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Preview	Issue Date	Title	Author(s)
	2015	Novel IL1RAPL1 mutations associated with intellectual disability impair synaptogenesis	Ramos-Brossier, M.; Montani, C.; Lebrun, N.; Gritti, L.; Martin, C.; Seminatore-Nole, C.; Toussaint, A.; Moreno, S.; Poirier, K.; Dorseuil, O.; Chelly, J.; Hackett, A.; Gecz, J.; Bieth, E.; Faudet, A.; Heron, D.; Kooy, R.; Loeys, B.; Humeau, Y.; Sala, C.; et al.
	2012	A genome-wide association search for type 2 diabetes genes in African Americans	Palmer, N.; McDonough, C.; Hicks, P.; Roh, B.; Wing, M.; Sandy An, S.; Hester, J.; Cooke, J.; Bostrom, M.; Rudock, M.; Talbert, M.; Lewis, J.; DIAGRAM Consortium,; MAGIC Consortium,; Ferrara, A.; Lu, L.; Ziegler, J.; Sale, M.; Divers, J.; Shriner, D.; et al.; Kronenberg, F.
	2016	A splicing-regulatory polymorphism in DRD2 disrupts ZRANB2 binding, impairs cognitive functioning and increases risk for schizophrenia in six Han Chinese samples	Cohen, O.; Weickert, T.; Hess, J.; Paish, L.; McCoy, S.; Rothmond, D.; Galletly, C.; Liu, D.; Weinberg, D.; Huang, X.; Xu, Q.; Shen, Y.; Zhang, D.; Yue, W.; Yan, J.; Wang, L.; Lu, T.; He, L.; Shi, Y.; Xu, M.; et al.
	2014	Novel approach identifies SNPs in SLC2A10 and KCNK9 with evidence for parent-of-origin effect on Body Mass Index	Hoggart, C.; Venturini, G.; Mangino, M.; Gomez, F.; Ascari, G.; Zhao, J.; Teumer, A.; Winkler, T.; Tšernikova, N.; Luan, J.; Mihailov, E.; Ehret, G.; Zhang, W.; Lamparter, D.; Esko, T.; Macé, A.; Rüeger, S.; Bochud, P.; Barcella, M.; Dauvilliers, Y.; et al.; Visscher, P.
	2015	The International SSRI Pharmacogenomics Consortium (ISPC): a genome-wide association study of antidepressant treatment response	Biernacka, J.; Sangkuhl, K.; Jenkins, G.; Whaley, R.; Barman, P.; Batzler, A.; Altman, R.; Arolt, V.; Brockmöller, J.; Chen, C.; Domschke, K.; Hall-Flavin, D.; Hong, C.; Illi, A.; Ji, Y.; Kampman, O.; Kinoshita, T.; Leinonen, E.; Liou, Y.; Mushiroda, T.; et al.
	2012	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women	Palmer, L.; Fox, C.S.; Liu, Y.; White, C.C.; Feitosa, M.; Smith, A.V.; Heard-Costa, N.; Lohman, K.; GIANT Consortium,; MAGIC Consortium,; GLGC Consortium,; Johnson, A.D.; Foster, M.C.; Greenawalt, D.M.; Griffin, P.; Ding, J.; Newman, A.B.; Tylavsky, F.; Miljkovic, I.; Kritchevsky, S.B.; et al.; Bray, M.
	2011	Association of genetic variation with systolic and diastolic blood pressure among African Americans: the Candidate Gene Association Resource Study	Fox, E.; Young, J.; Li, Y.; Dreisbach, A.; Keating, B.; Musani, S.; Liu, K.; Morrison, A.; Ganesh, S.; Kutlar, A.; Ramachandran, V.; Polak, J.; Fabsitz, R.; Dries, D.; Farlow, D.; Redline, S.; Adeyemo, A.; Hirschorn, J.; Sun, Y.; Wyatt, S.; et al.
	2011	Genome-wide association identifies nine common variants associated with fasting proinsulin levels and provides new insights into the pathophysiology of type 2 diabetes	Strawbridge, R.; Dupuis, J.; Prokopenko, I.; Barker, A.; Ahlqvist, E.; Rybin, D.; Petrie, J.; Travers, M.; Bouatia-Naji, N.; Dimas, A.; Nica, A.; Wheeler, E.; Chen, H.; Voight, B.; Taneera, J.; Kanoni, S.; Peden, J.; Turrini, F.; Gustafsson, S.; Zabena, C.; et al.
	2011	A genome-wide significant linkage for severe depression on chromosome 3: the depression network study	Breen, G.; Webb, B.; Butler, A.; van den Oord, E.; Tozzi, F.; Craddock, N.; Gill, M.; Korszun, A.; Maier, W.; Middleton, L.; Mors, O.; Owen, M.; Cohen-Woods, S.; Perry, J.; Galwey, N.; Upmanyu, R.; Craig, I.; Lewis, C.; Ng, M.; Brewster, S.; et al.
	2015	A genome-wide association study of susceptibility to acute lymphoblastic leukemia in adolescents and young adults	Perez-Andreu, V.; Roberts, K.; Xu, H.; Smith, C.; Zhang, H.; Yang, W.; Harvey, R.; Payne-Turner, D.; Devidas, M.; Cheng, I.; Carroll, W.; Heerema, N.; Carroll, A.; Raetz, E.; Gastier-Foster, J.; Marcucci, G.; Bloomfield, C.; Mrozek, K.; Kohlschmidt, J.; Stock, W.; et al.