Rahmioglu N, Macgregor S, Drong AW, et al. Genome-wide enrichment analysis between endometriosis and obesity-related traits reveals novel susceptibility loci. Hum Mol Genet. 2015;24(4):1185-99. doi:10.1093/hmg/ddu516
Dunn EC, Brown RC, Dai Y, et al. Genetic determinants of depression: recent findings and future directions. Harv Rev Psychiatry. 2015;23(1):1-18. doi:10.1097/HRP.0000000000000054
Galizia EC, Myers CT, Leu C, et al. CHD2 variants are a risk factor for photosensitivity in epilepsy. Brain. 2015;138(Pt 5):1198-207. doi:10.1093/brain/awv052
Pendergraft WF, Nachman PH. Recent pathogenetic advances in ANCA-associated vasculitis. Presse Med. 2015;44(6 Pt 2):e223-9. doi:10.1016/j.lpm.2015.04.007
Stachler MD, Taylor-Weiner A, Peng S, et al. Paired exome analysis of Barrett’s esophagus and adenocarcinoma. Nat Genet. 2015;47(9):1047-55. doi:10.1038/ng.3343
Yarwood A, Viatte S, Okada Y, et al. Loci associated with N-glycosylation of human IgG are not associated with rheumatoid arthritis: a Mendelian randomisation study. Ann Rheum Dis. 2016;75(1):317-20. doi:10.1136/annrheumdis-2014-207210
McLaren PJ, Coulonges C, Bartha I, et al. Polymorphisms of large effect explain the majority of the host genetic contribution to variation of HIV-1 virus load. Proc Natl Acad Sci U S A. 2015;112(47):14658-63. doi:10.1073/pnas.1514867112
Diamandis P, Ferrer-Luna R, Huang RY, et al. Case Report: Next generation sequencing identifies a NAB2-STAT6 fusion in Glioblastoma. Diagn Pathol. 2016;11:13. doi:10.1186/s13000-016-0455-9
Leu C, Balestrini S, Maher B, et al. Genome-wide Polygenic Burden of Rare Deleterious Variants in Sudden Unexpected Death in Epilepsy. EBioMedicine. 2015;2(9):1063-70. doi:10.1016/j.ebiom.2015.07.005
Rioux JD, Daly MJ, Green T, et al. Absence of linkage between inflammatory bowel disease and selected loci on chromosomes 3, 7, 12, and 16. Gastroenterology. 1998;115(5):1062-5.