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Results 31-40 of 62 (Search time: 0.003 seconds).
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PreviewIssue DateTitleAuthor(s)
2021HLA-DRB1 and HLA-DQB1 genetic diversity modulates response to lithium in bipolar affective disordersLe Clerc, S.; Lombardi, L.; Baune, B.T.; Amare, A.T.; Schubert, K.O.; Hou, L.; Clark, S.R.; Papiol, S.; Cearns, M.; Heilbronner, U.; Degenhardt, F.; Tekola-Ayele, F.; Hsu, Y.-H.; Shekhtman, T.; Adli, M.; Akula, N.; Akiyama, K.; Ardau, R.; Arias, B.; Aubry, J.-M.; et al.
2021Combining schizophrenia and depression polygenic risk scores improves the genetic prediction of lithium response in bipolar disorder patientsSchubert, K.O.; Thalamuthu, A.; Amare, A.T.; Frank, J.; Streit, F.; Adl, M.; Akula, N.; Akiyama, K.; Ardau, R.; Arias, B.; Aubry, J.-M.; Backlund, L.; Bhattacharjee, A.K.; Bellivier, F.; Benabarre, A.; Bengesser, S.; Biernacka, J.M.; Birner, A.; Marie-Claire, C.; Cearns, M.; et al.
2013Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architectureBerndt, S.; Gustafsson, S.; Mägi, R.; Ganna, A.; Wheeler, E.; Feitosa, M.; Justice, A.; Monda, K.; Croteau-Chonka, D.; Day, F.; Esko, T.; Fall, T.; Ferreira, T.; Gentilini, D.; Jackson, A.; Luan, J.; Randall, J.; Vedantam, S.; Willer, C.; Winkler, T.; et al.
2009Sequence variants affecting eosinophil numbers associate with asthma and myocardial infarctionGudbjartsson, D.; Bjornsdottir, U.; Halapi, E.; Helgadottir, A.; Sulem, P.; Jonsdottir, G.; Thorleifsson, G.; Helgadottir, H.; Steinthorsdottir, V.; Stefansson, H.; Williams, C.; Hui, J.; Beilby, J.; Warrington, N.; James, A.; Palmer, L.; Koppelman, G.; Heinzmann, A.; Krueger, M.; Boezen, H.; et al.
2014Refining analyses of copy number variation identifies specific genes associated with developmental delayCoe, B.; Witherspoon, K.; Rosenfeld, J.; van Bon, B.; Vulto-van Silfhout, A.; Bosco, P.; Friend, K.; Baker, C.; Buono, S.; Vissers, L.; Schuurs-Hoeijmakers, J.; Hoischen, A.; Pfundt, R.; Krumm, N.; Carvill, G.; Li, D.; Amaral, D.; Brown, N.; Lockhart, P.; Scheffer, I.; et al.
2012A genome-wide association meta-analysis identifies new childhood obesity lociBradfield, J.; Taal, H.; Timpson, N.; Scherag, A.; Lecoeur, C.; Warrington, N.; Hypponen, E.; Holst, C.; Valcarcel, B.; Thiering, E.; Salem, R.; Schumacher, F.; Cousminer, D.; Sleiman, P.; Jianhua, Z.; Berkowitz, R.; Vimaleswaran, K.; Ivonne, J.; Pennell, C.; Evans, D.; et al.
2023Heritable defects in telomere and mitotic function selectively predispose to sarcomasBallinger, M.L.; Pattnaik, S.; Mundra, P.A.; Zaheed, M.; Rath, E.; Priestley, P.; Baber, J.; Ray-Coquard, I.; Isambert, N.; Causeret, S.; van der Graaf, W.T.A.; Puri, A.; Duffaud, F.; Le Cesne, A.; Seddon, B.; Chandrasekar, C.; Schiffman, J.D.; Brohl, A.S.; James, P.A.; Kurtz, J.-E.; et al.
2015Association of the colorectal CpG island methylator phenotype with molecular features, risk factors, and family historyWeisenberger, D.; Levine, A.; Long, T.; Buchanan, D.; Walters, R.; Clendenning, M.; Rosty, C.; Joshi, A.; Stern, M.; Le Marchand, L.; Lindor, N.; Daftary, D.; Gallinger, S.; Selander, T.; Bapat, B.; Newcomb, P.; Campbell, P.; Casey, G.; Ahnen, D.; Baron, J.; et al.
2010Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studiesElks, C.; Perry, J.; Sulem, P.; Chasman, D.; Franceschini, N.; He, C.; Lunetta, K.; Visser, J.; Byrne, E.; Cousminer, D.; Gudbjartsson, D.; Esko, T.; Feenstra, B.; Hottenga, J.; Koller, D.; Kutalik, Z.; Lin, P.; Mangino, M.; Marongiu, M.; McArdle, P.; et al.
2011A novel recurrent mutation in MITF predisposes to familial and sporadic melanomaYokoyama, S.; Woods, S.; Boyle, G.; Aoude, L.; MacGregor, S.; Zismann, V.; Gartside, M.; Cust, A.; Haq, R.; Harland, M.; Taylor, J.; Duffy, D.; Holohan, K.; Dutton-Regester, K.; Palmer, J.; Bonazzi, V.; Stark, M.; Symmons, J.; Law, M.; Schmidt, C.; et al.

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