuregulin provide a pathogenesis model? Harv Rev Psychiatry. 2006;14(2):64-77. doi:10.1080/10673220600642960