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Results 1201-1210 of 3088 (Search time: 0.004 seconds).
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PreviewIssue DateTitleAuthor(s)
2012Using tumour pathology to identify people at high genetic risk of breast and colorectal cancersHopper, J.; Jenkins, M.; Dowty, J.; Dite, G.; Apicella, C.; Keogh, L.; Win, A.; Young, J.; Buchanan, D.; Walsh, M.; Rosty, C.; Baglietto, L.; Severi, G.; Phillips, K.; Wong, E.; Dobrovic, A.; Waring, P.; Winship, I.; Ramus, S.; Giles, G.; et al.
2011Genome-wide association analysis identifies variants associated with nonalcoholic fatty liver disease that have distinct effects on metabolic traitsSpeliotes, E.; Yerges-Armstrong, L.; Wu, J.; Hernaez, R.; Kim, L.; Palmer, C.; Gudnason, V.; Eiriksdottir, G.; Garcia, M.; Launer, L.; Nalls, M.; Clark, J.; Mitchell, B.; Shuldiner, A.; Butler, J.; Tomas, M.; Hoffmann, U.; Hwang, S.; Massaro, J.; O’Donnell, C.; et al.; McCarthy, M.I.
2014HLA-DQA1-HLA-DRB1 variants confer susceptibility to pancreatitis induced by thiopurine immunosuppressantsHeap, G.; Weedon, M.; Bewshea, C.; Singh, A.; Chen, M.; Satchwell, J.; Vivian, J.; So, K.; Dubois, P.; Andrews, J.; Annese, V.; Bampton, P.; Barnardo, M.; Bell, S.; Cole, A.; Connor, S.; Creed, T.; Cummings, F.; D'Amato, M.; Daneshmend, T.; et al.
2021Different types of disease-causing non-coding variants revealed by genomic and gene expression analyses in families with X-linked intellectual disabilityField, M.J.; Sharma, R.; Hackett, A.; Kayumi, S.; Shoubridge, C.; Ewans, L.J.; Ivancevic, A.M.; Dudding-Byth, T.; Carroll, R.; Kroes, T.; Gardner, A.E.; Sullivan, P.; Ha, T.T.; Schwartz, C.E.; Cowley, M.J.; Dinger, M.E.; Palmer, E.E.; Christie, L.; Shaw, M.; Roscioli, T.; et al.
2019Monte Carlo studies for the optimisation of the Cherenkov Telescope Array layoutAcharyya, A.; Agudo, I.; Angüner, E.O.; Alfaro, R.; Alfaro, J.; Alispach, C.; Aloisio, R.; Alves Batista, R.; Amans, J.P.; Amati, L.; Amato, E.; Ambrosi, G.; Antonelli, L.A.; Aramo, C.; Armstrong, T.; Arqueros, F.; Arrabito, L.; Asano, K.; Ashkar, H.; Balazs, C.; et al.
2018Maternal smoking during pregnancy and offspring overweight: is there a dose-response relationship? An individual patient data meta-analysisAlbers, L.; Sobotzki, C.; Kuß, O.; Ajslev, T.; Batista, R.; Bettiol, H.; Brabin, B.; Buka, S.; Cardoso, V.; Clifton, V.; Devereux, G.; Gilman, S.; Grzeskowiak, L.; Heinrich, J.; Hummel, S.; Jacobsen, G.; Jones, G.; Koshy, G.; Morgen, C.; Oken, E.; et al.
2017Search for photons with energies above 10¹⁸ eV using the hybrid detector of the Pierre Auger ObservatoryAab, A.; Abreu, P.; Aglietta, M.; Al Samarai, I.; Albuquerque, I.; Allekotte, I.; Almela, A.; Alvarez Castillo, J.; Alvarez-Muñiz, J.; Anastasi, G.; Anchordoqui, L.; Andrada, B.; Andringa, S.; Aramo, C.; Arqueros, F.; Arsene, N.; Asorey, H.; Assis, P.; Aublin, J.; Avila, G.; et al.
2017Association of delirium with cognitive decline in late life: a neuropathologic study of 3 population-based cohort studiesDavis, D.H.J.; Muniz-Terrera, G.; Keage, H.A.D.; Stephan, B.C.M.; Fleming, J.; Ince, P.G.; Matthews, F.E.; Cunningham, C.; Ely, E.W.; MacLullich, A.M.J.; Brayne, C.; McKeith, I.; Polvikoski, T.; Sulkava, R.; Hardy, J.; Melzer, D.; Myllykangas, L.; Nicoll, J.; Singleton, A.; Tienari, P.; et al.
2015Novel IL1RAPL1 mutations associated with intellectual disability impair synaptogenesisRamos-Brossier, M.; Montani, C.; Lebrun, N.; Gritti, L.; Martin, C.; Seminatore-Nole, C.; Toussaint, A.; Moreno, S.; Poirier, K.; Dorseuil, O.; Chelly, J.; Hackett, A.; Gecz, J.; Bieth, E.; Faudet, A.; Heron, D.; Kooy, R.; Loeys, B.; Humeau, Y.; Sala, C.; 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.

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