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Results 1-10 of 99 (Search time: 0.002 seconds).
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PreviewIssue DateTitleAuthor(s)
2015Fine mapping of type 1 diabetes susceptibility loci and evidence for colocalization of causal variants with lymphoid gene enhancersOnengut-Gumuscu, S.; Chen, W.-M.; Burren, O.; Cooper, N.J.; Quinlan, A.R.; Mychaleckyj, J.C.; Farber, E.; Bonnie, J.K.; Szpak, M.; Schofield, E.; Achuthan, P.; Guo, H.; Fortune, M.D.; Stevens, H.; Walker, N.M.; Ward, L.D.; Kundaje, A.; Kellis, M.; Daly, M.J.; Barrett, J.C.; et al.
2015Exome sequencing identifies rare LDLR and APOA5 alleles conferring risk for myocardial infarctionDo, R.; Stitziel, N.O.; Won, H.H.; Jørgensen, A.B.; Duga, S.; Merlini, P.A.; Kiezun, A.; Farrall, M.; Goel, A.; Zuk, O.; Guella, I.; Asselta, R.; Lange, L.A.; Peloso, G.M.; Auer, P.L.; Girelli, D.; Martinelli, N.; Farlow, D.N.; DePristo, M.A.; Roberts, R.; et al.
2015Essential versus accessory aspects of cell death: recommendations of the NCCD 2015Galluzzi, L.; Bravo-San Pedro, J.; Vitale, I.; Aaronson, S.; Abrams, J.; Adam, D.; Alnemri, E.; Altucci, L.; Andrews, D.; Annicchiarico-Petruzzelli, M.; Baehrecke, E.; Bazan, N.; Bertrand, M.; Bianchi, K.; Blagosklonny, M.; Blomgren, K.; Borner, C.; Bredesen, D.; Brenner, C.; Campanella, M.; et al.
2015Multimodal imaging of a tescalcin (TESC)-regulating polymorphism (rs7294919)-specific effects on hippocampal gray matter structureDannlowski, U.; Grabe, H.; Wittfeld, K.; Klaus, J.; Konrad, C.; Grotegerd, D.; Redlich, R.; Suslow, T.; Opel, N.; Ohrmann, P.; Bauer, J.; Zwanzger, P.; Laeger, I.; Hohoff, C.; Arolt, V.; Heindel, W.; Deppe, M.; Domschke, K.; Hegenscheid, K.; Völzke, H.; et al.
2015Fine-mapping of the HNF1B multicancer locus identifies candidate variants that mediate endometrial cancer riskPainter, 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.
2015Randomized comparison of nifedipine and placebo in fibronectin-negative women with symptoms of preterm labor and a short cervix (APOSTEL-I Trial)Vis, J.; Van Baaren, G.; Wilms, F.; Oudijk, M.; Kwee, A.; Porath, M.; Scheepers, H.; Spaanderman, M.; Bloemenkamp, K.; Van Lith, J.; Bolte, A.; Bax, C.; Cornette, J.; Duvekot, J.; Nij Bijvank, S.; Van Eyck, J.; Franssen, M.; Sollie, K.; Woiski, M.; Vandenbussche, F.; et al.
2015COMMD1 is linked to the WASH complex and regulates endosomal trafficking of the copper transporter ATP7APhillips-Krawczak, C.; Singla, A.; Starokadomskyy, P.; Deng, Z.; Osborne, D.; Li, H.; Dick, C.; Gomez, T.; Koenecke, M.; Zhang, J.; Dai, H.; Sifuentes-Dominguez, L.; Geng, L.; Kaufmann, S.; Hein, M.; Wallis, M.; McGaughran, J.; Gecz, J.; Van De Sluis, B.; Billadeau, D.; et al.; Gruenberg, J.E.
2015Role of tumour molecular and pathology features to estimate colorectal cancer risk for first-degree relativesWin, 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.
2015Genome-wide association study for sight-threatening diabetic retinopathy reveals association with genetic variation near the GRB2 geneBurdon, K.; Fogarty, R.; Shen, W.; Abhary, S.; Kaidonis, G.; Appukuttan, B.; Hewitt, A.; Sharma, S.; Daniell, M.; Essex, R.; Chang, J.; Klebe, S.; Lake, S.; Pal, B.; Jenkins, A.; Govindarjan, G.; Sundaresan, P.; Lamoureux, E.; Ramasamy, K.; Pefkianaki, M.; et al.
2015Agreement between routine and research measurement of infant height and weightBryant, M.; Santorelli, G.; Fairley, L.; Petherick, E.; Bhopal, R.; Lawlor, D.; Tilling, K.; Howe, L.; Farrar, D.; Cameron, N.; Mohammed, M.; Wright, J.; Born in Bradford Childhood Obesity Scientific Group,; Farrin, A.; Ball, H.; Summerbell, C.; Barber, S.; Hill, A.; Small, N.; Raynor, P.; et al.

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