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Preview	Issue Date	Title	Author(s)
	2010	Familial concordance of breast cancer pathology as an indicator of genotype in multiple-case families	Balleine, R.; Provan, P.; Pupo, G.; Pathmanathan, N.; Cummings, M.; Farshid, G.; Salisbury, E.; Bilous, A.; Byth, K.; Mann, G.
	2010	Hundreds of variants clustered in genomic loci and biological pathways affect human height	Allen, H.; Estrada, K.; Lettre, G.; Berndt, S.; Weedon, M.; Rivadeneira, F.; Willer, C.; Jackson, A.; Vedantam, S.; Raychaudhuri, S.; Ferreira, T.; Wood, A.; Weyant, R.; Segre, A.; Speliotes, E.; Wheeler, E.; Soranzo, N.; Park, J.-H.; Yang, J.; Gudbjartsson, D.; et al.
	2010	A recurrent 16p12.1 microdeletion supports a two-hit model for severe developmental delay	Haan, E.; Gecz, J.
	2010	Genome-wide pharmacogenetics of antidepressant response in the GENDEP project	Uher, R.; Perroud, N.; Ng, M.; Hauser, J.; Henigsberg, N.; Maier, W.; Mors, O.; Placentino, A.; Rietschel, M.; Souery, D.; Zagar, T.; Czerski, P.; Jerman, B.; Larsen, E.; Schulze, T.; Zobel, A.; Cohen-Woods, S.; Pirlo, K.; Butler, A.; Muglia, P.; et al.
	2010	Genomic hotspots for adaptation: the population genetics of Müllerian mimicry in Heliconius erato	Counterman, B.; Araujo-Perez, F.; Hines, H.; Baxter, S.; Morrison, C.; Lindstrom, D.; Papa, R.; Ferguson, L.; Joron, M.; ffrench-Constant, R.; Smith, C.; Nielsen, D.; Chen, R.; Jiggins, C.; Reed, R.; Halder, G.; Mallet, J.; McMillan, W.; Nachman, M.W.
	2010	Bayesian methods for meta-analysis of causal relationships estimated using genetic instrumental variables	Thompson, S.; Burgess, S.; CRP CHD Genetics Collaboration,
	2010	A novel syndrome of paediatric cataract, dysmorphism, ectodermal features, and developmental delay in Australian Aboriginal family maps to 1p35.3-p36.32	Hattersley, K.; Laurie, K.; Liebelt, J.; Gecz, J.; Durkin, S.; Craig, J.; Burden, K.