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Preview	Issue Date	Title	Author(s)
	2016	TBC1D24 genotype-phenotype correlation	Balestrini, S.; Milh, M.; Castiglioni, C.; Lüthy, K.; Finelli, M.; Verstreken, P.; Cardon, A.; Stražišar, B.; Holder, J.; Lesca, G.; Mancardi, M.; Poulat, A.; Repetto, G.; Banka, S.; Bilo, L.; Birkeland, L.; Bosch, F.; Brockmann, K.; Cross, J.; Doummar, D.; et al.
	2020	ENIGMA and global neuroscience: A decade of large-scale studies of the brain in health and disease across more than 40 countries	Thompson, P.M.; Jahanshad, N.; Ching, C.R.K.; Salminen, L.E.; Thomopoulos, S.I.; Bright, J.; Baune, B.T.; Bertolín, S.; Bralten, J.; Bruin, W.B.; Bülow, R.; Chen, J.; Chye, Y.; Dannlowski, U.; de Kovel, C.G.F.; Donohoe, G.; Eyler, L.T.; Faraone, S.V.; Favre, P.; Filippi, C.A.; et al.
	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.
	2017	Antenatal suppression of il-1 protects against inflammation-induced fetal injury and improves neonatal and developmental outcomes in mice	Nadeau-Vallée, M.; Chin, P.; Belarbi, L.; Brien, M.; Pundir, S.; Berryer, M.; Beaudry-Richard, A.; Madaan, A.; Sharkey, D.; Lupien-Meilleur, A.; Hou, X.; Quiniou, C.; Beaulac, A.; Boufaied, I.; Boudreault, A.; Carbonaro, A.; Doan, N.; Joyal, J.; Lubell, W.; Olson, D.; et al.
	2020	ENIGMA MDD: seven years of global neuroimaging studies of major depression through worldwide data sharing	Schmaal, L.; Pozzi, E.; C Ho, T.; van Velzen, L.S.; Veer, I.M.; Opel, N.; Van Someren, E.J.W.; Han, L.K.M.; Aftanas, L.; Aleman, A.; Baune, B.T.; Berger, K.; Blanken, T.F.; Capitão, L.; Couvy-Duchesne, B.; R Cullen, K.; Dannlowski, U.; Davey, C.; Erwin-Grabner, T.; Evans, J.; et al.
	2021	Brain structural abnormalities in obesity: relation to age, genetic risk, and common psychiatric disorders: evidence through univariate and multivariate mega-analysis including 6420 participants from the ENIGMA MDD working group	Opel, N.; Thalamuthu, A.; Milaneschi, Y.; Grotegerd, D.; Flint, C.; Leenings, R.; Goltermann, J.; Richter, M.; Hahn, T.; Woditsch, G.; Berger, K.; Hermesdorf, M.; McIntosh, A.; Whalley, H.C.; Harris, M.A.; MacMaster, F.P.; Walter, H.; Veer, I.M.; Frodl, T.; Carballedo, A.; et al.
	2021	A Brain Capital Grand Strategy: toward economic reimagination	Smith, E.; Ali, D.; Wilkerson, B.; Dawson, W.D.; Sobowale, K.; Reynolds, C.; Berk, M.; Lavretsky, H.; Jeste, D.; Ng, C.H.; Soares, J.C.; Aragam, G.; Wainer, Z.; Manji, H.K.; Licinio, J.; Lo, A.W.; Storch, E.; Fu, E.; Leboyer, M.; Tarnanas, I.; et al.
	2020	Common genetic variation indicates separate causes for periventricular and deep white matter hyperintensities	Armstrong, N.J.; Mather, K.A.; Sargurupremraj, M.; Knol, M.J.; Malik, R.; Satizabal, C.L.; Yanek, L.R.; Wen, W.; Gudnason, V.G.; Dueker, N.D.; Elliott, L.T.; Hofer, E.; Hofer, E.; Bis, J.; Jahanshad, N.; Li, S.; Logue, M.A.; Logue, M.A.; Luciano, M.; Scholz, M.; et al.
	2013	A novel prion disease associated with diarrhea and autonomic neuropathy	Mead, S.; Gandhi, S.; Beck, J.; Caine, D.; Gallujipali, D.; Carswell, C.; Hyare, H.; Joiner, S.; Ayling, H.; Lashley, T.; Linehan, J.M.; Al-Doujaily, H.; Sharps, B.; Revesz, T.; Sandberg, M.K.; Reilly, M.M.; Koltzenburg, M.; Forbes, A.; Rudge, P.; Brandner, S.; et al.
	2016	A genome-wide association study in multiple system atrophy	Sailer, A.; Scholz, S.W.; Nalls, M.A.; Schulte, C.; Federoff, M.; Price, T.R.; Lees, A.; Ross, O.A.; Dickson, D.W.; Mok, K.; Mencacci, N.E.; Schottlaender, L.; Chelban, V.; Ling, H.; O'Sullivan, S.S.; Wood, N.W.; Traynor, B.J.; Ferrucci, L.; Federoff, H.J.; Mhyre, T.R.; et al.