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Results 1-10 of 188 (Search time: 0.002 seconds).
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PreviewIssue DateTitleAuthor(s)
2010FunctSNP: an R package to link SNPs to functional knowledge and dbAutoMaker: a suite of Perl scripts to build SNP databasesGoodswen, S.; Gondro, C.; Watson-Haigh, N.; Kadarmideen, H.
2010Genetic variants regulating insulin receptor signalling are associated with the severity of liver damage in patients with non-alcoholic fatty liver diseaseDongiovanni, P.; Valenti, L.; Rametta, R.; Daly, A.; Nobili, V.; Mozzi, E.; Leathart, J.; Pietrobattista, A.; Burt, A.; Maggioni, M.; Fracanzani, A.; Lattuada, E.; Zappa, M.; Roviaro, G.; Marchesini, G.; Day, C.; Fargion, S.
2017Increased genomic prediction accuracy in wheat breeding using a large Australian panelTaylor, J.D.; Norman, A.; Tanaka, E.; Telfer, P.; Edwards, J.; Martinant, J.P.; Kuchel, H.
2013Common variants in mendelian kidney disease genes and their association with renal functionParsa, A.; Fuchsberger, C.; Köttgen, A.; O'Seaghdha, C.; Pattaro, C.; De Andrade, M.; Chasman, D.; Teumer, A.; Endlich, K.; Olden, M.; Chen, M.; Tin, A.; Kim, Y.; Taliun, D.; Li, M.; Feitosa, M.; Gorski, M.; Yang, Q.; Hundertmark, C.; Foster, M.; et al.
2015Fine mapping of type 1 diabetes susceptibility loci and evidence for colocalization of causal variants with lymphoid gene enhancersOnengut-Gumuscu, S.; Chen, W.-M.; Burren, O.; Cooper, N.J.; Quinlan, A.R.; Mychaleckyj, J.C.; Farber, E.; Bonnie, J.K.; Szpak, M.; Schofield, E.; Achuthan, P.; Guo, H.; Fortune, M.D.; Stevens, H.; Walker, N.M.; Ward, L.D.; Kundaje, A.; Kellis, M.; Daly, M.J.; Barrett, J.C.; et al.
2017A latent genetic subtype of major depression identified by whole-exome genotyping data in a Mexican-American cohortYu, C.; Arcos-Burgos, M.; Licinio, J.; Wong, M.
2019The impact of genetic adaptation on chimpanzee subspecies differentiationSchmidt, J.M.; de Manuel, M.; Marques-Bonet, T.; Castellano, S.; Andrés, A.M.; Gojobori, T.
2018A C6orf10/LOC101929163 locus is associated with age of onset in C9orf72 carriersZhang, M.; Ferrari, R.; Tartaglia, M.C.; Keith, J.; Surace, E.I.; Wolf, U.; Sato, C.; Grinberg, M.; Liang, Y.; Xi, Z.; Dupont, K.; McGoldrick, P.; Weichert, A.; McKeever, P.M.; Schneider, R.; McCorkindale, M.D.; Manzoni, C.; Rademakers, R.; Graff-Radford, N.R.; Dickson, D.W.; et al.
2016Role of genetic susceptibility variants in predicting clinical course in multiple sclerosis: A cohort studyPan, G.; Simpson, S.; van der Mei, I.; Charlesworth, J.C.; Lucas, R.; Ponsonby, A.L.; Zhou, Y.; Wu, F.; Taylor, B.V.; Dear, K.; Dwyer, T.; Blizzard, L.; Broadley, S.; Kilpatrick, T.; Williams, D.; Lechner-Scott, J.; Shaw, C.; Chapman, C.; Coulthard, A.; Valery, P.
2017Epiregulin and EGFR interactions are involved in pain processingMartin, L.J.; Smith, S.B.; Khoutorsky, A.; Magnussen, C.A.; Samoshkin, A.; Sorge, R.E.; Cho, C.; Yosefpour, N.; Sivaselvachandran, S.; Tohyama, S.; Cole, T.; Khuong, T.M.; Mir, E.; Gibson, D.G.; Wieskopf, J.S.; Sotocinal, S.G.; Austin, J.S.; Meloto, C.B.; Gitt, J.H.; Gkogkas, C.; et al.

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