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Preview	Issue Date	Title	Author(s)
	1997	The genome organisation of the Fanconi Anemia Group A (FAA) Gene	Ianzano, L.; d'Apolito, M.; Centra, M.; Savino, M.; Levran, O.; Auerbach, A.; Cleton-Jansen, A.M.; Doggett, N.; Pronk, J.; Tipping, A.; Gibson, R.; Mathew, C.; Whitmore, S.; Apostolou, S.; Callen, D.; Zelante, L.; Savoia, A.
	1997	Gene structure and subcellular localisation of FMR2, a member of a new family of putative transcription activators	Gecz, J.; Bielby, S.; Sutherland, G.; Mulley, J.
	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.
	1997	A high-resolution genetic map of the familial Mediterranean fever candidate region allows identification of haplotype-sharing among ethnic groups	Balow Jnr., J.; Shelton, D.; Orsborn, A.; Mangelsdorf, M.; Aksentijevich, I.; Blake, T.; Sood, R.; Gardner, D.; Liu, R.; Pras, E.; Levy, E.; Centola, M.; Deng, Z.; Zaks, N.; Wood, G.; Chen, X.; Richards, N.; Shohat, M.; Livneh, A.; Pras, M.; et al.
	2018	Analysis of 182 cerebral palsy transcriptomes points to dysregulation of trophic signalling pathways and overlap with autism	Van Eyk, C.; Corbett, M.; Gardner, A.; Van Bon, B.; Broadbent, J.; Harper, K.; MacLennan, A.; Gecz, J.
	1997	Chromosomal localisation of the human P2y6 purinoceptor gene and phylogenetic analysis of the P2y purinoceptor family	Somers, G.; Hammet, F.; Woollatt, E.; Richards, R.; Southey, M.; Venter, D.
	1999	The PISSLRE Gene: structure, exon skipping, and exclusion as tumor suppressor in breast cancer	Crawford, J.; Ianzano, L.; Savino, M.; Whitmore, S.; Cleton-Jansen, A.M.; Settasatian, C.; d'Apolito, M.; Seshadri, R.; Pronk, J.; Auerbach, A.; Verlander, P.; Mathew, C.; Tipping, A.; Doggett, N.; Zelante, L.; Callen, D.; Savoia, A.
	2017	Single-nucleotide variant proportion in genes: a new concept to explore major depression based on DNA sequencing data	Yu, C.; Baune, B.; Licinio, J.; Wong, M.
	2017	Gonadal mosaicism of a novel IQSEC2 variant causing female limited intellectual disability and epilepsy	Ewans, L.J.; Field, M.; Zhu, Y.; Turner, G.; Leffler, M.; Dinger, M.E.; Cowley, M.J.; Buckley, M.F.; Scheffer, I.E.; Jackson, M.R.; Roscioli, T.; Shoubridge, C.
	2014	From cheek swabs to consensus sequences: an A to Z protocol for high-throughput DNA sequencing of complete human mitochondrial genomes	Clarke, A.; Prost, S.; Stanton, J.; White, W.; Kaplan, M.; Matisoo-Smith, E.; Genographic Consortium,