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PreviewIssue DateTitleAuthor(s)
2008X-linked protocadherin 19 mutations cause female-limited epilepsy and cognitive impairmentDibbens, L.; Tarpey, P.; Hynes, K.; Bayly, M.; Scheffer, I.; Smith, R.; Bomar, J.; Sutton, E.; Vandeleur, L.; Shoubridge, C.; Edkins, S.; Turner, S.; Stevens, C.; O'Meara, S.; Tofts, C.; Barthorpe, S.; Buck, G.; Cole, J.; Halliday, K.; Jones, D.; et al.
2007Epidemiological comparisons of problems and positive qualities reported by adolescents in 24 countriesRescorla, L.; Achenbach, T.; Ivanova, M.; Dumenci, L.; Almqvist, F.; Bilenberg, N.; Bird, H.; Broberg, A.; Dobrean, A.; Dopfner, M.; Erol, N.; Forns, M.; Hannesdottir, H.; Kanbayashi, Y.; Lambert, M.; Leung, P.; Minaei, A.; Mulatu, M.; Novik, T.; Oh, K.; et al.
1997A unique point mutation in the fibroblast growth factor receptor 3 gene (FGFR3) defines a new craniosynostosis syndromeMuenke, M.; Gripp, K.; McDonald-McGinn, D.; Gaudenz, K.; Whitaker, L.; Bartlett, S.; Markowitz, R.; Robin, N.; Nwokoro, N.; Mulvihill, J.; Losken, H.; Mulliken, J.; Guttmacher, A.; Wilroy, R.; Clarke, L.; Hollway, G.; Ades, L.; Haan, E.; Mulley, J.; Cohen, M.; et al.
2007Mutations in ZDHHC9, which encodes a palmitoyltransferase of NRAS and HRAS, cause X-linked mental retardation associated with a marfanoid habitusRaymond, F.; Tarpey, P.; Edkins, S.; Tofts, C.; O'Meara, S.; Teague, J.; Butler, A.; Stevens, C.; Barthorpe, S.; Buck, G.; Cole, J.; Dicks, E.; Gray, K.; Harrison, R.; Hills, K.; Hinton, J.; Jones, D.; Menzies, A.; Perry, J.; Raine, K.; et al.
2019Preferred learning modalities and practice for critical skills: a global survey of paediatric emergency medicine cliniciansCraig, S.S.; Auerbach, M.; Cheek, J.A.; Babl, F.E.; Oakley, E.; Nguyen, L.; Rao, A.; Dalton, S.; Lyttle, M.D.; Mintegi, S.; Nagler, J.; Mistry, R.D.; Dixon, A.; Rino, P.; Kohn-Loncarica, G.; Dalziel, S.R.; Tzimenatos, L.; Mistry, R.; Brown, K.; Powell, E.; et al.
2018A C6orf10/LOC101929163 locus is associated with age of onset in C9orf72 carriersZhang, M.; Ferrari, R.; Tartaglia, M.C.; Keith, J.; Surace, E.I.; Wolf, U.; Sato, C.; Grinberg, M.; Liang, Y.; Xi, Z.; Dupont, K.; McGoldrick, P.; Weichert, A.; McKeever, P.M.; Schneider, R.; McCorkindale, M.D.; Manzoni, C.; Rademakers, R.; Graff-Radford, N.R.; Dickson, D.W.; et al.
2020Top 10 priorities for future infertility research: an international consensus development studyDuffy, J.M.N.; Adamson, G.D.; Benson, E.; Bhattacharya, S.; Bhattacharya, S.; Bofill, M.; Brian, K.; Collura, B.; Curtis, C.; Evers, J.L.H.; Farquharson, R.G.; Fincham, A.; Franik, S.; Giudice, L.C.; Glanville, E.; Hickey, M.; Horne, A.W.; Hull, M.L.; Johnson, N.P.; Jordan, V.; et al.
2020Top 10 priorities for future infertility research: an international consensus development studyDuffy, J.M.N.; Adamson, G.D.; Benson, E.; Bhattacharya, S.; Bhattacharya, S.; Bofill, M.; Brian, K.; Collura, B.; Curtis, C.; Evers, J.L.H.; Farquharson, R.G.; Fincham, A.; Franik, S.; Giudice, L.C.; Glanville, E.; Hickey, M.; Horne, A.W.; Hull, M.L.; Johnson, N.P.; Jordan, V.; et al.
2021Implementing gene curation for hereditary cancer susceptibility in Australia: achieving consensus on genes with clinical utilityTudini, E.; Davidson, A.L.; Dressel, U.; Andrews, L.; Antill, Y.; Crook, A.; Field, M.; Gattas, M.; Harris, R.; Kirk, J.; Pachter, N.; Salmon, L.; Susman, R.; Townshend, S.; Trainer, A.H.; Tucker, K.M.; Mitchell, G.; James, P.A.; Ward, R.L.; Mar Fan, H.; et al.
2018Maternal smoking during pregnancy and offspring overweight: is there a dose-response relationship? An individual patient data meta-analysisAlbers, L.; Sobotzki, C.; Kuß, O.; Ajslev, T.; Batista, R.; Bettiol, H.; Brabin, B.; Buka, S.; Cardoso, V.; Clifton, V.; Devereux, G.; Gilman, S.; Grzeskowiak, L.; Heinrich, J.; Hummel, S.; Jacobsen, G.; Jones, G.; Koshy, G.; Morgen, C.; Oken, E.; et al.

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