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PreviewIssue DateTitleAuthor(s)
2014Ancient human genomes suggest three ancestral populations for present-day EuropeansLazaridis, I.; Patterson, N.; Mittnik, A.; Renaud, G.; Mallick, S.; Kirsanow, K.; Sudmant, P.; Schraiber, J.; Castellano, S.; Lipson, M.; Berger, B.; Economou, C.; Bollongino, R.; Fu, Q.; Bos, K.; Nordenfelt, S.; Li, H.; De Filippo, C.; Prüfer, K.; Sawyer, S.; et al.
2016Inherited determinants of Crohn's disease and ulcerative colitis phenotypes: a genetic association studyCleynen, I.; Boucher, G.; Jostins, L.; Schumm, L.; Zeissig, S.; Ahmad, T.; Andersen, V.; Andrews, J.; Annese, V.; Brand, S.; Brant, S.; Cho, J.; Daly, M.; Dubinsky, M.; Duerr, R.; Ferguson, L.; Franke, A.; Gearry, R.; Goyette, P.; Hakonarson, H.; et al.
2016Stillbirths: recall to action in high-income countriesFlenady, V.; Wojcieszek, A.; Middleton, P.; Ellwood, D.; Erwich, J.; Coory, M.; Khong, T.; Silver, R.; Smith, G.; Boyle, F.; Lawn, J.; Blencowe, H.; Leisher, S.; Gross, M.; Horey, D.; Farrales, L.; Bloomfield, F.; McCowan, L.; Brown, S.; Joseph, K.; et al.
2015Mutations in DDX3X are a common cause of unexplained intellectual disability with gender-specific effects on Wnt signalingSnijders 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.
2015Candidate locus analysis of the TERT–CLPTM1L cancer risk region on chromosome 5p15 identifies multiple independent variants associated with endometrial cancer riskCarvajal-Carmona, L.; O Mara, T.; Painter, J.; Lose, F.; Dennis, J.; Michailidou, K.; Tyrer, J.; Ahmed, S.; Ferguson, K.; Healey, C.; Pooley, K.; Beesley, J.; Cheng, T.; Jones, A.; Howarth, K.; Martin, L.; Gorman, M.; Hodgson, S.; National Study of Endometrial Cancer Genetics Group (NSECG),; The Australian National Endometrial Cancer Study Group (ANECS); et al.

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