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Preview	Issue Date	Title	Author(s)
	2016	CXCR5⁺ follicular cytotoxic T cells control viral infection in B cell follicles	Leong, Y.; Chen, Y.; Ong, H.; Wu, D.; Man, K.; Deleage, C.; Minnich, M.; Meckiff, B.; Wei, Y.; Hou, Z.; Zotos, D.; Fenix, K.; Atnerkar, A.; Preston, S.; Chipman, J.; Beilman, G.; Allison, C.; Sun, L.; Wang, P.; Xu, J.; et al.
	2004	Interlaboratory comparison of results of susceptibility testing with caspofungin against candida and aspergillus species	Odds, F.; Motyl, M.; Andrade, R.; Bille, J.; Canton, E.; Cuenca-Estrella, M.; Davidson, A.; Durussel, C.; Ellis, D.; Foraker, E.; Fothergill, A.; Ghannoum, M.; Giacobbe, R.; Gobernado, M.; Handke, R.; Laverdiere, M.; Lee-Yang, W.; Merz, W.; Ostrosky-Zeichner, L.; Peman, J.; et al.
	2007	Mutations in the BRWD3 gene cause X-linked mental retardation associated with macrocephaly	Field, M.; Tarpey, P.; Smith, R.; Edkins, S.; O'Meara, S.; Stevens, C.; Tofts, C.; Teague, J.; Butler, A.; Dicks, E.; Barthorpe, S.; Buck, G.; Cole, J.; Gray, K.; Halliday, K.; Hills, K.; Jenkinson, A.; Jones, D.; Menzies, A.; Mironenko, T.; et al.
	1998	Construction of an ~700-kb transcript map around the Familial Mediterranean Fever locus on human chromosome 16p13.3	Centola, M.; Chen, X.; Sood, R.; Deng, Z.; Aksentijevich, I.; Blake, T.; Ricke, D.; Chen, X.; Wood, G.; Zaks, N.; Richards, N.; Krizman, D.; Mansfield, E.; Apostolou, S.; Liu, J.; Shafran, N.; Vedula, A.; Hamon, M.; Cercek, A.; Kahan, T.; et al.
	2004	Proceedings of the Oxygen Homeostasis/Hypoxia Meeting	Kaufman, B.; Scharf, O.; Arbeit, J.; Ashcroft, M.; Brown, J.; Bruick, R.; Chapman, J.; Evans, S.; Giaccia, A.; Harris, A.; Huang, E.; Johnson, R.; Kaelin Jr., W.; Koch, C.; Maxwell, P.; Mitchell, J.; Neckers, L.; Powis, G.; Rajendran, J.; Semenza, G.; et al.
	2007	Mutations in UPF3B, a member of the nonsense-mediated mRNA decay complex, cause syndromic and nonsyndromic mental retardation	Tarpey, P.; Raymond, F.; Nguyen, L.; Rodriguez, J.; Hackett, A.; Vandeleur, L.; Smith, R.; Shoubridge, C.; Edkins, S.; Stevens, C.; O'Meara, S.; Tofts, C.; Barthorpe, S.; Buck, G.; Cole, J.; Halliday, K.; Hills, K.; Jones, D.; Mironenko, T.; Perry, J.; et al.
	2020	Genetic comorbidity between major depression and cardio-metabolic traits, stratified by age at onset of major depression	Hagenaars, S.P.; Coleman, J.R.I.; Choi, S.W.; Gaspar, H.; Adams, M.J.; Howard, D.M.; Hodgson, K.; Traylor, M.; Air, T.M.; Andlauer, T.F.M.; Arolt, V.; Baune, B.T.; Binder, E.B.; Blackwood, D.H.R.; Boomsma, D.I.; Campbell, A.; Cearns, M.; Czamara, D.; Dannlowski, U.; Domschke, K.; et al.
	2018	A global cline in a colour polymorphism suggests a limited contribution of gene flow towards the recovery of a heavily exploited marine mammal	Hoffman, J.I.; Bauer, E.; Paijmans, A.J.; Humble, E.; Beckmann, L.M.; Kubetschek, C.; Christaller, F.; Kröcker, N.; Fuchs, B.; Moreras, A.; Shihlomule, Y.D.; Bester, M.N.; Cleary, A.C.; De Bruyn, P.J.N.; Forcada, J.; Goebel, M.E.; Goldsworthy, S.D.; Guinet, C.; Hoelzel, A.R.; Lydersen, C.; 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.
	2020	Repurposing a neurodegenerative disease drug to treat Gram-negative antibiotic-resistant bacterial sepsis	De Oliveira, D.M.P.; Bohlmann, L.; Conroy, T.; Jen, F.E.-C.; Everest-Dass, A.; Hansford, K.A.; Bolisetti, R.; El-Deeb, I.M.; Forde, B.M.; Phan, M.-D.; Lacey, J.A.; Tan, A.; Rivera-Hernandez, T.; Brouwer, S.; Keller, N.; Kidd, T.J.; Cork, A.J.; Bauer, M.J.; Cook, G.M.; Davies, M.R.; et al.