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Preview	Issue Date	Title	Author(s)
	2018	Cortical abnormalities in bipolar disorder: an MRI analysis of 6503 individuals from the ENIGMA Bipolar Disorder Working Group	Hibar, D.; Westlye, L.; Doan, N.; Jahanshad, N.; Cheung, J.; Ching, C.; Versace, A.; Bilderbeck, A.; Uhlmann, A.; Mwangi, B.; Krämer, B.; Overs, B.; Hartberg, C.; Abé, C.; Dima, D.; Grotegerd, D.; Sprooten, E.; Bøen, E.; Jimenez, E.; Howells, F.; et al.
	2019	GooD4Mum: a general practice-based quality improvement collaborative for diabetes prevention in women with previous gestational diabetes	O'Reilly, S.L.; Dunbar, J.A.; Best, J.D.; Versace, V.; Ford, D.; Young, A.; Shih, S.; Bills, R.; Shepherdley, W.; Janus, E.D.; Carter, R.; Oats, J.; Skinner, T.; Ackland, M.; Phillips, P.; Nankervis, A.; Johnson, G.; Catford, J.; Jeffries, B.; Rasa, J.; et al.
	2019	Preferred learning modalities and practice for critical skills: a global survey of paediatric emergency medicine clinicians	Craig, S.S.; Auerbach, M.; Cheek, J.A.; Babl, F.E.; Oakley, E.; Nguyen, L.; Rao, A.; Dalton, S.; Lyttle, M.D.; Mintegi, S.; Nagler, J.; Mistry, R.D.; Dixon, A.; Rino, P.; Kohn-Loncarica, G.; Dalziel, S.R.; Tzimenatos, L.; Mistry, R.; Brown, K.; Powell, E.; et al.
	2019	Intronic ATTTC repeat expansions in STARD7 in familial adult myoclonic epilepsy linked to chromosome 2	Corbett, M.A.; Kroes, T.; Veneziano, L.; Bennett, M.F.; Florian, R.; Schneider, A.L.; Coppola, A.; Licchetta, L.; Franceschetti, S.; Suppa, A.; Wenger, A.; Mei, D.; Pendziwiat, M.; Kaya, S.; Delledonne, M.; Straussberg, R.; Xumerle, L.; Regan, B.; Crompton, D.; van Rootselaar, A.-F.; et al.
	2019	Association of HIV preexposure prophylaxis with incidence of sexually transmitted infections among individuals at high risk of HIV infection	Traeger, M.W.; Cornelisse, V.J.; Asselin, J.; Price, B.; Roth, N.J.; Willcox, J.; Tee, B.K.; Fairley, C.K.; Chang, C.C.; Armishaw, J.; Vujovic, O.; Penn, M.; Cundill, P.; Forgan-Smith, G.; Gall, J.; Pickett, C.; Lal, L.; Mak, A.; Spelman, T.D.; Long, N.; et al.
	2019	Association of chromosome 9p21 with subsequent coronary heart disease events A GENIUS-CHD study of individual participant data	Patel, R.S.; Schmidt, A.F.; Tragante, V.; McCubrey, R.O.; Holmes, M.; Howe, L.J.; Direk, K.; Akerblom, A.; Leander, K.; Virani, S.S.; Kaminski, K.A.; Muehlschlegel, J.D.; Dube, M.-P.; Allayee, H.; Almgren, P.; Alver, M.; Baranova, E.; Behlouli, H.; Boeckx, B.; Braund, P.S.; et al.
	2017	Developing consensus-based priority outcome domains for trials in kidney transplantation: a multinational Delphi Survey with patients, caregivers, and health professionals	Sautenet, B.; Tong, A.; Manera, K.; Chapman, J.; Warrens, A.; Rosenbloom, D.; Wong, G.; Gill, J.; Budde, K.; Rostaing, L.; Marson, L.; Josephson, M.; Reese, P.; Pruett, T.; Hanson, C.; O'Donoghue, D.; Tam-Tham, H.; Halimi, J.; Shen, J.; Kanellis, J.; et al.
	2018	A four-gene lincRNA expression signature predicts risk in multiple cohorts of acute myeloid leukemia patients	Beck, D.; Thoms, J.; Palu, C.; Herold, T.; Shah, A.; Olivier, J.; Boelen, L.; Huang, Y.; Chacon, D.; Brown, A.; Babic, M.; Hahn, C.; Perugini, M.; Zhou, X.; Huntly, B.; Schwarzer, A.; Klusmann, J.-H.; Berdel, W.; Wörmann, B.; Büchner, T.; et al.
	2014	Inactivating mutations in NPC1L1 and protection from coronary heart disease	Stitziel, N.O.; Won, H.H.; Morrison, A.C.; Peloso, G.M.; Do, R.; Lange, L.A.; Fontanillas, P.; Gupta, N.; Duga, S.; Goel, A.; Farrall, M.; Saleheen, D.; Ferrario, P.; König, I.; Asselta, R.; Merlini, P.A.; Marziliano, N.; Notarangelo, M.F.; Schick, U.; Auer, P.; et al.
	2014	Tumor mismatch repair immunohistochemistry and DNA MLH1 methylation testing of patients with endometrial cancer diagnosed at age younger than 60 years optimizes triage for population-level germline mismatch repair gene mutation testing	Buchanan, D.; Tan, Y.; Walsh, M.; Clendenning, M.; Metcalf, A.; Ferguson, K.; Arnold, S.; Thompson, B.; Lose, F.; Parsons, M.; Walters, R.; Pearson, S.; Cummings, M.; Oehler, M.; Blomfield, P.; Quinn, M.; Kirk, J.; Stewart, C.; Obermair, A.; Young, J.; et al.