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Preview	Issue Date	Title	Author(s)
	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.
	2006	Exploration of the genetic architecture of idiopathic generalized epilepsies	Hempelmann, A.; Taylor, K.; Heils, A.; Lorenz, S.; Prud'Homme, J.; Nabbout, R.; Dulac, O.; Rudolf, G.; Zara, F.; Bianchi, A.; Robinson, R.; Gardiner, R.; Covanis, A.; Lindhout, D.; Stephani, U.; Elger, C.; Weber, Y.; Lerche, H.; Nurnberg, P.; Kron, K.; et al.
	2006	Implantation of the human embryo: Research lines and models	Bischof, P.; Aplin, J.; Bentin-Ley, U.; Brannstrom, M.; Casslen, B.; Castrillo, J.; Classen-Linke, I.; Critchley, H.; Devoto, L.; D'Hooghe, T.; Horcajadas, J.; Groothuis, P.; Ivell, R.; Pongrantz, I.; Macklon, N.; Sharkey, A.; Vicovac, L.; White, J.; Winterhager, E.; von Wolff, M.; et al.
	2015	Integrated genomic and transcriptomic analysis of human brain metastases identifies alterations of potential clinical significance	Saunus, J.; Quinn, M.; Patch, A.; Pearson, J.; Bailey, P.; Nones, K.; McCart Reed, A.; Miller, D.; Wilson, P.; Al-Ejeh, F.; Mariasegaram, M.; Lau, Q.; Withers, T.; Jeffree, R.; Reid, L.; Da Silva, L.; Matsika, A.; Niland, C.; Cummings, M.; Bruxner, T.; et al.
	2012	Prognostically significant fusion oncogenes in Pakistani patients with adult acute lymphoblastic leukemia and their association with disease biology and outcome	Sabir, N.; Iqbal, Z.; Aleem, A.; Awan, T.; Naeem, T.; Asad, S.; Tahir, A.; Absar, M.; Hasanato, R.; Basit, S.; Chishti, M.; Ul-Haque, M.; Khalid, A.; Sabar, M.; Rasool, M.; Karim, S.; Khan, M.; Samreen, B.; Akram, A.; Siddiqi, M.; et al.
	2017	YY1 haploinsufficiency causes an intellectual disability syndrome featuring transcriptional and chromatin dysfunction	Gabriele, M.; Vulto-van Silfhout, A.; Germain, P.; Vitriolo, A.; Kumar, R.; Douglas, E.; Haan, E.; Kosaki, K.; Takenouchi, T.; Rauch, A.; Steindl, K.; Frengen, E.; Misceo, D.; Pedurupillay, C.; Stromme, P.; Rosenfeld, J.; Shao, Y.; Craigen, W.; Schaaf, C.; Rodriguez-Buritica, D.; 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	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.
	2016	A principal component meta-analysis on multiple anthropometric traits identifies novel loci for body shape	Ried, J.; Jeff, J.; Chu, A.; Bragg-Gresham, J.; Van Dongen, J.; Huffman, J.; Ahluwalia, T.; Cadby, G.; Eklund, N.; Eriksson, J.; Esko, T.; Feitosa, M.; Goel, A.; Gorski, M.; Hayward, C.; Heard-Costa, N.; Jackson, A.; Jokinen, E.; Kanoni, S.; Kristiansson, K.; et al.
	2015	A meta-analysis of gene expression signatures of blood pressure and hypertension	Huan, T.; Esko, T.; Peters, M.; Pilling, L.; Schramm, K.; Schurmann, C.; Chen, B.; Liu, C.; Joehanes, R.; Johnson, A.; Yao, C.; Ying, S.; Courchesne, P.; Milani, L.; Raghavachari, N.; Wang, R.; Liu, P.; Reinmaa, E.; Dehghan, A.; Hofman, A.; et al.; McCarthy, M.