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Preview	Issue Date	Title	Author(s)
	2016	A splicing-regulatory polymorphism in DRD2 disrupts ZRANB2 binding, impairs cognitive functioning and increases risk for schizophrenia in six Han Chinese samples	Cohen, O.; Weickert, T.; Hess, J.; Paish, L.; McCoy, S.; Rothmond, D.; Galletly, C.; Liu, D.; Weinberg, D.; Huang, X.; Xu, Q.; Shen, Y.; Zhang, D.; Yue, W.; Yan, J.; Wang, L.; Lu, T.; He, L.; Shi, Y.; Xu, M.; et al.
	2016	Identity by descent fine mapping of familial adult myoclonus epilepsy (FAME) to 2p11.2–2q11.2	Henden, L.; Freytag, S.; Afawi, Z.; Baldassari, S.; Berkovic, S.; Bisulli, F.; Canafoglia, L.; Casari, G.; Crompton, D.; Depienne, C.; Gecz, J.; Guerrini, R.; Helbig, I.; Hirsch, E.; Keren, B.; Klein, K.; Labauge, P.; LeGuern, E.; Licchetta, L.; Mei, D.; et al.
	2015	Patient controlled analgesia with remifentanil versus epidural analgesia in labour: Randomised multicentre equivalence trial	Freeman, L.; Bloemenkamp, K.; Franssen, M.; Papatsonis, D.; Hajenius, P.; Hollmann, M.; Woiski, M.; Porath, M.; Van Den Berg, H.; Van Beek, E.; Borchert, O.; Schuitemaker, N.; Sikkema, J.; Kuipers, A.; Logtenberg, S.; Van Der Salm, P.; Rengerink, K.; Lopriore, E.; Van Den Akker-van Marle, M.; Le Cessie, S.; et al.
	2014	Antepartum dalteparin versus no antepartum dalteparin for the prevention of pregnancy complications in pregnant women with thrombophilia (TIPPS): a multinational open-label randomised trial	Rodger, M.; Hague, W.; Kingdom, J.; Kahn, S.; Karovitch, A.; Sermer, M.; Clement, A.; Coat, S.; Chan, W.; Said, J.; Rey, E.; Robinson, S.; Khurana, R.; Demers, C.; Kovacs, M.; Solymoss, S.; Hinshaw, K.; Dwyer, J.; Smith, G.; McDonald, S.; et al.
	2010	Lynch syndrome-associated breast cancers: Clinicopathologic characteristics of a case series from the colon cancer family registry	Walsh, M.; Buchanan, D.; Cummings, M.; Pearson, S.; Arnold, S.; Clendenning, M.; Walters, R.; McKeone, D.; Spurdle, A.; Hopper, J.; Jenkins, M.; Phillips, K.; Suthers, G.; George, J.; Goldblatt, J.; Muir, A.; Tucker, K.; Pelzer, E.; Gattas, M.; Woodall, S.; et al.
	2015	Fibrosis, gene expression and orbital inflammatory disease	Rosenbaum, J.; Choi, D.; Wilson, D.; Grossniklaus, H.; Harrington, C.; Dailey, R.; Ng, J.; Steele, E.; Czyz, C.; Foster, J.; Tse, D.; Alabiad, C.; Dubovy, S.; Parekh, P.; Harris, G.; Kazim, M.; Patel, P.; White, V.; Dolman, P.; Edward, D.; et al.
	2016	X chromosome dose and sex bias in autoimmune diseases: increased prevalence of 47,XXX in systemic lupus erythematosus and Sjögren's syndrome	Liu, K.; Kurien, B.; Zimmerman, S.; Kaufman, K.; Taft, D.; Kottyan, L.; Lazaro, S.; Weaver, C.; Ice, J.; Adler, A.; Chodosh, J.; Radfar, L.; Rasmussen, A.; Stone, D.; Lewis, D.; Li, S.; Koelsch, K.; Igoe, A.; Talsania, M.; Kumar, J.; et al.
	2012	Loss-of-function germline GATA2 mutations in patients with MDS/AML or MonoMAC syndrome and primary lymphedema reveal a key role for GATA2 in the lymphatic vasculature	Kazenwadel, J.; Secker, G.; Liu, Y.; Rosenfeld, J.; Wildin, R.; Cuellar-Rodriguez, J.; Hsu, A.; Dyack, S.; Fernandez, C.; Chong, C.; Babic, M.; Bardy, P.; Shimamura, A.; Zhang, M.; Walsh, T.; Holland, S.; Hickstein, D.; Horwitz, M.; Hahn, C.; Scott, H.; et al.
	2015	Aspirin, ibuprofen, and the risk of colorectal cancer in Lynch Syndrome	Ait Ouakrim, D.; Dashti, S.; Chau, R.; Buchanan, D.; Clendenning, M.; Rosty, C.; Winship, I.; Young, J.; Giles, G.; Leggett, B.; Macrae, F.; Ahnen, D.; Casey, G.; Gallinger, S.; Haile, R.; Le Marchand, L.; Thibodeau, S.; Lindor, N.; Newcomb, P.; Potter, J.; et al.
	2013	Evidence for a retroviral insertion in TRPM1 as the cause of congenital stationary night blindness and leopard complex spotting in the horse	Bellone, R.; Holl, H.; Sealuri, V.; Devi, S.; Maddodi, N.; Archer, S.; Sandmeyer, L.; Ludwig, A.; Foerster, D.; Pruvost, M.; Reissmann, M.; Bortfeldt, R.; Adelson, D.; Lim, S.; Nelson, J.; Haase, B.; Engensteiner, M.; Leeb, T.; Forsyth, G.; Mienaltowski, M.; et al.