Fraser HB, Xie X. Common polymorphic transcript variation in human disease. Genome Res. 2009;19(4):567-75. doi:10.1101/gr.083477.108
Brockman W, Alvarez P, Young S, et al. Quality scores and SNP detection in sequencing-by-synthesis systems. Genome Res. 2008;18(5):763-70. doi:10.1101/gr.070227.107
Dutt A, Beroukhim R. Single nucleotide polymorphism array analysis of cancer. Curr Opin Oncol. 2007;19(1):43-9. doi:10.1097/CCO.0b013e328011a8c1
Altshuler D, Clark AG. Genetics. Harvesting medical information from the human family tree. Science. 2005;307(5712):1052-3. doi:10.1126/science.1109682
Mather KJ, Christophi CA, Jablonski KA, et al. Common variants in genes encoding adiponectin (ADIPOQ) and its receptors (ADIPOR1/2), adiponectin concentrations, and diabetes incidence in the Diabetes Prevention Program. Diabet Med. 2012;29(12):1579-88. doi:10.1111/j.1464-5491.2012.03662.x
Rueckert EH, Barker D, Ruderfer D, et al. Cis-acting regulation of brain-specific ANK3 gene expression by a genetic variant associated with bipolar disorder. Mol Psychiatry. 2013;18(8):922-9. doi:10.1038/mp.2012.104
de Miguel-Yanes JM, Porneala B, Pencina MJ, et al. Lack of interaction of beta-cell-function-associated variants with hypertension on change in fasting glucose and diabetes risk: the Framingham Offspring Study. J Hypertens. 2013;31(5):1001-9. doi:10.1097/HJH.0b013e32835f5a83
Patsopoulos NA, Barcellos LF, Hintzen RQ, et al. Fine-mapping the genetic association of the major histocompatibility complex in multiple sclerosis: HLA and non-HLA effects. PLoS Genet. 2013;9(11):e1003926. doi:10.1371/journal.pgen.1003926
Fowler SA, Ananthakrishnan AN, Gardet A, et al. SMAD3 gene variant is a risk factor for recurrent surgery in patients with Crohn’s disease. J Crohns Colitis. 2014;8(8):845-51. doi:10.1016/j.crohns.2014.01.003
Lee MN, Ye C, Villani AC, et al. Common genetic variants modulate pathogen-sensing responses in human dendritic cells. Science. 2014;343(6175):1246980. doi:10.1126/science.1246980