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Results 61-70 of 275 (Search time: 0.002 seconds).
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PreviewIssue DateTitleAuthor(s)
2015A recurrent de novo mutation in KCNC1 causes progressive myoclonus epilepsyMuona, M.; Berkovic, S.; Dibbens, L.; Oliver, K.; Maljevic, S.; Bayly, M.; Joensuu, T.; Canafoglia, L.; Franceschetti, S.; Michelucci, R.; Markkinen, S.; Heron, S.; Hildebrand, M.; Andermann, E.; Andermann, F.; Gambardella, A.; Tinuper, P.; Licchetta, L.; Scheffer, I.; Criscuolo, C.; 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.
2015Cova del Rinoceront (Castelldefels, Barcelona): a terrestrial record for the Last Interglacial period (MIS 5) in the Mediterranean coast of the Iberian PeninsulaDaura, J.; Sanz, M.; Julià, R.; García-Fernández, D.; Fornós, J.J.; Vaquero, M.; Allué, E.; López-García, J.M.; Blain, H.A.; Ortiz, J.E.; Torres, T.; Albert, R.M.; Rodríguez-Cintas, À.; Sánchez-Marco, A.; Cerdeño, E.; Skinner, A.R.; Asmeron, Y.; Polyak, V.J.; Garcés, M.; Arnold, L.J.; et al.
2015Integrated genomic and transcriptomic analysis of human brain metastases identifies alterations of potential clinical significanceSaunus, J.; Quinn, M.; Patch, A.; Pearson, J.; Bailey, P.; Nones, K.; McCart Reed, A.; Miller, D.; Wilson, P.; Al-Ejeh, F.; Mariasegaram, M.; Lau, Q.; Withers, T.; Jeffree, R.; Reid, L.; Da Silva, L.; Matsika, A.; Niland, C.; Cummings, M.; Bruxner, T.; 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.
2015Increased STAG2 dosage defines a novel cohesinopathy with intellectual disability and behavioral problemsKumar, R.; Corbett, M.; Van Bon, B.; Gardner, A.; Woenig, J.; Jolly, L.; Douglas, E.; Friend, K.; Tan, C.; Van Esch, H.; Holvoet, M.; Raynaud, M.; Field, M.; Leffler, M.; Budny, B.; Wisniewska, M.; Badura-Stronka, M.; Latos-Bieleńska, A.; Batanian, J.; Rosenfeld, J.; 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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