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Preview	Issue Date	Title	Author(s)
	2013	A suppressor screen in Mecp2 mutant mice implicates cholesterol metabolism in Rett syndrome	Buchovecky, C.; Turley, S.; Brown, H.; Kyle, S.; McDonald, J.; Liu, B.; Pieper, A.; Huang, W.; Katz, D.; Russell, D.; Shendure, J.; Justice, M.
	2013	A tudor domain protein SPINDLIN1 interacts with the mRNA-binding protein SERBP1 and is involved in mouse oocyte meiotic resumption	Chew, T.; Peaston, A.; Lim, A.; Lorthongpanich, C.; Knowles, B.; Solter, D.; Sun, Q.-Y.
	2004	Mouse orthologue of ARX, a gene mutated in several X-linked forms of mental retardation and epilepsy, is a marker of adult neural stem cells and forebrain GABAergic neurons	Colombo, E.; Galli, R.; Cossu, G.; Gecz, J.; Broccoli, V.
	2013	ZC4H2 mutations are associated with arthrogryposis multiplex congenita and intellectual disability through impairment of central and peripheral synaptic plasticity	Hirata, H.; McMichael, G.; Haan, E.; MacLennan, A.; Yap, T.; Nguyen, L.; Shaw, M.; Gecz, J.
	2012	A noncoding, regulatory mutation implicates HCFC1 in nonsyndromic intellectual disability	Huang, L.; Jolly, L.; Willis-Owen, S.; Gardner, A.; Sharma, R.; Douglas, E.; Shoubridge, C.; Wieczorek, D.; Tzschach, A.; Cohen, M.; Hackett, A.; Field, M.; Froyen, G.; Hu, H.; Haas, S.; Ropers, H.; Kalscheuer, V.; Corbett, M.; Gecz, J.
	2008	An integrated genetic and functional analysis of the role of type II transmembrane serine proteases (TMPRSSs) in hearing loss	Guipponi, M.; Toh, M.; Tan, J.; Park, D.; Hanson, K.; Ballana, E.; Kwong, D.; Cannon, P.; Wu, Q.; Gout, A.; Delorenzi, M.; Speed, T.; Smith, R.; Dahl, H.; Petersen, M.; Teasdale, R.; Estivill, X.; Park, W.; Scott, H.
	2015	DAT isn’t all that: cocaine reward and reinforcement require Toll-like receptor 4 signaling	Northcutt, A.; Hutchinson, M.; Wang, X.; Baratta, M.; Hiranita, T.; Cochran, T.; Pomrenze, M.; Galer, E.; Kopajtic, T.; Li, C.; Amat, J.; Larson, G.; Cooper, D.; Huang, Y.; O'Neill, C.; Yin, H.; Zahniser, N.; Katz, J.; Rice, K.; Maier, S.; et al.
	2015	HCFC1 loss-of-function mutations disrupt neuronal and neural progenitor cells of the developing brain.	Jolly, L.; Nguyen, L.; Domingo, D.; Sun, Y.; Barry, S.; Hancarova, M.; Plevova, P.; Vlckova, M.; Havlovicova, M.; Kalscheuer, V.; Graziano, C.; Pippucci, T.; Bonora, E.; Sedlacek, Z.; Gecz, J.
	2013	A transcription factor contributes to pathogenesis and virulence in streptococcus pneumoniae	Mahdi, L.; Ebrahimie, E.; Adelson, D.; Paton, J.; Ogunniyi, A.; Skurnik, M.
	2003	Nova regulates GABA(A) receptor gamma 2 alternative splicing via a distal downstream UCAU-rich intronic splicing enhancer	Dredge, B.; Darnell, R.