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Results 31-40 of 254 (Search time: 0.006 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.
2017Hotspots of missense mutation identify neurodevelopmental disorder genes and functional domainsGeisheker, M.; Heymann, G.; Wang, T.; Coe, B.; Turner, T.; Stessman, H.; Hoekzema, K.; Kvarnung, M.; Shaw, M.; Friend, K.; Liebelt, J.; Barnett, C.; Thompson, E.; Haan, E.; Guo, H.; Anderlid, B.; Nordgren, A.; Lindstrand, A.; Vandeweyer, G.; Alberti, A.; et al.
2011Bile leakage after hepatobiliary and pancreatic surgery: A definition and grading of severity by the International Study Group of Liver SurgeryKoch, M.; Garden, J.; Padbury, R.; Rahbari, N.; Adam, R.; Capussotti, L.; Sheung, T.; Yokoyama, Y.; Crawford, M.; Makuuchi, M.; Christophi, C.; Banting, S.; Brooke-Smith, M.; Usatoff, V.; Nagino, M.; Maddern, G.; Hugh, T.; Vauthey, J.; Greig, P.; Rees, M.; et al.
2018Augmented capacity for peripheral serotonin release in human obesityYoung, R.; Lumsden, A.; Martin, A.; Schober, G.; Pezos, N.; Thazhath, S.; Isaacs, N.; Cvijanovic, N.; Sun, E.; Wu, T.; Rayner, C.; Nguyen, Q.; Fontgalland, D.; Rabbitt, P.; Hollington, P.; Sposato, L.; Due, S.; Wattchow, D.; Liou, A.; Jackson, V.; et al.
2018Integrative genomic analysis reveals cancer-associated mutations at diagnosis of CML in patients with high-risk diseaseBranford, S.; Wang, P.; Yeung, D.T.; Thomson, D.; Purins, A.; Wadham, C.; Shahrin, N.H.; Marum, J.E.; Nataren, N.; Parker, W.T.; Geoghegan, J.; Feng, J.; Shanmuganathan, N.; Mueller, M.C.; Dietz, C.; Stangl, D.; Donaldson, Z.; Altamura, H.; Georgievski, J.; Braley, J.; et al.
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)
2011SHP-1 expression accounts for resistance to imatinib treatment in Philadelphia chromosome-positive cells derived from patients with chronic myeloid leukemiaEsposito, N.; Colavita, I.; Quintarelli, C.; Sica, A.; Peluso, A.; Luciano, L.; Picardi, M.; Vecchio, L.; Buonomo, T.; Hughes, T.; White, D.; Radich, J.; Russo, D.; Branford, S.; Saglio, G.; Vaz de Melo, J.; Martinelli, R.; Ruoppolo, M.; Kalebic, T.; Martinelli, G.; et al.
2015Association of cardiometabolic multimorbidity with mortalityEmerging Risk Factors Collaboration; Di Angelantonio, E.; Kaptoge, S.; Wormser, D.; Willeit, P.; Butterworth, A.; Bansal, N.; O'Keeffe, L.; Gao, P.; Wood, A.; Burgess, S.; Freitag, D.; Pennells, L.; Peters, S.; Hart, C.; Haheim, L.; Gillum, R.; Nordestgaard, B.; Psaty, B.; Yeap, B.; et al.
2016Protocol of the Australasian malignant pleural effusion-2 (AMPLE-2) trial: amulticentre randomised study of aggressive versus symptom-guided drainage via indwelling pleural cathetersAzzopardi, M.; Thomas, R.; Muruganandan, S.; Lam, D.C.L.; Garske, L.A.; Kwan, B.C.H.; Rashid Ali, M.R.S.; Nguyen, P.T.; Yap, E.; Horwood, F.C.; Ritchie, A.J.; Bint, M.; Tobin, C.L.; Shrestha, R.; Piccolo, F.; De Chaneet, C.C.; Creaney, J.; Newton, R.U.; Hendrie, D.; Murray, K.; et al.