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Preview	Issue Date	Title	Author(s)
	2018	A global cline in a colour polymorphism suggests a limited contribution of gene flow towards the recovery of a heavily exploited marine mammal	Hoffman, J.I.; Bauer, E.; Paijmans, A.J.; Humble, E.; Beckmann, L.M.; Kubetschek, C.; Christaller, F.; Kröcker, N.; Fuchs, B.; Moreras, A.; Shihlomule, Y.D.; Bester, M.N.; Cleary, A.C.; De Bruyn, P.J.N.; Forcada, J.; Goebel, M.E.; Goldsworthy, S.D.; Guinet, C.; Hoelzel, A.R.; Lydersen, C.; et al.
	2017	YY1 haploinsufficiency causes an intellectual disability syndrome featuring transcriptional and chromatin dysfunction	Gabriele, M.; Vulto-van Silfhout, A.; Germain, P.; Vitriolo, A.; Kumar, R.; Douglas, E.; Haan, E.; Kosaki, K.; Takenouchi, T.; Rauch, A.; Steindl, K.; Frengen, E.; Misceo, D.; Pedurupillay, C.; Stromme, P.; Rosenfeld, J.; Shao, Y.; Craigen, W.; Schaaf, C.; Rodriguez-Buritica, D.; et al.
	2017	Hotspots of missense mutation identify neurodevelopmental disorder genes and functional domains	Geisheker, M.; Heymann, G.; Wang, T.; Coe, B.; Turner, T.; Stessman, H.; Hoekzema, K.; Kvarnung, M.; Shaw, M.; Friend, K.; Liebelt, J.; Barnett, C.; Thompson, E.; Haan, E.; Guo, H.; Anderlid, B.; Nordgren, A.; Lindstrand, A.; Vandeweyer, G.; Alberti, A.; et al.
	2011	Abdominal aortic aneurysm is associated with a variant in low-density lipoprotein receptor-related protein 1	Bown, M.J.; Jones, G.T.; Harrison, S.C.; Wright, B.J.; Bumpstead, S.; Baas, A.F.; Gretarsdottir, S.; Badger, S.A.; Bradley, D.T.; Burnand, K.; Child, A.H.; Clough, R.E.; Cockerill, G.; Hafez, H.; Scott, D.J.A.; Futers, S.; Johnson, A.; Sohrabi, S.; Smith, A.; Thompson, M.M.; et al.
	2019	Quantifying between-cohort and between-sex genetic heterogeneity in major depressive disorder	Trzaskowski, M.; Mehta, D.; Peyrot, W.J.; Hawkes, D.; Davies, D.; Howard, D.M.; Kemper, K.E.; Sidorenko, J.; Maier, R.; Ripke, S.; Mattheisen, M.; Baune, B.T.; Grabe, H.J.; Heath, A.C.; Jones, L.; Jones, I.; Madden, P.A.F.; McIntosh, A.M.; Breen, G.; Lewis, C.M.; et al.
	2017	Discovery and functional prioritization of Parkinson's disease candidate genes from large-scale whole exome sequencing	Jansen, I.E.; Ye, H.; Heetveld, S.; Lechler, M.C.; Michels, H.; Seinstra, R.I.; Lubbe, S.J.; Drouet, V.; Lesage, S.; Majounie, E.; Gibbs, J.R.; Nalls, M.A.; Ryten, M.; Botia, J.A.; Vandrovcova, J.; Simon-Sanchez, J.; Castillo-Lizardo, M.; Rizzu, P.; Blauwendraat, C.; Chouhan, A.K.; et al.
	2018	Genome-wide gene-environment interaction in depression: a systematic evaluation of candidate genes: the childhood trauma working-group of PGC-MDD	Van der Auwera, S.; Peyrot, W.; Milaneschi, Y.; Hertel, J.; Baune, B.; Breen, G.; Byrne, E.; Dunn, E.; Fisher, H.; Homuth, G.; Levinson, D.; Lewis, C.; Mills, N.; Mullins, N.; Nauck, M.; Pistis, G.; Preisig, M.; Rietschel, M.; Ripke, S.; Sullivan, P.; et al.
	2018	Developing reproducible bioinformatics analysis workflows for heterogeneous computing environments to support African genomics	Baichoo, S.; Souilmi, Y.; Panji, S.; Botha, G.; Meintjes, A.; Hazelhurst, S.; Bendou, H.; de Beste, E.; Mpangase, P.; Souiai, O.; Alghali, M.; Yi, L.; O'Connor, B.; Crusoe, M.; Armstrong, D.; Aron, S.; Joubert, F.; Ahmed, A.; Mbiyavanga, M.; van Heusden, P.; et al.
	2014	Genetic analysis implicates APOE, SNCA and suggests lysosomal dysfunction in the etiology of dementia with Lewy bodies	Bras, J.; Guerreiro, R.; Darwent, L.; Parkkinen, L.; Ansorge, O.; Escott-Price, V.; Hernandez, D.G.; Nalls, M.A.; Clark, L.N.; Honig, L.S.; Marder, K.; Van Der Flier, W.M.; Lemstra, A.; Scheltens, P.; Rogaeva, E.; St George-Hyslop, P.; Londos, E.; Zetterberg, H.; Ortega-Cubero, S.; Pastor, P.; et al.
	2012	Prognostically significant fusion oncogenes in Pakistani patients with adult acute lymphoblastic leukemia and their association with disease biology and outcome	Sabir, N.; Iqbal, Z.; Aleem, A.; Awan, T.; Naeem, T.; Asad, S.; Tahir, A.; Absar, M.; Hasanato, R.; Basit, S.; Chishti, M.; Ul-Haque, M.; Khalid, A.; Sabar, M.; Rasool, M.; Karim, S.; Khan, M.; Samreen, B.; Akram, A.; Siddiqi, M.; et al.