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Preview	Issue Date	Title	Author(s)
	2011	A genome-wide significant linkage for severe depression on chromosome 3: the depression network study	Breen, G.; Webb, B.; Butler, A.; van den Oord, E.; Tozzi, F.; Craddock, N.; Gill, M.; Korszun, A.; Maier, W.; Middleton, L.; Mors, O.; Owen, M.; Cohen-Woods, S.; Perry, J.; Galwey, N.; Upmanyu, R.; Craig, I.; Lewis, C.; Ng, M.; Brewster, S.; et al.
	2012	Copy-number gains of HUWE1 due to replication-and recombination-based rearrangements	Froyen, G.; Belet, S.; Martinez, F.; Santos-Reboucas, C.; Declercq, M.; Verbeeck, J.; Donckers, L.; Berland, S.; Mayo, S.; Rosello, M.; Pimentel, M.; Fintelman-Rodrigues, N.; Hovland, R.; dos Santos, S.; Raymond, F.; Sundernathan, T.; Corbett, M.; Sheffield, L.; van Ravenswaaij-Arts, C.; Dijkhuizen, T.; et al.
	2008	Identifying genetic traces of historical expansions: Phoenician footprints in the Mediterranean	Zalloua, P.; Platt, D.; El Sibai, M.; Khalife, J.; Makhoul, N.; Haber, M.; Xue, Y.; Izaabel, H.; Bosch, E.; Adams, S.; Arroyo, E.; Lopez-Parra, A.; Aler, M.; Picornell, A.; Ramon, M.; Jobling, M.; Comas, D.; Bertranpetit, J.; Spencer Wells, R.; Tyler-Smith, C.; et al.; Cooper, Alan
	2008	Y-chromosomal diversity in Lebanon is structured by recent historical events	Zalloua, P.; Xue, Y.; Khalife, J.; Makhoul, N.; Debiane, L.; Platt, D.; Royyuru, A.; Herrera, R.; Hernanz, D.; Blue-Smith, J.; Spencer Wells, R.; Comas, D.; Bertranpetit, J.; Tyler-Smith, C.; Schurr, T.; Santos, F.; Quintana-Murci, L.; Balanovska, E.; Balanovsky, O.; Behar, D.; et al.; Cooper, Alan
	2007	Genome wide association study identifies novel breat cancer susceptibility loci	Easton, D.; Pooley, K.; Pharoah, P.; Thompson, D.; Ballinger, D.; Struewing, J.; Morrison, J.; Field, H.; Luben, R.; Wareham, N.; Ahmed, S.; Healey, C.; Bowman, R.; Luccarini, C.; Conroy, D.; Shah, M.; Munday, H.; Jordan, C.; Perkins, B.; West, J.; et al.
	2007	Multicentre search for genetic susceptibility loci in sporadic epilepsy syndrome and seizure types: a case-control study	Cavalleri, G.; Weale, M.; Shianna, K.; Singh, R.; Lynch, J.; Grinton, B.; Szoeke, C.; Murphy, K.; Kinirons, P.; O'Rourke, D.; Ge, D.; Depondt, C.; Claeys, K.; Pandolfo, M.; Gumbs, C.; Walley, N.; McNamara, J.; Mulley, J.; Linney, K.; Sheffield, L.; et al.
	2011	Genome-wide association study identifies susceptibility loci for open angle glaucoma at TMCO1 and CDKN2B-AS1	Burdon, K.; MacGregor, S.; Hewitt, A.; Sharma, S.; Chidlow, G.; Mills, R.; Danoy, P.; Casson, R.; Viswanathan, A.; Liu, J.; Landers, J.; Henders, A.; Wood, J.; Souzeau, E.; Crawford, A.; Leo, P.; Wang, J.; Rochtchina, E.; Nyholt, D.; Martin, N.; et al.
	2011	Heritable GATA2 mutations associated with familial myelodysplastic syndrome and acute myeloid leukemia	Hahn, C.; Chong, C.; Carmichael, C.; Wilkins, E.; Brautigan, P.; Li, X.; Babic, M.; Lin, M.; Carmagnac, A.; Lee, Y.; Kok, C.; Gagliardi, L.; Friend, K.; Ekert, P.; Butcher, C.; Brown, A.; Lewis, I.; To, L.; Timms, A.; Storek, J.; et al.
	2008	Estimating the ancestral recombinations graph (ARG) as compatible networks of SNP patterns	Parida, L.; Mele, M.; Calafell, F.; Bertranpetit, J.; Schurr, T.; Santos, F.; Quintana-Murci, L.; Comas, D.; Tyler-Smith, C.; Zalloua, P.; Balanovska, E.; Balanovsky, O.; Behar, D.; Mitchell, R.; Jin, L.; Soodyall, H.; Pitchappan, R.; Cooper, A.; Royyuru, A.; Rosset, S.; et al.; Cooper, Alan
	2007	A multicenter study of BRD2 as a risk factor for juvenile myoclonic epilepsy	Cavalleri, G.; Walley, N.; Soranzo, N.; Mulley, J.; Doherty, C.; Kapoor, A.; Depondt, C.; Lynch, J.; Scheffer, I.; Heils, A.; Gehrmann, A.; Kinirons, P.; Gandhi, S.; Satishchandra, P.; Wood, N.; Anand, A.; Sander, T.; Berkovic, S.; Delanty, N.; Goldstein, D.; et al.