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Preview	Issue Date	Title	Author(s)
	2013	Common variants in mendelian kidney disease genes and their association with renal function	Parsa, 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.
	2018	Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection	Pardiñas, A.; Holmans, P.; Pocklington, A.; Escott-Price, V.; Ripke, S.; Carrera, N.; Legge, S.; Bishop, S.; Cameron, D.; Hamshere, M.; Han, J.; Hubbard, L.; Lynham, A.; Mantripragada, K.; Rees, E.; MacCabe, J.; McCarroll, S.; Baune, B.; Breen, G.; Byrne, E.; et al.
	2013	A pathway-based analysis provides additional support for an immune-related genetic susceptibility to Parkinsons disease	Holmans, P.; Moskvina, V.; Jones, L.; Sharma, M.; Vedernikov, A.; Buchel, F.; Sadd, M.; Bras, J.M.; Bettella, F.; Nicolaou, N.; Simon-Sanchez, J.; Mittag, F.; Gibbs, J.R.; Schulte, C.; Durr, A.; Guerreiro, R.; Hernandez, D.; Brice, A.; Stefansson, H.; Majamaa, K.; et al.
	2019	GWAS on longitudinal growth traits reveals different genetic factors influencing infant, child, and adult BMI	Alves, A.C.; De Silva, N.M.G.; Karhunen, V.; Sovio, U.; Das, S.; Rob Taal, H.; Warrington, N.M.; Lewin, A.M.; Kaakinen, M.; Cousminer, D.L.; Thiering, E.; Timpson, N.J.; Bond, T.A.; Lowry, E.; Brown, C.D.; Estivill, X.; Lindi, V.; Bradfield, J.P.; Geller, F.; Speed, D.; et al.
	2020	Multitrait analysis of glaucoma identifies new risk loci and enables polygenic prediction of disease susceptibility and progression	Craig, J.E.; Han, X.; Qassim, A.; Hassall, M.; Cooke Bailey, J.N.; Kinzy, T.G.; Khawaja, A.P.; An, J.; Marshall, H.; Gharahkhani, P.; Igo, R.P.; Graham, S.L.; Healey, P.R.; Ong, J.-S.; Zhou, T.; Siggs, O.; Law, M.H.; Souzeau, E.; Ridge, B.; Hysi, P.G.; et al.
	2020	The Genetics of the Mood Disorder Spectrum: Genome-wide Association Analyses of More Than 185,000 Cases and 439,000 Controls	Coleman, J.R.I.; Gaspar, H.A.; Bryois, J.; Byrne, E.M.; Forstner, A.J.; Holmans, P.A.; de Leeuw, C.A.; Mattheisen, M.; McQuillin, A.; Whitehead Pavlides, J.M.; Pers, T.H.; Ripke, S.; Stahl, E.A.; Steinberg, S.; Trubetskoy, V.; Trzaskowski, M.; Wang, Y.; Abbott, L.; Abdellaoui, A.; Adams, M.J.; et al.
	2020	The genetic architecture of the human cerebral cortex	Grasby, K.L.; Jahanshad, N.; Painter, J.N.; Colodro-Conde, L.; Bralten, J.; Hibar, D.P.; Lind, P.A.; Pizzagalli, F.; Ching, C.R.K.; McMahon, M.A.B.; Shatokhina, N.; Zsembik, L.C.P.; Thomopoulos, S.I.; Zhu, A.H.; Strike, L.T.; Agartz, I.; Alhusaini, S.; Almeida, M.A.A.; Alnæs, D.; Amlien, I.K.; et al.
	2020	Common genetic variation indicates separate causes for periventricular and deep white matter hyperintensities	Armstrong, N.J.; Mather, K.A.; Sargurupremraj, M.; Knol, M.J.; Malik, R.; Satizabal, C.L.; Yanek, L.R.; Wen, W.; Gudnason, V.G.; Dueker, N.D.; Elliott, L.T.; Hofer, E.; Hofer, E.; Bis, J.; Jahanshad, N.; Li, S.; Logue, M.A.; Logue, M.A.; Luciano, M.; Scholz, M.; et al.
	2014	Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease	Nalls, M.A.; Pankratz, N.; Lill, C.M.; Do, C.B.; Hernandez, D.G.; Saad, M.; DeStefano, A.L.; Kara, E.; Bras, J.; Sharma, M.; Schulte, C.; Keller, M.F.; Arepalli, S.; Letson, C.; Edsall, C.; Stefansson, H.; Liu, X.; Pliner, H.; Lee, J.H.; Cheng, R.; et al.
	2018	Investigating the genetic architecture of dementia with Lewy bodies: a two-stage genome-wide association study	Guerreiro, R.; Ross, O.A.; Kun-Rodrigues, C.; Hernandez, D.G.; Orme, T.; Eicher, J.D.; Shepherd, C.E.; Parkkinen, L.; Darwent, L.; Heckman, M.G.; Scholz, S.W.; Troncoso, J.C.; Pletnikova, O.; Ansorge, O.; Clarimon, J.; Lleo, A.; Morenas-Rodriguez, E.; Clark, L.; Honig, L.S.; Marder, K.; et al.