| Preview | Issue Date | Title | Author(s) |
| 2013 | Expression of an anti-CD4 single-chain antibody fragment from the donor cornea can prolong corneal allograft survival in inbred rats | Appleby, S.; Jessup, C.; Mortimer, L.; Kirk, K.; Brereton, H.; Coster, D.; Tan, C.; Williams, K. |
| 2015 | Homozygous mutation of STXBP5L explains an autosomal recessive infantile-onset neurodegenerative disorder | Kumar, R.; Corbett, M.; Smith, N.; Jolly, L.; Tan, C.; Keating, D.; Duffield, M.; Utsumi, T.; Moriya, K.; Smith, K.; Hoischen, A.; Abbott, K.; Harbord, M.; Compton, A.; Woenig, J.; Arts, P.; Kwint, M.; Wieskamp, N.; Gijsen, S.; Veltman, J.; et al. |
| 2015 | Increased STAG2 dosage defines a novel cohesinopathy with intellectual disability and behavioral problems | Kumar, R.; Corbett, M.; Van Bon, B.; Gardner, A.; Woenig, J.; Jolly, L.; Douglas, E.; Friend, K.; Tan, C.; Van Esch, H.; Holvoet, M.; Raynaud, M.; Field, M.; Leffler, M.; Budny, B.; Wisniewska, M.; Badura-Stronka, M.; Latos-Bieleńska, A.; Batanian, J.; Rosenfeld, J.; et al. |
| 2007 | Lentivirus-mediated gene transfer to the rat, ovine and human cornea | Parker, D.; Kaufmann, C.; Brereton, H.; Anson, D.; Francis-Staite, L.; Jessup, C.; Marshall, K.; Tan, C.; Koldej, R.; Coster, D.; Williams, K. |
| 2022 | Non-invasive, label-free optical analysis to detect aneuploidy within the inner cell mass of the preimplantation embryo | Tan, C.; Mahbub, S.; Campbell, J.; Habibalahi, A.; Campugan, C.; Rose, R.; Chow, D.; Mustafa, S.; Goldys, E.; Dunning, K. |
| 2015 | THOC2 mutations implicate mRNA-export pathway in X-linked intellectual disability | Kumar, R.; Corbett, M.; Van Bon, B.; Woenig, J.; Weir, L.; Douglas, E.; Friend, K.; Gardner, A.; Shaw, M.; Jolly, L.; Tan, C.; Hunter, M.; Hackett, A.; Field, M.; Palmer, E.; Leffler, M.; Rogers, C.; Boyle, J.; Bienek, M.; Jensen, C.; et al. |
