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Results 1-10 of 46 (Search time: 0.004 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.
2016Identity by descent fine mapping of familial adult myoclonus epilepsy (FAME) to 2p11.2–2q11.2Henden, L.; Freytag, S.; Afawi, Z.; Baldassari, S.; Berkovic, S.; Bisulli, F.; Canafoglia, L.; Casari, G.; Crompton, D.; Depienne, C.; Gecz, J.; Guerrini, R.; Helbig, I.; Hirsch, E.; Keren, B.; Klein, K.; Labauge, P.; LeGuern, E.; Licchetta, L.; Mei, D.; et al.
2015Fine-mapping of the HNF1B multicancer locus identifies candidate variants that mediate endometrial cancer riskPainter, J.; O'Mara, T.; Batra, J.; Cheng, T.; Lose, F.; Dennis, J.; Michailidou, K.; Tyrer, J.; Ahmed, S.; Ferguson, K.; Healey, C.; Kaufmann, S.; Hillman, K.; Walpole, C.; Moya, L.; Pollock, P.; Jones, A.; Howarth, K.; Martin, L.; Gorman, M.; et al.
2014Common variants near ABCA1, AFAP1 and GMDS confer risk of primary open-angle glaucomaGharahkhani, P.; Burdon, K.; Fogarty, R.; Sharma, S.; Hewitt, A.; Martin, S.; Law, M.; Cremin, K.; Bailey, J.; Loomis, S.; Pasquale, L.; Haines, J.; Hauser, M.; Viswanathan, A.; McGuffin, P.; Topouzis, F.; Foster, P.; Graham, S.; Casson, R.; Chehade, M.; 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.
2012Impact of common variation in bone-related genes on type 2 diabetes and related traitsBillings, L.; Hsu, Y.; Ackerman, R.; Dupuis, J.; Voight, B.; Rasmussen-Torvik, L.; Hercberg, S.; Lathrop, M.; Barnes, D.; Langenberg, C.; Hui, J.; Fu, M.; Bouatia-Naji, N.; Lecoeur, C.; An, P.; Magnusson, P.; Surakka, I.; Ripatti, S.; Christiansen, L.; Dalgard, C.; et al.
2012Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in womenPalmer, L.; Fox, C.S.; Liu, Y.; White, C.C.; Feitosa, M.; Smith, A.V.; Heard-Costa, N.; Lohman, K.; GIANT Consortium; MAGIC Consortium; GLGC Consortium; Johnson, A.D.; Foster, M.C.; Greenawalt, D.M.; Griffin, P.; Ding, J.; Newman, A.B.; Tylavsky, F.; Miljkovic, I.; Kritchevsky, S.B.; et al.; Bray, M.
2013Epigenetic analysis leads to identification of HNF1B as a subtype-specific susceptibility gene for ovarian cancerShen, H.; Fridley, B.; Song, H.; Lawrenson, K.; Cunningham, J.; Ramus, S.; Cicek, M.; Tyrer, J.; Stram, D.; Larson, M.; Köbel, M.; PRACTICAL Consortium; Ziogas, A.; Zheng, W.; Yang, H.; Wu, A.; Wozniak, E.; Ling Woo, Y.; Winterhoff, B.; Wik, E.; et al.
2016Characterization of leukemias with ETV6-ABL1 fusionZaliova, M.; Moorman, A.; Cazzaniga, G.; Stanulla, M.; Harvey, R.; Roberts, K.; Heatley, S.; Loh, M.; Konopleva, M.; Chen, I.; Zimmermannova, O.; Schwab, C.; Smith, O.; Mozziconacci, M.; Chabannon, C.; Kim, M.; Frederik Falkenburg, J.; Norton, A.; Marshall, K.; Haas, O.; et al.; Annual Meeting of the American-Society-of-Hematology (5 Dec 2015 - 8 Dec 2015 : Orlando, FL)
2018Association of serotonin transporter gene AluJb methylation with major depression, amygdala responsiveness, 5-HTTLPR/rs25531 polymorphism, and stressSchneider, I.; Kugel, H.; Redlich, R.; Grotegerd, D.; Bürger, C.; Bürkner, P.-C.; Opel, N.; Dohm, K.; Zaremba, D.; Meinert, S.; Schröder, N.; Straßburg, A.; Schwarte, K.; Schettler, C.; Ambrée, O.; Rust, S.; Domschke, K.; Arolt, V.; Heindel, W.; Baune, B.; et al.

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