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Preview	Issue Date	Title	Author(s)
	2015	The International SSRI Pharmacogenomics Consortium (ISPC): a genome-wide association study of antidepressant treatment response	Biernacka, J.; Sangkuhl, K.; Jenkins, G.; Whaley, R.; Barman, P.; Batzler, A.; Altman, R.; Arolt, V.; Brockmöller, J.; Chen, C.; Domschke, K.; Hall-Flavin, D.; Hong, C.; Illi, A.; Ji, Y.; Kampman, O.; Kinoshita, T.; Leinonen, E.; Liou, Y.; Mushiroda, T.; et al.
	2009	Analyses of associations with asthma in four asthma population samples from Canada and Australia	Daly, D.; Lemire, M.; Akhabir, L.; Chan-Yeung, M.; He, J.; McDonald, T.; Stanford, A.; Stefanowicz, D.; Tripp, B.; Zamar, D.; Bosse, Y.; Ferretti, V.; Montpetit, A.; Tessier, M.; Becker, A.; Kozyrskyj, A.; Beilby, J.; McCaskie, P.; Musk, A.; Warrington, N.; et al.
	2009	Sequence variants in three loci influence monocyte counts and erythrocyte volume	Ferreira, M.; Hottenga, J.; Warrington, N.; Medland, S.; Willemsen, G.; Lawrence, R.; Gordon, S.; de Geus, E.; Henders, A.; Smit, J.; Campbell, M.; Wallace, L.; Evans, D.; Wright, M.; Nyholt, D.; James, A.; Beilby, J.; Penninx, B.; Palmer, L.; Frazer, I.; et al.
	2012	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women	Palmer, L.; Fox, C.S.; Liu, Y.; White, C.C.; Feitosa, M.; Smith, A.V.; Heard-Costa, N.; Lohman, K.; GIANT Consortium,; MAGIC Consortium,; GLGC Consortium,; Johnson, A.D.; Foster, M.C.; Greenawalt, D.M.; Griffin, P.; Ding, J.; Newman, A.B.; Tylavsky, F.; Miljkovic, I.; Kritchevsky, S.B.; et al.; Bray, M.
	2012	FTO genotype is associated with phenotypic variability of body mass index	Yang, J.; Loos, R.; Powell, J.; Medland, S.; Speliotes, E.; Chasman, D.; Rose, L.; Thorleifsson, G.; Steinthorsdottir, V.; Mägi, R.; Waite, L.; Smith, A.; Yerges-Armstrong, L.; Monda, K.; Hadley, D.; Mahajan, A.; Li, G.; Kapur, K.; Vitart, V.; Huffman, J.; et al.
	2010	Genome-wide association study identifies five loci associated with lung function	Repapi, E.; Sayers, I.; Wain, L.; Burton, P.; Johnson, T.; Obeidat, M.; Zhao J-, H.; Ramasamy, A.; Zhai, G.; Vitart, V.; Huffman, J.; Igl, W.; Albrecht, E.; Deloukas, P.; Henderson, J.; Granell, R.; McArdle, W.; Rudnicka, A.; Wellcome Trust Case Control Consortium,; Barroso, I.; et al.
	2012	Common variants at 12q15 and 12q24 are associated with infant head circumference	Taal, H.; St Pourcain, B.; Thiering, E.; Das, S.; Mook-Kanamori, D.; Warrington, N.; Kaakinen, M.; Kreiner-Møller, E.; Bradfield, J.; Freathy, R.; Geller, F.; Guxens, M.; Cousminer, D.; Kerkhof, M.; Timpson, N.; Arfan Ikram, M.; Beilin, L.; Bønnelykke, K.; Buxton, J.; Charoen, P.; et al.
	2013	GWAS of 126,559 individuals identifies genetic variants associated with educational attainment	Rietveld, C.; Medland, S.; Derringer, J.; Yang, J.; Esko, T.; Martin, N.; Westra, H.-J.; Shakhbazov, K.; Abdellaoui, A.; Agrawal, A.; Albrecht, E.; Alizadeh, B.; Amin, N.; Barnard, J.; Baumeister, S.; Benke, K.; Bielak, L.; Boatman, J.; Boyle, P.; Davies, G.; et al.
	2011	Association of genetic variation with systolic and diastolic blood pressure among African Americans: the Candidate Gene Association Resource Study	Fox, E.; Young, J.; Li, Y.; Dreisbach, A.; Keating, B.; Musani, S.; Liu, K.; Morrison, A.; Ganesh, S.; Kutlar, A.; Ramachandran, V.; Polak, J.; Fabsitz, R.; Dries, D.; Farlow, D.; Redline, S.; Adeyemo, A.; Hirschorn, J.; Sun, Y.; Wyatt, S.; et al.
	2014	Refining analyses of copy number variation identifies specific genes associated with developmental delay	Coe, 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.