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Preview	Issue Date	Title	Author(s)
	2023	Distinct Assemblies of Heterodimeric Cytokine Receptors Govern Stemness Programs in Leukemia	Kan, W.L.; Dhagat, U.; Hercus, T.R.; Kaufmann, K.B.; Nero, T.L.; Zeng, A.G.X.; Toubia, J.; Barry, E.F.; Broughton, S.E.; Gomez, G.A.; Dottore, M.; Cheung Tung Shing, K.S.; Thomas, D.; Benard, B.; Simpson, K.J.; Schoof, E.; Goodall, G.J.; Begley, C.G.; Ekert, P.G.; Tvorogov, D.; et al.
	2020	RUNX1-mutated families show phenotype heterogeneity and a somatic mutation profile unique to germline predisposed AML	Brown, A.L.; Arts, P.; Carmichael, C.L.; Babic, M.; Dobbins, J.; Chong, C.-E.; Schreiber, A.W.; Feng, J.; Phillips, K.; Wang, P.P.S.; Ha, T.; Homan, C.C.; King-Smith, S.L.; Rawlings, L.; Vakulin, C.; Dubowsky, A.; Burdett, J.; Moore, S.; McKavanagh, G.; Henry, D.; et al.
	2020	Intravenous alteplase for stroke with unknown time of onset guided by advanced imaging: systematic review and meta-analysis of individual patient data	Thomalla, G.; Boutitie, F.; Ma, H.; Koga, M.; Ringleb, P.; Schwamm, L.H.; Wu, O.; Bendszus, M.; Bladin, C.F.; Campbell, B.C.V.; Cheng, B.; Churilov, L.; Ebinger, M.; Endres, M.; Fiebach, J.B.; Fukuda-Doi, M.; Inoue, M.; Kleinig, T.J.; Latour, L.L.; Lemmens, R.; et al.
	2020	An investigation of antihypertensive class, dementia, and cognitive decline	Peters, R.; Yasar, S.; Anderson, C.S.; Andrews, S.; Antikainen, R.; Arima, H.; Beckett, N.; Beer, J.C.; Bertens, A.S.; Booth, A.; van Boxtel, M.; Brayne, C.; Brodaty, H.; Carlson, M.C.; Chalmers, J.; Corrada, M.; DeKosky, S.; Derby, C.; Dixon, R.A.; Forette, F.; 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.
	2020	Multitrait analysis of glaucoma identifies new risk loci and enables polygenic prediction of disease susceptibility and progression	Craig, J.E.; Han, X.; Qassim, A.; Hassall, M.; Cooke Bailey, J.N.; Kinzy, T.G.; Khawaja, A.P.; An, J.; Marshall, H.; Gharahkhani, P.; Igo, R.P.; Graham, S.L.; Healey, P.R.; Ong, J.-S.; Zhou, T.; Siggs, O.; Law, M.H.; Souzeau, E.; Ridge, B.; Hysi, P.G.; et al.
	2020	Genome sequencing in persistently unsolved white matter disorders	Helman, G.; Lajoie, B.R.; Crawford, J.; Takanohashi, A.; Walkiewicz, M.; Dolzhenko, E.; Gross, A.M.; Gainullin, V.G.; Bent, S.J.; Jenkinson, E.M.; Ferdinandusse, S.; Waterham, H.R.; Dorboz, I.; Bertini, E.; Miyake, N.; Wolf, N.I.; Abbink, T.E.M.; Kirwin, S.M.; Tan, C.M.; Hobson, G.M.; et al.
	2020	The genetic architecture of the human cerebral cortex	Grasby, K.L.; Jahanshad, N.; Painter, J.N.; Colodro-Conde, L.; Bralten, J.; Hibar, D.P.; Lind, P.A.; Pizzagalli, F.; Ching, C.R.K.; McMahon, M.A.B.; Shatokhina, N.; Zsembik, L.C.P.; Thomopoulos, S.I.; Zhu, A.H.; Strike, L.T.; Agartz, I.; Alhusaini, S.; Almeida, M.A.A.; Alnæs, D.; Amlien, I.K.; et al.
	2020	Evaluation of implementation of risk management guidelines for carriers of pathogenic variants in mismatch repair genes: a nationwide audit of familial cancer clinics	Meiser, B.; Kaur, R.; Kirk, J.; Morrow, A.; Peate, M.; Wong, W.K.T.; McPike, E.; Cops, E.; Dowson, C.; Austin, R.; Fine, M.; Thrupp, L.; Ward, R.; Macrae, F.; Hiller, J.E.; Trainer, A.H.; Mitchell, G.; Susman, R.; Pachter, N.; Goodwin, A.; et al.
	2020	Effect of intravenous tenecteplase dose on cerebral reperfusion before thrombectomy in patients with large vessel occlusion ischemic stroke: the EXTEND-IA TNK part 2 randomized clinical trial	Campbell, B.C.V.; Mitchell, P.J.; Churilov, L.; Yassi, N.; Kleinig, T.J.; Dowling, R.J.; Yan, B.; Bush, S.J.; Thijs, V.; Scroop, R.; Simpson, M.; Brooks, M.; Asadi, H.; Wu, T.Y.; Shah, D.G.; Wijeratne, T.; Zhao, H.; Alemseged, F.; Ng, F.; Bailey, P.; et al.