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Results 11-20 of 78 (Search time: 0.002 seconds).
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PreviewIssue DateTitleAuthor(s)
2016A splicing-regulatory polymorphism in DRD2 disrupts ZRANB2 binding, impairs cognitive functioning and increases risk for schizophrenia in six Han Chinese samplesCohen, O.; Weickert, T.; Hess, J.; Paish, L.; McCoy, S.; Rothmond, D.; Galletly, C.; Liu, D.; Weinberg, D.; Huang, X.; Xu, Q.; Shen, Y.; Zhang, D.; Yue, W.; Yan, J.; Wang, L.; Lu, T.; He, L.; Shi, Y.; Xu, M.; et al.
2016Inherited determinants of Crohn's disease and ulcerative colitis phenotypes: a genetic association studyCleynen, I.; Boucher, G.; Jostins, L.; Schumm, L.; Zeissig, S.; Ahmad, T.; Andersen, V.; Andrews, J.; Annese, V.; Brand, S.; Brant, S.; Cho, J.; Daly, M.; Dubinsky, M.; Duerr, R.; Ferguson, L.; Franke, A.; Gearry, R.; Goyette, P.; Hakonarson, H.; et al.
2016Combined genetic and splicing analysis of BRCA1 c.[594-2A>C; 641A>G] highlights the relevance of naturally occurring in-frame transcripts for developing disease gene variant classification algorithmsde la Hoya, M.; Soukarieh, O.; López-Perolio, I.; Vega, A.; Walker, L.C.; van Ierland, Y.; Baralle, D.; Santamariña, M.; Lattimore, V.; Wijnen, J.; Whiley, P.; Blanco, A.; Raponi, M.; Hauke, J.; Wappenschmidt, B.; Becker, A.; Hansen, T.V.O.; Behar, R.; KConFaB, I.; Niederacher, D.; et al.
2016Point mutations in Exon 1B of APC reveal gastric adenocarcinoma and proximal polyposis of the stomach as a familial adenomatous polyposis variantLi, J.; Woods, S.; Healey, S.; Beesley, J.; Chen, X.; Lee, J.; Sivakumaran, H.; Wayte, N.; Nones, K.; Waterfall, J.; Pearson, J.; Patch, A.; Senz, J.; Ferreira, M.; Kaurah, P.; MacKenzie, R.; Heravi-Moussavi, A.; Hansford, S.; Lannagan, T.; Spurdle, A.; et al.
2016X chromosome dose and sex bias in autoimmune diseases: increased prevalence of 47,XXX in systemic lupus erythematosus and Sjögren's syndromeLiu, K.; Kurien, B.; Zimmerman, S.; Kaufman, K.; Taft, D.; Kottyan, L.; Lazaro, S.; Weaver, C.; Ice, J.; Adler, A.; Chodosh, J.; Radfar, L.; Rasmussen, A.; Stone, D.; Lewis, D.; Li, S.; Koelsch, K.; Igoe, A.; Talsania, M.; Kumar, J.; et al.
2016Choline kinase alpha as an androgen receptor chaperone and prostate cancer therapeutic targetAsim, M.; Massie, C.; Orafidiya, F.; Pértega-Gomes, N.; Warren, A.; Esmaeili, M.; Selth, L.; Zecchini, H.; Luko, K.; Qureshi, A.; Baridi, A.; Menon, S.; Madhu, B.; Escriu, C.; Lyons, S.; Vowler, S.; Zecchini, V.; Shaw, G.; Hessenkemper, W.; Russell, R.; et al.
2016Novel germ line DDX41 mutations define families with a lower age of MDS/AML onset and lymphoid malignanciesLewinsohn, M.; Brown, A.L.; Weinel, L.M.; Phung, C.; Rafidi, G.; Lee, M.K.; Schreiber, A.W.; Feng, J.; Babic, M.; Chong, C.E.; Lee, Y.; Yong, A.; Suthers, G.K.; Poplawski, N.; Altree, M.; Phillips, K.; Jaensch, L.; Fine, M.; D'Andrea, R.J.; Lewis, I.D.; et al.
2016Replication of association of the apolipoprotein A1-C3-A4 gene cluster with the risk of goutRasheed, H.; Phipps-Green, A.J.; Topless, R.; Smith, M.D.; Hill, C.; Lester, S.; Rischmueller, M.; Janssen, M.; Jansen, T.L.; Joosten, L.A.; Radstake, T.R.; Riches, P.L.; Tausche, A.K.; Lioté, F.; So, A.; Van Rij, A.; Jones, G.T.; McCormick, S.P.; Harrison, A.A.; Stamp, L.K.; et al.
2016Compound mutations in BCR-ABL1 are not major drivers of primary or secondary resistance to ponatinib in CP-CML patientsDeininger, M.; Hodgson, J.; Shah, N.; Cortes, J.; Kim, D.; Nicolini, F.; Talpaz, M.; Baccarani, M.; Müller, M.; Li, J.; Parker, W.; Lustgarten, S.; Clackson, T.; Haluska, F.; Guilhot, F.; Kantarjian, H.; Soverini, S.; Hochhaus, A.; Hughes, T.; Rivera, V.; et al.
2016Dclk1 defines quiescent pancreatic progenitors that promote injury-induced regeneration and tumorigenesisWestphalen, C.; Takemoto, Y.; Tanaka, T.; Macchini, M.; Jiang, Z.; Renz, B.; Chen, X.; Ormanns, S.; Nagar, K.; Tailor, Y.; May, R.; Cho, Y.; Asfaha, S.; Worthley, D.; Hayakawa, Y.; Urbanska, A.; Quante, M.; Reichert, M.; Broyde, J.; Subramaniam, P.; et al.