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Results 61-70 of 308 (Search time: 0.003 seconds).
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PreviewIssue DateTitleAuthor(s)
2013The Val158Met COMT polymorphism is a modifier of the age at onset in Parkinson's disease with a sexual dimorphismKlebe, S.; Golmard, J.-L.; Nalls, M.A.; Saad, M.; Singleton, A.B.; Bras, J.M.; Hardy, J.; Simon-Sanchez, J.; Heutink, P.; Kuhlenbaeumer, G.; Charfi, R.; Klein, C.; Hagenah, J.; Gasser, T.; Wurster, I.; Lesage, S.; Lorenz, D.; Deuschl, G.; Durif, F.; Pollak, P.; et al.
2018Plasmacytoid dendritic cells protect from viral bronchiolitis and asthma through semaphorin 4a-mediated T reg expansionLynch, J.; Werder, R.; Loh, Z.; Sikder, M.; Curren, B.; Zhang, V.; Rogers, M.; Lane, K.; Simpson, J.; Mazzone, S.; Spann, K.; Hayball, J.; Diener, K.; Everard, M.; Blyth, C.; Forstner, C.; Dennis, P.; Murtaza, N.; Morrison, M.; Cuív, P.; et al.
2020An investigation of antihypertensive class, dementia, and cognitive declinePeters, R.; Yasar, S.; Anderson, C.S.; Andrews, S.; Antikainen, R.; Arima, H.; Beckett, N.; Beer, J.C.; Bertens, A.S.; Booth, A.; van Boxtel, M.; Brayne, C.; Brodaty, H.; Carlson, M.C.; Chalmers, J.; Corrada, M.; DeKosky, S.; Derby, C.; Dixon, R.A.; Forette, F.; et al.
2020Genome sequencing in persistently unsolved white matter disordersHelman, G.; Lajoie, B.R.; Crawford, J.; Takanohashi, A.; Walkiewicz, M.; Dolzhenko, E.; Gross, A.M.; Gainullin, V.G.; Bent, S.J.; Jenkinson, E.M.; Ferdinandusse, S.; Waterham, H.R.; Dorboz, I.; Bertini, E.; Miyake, N.; Wolf, N.I.; Abbink, T.E.M.; Kirwin, S.M.; Tan, C.M.; Hobson, G.M.; et al.
2019Epidemiology of childhood death in Australian and New Zealand intensive care unitsMoynihan, K.M.; Alexander, P.M.A.; Schlapbach, L.J.; Millar, J.; Jacobe, S.; Ravindranathan, H.; Croston, E.J.; Staffa, S.J.; Burns, J.P.; Gelbart, B.; Erickson, S.; Barr, S.; Schlapbach, L.; Schibler, A.; Long, D.; Alexander, J.; Ganeshalingam, A.; Sherring, C.; Williams, G.; Smith, V.; et al.
2019Alternative splicing in a presenilin 2 variant associated with Alzheimer diseaseBraggin, J.E.; Bucks, S.A.; Course, M.M.; Smith, C.L.; Sopher, B.; Osnis, L.; Shuey, K.D.; Domoto-Reilly, K.; Caso, C.; Kinoshita, C.; Scherpelz, K.P.; Cross, C.; Grabowski, T.; Nik, S.H.M.; Newman, M.; Garden, G.A.; Leverenz, J.B.; Tsuang, D.; Latimer, C.; Gonzalez-Cuyar, L.F.; et al.
2020Genome-wide gene-environment analyses of major depressive disorder and reported lifetime traumatic experiences in UK BiobankColeman, J.R.I.; Peyrot, W.J.; Purves, K.L.; Davis, K.A.S.; Rayner, C.; Choi, S.W.; Hübel, C.; Gaspar, H.A.; Kan, C.; Van der Auwera, S.; Adams, M.J.; Lyall, D.M.; Choi, K.W.; Wray, N.R.; Ripke, S.; Mattheisen, M.; Trzaskowski, M.; Byrne, E.M.; Abdellaoui, A.; Adams, M.J.; et al.
2020Genetic history from the Middle Neolithic to present on the Mediterranean island of SardiniaMarcus, J.H.; Posth, C.; Ringbauer, H.; Lai, L.; Skeates, R.; Sidore, C.; Beckett, J.; Furtwängler, A.; Olivieri, A.; Chiang, C.W.K.; Al-Asadi, H.; Dey, K.; Joseph, T.A.; Liu, C.-C.; Der Sarkissian, C.; Radzevičiūtė, R.; Michel, M.; Gradoli, M.G.; Marongiu, P.; Rubino, S.; et al.
2020An intraocular pressure polygenic risk score stratifies multiple primary open-angle glaucoma parameters including treatment intensityQassim, A.; Souzeau, E.; Siggs, O.M.; Hassall, M.M.; Han, X.; Griffiths, H.L.; Frost, N.A.; Vallabh, N.A.; Kirwan, J.F.; Menon, G.; Cree, A.J.; Galanopoulos, A.; Agar, A.; Healey, P.R.; Graham, S.L.; Landers, J.; Casson, R.J.; Gharahkhani, P.; Willoughby, C.E.; Hewitt, A.W.; et al.
2020Evaluation of implementation of risk management guidelines for carriers of pathogenic variants in mismatch repair genes: a nationwide audit of familial cancer clinicsMeiser, B.; Kaur, R.; Kirk, J.; Morrow, A.; Peate, M.; Wong, W.K.T.; McPike, E.; Cops, E.; Dowson, C.; Austin, R.; Fine, M.; Thrupp, L.; Ward, R.; Macrae, F.; Hiller, J.E.; Trainer, A.H.; Mitchell, G.; Susman, R.; Pachter, N.; Goodwin, A.; et al.

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