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Preview	Issue Date	Title	Author(s)
	2014	Common variants near ABCA1, AFAP1 and GMDS confer risk of primary open-angle glaucoma	Gharahkhani, P.; Burdon, K.; Fogarty, R.; Sharma, S.; Hewitt, A.; Martin, S.; Law, M.; Cremin, K.; Bailey, J.; Loomis, S.; Pasquale, L.; Haines, J.; Hauser, M.; Viswanathan, A.; McGuffin, P.; Topouzis, F.; Foster, P.; Graham, S.; Casson, R.; Chehade, M.; 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.
	2016	Novel germ line DDX41 mutations define families with a lower age of MDS/AML onset and lymphoid malignancies	Lewinsohn, M.; Brown, A.L.; Weinel, L.M.; Phung, C.; Rafidi, G.; Lee, M.K.; Schreiber, A.W.; Feng, J.; Babic, M.; Chong, C.E.; Lee, Y.; Yong, A.; Suthers, G.K.; Poplawski, N.; Altree, M.; Phillips, K.; Jaensch, L.; Fine, M.; D'Andrea, R.J.; Lewis, I.D.; 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.
	2010	Variants in ADCY5 and near CCNL1 are associated with fetal growth and birth weight	Freathy, R.; Mook-Kanamori, D.; Sovio, U.; Prokopenko, I.; Timpson, N.; Berry, D.; Warrington, N.; Widen, E.; Jan Hottenga, J.; Kaakinen, M.; Lange, L.; Bradfield, J.; Kerkhof, M.; Marsh, J.; Mägi, R.; Chen, C.-M.; Lyon, H.; Kirin, M.; Adair, L.; Aulchenko, Y.; 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.
	2013	Mutations in DEPDC5 cause familial focal epilepsy with variable foci	Dibbens, L.; de Vries, B.; Donatello, S.; Heron, S.; Hodgson, B.; Chintawar, S.; Crompton, D.; Hughes, J.; Bellows, S.; Klein, K.; Callenbach, P.; Corbett, M.; Gardner, A.; Kivity, S.; Iona, X.; Regan, B.; Weller, C.; Crimmins, D.; O'Brien, T.; Guerrero-Lopez, R.; et al.
	2011	Progesterone receptor gene variants and risk of endometrial cancer	O'Mara, T.; Fahey, P.; Ferguson, K.; Marquart, L.; Lambrechts, D.; Despierre, E.; Vergote, I.; Amant, F.; Hall, P.; Liu, J.; Czene, K.; SASBAC,; Rebbeck, T.; WISE Study Group,; AOCS Management Group,; SEARCH,; Ahmed, S.; Dunning, A.; Gregory, C.; Shah, M.; et al.