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Preview	Issue Date	Title	Author(s)
	2015	Human-assisted invasions of Pacific islands by Litoria frogs: a case study of the bleating tree frog on Lord Howe Island	Plenderleith, T.; Smith, K.; Donnellan, S.; Reina, R.; Chapple, D.; Patterson, H.
	1997	Ancient missense mutations in a new member of the RoRet gene family are likely to cause Familial Mediterranean Fever	Aksentijevich, I.; Centola, M.; Deng, Z.; Sood, R.; Balow, J.; Wood, G.; Zaks, N.; Mansfield, E.; Chen, X.; Eisenberg, S.; Vedula, A.; Shafran, N.; Raben, N.; Pras, E.; Pras, M.; Kastner, D.; Blake, T.; Baxevanis, A.; Robbins, C.; Krizman, D.; et al.
	2011	Double-stranded RNA is pathogenic in Drosophila models of expanded repeat neurodegenerative diseases	Lawlor, K.; O'Keefe, L.; Samaraweera, S.; van Eyk, C.; McLeod, C.; Maloney, C.; Dang, T.; Suter, C.; Richards, R.
	2011	Identification of SOX3 as an XX male sex reversal gene in mice and humans	Sutton, E.; Hughes, J.; White, S.; Sekido, R.; Tan, J.; Arboleda, V.; Rogers, N.; Knower, K.; Rowley, L.; Eyre, H.; Rizzoti, K.; McAninch, D.; Golcalves, J.; Slee, J.; Turbitt, E.; Bruno, D.; Bengtsson, H.; Harley, V.; Vilain, E.; Sinclair, A.; et al.
	1998	PAK3 mutation in nonsyndromic X-linked mental retardation	Allen, K.; Gleeson, J.; Bagrodia, S.; Partington, M.; MacMillan, J.; Cerione, R.; Mulley, J.; Walsh, C.
	1998	The identification and localisation of a human gene with sequence similarity to Polycomblike of Drosophila melanogaster	Coulson, M.; Robert, S.; Eyre, H.; Saint, R.
	2017	Mitochondrion to endoplasmic reticulum apposition length in zebrafish embryo spinal progenitors is unchanged in response to perturbations associated with Alzheimer’s disease	Newman, M.; Halter, L.; Lim, A.; Lardelli, M.; Lakshmana, M.
	1998	Localisation of the human NMDAR2D receptor subunit gene (GRIN2D) to 19q13.1-qter, the NMDAR2A subunit gene to 16p13.2 (GRIN2A), and the NMDAR2C subunit gene (GRIN2C) to 17q24-q25 using somatic cell hybrid and radiation hybrid mapping panels.	Kalsi, G.; Whiting, P.; Bourdelles, B.; Callen, D.; Barnard, E.; Gurling, H.
	1998	The human dead ringer/bright homolog, DRIL1: cDNA cloning, gene structure, and mapping to D19S886, a marker on 19p13.3 that is strictly linked to the Peutz-Jeghers Syndrome.	Kortschak, R.; Reimann, H.; Zimmer, M.; Eyre, H.; Saint, R.; Jenne, D.
	2023	The impact of the cytoplasmic ubiquitin ligase TNFAIP3 gene variation on transcription factor NF-κB activation in acute kidney injury	Rogers, N.M.; Zammit, N.; Nguyen-Ngo, D.; Souilmi, Y.; Minhas, N.; Meijles, D.N.; Self, E.; Walters, S.N.; Warren, J.; Cultrone, D.; El-Rashid, M.; Li, J.; Chtanova, T.; O'Connell, P.J.; Grey, S.T.