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PreviewIssue DateTitleAuthor(s)
2019Disruptive variants of CSDE1 associate with autism and interfere with neuronal development and synaptic transmissionGuo, H.; Li, Y.; Shen, L.; Wang, T.; Jia, X.; Liu, L.; Xu, T.; Ou, M.; Hoekzema, K.; Wu, H.; Gillentine, M.A.; Liu, C.; Ni, H.; Peng, P.; Zhao, R.; Zhang, Y.; Phornphutkul, C.; Stegmann, A.P.A.; Prada, C.E.; Hopkin, R.J.; et al.
2021Targeted gene panels identify a high frequency of pathogenic germline variants in patients diagnosed with a hematological malignancy and at least one other independent cancerSinghal, D.; Hahn, C.N.; Feurstein, S.; Wee, L.Y.A.; Moma, L.; Kutyna, M.M.; Chhetri, R.; Eshraghi, L.; Schreiber, A.W.; Feng, J.; Wang, P.P.-S.; Babic, M.; Parker, W.T.; Gao, S.; Moore, S.; Das, S.; Thomas, D.; Pattnaik, S.; Brown, A.L.; D'Andrea, R.J.; et al.
2012A genome-wide association meta-analysis identifies new childhood obesity lociBradfield, J.; Taal, H.; Timpson, N.; Scherag, A.; Lecoeur, C.; Warrington, N.; Hypponen, E.; Holst, C.; Valcarcel, B.; Thiering, E.; Salem, R.; Schumacher, F.; Cousminer, D.; Sleiman, P.; Jianhua, Z.; Berkowitz, R.; Vimaleswaran, K.; Ivonne, J.; Pennell, C.; Evans, D.; et al.
2011A novel recurrent mutation in MITF predisposes to familial and sporadic melanomaYokoyama, S.; Woods, S.; Boyle, G.; Aoude, L.; MacGregor, S.; Zismann, V.; Gartside, M.; Cust, A.; Haq, R.; Harland, M.; Taylor, J.; Duffy, D.; Holohan, K.; Dutton-Regester, K.; Palmer, J.; Bonazzi, V.; Stark, M.; Symmons, J.; Law, M.; Schmidt, C.; et al.
2011A genome-wide significant linkage for severe depression on chromosome 3: the depression network studyBreen, G.; Webb, B.; Butler, A.; van den Oord, E.; Tozzi, F.; Craddock, N.; Gill, M.; Korszun, A.; Maier, W.; Middleton, L.; Mors, O.; Owen, M.; Cohen-Woods, S.; Perry, J.; Galwey, N.; Upmanyu, R.; Craig, I.; Lewis, C.; Ng, M.; Brewster, S.; et al.
2013Mutations in DEPDC5 cause familial focal epilepsy with variable fociDibbens, L.; de Vries, B.; Donatello, S.; Heron, S.; Hodgson, B.; Chintawar, S.; Crompton, D.; Hughes, J.; Bellows, S.; Klein, K.; Callenbach, P.; Corbett, M.; Gardner, A.; Kivity, S.; Iona, X.; Regan, B.; Weller, C.; Crimmins, D.; O'Brien, T.; Guerrero-Lopez, R.; et al.
2015A genome-wide association study of susceptibility to acute lymphoblastic leukemia in adolescents and young adultsPerez-Andreu, V.; Roberts, K.; Xu, H.; Smith, C.; Zhang, H.; Yang, W.; Harvey, R.; Payne-Turner, D.; Devidas, M.; Cheng, I.; Carroll, W.; Heerema, N.; Carroll, A.; Raetz, E.; Gastier-Foster, J.; Marcucci, G.; Bloomfield, C.; Mrozek, K.; Kohlschmidt, J.; Stock, W.; et al.
2011Progesterone receptor gene variants and risk of endometrial cancerO'Mara, T.; Fahey, P.; Ferguson, K.; Marquart, L.; Lambrechts, D.; Despierre, E.; Vergote, I.; Amant, F.; Hall, P.; Liu, J.; Czene, K.; SASBAC,; Rebbeck, T.; WISE Study Group,; AOCS Management Group,; SEARCH,; Ahmed, S.; Dunning, A.; Gregory, C.; Shah, M.; et al.

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