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Preview	Issue Date	Title	Author(s)
	2016	TBC1D24 genotype-phenotype correlation	Balestrini, S.; Milh, M.; Castiglioni, C.; Lüthy, K.; Finelli, M.; Verstreken, P.; Cardon, A.; Stražišar, B.; Holder, J.; Lesca, G.; Mancardi, M.; Poulat, A.; Repetto, G.; Banka, S.; Bilo, L.; Birkeland, L.; Bosch, F.; Brockmann, K.; Cross, J.; Doummar, D.; et al.
	2023	Machine learning to predict poor school performance in paediatric survivors of intensive care: a population-based cohort study	Gilholm, P.; Gibbons, K.; Brüningk, S.; Klatt, J.; Vaithianathan, R.; Long, D.; Millar, J.; Tomaszewski, W.; Schlapbach, L.J.; Ganeshalingam, A.; Sherring, C.; Erickson, S.; Barr, S.; Raman, S.; Long, D.; Schlapbach, L.; Gibbons, K.; George, S.; Singh, P.; Smith, V.; et al.
	2020	Androgens In Men Study (AIMS): protocol for meta-analyses of individual participant data investigating associations of androgens with health outcomes in men	Yeap, B.B.; Marriott, R.J.; Adams, R.J.; Antonio, L.; Ballantyne, C.M.; Bhasin, S.; Cawthon, P.M.; Couper, D.J.; Dobs, A.S.; Flicker, L.; Karlsson, M.; Martin, S.A.; Matsumoto, A.M.; Mellström, D.; Norman, P.E.; Ohlsson, C.; Orwoll, E.S.; O'Neill, T.W.; Shores, M.M.; Travison, T.G.; et al.
	2017	Relations between lipoprotein(a) concentrations, LPA genetic variants, and the risk of mortality in patients with established coronary heart disease: a molecular and genetic association study	Zewinger, S.; Kleber, M.E.; Tragante, V.; McCubrey, R.O.; Schmidt, A.F.; Direk, K.; Laufs, U.; Werner, C.; Koenig, W.; Rothenbacher, D.; Mons, U.; Breitling, L.P.; Brenner, H.; Jennings, R.T.; Petrakis, I.; Triem, S.; Klug, M.; Filips, A.; Blankenberg, S.; Waldeyer, C.; et al.
	2021	Clonal evolution and clinical implications of genetic abnormalities in blastic transformation of chronic myeloid leukaemia	Ochi, Y.; Yoshida, K.; Huang, Y.-J.; Kuo, M.-C.; Nannya, Y.; Sasaki, K.; Mitani, K.; Hosoya, N.; Hiramoto, N.; Ishikawa, T.; Branford, S.; Shanmuganathan, N.; Ohyashiki, K.; Takahashi, N.; Takaku, T.; Tsuchiya, S.; Kanemura, N.; Nakamura, N.; Ueda, Y.; Yoshihara, S.; et al.
	2018	Investigating the genetic architecture of dementia with Lewy bodies: a two-stage genome-wide association study	Guerreiro, R.; Ross, O.A.; Kun-Rodrigues, C.; Hernandez, D.G.; Orme, T.; Eicher, J.D.; Shepherd, C.E.; Parkkinen, L.; Darwent, L.; Heckman, M.G.; Scholz, S.W.; Troncoso, J.C.; Pletnikova, O.; Ansorge, O.; Clarimon, J.; Lleo, A.; Morenas-Rodriguez, E.; Clark, L.; Honig, L.S.; Marder, K.; et al.
	2016	A genome-wide association study in multiple system atrophy	Sailer, A.; Scholz, S.W.; Nalls, M.A.; Schulte, C.; Federoff, M.; Price, T.R.; Lees, A.; Ross, O.A.; Dickson, D.W.; Mok, K.; Mencacci, N.E.; Schottlaender, L.; Chelban, V.; Ling, H.; O'Sullivan, S.S.; Wood, N.W.; Traynor, B.J.; Ferrucci, L.; Federoff, H.J.; Mhyre, T.R.; et al.
	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.
	2015	Role of tumour molecular and pathology features to estimate colorectal cancer risk for first-degree relatives	Win, A.; Buchanan, D.; Rosty, C.; MacInnis, R.; Dowty, J.; Dite, G.; Giles, G.; Southey, M.; Young, J.; Clendenning, M.; Walsh, M.; Walters, R.; Boussioutas, A.; Smyrk, T.; Thibodeau, S.; Baron, J.; Potter, J.; Newcomb, P.; Le Marchand, L.; Haile, R.; et al.
	2013	Gene-centric meta-analyses of 108 912 individuals confirm known body mass index loci and reveal three novel signals	Guo, Y.; Lanktree, M.; Taylor, K.; Hakonarson, H.; Lange, L.; Keating, B.; Guo, Y.; Taylor, K.; Fairfax, B.; Elbers, C.; Barnard, J.; Farrall, M.; Padmanabhan, S.; Baumert, J.; Castillo, B.; Gaunt, T.; Gong, Y.; Rajagopalan, R.; Romaine, S.; Kumari, M.; et al.