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Results 61-70 of 136 (Search time: 0.003 seconds).
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PreviewIssue DateTitleAuthor(s)
2015Endovascular therapy for ischemic stroke with perfusion-imaging selectionCampbell, B.; Mitchell, P.; Kleinig, T.; Dewey, H.; Churilov, L.; Yassi, N.; Yan, B.; Dowling, R.; Parsons, M.; Oxley, T.; Wu, T.; Brooks, M.; Simpson, M.; Miteff, F.; Levi, C.; Krause, M.; Harrington, T.; Faulder, K.; Steinfort, B.; Priglinger, M.; et al.
2016X-exome sequencing of 405 unresolved families identifies seven novel intellectual disability genesHu, H.; Haas, S.; Chelly, J.; Van Esch, H.; Raynaud, M.; De Brouwer, A.; Weinert, S.; Froyen, G.; Frints, S.; Laumonnier, F.; Zemojtel, T.; Love, M.; Richard, H.; Emde, A.; Bienek, M.; Jensen, C.; Hambrock, M.; Fischer, U.; Langnick, C.; Feldkamp, M.; et al.
2016Disruptive de novo mutations of DYRK1A lead to a syndromic form of autism and IDvan Bon, B.W.M.; Coe, B.P.; Bernier, R.; Green, C.; Gerdts, J.; Witherspoon, K.; Kleefstra, T.; Willemsen, M.H.; Kumar, R.; Bosco, P.; Fichera, M.; Li, D.; Amaral, D.; Cristofoli, F.; Peeters, H.; Haan, E.; Romano, C.; Mefford, H.C.; Scheffer, I.; Gecz, J.; et al.
2012Pemetrexed versus pemetrexed and carboplatin as second-line chemotherapy in advanced non-small-cell lung cancer: Results of the GOIRC 02-2006 randomized phase II study and pooled analysis with the NVALT7 trialArdizzoni, A.; Tiseo, M.; Boni, L.; Vincent, A.; Passalacqua, R.; Buti, S.; Amoroso, D.; Camerini, A.; Labianca, R.; Genestreti, G.; Boni, C.; Ciuffreda, L.; Di Costanzo, F.; De Marinis, F.; Crino, L.; Santo, A.; Pazzola, A.; Barbieri, F.; Zilembo, N.; Colantonio, I.; et al.
2013Gain-of-function mutations in RIT1 cause Noonan syndrome, a RAS/MAPK pathway syndromeAoki, Y.; Niihori, T.; Banjo, T.; Okamoto, N.; Mizuno, S.; Kurosawa, K.; Ogata, T.; Takada, F.; Yano, M.; Ando, T.; Hoshika, T.; Barnett, C.; Ohashi, H.; Kawame, H.; Hasegawa, T.; Okutani, T.; Nagashima, T.; Hasegawa, S.; Funayama, R.; Nagashima, T.; 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.
2014Nonsense mutations in the shelterin complex genes ACD and TERF2IP in familial melanomaAoude, L.; Pritchard, A.; Robles-Espinoza, C.; Wadt, K.; Harland, M.; Choi, J.; Gartside, M.; Quesada, V.; Johansson, P.; Palmer, J.; Ramsay, A.; Zhang, X.; Jones, K.; Symmons, J.; Holland, E.; Schmid, H.; Bonazzi, V.; Woods, S.; Dutton-Regester, K.; Stark, M.; et al.
2010Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distributionHeid, I.; Jackson, A.; Randall, J.; Winkler, T.; Qi, L.; Steinthorsdottir, V.; Thorleifsson, G.; Zillikens, M.; Speliotes, E.; Magi, R.; Workalemahu, T.; White, C.; Bouatia-Naji, N.; Harris, T.; Berndt, S.; Ingelsson, E.; Willer, C.; Weedon, M.; Luan, J.; Vedantam, S.; et al.
2011Genome-wide association identifies nine common variants associated with fasting proinsulin levels and provides new insights into the pathophysiology of type 2 diabetesStrawbridge, R.; Dupuis, J.; Prokopenko, I.; Barker, A.; Ahlqvist, E.; Rybin, D.; Petrie, J.; Travers, M.; Bouatia-Naji, N.; Dimas, A.; Nica, A.; Wheeler, E.; Chen, H.; Voight, B.; Taneera, J.; Kanoni, S.; Peden, J.; Turrini, F.; Gustafsson, S.; Zabena, C.; et al.
2010Variants in ADCY5 and near CCNL1 are associated with fetal growth and birth weightFreathy, R.; Mook-Kanamori, D.; Sovio, U.; Prokopenko, I.; Timpson, N.; Berry, D.; Warrington, N.; Widen, E.; Jan Hottenga, J.; Kaakinen, M.; Lange, L.; Bradfield, J.; Kerkhof, M.; Marsh, J.; Mägi, R.; Chen, C.-M.; Lyon, H.; Kirin, M.; Adair, L.; Aulchenko, Y.; et al.

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