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Results 2591-2600 of 2600 (Search time: 0.006 seconds).
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PreviewIssue DateTitleAuthor(s)
2017Lost in translation: returning germline genetic results in genome-scale cancer researchJohns, A.; McKay, S.; Humphris, J.; Pinese, M.; Chantrill, L.; Mead, R.; Tucker, K.; Andrews, L.; Goodwin, A.; Leonard, C.; High, H.; Nones, K.; Waddell, N.; Patch, A.; Merrett, N.; Pavlakis, N.; Kassahn, K.; Samra, J.; Miller, D.; Chang, D.; et al.
2014Genome-wide DNA methylation patterns in pancreatic ductal adenocarcinoma reveal epigenetic deregulation of SLIT-ROBO, ITGA2 and MET signalingNones, K.; Waddell, N.; Song, S.; Patch, A.; Miller, D.; Johns, A.; Wu, J.; Kassahn, K.; Wood, D.; Bailey, P.; Fink, L.; Manning, S.; Christ, A.; Nourse, C.; Kazakoff, S.; Taylor, D.; Leonard, C.; Chang, D.; Jones, M.; Thomas, M.; et al.
2012qpure: A tool to estimate tumor cellularity from genome-wide single-nucleotide polymorphism profilesSong, S.; Nones, K.; Miller, D.; Harliwong, I.; Kassahn, K.S.; Pinese, M.; Pajic, M.; Gill, A.J.; Johns, A.L.; Anderson, M.; Holmes, O.; Leonard, C.; Taylor, D.; Wood, S.; Xu, Q.; Newell, F.; Cowley, M.J.; Wu, J.; Wilson, P.; Fink, L.; et al.; Ting, A.H.
2013Clinical and molecular characterization of HER2 amplified-pancreatic cancerChou, A.; Waddell, N.; Cowley, M.; Gill, A.; Chang, D.; Patch, A.; Nones, K.; Wu, J.; Pinese, M.; Johns, A.; Miller, D.; Kassahn, K.; Nagrial, A.; Wasan, H.; Goldstein, D.; Toon, C.; Chin, V.; Chantrill, L.; Humphris, J.; Mead, R.; et al.
2015Whole-genome characterization of chemoresistant ovarian cancerPatch, A.; Christie, E.; Etemadmoghadam, D.; Garsed, D.; George, J.; Fereday, S.; Nones, K.; Cowin, P.; Alsop, K.; Bailey, P.; Kassahn, K.; Newell, F.; Quinn, M.; Kazakoff, S.; Quek, K.; Wilhelm-Benartzi, C.; Curry, E.; Leong, H.; Australian Ovarian Cancer Study Group,; Hamilton, A.; et al.
2013Somatic point mutation calling in low cellularity tumorsKassahn, K.; Holmes, O.; Nones, K.; Patch, A.; Miller, D.; Christ, A.; Harliwong, I.; Bruxner, T.; Xu, Q.; Anderson, M.; Wood, S.; Leonard, C.; Taylor, D.; Newell, F.; Song, S.; Idrisoglu, S.; Nourse, C.; Nourbakhsh, E.; Manning, S.; Wani, S.; et al.; Jordan, I.
2013Computational approaches to identify functional genetic variants in cancer genomesGonzalez-Perez, A.; Mustonen, V.; Reva, B.; Ritchie, G.; Creixell, P.; Karchin, R.; Vazquez, M.; Fink, J.; Kassahn, K.; Pearson, J.; Bader, G.; Boutros, P.; Muthuswamy, L.; Ouellette, B.; Reimand, J.; Linding, R.; Shibata, T.; Valencia, A.; Butler, A.; Dronov, S.; et al.
2019Searches for continuous gravitational waves from 15 supernova remnants and Fomalhaut b with Advanced LIGOAbbott, B.P.; Abbott, R.; Abbott, T.D.; Abraham, S.; Acernese, F.; Ackley, K.; Adams, C.; Adhikari, R.X.; Adya, V.B.; Affeldt, C.; Agathos, M.; Agatsuma, K.; Aggarwal, N.; Aguiar, O.D.; Aiello, L.; Ain, A.; Ajith, P.; Allen, G.; Allocca, A.; Aloy, M.A.; et al.
2019A new microdeletion syndrome involving TBC1D24, ATP6V0C, and PDPK1 causes epilepsy, microcephaly, and developmental delayMucha, B.E.; Banka, S.; Ajeawung, N.F.; Molidperee, S.; Chen, G.G.; Koenig, M.K.; Adejumo, R.B.; Till, M.; Harbord, M.; Perrier, R.; Lemyre, E.; Boucher, R.M.; Skotko, B.G.; Waxler, J.L.; Thomas, M.A.; Hodge, J.C.; Gecz, J.; Nicholl, J.; McGregor, L.; Linden, T.; et al.
2020Mutations disrupting neuritogenesis genes confer risk for cerebral palsyJin, S.C.; Lewis, S.A.; Bakhtiari, S.; Zeng, X.; Sierant, M.C.; Shetty, S.; Nordlie, S.M.; Elie, A.; Corbett, M.A.; Norton, B.Y.; van Eyk, C.L.; Haider, S.; Guida, B.S.; Magee, H.; Liu, J.; Pastore, S.; Vincent, J.B.; Brunstrom-Hernandez, J.; Papavasileiou, A.; Fahey, M.C.; et al.

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