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Preview	Issue Date	Title	Author(s)
	2018	The Beaker phenomenon and the genomic transformation of northwest Europe	Olalde, I.; Brace, S.; Allentoft, M.E.; Armit, I.; Kristiansen, K.; Booth, T.; Rohland, N.; Mallick, S.; Szécsényi-Nagy, A.; Mittnik, A.; Altena, E.; Lipson, M.; Lazaridis, I.; Harper, T.K.; Patterson, N.; Broomandkhoshbacht, N.; Diekmann, Y.; Faltyskova, Z.; Fernandes, D.; Ferry, M.; et al.
	2016	The genetic history of Peruvian Quechua-Lamistas and Chankas: uniparental DNA Patterns among autochthonous Amazonian and Andean populations	Sandoval, J.; Lacerda, D.; Acosta, O.; Jota, M.; Robles-Ruiz, P.; Salazar-Granara, A.; Vieira, P.; Paz-y-Miño, C.; Fujita, R.; Santos, F.; Jin, L.; Li, H.; Li, S.; Swamikrishnan, P.; Javed, A.; Parida, L.; Royyuru, A.; Mitchell, R.; Zalloua, P.; Adhikarla, S.; et al.
	2014	The sheep genome illuminates biology of the rumen and lipid metabolism	Jiang, Y.; Xie, M.; Chen, W.; Talbot, R.; Maddox, J.; Faraut, T.; Wu, C.; Muzny, D.; Li, Y.; Zhang, W.; Stanton, J.; Brauning, R.; Barris, W.; Hourlier, T.; Aken, B.; Searle, S.; Adelson, D.; Bian, C.; Cam, G.; Chen, Y.; et al.
	2014	Fifty thousand years of Arctic vegetation and megafaunal diet	Willerslev, E.; Davison, J.; Moora, M.; Zobel, M.; Coissac, E.; Edwards, M.; Lorenzen, E.; Vestergård, M.; Gussarova, G.; Haile, J.; Craine, J.; Gielly, L.; Boessenkool, S.; Epp, L.; Pearman, P.; Cheddadi, R.; Murray, D.; Bråthen, K.; Yoccoz, N.; Binney, H.; et al.
	2016	A principal component meta-analysis on multiple anthropometric traits identifies novel loci for body shape	Ried, J.; Jeff, J.; Chu, A.; Bragg-Gresham, J.; Van Dongen, J.; Huffman, J.; Ahluwalia, T.; Cadby, G.; Eklund, N.; Eriksson, J.; Esko, T.; Feitosa, M.; Goel, A.; Gorski, M.; Hayward, C.; Heard-Costa, N.; Jackson, A.; Jokinen, E.; Kanoni, S.; Kristiansson, K.; et al.
	2011	Identification of SOX3 as an XX male sex reversal gene in mice and humans	Sutton, E.; Hughes, J.; White, S.; Sekido, R.; Tan, J.; Arboleda, V.; Rogers, N.; Knower, K.; Rowley, L.; Eyre, H.; Rizzoti, K.; McAninch, D.; Golcalves, J.; Slee, J.; Turbitt, E.; Bruno, D.; Bengtsson, H.; Harley, V.; Vilain, E.; Sinclair, A.; et al.
	2017	Targeted sequencing identifies 91 neurodevelopmental-disorder risk genes with autism and developmental-disability biases	Stessman, H.; Xiong, B.; Coe, B.; Wang, T.; Hoekzema, K.; Fenckova, M.; Kvarnung, M.; Gerdts, J.; Trinh, S.; Cosemans, N.; Vives, L.; Lin, J.; Turner, T.; Santen, G.; Ruivenkamp, C.; Kriek, M.; Van Haeringen, A.; Aten, E.; Friend, K.; Liebelt, J.; et al.
	2018	A genotype-first approach identifies an intellectual disability-overweight syndrome caused by PHIP haploinsufficiency	Jansen, S.; Hoischen, A.; Coe, B.; Carvill, G.; van Esch, H.; Bosch, D.; Andersen, U.; Baker, C.; Bauters, M.; Bernier, R.; van Bon, B.; Claahsen-van der Grinten, H.; Gecz, J.; Gilissen, C.; Grillo, L.; Hackett, A.; Kleefstra, T.; Koolen, D.; Kvarnung, M.; Larsen, M.; et al.
	2017	A recurrent de novo nonsense variant in ZSWIM6 results in severe intellectual disability without frontonasal or limb malformations	Palmer, E.E.; Kumar, R.; Gordon, C.T.; Shaw, M.; Hubert, L.; Carroll, R.; Rio, M.; Murray, L.; Leffler, M.; Dudding-Byth, T.; Oufadem, M.; Lalani, S.R.; Lewis, A.M.; Xia, F.; Tam, A.; Webster, R.; Brammah, S.; Filippini, F.; Pollard, J.; Spies, J.; et al.
	2016	A method to exploit the structure of genetic ancestry space to enhance case-control studies	Bodea, C.A.; Neale, B.M.; Ripke, S.; Barclay, M.; Peyrin-Biroulet, L.; Chamaillard, M.; Colombel, J.F.; Cottone, M.; Croft, A.; D'Incà, R.; Halfvarson, J.; Hanigan, K.; Henderson, P.; Hugot, J.P.; Karban, A.; Kennedy, N.A.; Khan, M.A.; Lémann, M.; Levine, A.; Massey, D.; et al.