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Preview	Issue Date	Title	Author(s)
	2023	TP53 mutation variant allele frequency of ≥10% is associated with poor prognosis in therapy-related myeloid neoplasms	Shah, M.V.; Tran, E.N.H.; Shah, S.; Chhetri, R.; Baranwal, A.; Ladon, D.; Shultz, C.; Al-Kali, A.; Brown, A.L.; Chen, D.; Scott, H.S.; Greipp, P.; Thomas, D.; Alkhateeb, H.B.; Singhal, D.; Gangat, N.; Kumar, S.; Patnaik, M.M.; Hahn, C.N.; Kok, C.H.; et al.
	2009	Long-term effects of a very low-carbohydrate diet and a low-fat diet on mood and cognitive function	Brinkworth, G.; Buckley, J.; Noakes, M.; Clifton, P.; Wilson, C.
	2013	Axl mediates acquired resistance of head and neck cancer cells to the epidermal growth factor receptor inhibitor erlotinib	Giles, K.; Kalinowski, F.; Candy, P.; Epis, M.; Zhang, P.; Redfern, A.; Stuart, L.; Goodall, G.; Leedman, P.
	2013	Rare variants in single-minded 1 (SIM1) are associated with severe obesity	Ramachandrappa, S.; Raimondo, A.; Cali, A.; Keogh, J.; Henning, E.; Saeed, S.; Thompson, A.; Garg, S.; Bochukova, E.; Brage, S.; Trowse, V.; Wheeler, E.; Sullivan, A.; Dattani, M.; Clayton, P.; Datta, V.; Bruning, J.; Wareham, N.; O'Rahilly, S.; Peet, D.; et al.
	2004	Benign familial neonatal-infantile seizures: Characterization of a new sodium channelopathy	Berkovic, S.; Heron, S.; Giordano, L.; Marini, C.; Guerrini, R.; Kaplan, R.; Gambardella, A.; Steinlein, O.; Grinton, B.; Dean, J.; Bordo, L.; Hodgson, B.; Yamamoto, T.; Mulley, J.; Zara, F.; Scheffer, I.
	2013	Loss-of-function mutations in SIM1 contribute to obesity and Prader-Willi-like features	Bonnefond, A.; Raimondo, A.; Stutzmann, F.; Ghoussaini, M.; Ramachandrappa, S.; Bersten, D.; Durand, E.; Vatin, V.; Balkau, B.; Lantieri, O.; Raverdy, V.; Pattou, F.; Van Hul, W.; Van Gaal, L.; Peet, D.; Weill, J.; Miller, J.; Horber, F.; Goldstone, A.; Driscoll, D.; et al.
	2003	X-linked mild non-syndromic mental retardation with neuropsychiatric problems and the missense mutation A365E in PAK3	Gedeon, A.; Nelson, J.; Gecz, J.; Mulley, J.
	2005	Intrahepatic gene expression profiles and alpha-smooth muscle actin patterns in hepatitis C virus induced fibrosis	Lau, D.; Luxon, B.; Xiao, S.; Beard, M.; Lemon, S.
	2006	Influence of CTLA4 haplotypes on susceptibility and some extraglandular manifestations in primary Sjogren's syndrome	Downie-Doyle, S.; Bayat, N.; Rischmueller, M.; Lester, S.
	2010	MicroRNA profiling of Barrett's oesophagus and oesophageal adenocarcinoma	Wijnhoven, B.; Hussey, D.; Watson, D.; Tsykin, A.; Smith, C.; Michael, M.