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Preview	Issue Date	Title	Author(s)
	2017	NAD deficiency, congenital malformations, and niacin supplementation	Shi, H.; Enriquez, A.; Rapadas, M.; Martin, E.; Wang, R.; Moreau, J.; Lim, C.; Szot, J.; Ip, E.; Hughes, J.; Sugimoto, K.; Humphreys, D.; McInerney-Leo, A.; Leo, P.; Maghzal, G.; Halliday, J.; Smith, J.; Colley, A.; Mark, P.; Collins, F.; et al.
	2017	Dominant protection from HLA-linked autoimmunity by antigen-specific regulatory T cells	Ooi, J.; Petersen, J.; Tan, Y.; Huynh, M.; Willett, Z.; Ramarathinam, S.; Eggenhuizen, P.; Loh, K.; Watson, K.; Gan, P.; Alikhan, M.; Dudek, N.; Handel, A.; Hudson, B.; Fugger, L.; Power, D.; Holt, S.; Coates, P.; Gregersen, J.; Purcell, A.; et al.
	2017	Electrophysiological, cognitive and clinical profiles of at-risk mental state: the longitudinal minds in transition (MinT) study	Atkinson, R.J.; Fulham, W.R.; Michie, P.T.; Ward, P.B.; Todd, J.; Stain, H.; Langdon, R.; Thienel, R.; Paulik, G.; Cooper, G.; Anthes, L.; Bowen, D.; Case, V.; Clark, S.; Collins-Langworthy, J.; Curtis, J.; Ehlkes, T.; Haddow, T.; Lawrence, C.; Logan, S.; et al.; Hashimoto, K.
	2017	Antenatal suppression of il-1 protects against inflammation-induced fetal injury and improves neonatal and developmental outcomes in mice	Nadeau-Vallée, M.; Chin, P.; Belarbi, L.; Brien, M.; Pundir, S.; Berryer, M.; Beaudry-Richard, A.; Madaan, A.; Sharkey, D.; Lupien-Meilleur, A.; Hou, X.; Quiniou, C.; Beaulac, A.; Boufaied, I.; Boudreault, A.; Carbonaro, A.; Doan, N.; Joyal, J.; Lubell, W.; Olson, D.; et al.
	2017	Hotspots of missense mutation identify neurodevelopmental disorder genes and functional domains	Geisheker, M.; Heymann, G.; Wang, T.; Coe, B.; Turner, T.; Stessman, H.; Hoekzema, K.; Kvarnung, M.; Shaw, M.; Friend, K.; Liebelt, J.; Barnett, C.; Thompson, E.; Haan, E.; Guo, H.; Anderlid, B.; Nordgren, A.; Lindstrand, A.; Vandeweyer, G.; Alberti, A.; et al.
	2017	Long-term efficacy and safety of α1 proteinase inhibitor treatment for emphysema caused by severe α1 antitrypsin deficiency: an open-label extension trial (RAPID-OLE)	McElvaney, N.; Burdon, J.; Holmes, M.; Glanville, A.; Wark, P.; Thompson, P.; Hernandez, P.; Chlumsky, J.; Teschler, H.; Ficker, J.; Seersholm, N.; Altraja, A.; Mäkitaro, R.; Chorostowska-Wynimko, J.; Sanak, M.; Stoicescu, P.; Piitulainen, E.; Vit, O.; Wencker, M.; Tortorici, M.; et al.
	2017	Docosahexaenoic acid and bronchopulmonary dysplasia in preterm infants	Collins, C.; Makrides, M.; McPhee, A.; Sullivan, T.; Davis, P.; Thio, M.; Simmer, K.; Rajadurai, V.; Travadi, J.; Berry, M.; Liley, H.; Opie, G.; Tan, K.; Lui, K.; Morris, S.; Stack, J.; Stark, M.; Chua, M.; Jayagobi, P.; Holberton, J.; et al.
	2017	Targeted sequencing identifies 91 neurodevelopmental-disorder risk genes with autism and developmental-disability biases	Stessman, H.; Xiong, B.; Coe, B.; Wang, T.; Hoekzema, K.; Fenckova, M.; Kvarnung, M.; Gerdts, J.; Trinh, S.; Cosemans, N.; Vives, L.; Lin, J.; Turner, T.; Santen, G.; Ruivenkamp, C.; Kriek, M.; Van Haeringen, A.; Aten, E.; Friend, K.; Liebelt, J.; et al.
	2017	Laparoscopy to predict the result of primary cytoreductive surgery in patients with advanced ovarian cancer: a randomized controlled trial	Rutten, M.; Van Meurs, H.; Van De Vrie, R.; Gaarenstroom, K.; Naaktgeboren, C.; Van Gorp, T.; Brugge, H.; Hofhuis, W.; Schreuder, H.; Arts, H.; Zusterzeel, P.; Pijnenborg, J.; Van Haaften, M.; Fons, G.; Engelen, M.; Boss, E.; Vos, M.; Gerestein, K.; Schutter, E.; Opmeer, B.; et al.
	2017	Adults with Philadelphia chromosome-like acute lymphoblastic leukemia frequently have IGH-CRLF2 and JAK2 mutations, persistence of minimal residual disease and poor prognosis	Herold, T.; Schneider, S.; Metzeler, K.; Neumann, M.; Hartmann, L.; Roberts, K.; Konstandin, N.; Greif, P.; Braeundl, K.; Ksienzyk, B.; Huk, N.; Schneider, I.; Zellmeier, E.; Jurinovic, V.; Mansmann, U.; Hiddemann, W.; Mullighan, C.; Bohlander, S.; Spiekermann, K.; Hoelzer, D.; et al.