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Preview	Issue Date	Title	Author(s)
	2014	Inactivating mutations in NPC1L1 and protection from coronary heart disease	Stitziel, N.O.; Won, H.H.; Morrison, A.C.; Peloso, G.M.; Do, R.; Lange, L.A.; Fontanillas, P.; Gupta, N.; Duga, S.; Goel, A.; Farrall, M.; Saleheen, D.; Ferrario, P.; König, I.; Asselta, R.; Merlini, P.A.; Marziliano, N.; Notarangelo, M.F.; Schick, U.; Auer, P.; et al.
	2014	MicroRNA related polymorphisms and breast cancer risk	Khan, S.; Greco, D.; Michailidou, K.; Milne, R.; Muranen, T.; Heikkinen, T.; Aaltonen, K.; Dennis, J.; Bolla, M.; Liu, J.; Hall, P.; Irwanto, A.; Humphreys, K.; Li, J.; Czene, K.; Chang-Claude, J.; Hein, R.; Rudolph, A.; Seibold, P.; Flesch-Janys, D.; et al.; Zhao, Z.
	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.
	2015	Fine-mapping of the HNF1B multicancer locus identifies candidate variants that mediate endometrial cancer risk	Painter, J.; O'Mara, T.; Batra, J.; Cheng, T.; Lose, F.; Dennis, J.; Michailidou, K.; Tyrer, J.; Ahmed, S.; Ferguson, K.; Healey, C.; Kaufmann, S.; Hillman, K.; Walpole, C.; Moya, L.; Pollock, P.; Jones, A.; Howarth, K.; Martin, L.; Gorman, M.; et al.
	2016	The obesity associated FTO gene variant and the risk of adverse pregnancy outcomes: evidence from the SCOPE study	Andraweera, P.; Dekker, G.; Leemaqz, S.; McCowan, L.; Roberts, C.
	2011	Association of vascular endothelial growth factor +936 C/T single-nucleotide polymorphism with pregnancies complicated by small-for-gestational-age babies	Andraweera, P.; Dekker, G.; Thompson, S.; Nowak, R.; Zhang, V.; McCowan, L.; North, R.; Roberts, C.
	2012	Dissecting the genetic heterogeneity of depression through age at onset	Power, R.; Cohen-Woods, S.
	2010	Association analysis of DAOA and DAO in bipolar disorder: results from two independent case-control studies	Gaysina, D.; Cohen-Woods, S.; Chow, P.; Martucci, L.; Schosser, A.; Ball, H.; Tozzi, F.; Perry, J.; Muglia, P.; Kennedy, J.; King, N.; Vincent, J.; Parikh, S.; Strauss, J.; Craig, I.; McGuffin, P.; Farmer, A.
	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.
	2012	The interaction between the maternal BMI and angiogenic gene polymorphisms associates with the risk of spontaneous preterm birth	Andraweera, P.; Dekker, G.; Thompson, S.; North, R.; McCowan, L.; Roberts, C.