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Preview	Issue Date	Title	Author(s)
	2012	The inSIGHT study: costs and effects of routine hysteroscopy prior to a first IVF treatment cycle. A randomised controlled trial	Smit, J.; Kasius, J.; Eijkemans, M.; Koks, C.; van Golde, R.; Oosterhuis, G.; Nap, A.; Scheffer, G.; Manger, P.; Hoek, A.; Kaplan, M.; Schoot, B.; van Heusden, A.; Kuchenbecker, W.; Perquin, D.; Fleischer, K.; Kaaijk, E.; Sluijmer, A.; Friederich, J.; Laven, J.; et al.
	2013	Induction of labour with a Foley catheter or oral misoprostol at term: The PROBAAT-II study, a multicentre randomised controlled trial	Ten Eikelder, M.; Neervoort, F.; Oude Rengerink, K.; Jozwiak, M.; de Leeuw, J.; de Graaf, I.; van Pampus, M.; Franssen, M.; Oudijk, M.; van der Salm, P.; Woiski, M.; Pernet, P.; Feitsma, A.; van Vliet, H.; Porath, M.; Roumen, F.; van Beek, E.; Versendaal, H.; Heres, M.; Mol, B.; et al.
	2010	Antenatal allopurinol for reduction of birth asphyxia induced brain damage (ALLO-Trial); a randomized double blind placebo controlled multicenter study	Kaandorp, J.; Benders, M.; Rademaker, C.; Torrance, H.; Oudijk, M.; de Haan, T.; Bloemenkamp, K.; Rijken, M.; van Pampus, M.; Bos, A.; Porath, M.; Bambang Oetomo, S.; Willekes, C.; Danilo Gavilanes, A.; Wouters, M.; van Elburg, R.; Huisjes, A.; Bakker, S.; van Meir, C.; von Lindern, J.; et al.
	2015	Increased STAG2 dosage defines a novel cohesinopathy with intellectual disability and behavioral problems	Kumar, R.; Corbett, M.; Van Bon, B.; Gardner, A.; Woenig, J.; Jolly, L.; Douglas, E.; Friend, K.; Tan, C.; Van Esch, H.; Holvoet, M.; Raynaud, M.; Field, M.; Leffler, M.; Budny, B.; Wisniewska, M.; Badura-Stronka, M.; Latos-Bieleńska, A.; Batanian, J.; Rosenfeld, J.; et al.
	2016	HUWE1 mutations in Juberg-Marsidi and Brooks syndromes: the results of an X-chromosome exome sequencing study	Friez, M.; Brooks, S.; Stevenson, R.; Field, M.; Basehore, M.; Adès, L.; Sebold, C.; Mcgee, S.; Saxon, S.; Skinner, C.; Craig, M.; Murray, L.; Simensen, R.; Yap, Y.; Shaw, M.; Gardner, A.; Corbett, M.; Kumar, R.; Bosshard, M.; Van Loon, B.; et al.
	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	High incidence of Noonan Syndrome features including short stature and pulmonic stenosis in patients carrying NF1 missense mutations affecting p.Arg1809: genotype-phenotype correlation	Rojnueangnit, K.; Xie, J.; Gomes, A.; Sharp, A.; Callens, T.; Chen, Y.; Liu, Y.; Cochran, M.; Abbott, M.; Atkin, J.; Babovic-Vuksanovic, D.; Barnett, C.; Crenshaw, M.; Bartholomew, D.; Basel, L.; Bellus, G.; Ben-Shachar, S.; Bialer, M.; Bick, D.; Blumberg, B.; et al.
	2012	Identification of cases with adverse neonatal outcome monitored by cardiotocography versus ST analysis: secondary analysis of a randomized trial	Westerhuis, M.; Porath, M.; Becker, J.; Van den Akker, E.; van Beek, E.; van Dessel, H.; Drogtrop, A.; van Geijn, H.; Graziosi, G.; Groenendaal, F.; van Lith, J.; Mol, B.; Moons, K.; Nijhuis, J.; Oei, S.; Oosterbaan, H.; Rijnders, R.; Schuitemaker, N.; Wijnberger, L.; Willekes, C.; et al.
	2014	Refining analyses of copy number variation identifies specific genes associated with developmental delay	Coe, B.; Witherspoon, K.; Rosenfeld, J.; van Bon, B.; Vulto-van Silfhout, A.; Bosco, P.; Friend, K.; Baker, C.; Buono, S.; Vissers, L.; Schuurs-Hoeijmakers, J.; Hoischen, A.; Pfundt, R.; Krumm, N.; Carvill, G.; Li, D.; Amaral, D.; Brown, N.; Lockhart, P.; Scheffer, I.; et al.
	2013	Enzyme replacement therapy for mucopolysaccharidosis VI: long-term cardiac effects of galsulfase (Naglazyme®) therapy	Braunlin, E.; Rosenfeld, H.; Kampmann, C.; Johnson, J.; Beck, M.; Giugliani, R.; Guffon, N.; Ketteridge, D.; Miranda, C.; Scarpa, M.; Schwartz, I.; Teles, E.; Wraith, J.; Barrios, P.; Dias da Silva, E.; Kurio, G.; Richardson, M.; Gildengorin, G.; Hopwood, J.; Imperiale, M.; et al.