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Preview	Issue Date	Title	Author(s)
	2015	shRNA off-target effects in vivo: impaired endogenous siRNA expression and spermatogenic defects	Song, H.; Bettegowda, A.; Oliver, D.; Yan, W.; Phan, M.; De Rooij, D.; Corbett, M.; Wilkinson, M.; White-Cooper, H.
	2015	Prevalence and predictors of alcohol use during pregnancy: findings from international multicentre cohort studies	O'Keeffe, L.; Kearney, P.; McCarthy, F.; Khashan, A.; Greene, R.; North, R.; Poston, L.; McCowan, L.; Baker, P.; Dekker, G.; Walker, J.; Taylor, R.; Kenny, L.
	2015	Mutations in DDX3X are a common cause of unexplained intellectual disability with gender-specific effects on Wnt signaling	Snijders Blok, L.; Madsen, E.; Juusola, J.; Gilissen, C.; Baralle, D.; Reijnders, M.; Venselaar, H.; Helsmoortel, C.; Cho, M.; Hoischen, A.; Vissers, L.; Koemans, T.; Wissink-Lindhout, W.; Eichler, E.; Romano, C.; Van Esch, H.; Stumpel, C.; Vreeburg, M.; Smeets, E.; Oberndorff, K.; et al.
	2015	A systematic review of transfusion-associated graft-versus-host disease	Kopolovic, I.; Ostro, J.; Tsubota, H.; Lin, Y.; Cserti-Gazdewich, C.; Messner, H.; Keir, A.; DenHollander, N.; Dzik, W.; Callum, J.
	2015	Temporal changes in blood product usage in preterm neonates born at less than 30 weeks' gestation in Canada	Keir, A.; Yang, J.; Harrison, A.; Pelausa, E.; Shah, P.
	2015	Mutations in the intellectual disability gene KDM5C reduce protein stability and demethylase activity	Brookes, E.; Laurent, B.; Õunap, K.; Carroll, R.; Moeschler, J.; Field, M.; Schwartz, C.; Gecz, J.; Shi, Y.
	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.
	2015	Pharmacokinetics of nifedipine slow-release during sustained tocolysis	ter Laak, M.; Roos, C.; Touw, D.; van Hattum, P.; Kwee, A.; Lotgering, F.; Mol, B.; van Pampus, M.; Porath, M.; Spaanderman, M.; van der Post, J.; Papatsonis, D.; van 't Veer, N.
	2015	Maternal and neonatal consequences of treated and untreated asymptomatic bacteriuria in pregnancy: a prospective cohort study with an embedded randomised controlled trial	Kazemier, B.; Koningstein, F.; Schneeberger, C.; Ott, A.; Bossuyt, P.; de Miranda, E.; Vogelvang, T.; Verhoeven, C.; Langenveld, J.; Woiski, M.; Oudijk, M.; van der Yen, J.; Vlegels, M.; Kuiper, P.; Feiertag, N.; Pajkrt, E.; de Groot, C.; Mol, B.; Geerlings, S.
	2015	Homozygous mutation of STXBP5L explains an autosomal recessive infantile-onset neurodegenerative disorder	Kumar, R.; Corbett, M.; Smith, N.; Jolly, L.; Tan, C.; Keating, D.; Duffield, M.; Utsumi, T.; Moriya, K.; Smith, K.; Hoischen, A.; Abbott, K.; Harbord, M.; Compton, A.; Woenig, J.; Arts, P.; Kwint, M.; Wieskamp, N.; Gijsen, S.; Veltman, J.; et al.