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Results 11-20 of 21 (Search time: 0.003 seconds).
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PreviewIssue DateTitleAuthor(s)
2017Targeted sequencing identifies 91 neurodevelopmental-disorder risk genes with autism and developmental-disability biasesStessman, H.; Xiong, B.; Coe, B.; Wang, T.; Hoekzema, K.; Fenckova, M.; Kvarnung, M.; Gerdts, J.; Trinh, S.; Cosemans, N.; Vives, L.; Lin, J.; Turner, T.; Santen, G.; Ruivenkamp, C.; Kriek, M.; Van Haeringen, A.; Aten, E.; Friend, K.; Liebelt, J.; et al.
2017High prevalence of relapse in children with Philadelphia-like acute lymphoblastic leukemia despite risk-adapted treatmentHeatley, S.L.; Sadras, T.; Kok, C.H.; Nievergall, E.; Quek, K.; Dang, P.; McClure, B.; Venn, N.; Moore, S.; Suttle, J.; Law, T.; Ng, A.; Muskovic, W.; Norris, M.D.; Revesz, T.; Osborn, M.; Moore, A.S.; Suppiah, R.; Fraser, C.; Alvaro, F.; et al.
2017Laparoscopy to predict the result of primary cytoreductive surgery in patients with advanced ovarian cancer: a randomized controlled trialRutten, M.; Van Meurs, H.; Van De Vrie, R.; Gaarenstroom, K.; Naaktgeboren, C.; Van Gorp, T.; Brugge, H.; Hofhuis, W.; Schreuder, H.; Arts, H.; Zusterzeel, P.; Pijnenborg, J.; Van Haaften, M.; Fons, G.; Engelen, M.; Boss, E.; Vos, M.; Gerestein, K.; Schutter, E.; Opmeer, B.; et al.
2017Adults with Philadelphia chromosome-like acute lymphoblastic leukemia frequently have IGH-CRLF2 and JAK2 mutations, persistence of minimal residual disease and poor prognosisHerold, T.; Schneider, S.; Metzeler, K.; Neumann, M.; Hartmann, L.; Roberts, K.; Konstandin, N.; Greif, P.; Braeundl, K.; Ksienzyk, B.; Huk, N.; Schneider, I.; Zellmeier, E.; Jurinovic, V.; Mansmann, U.; Hiddemann, W.; Mullighan, C.; Bohlander, S.; Spiekermann, K.; Hoelzer, D.; et al.
2017Parallel palaeogenomic transects reveal complex genetic history of early European farmersLipson, M.; Szécsényi-Nagy, A.; Mallick, S.; Pósa, A.; Stégmár, B.; Keerl, V.; Rohland, N.; Stewardson, K.; Ferry, M.; Michel, M.; Oppenheimer, J.; Broomandkhoshbacht, N.; Harney, E.; Nordenfelt, S.; Llamas, B.; Gusztáv, B.; Köhler, K.; Oross, K.; Bondár, M.; Marton, T.; et al.
2017A mutation in the viral sensor 2’-5’-oligoadenylate synthetase 2 causes failure of lactationOakes, S.R.; Gallego-Ortega, D.; Stanford, P.M.; Junankar, S.; Au, W.W.Y.; Kikhtyak, Z.; von Korff, A.; Sergio, C.M.; Law, A.M.K.; Castillo, L.E.; Allerdice, S.L.; Young, A.I.J.; Piggin, C.; Whittle, B.; Bertram, E.; Naylor, M.J.; Roden, D.L.; Donovan, J.; Korennykh, A.; Goodnow, C.C.; et al.; Wells, C.A.
2017Inhibition of Pol I transcription treats murine and human AML by targeting the leukemia-initiating cell populationHein, N.; Cameron, D.; Hannan, K.; Nguyen, N.; Fong, C.; Sornkom, J.; Wall, M.; Pavy, M.; Cullinane, C.; Diesch, J.; Devlin, J.; George, A.; Sanij, E.; Quin, J.; Poortinga, G.; Verbrugge, I.; Baker, A.; Drygin, D.; Harrison, S.; Rozario, J.; et al.
2017Aboriginal Australian mitochondrial genome variation - an increased understanding of population antiquity and diversityNagle, N.; Van Oven, M.; Wilcox, S.; Van Holst Pellekaan, S.; Tyler-Smith, C.; Xue, Y.; Ballantyne, K.; Wilcox, L.; Papac, L.; Cooke, K.; Van Oorschot, R.; McAllister, P.; Williams, L.; Kayser, M.; Mitchell, R.; Adhikarla, S.; Adler, C.; Balanovska, E.; Balanovsky, O.; Bertranpetit, J.; et al.
2017Global causes of blindness and distance vision impairment 1990–2020: a systematic review and meta-analysisFlaxman, S.R.; Bourne, R.R.A.; Resnikoff, S.; Ackland, P.; Braithwaite, T.; Cicinelli, M.V.; Das, A.; Jonas, J.B.; Keeffe, J.; Kempen, J.H.; Leasher, J.; Limburg, H.; Naidoo, K.; Pesudovs, K.; Silvester, A.; Stevens, G.A.; Tahhan, N.; Wong, T.Y.; Taylor, H.R.; Vision Loss Expert Group of the Global Burden of Disease Study,; et al.
2017Magnitude, temporal trends, and projections of the global prevalence of blindness and distance and near vision impairment: a systematic review and meta-analysisBourne, R.R.A.; Flaxman, S.R.; Braithwaite, T.; Cicinelli, M.V.; Das, A.; Jonas, J.B.; Keeffe, J.; Kempen, J.H.; Leasher, J.; Limburg, H.; Naidoo, K.; Pesudovs, K.; Resnikoff, S.; Silvester, A.; Stevens, G.A.; Tahhan, N.; Wong, T.Y.; Taylor, H.R.; Vision Loss Expert Group,; Ackland, P.; et al.