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Results 1-10 of 31 (Search time: 0.002 seconds).
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PreviewIssue DateTitleAuthor(s)
2019Physical Frailty: ICFSR International Clinical Practice Guidelines for Identification and ManagementDent, E.; Morley, J.E.; Cruz-Jentoft, A.J.; Woodhouse, L.; Rodríguez-Mañas, L.; Fried, L.P.; Woo, J.; Aprahamian, I.; Sanford, A.; Lundy, J.; Landi, F.; Beilby, J.; Martin, F.C.; Bauer, J.M.; Ferrucci, L.; Merchant, R.A.; Dong, B.; Arai, H.; Hoogendijk, E.O.; Won, C.W.; et al.
2014Tumor mismatch repair immunohistochemistry and DNA MLH1 methylation testing of patients with endometrial cancer diagnosed at age younger than 60 years optimizes triage for population-level germline mismatch repair gene mutation testingBuchanan, D.; Tan, Y.; Walsh, M.; Clendenning, M.; Metcalf, A.; Ferguson, K.; Arnold, S.; Thompson, B.; Lose, F.; Parsons, M.; Walters, R.; Pearson, S.; Cummings, M.; Oehler, M.; Blomfield, P.; Quinn, M.; Kirk, J.; Stewart, C.; Obermair, A.; Young, J.; et al.
2013A phase 2 trial of ponatinib in Philadelphia chromosome-positive leukemiasCortes, J.E.; Kim, D.W.; Pinilla-Ibarz, J.; Le Coutre, P.; Paquette, R.; Chuah, C.; Nicolini, F.E.; Apperley, J.F.; Khoury, H.J.; Talpaz, M.; DiPersio, J.; DeAngelo, D.J.; Abruzzese, E.; Rea, D.; Baccarani, M.; Müller, M.C.; Gambacorti-Passerini, C.; Wong, S.; Lustgarten, S.; Rivera, V.M.; et al.
2019Chromosomal abnormalities and prognosis in NPM1-mutated acute myeloid leukemia: a pooled analysis of individual patient data from nine international cohortsAngenendt, L.; Röllig, C.; Montesinos, P.; Martínez-Cuadrón, D.; Barragan, E.; García, R.; Botella, C.; Martínez, P.; Ravandi, F.; Kadia, T.; Kantarjian, H.M.; Cortes, J.; Juliusson, G.; Lazarevic, V.; Höglund, M.; Lehmann, S.; Recher, C.; Pigneux, A.; Bertoli, S.; Dumas, P.Y.; et al.
2018Long-term outcome of catheter ablation for treatment of bundle branch re-entrant tachycardiaPathak, R.; Fahed, J.; Santangeli, P.; Hyman, M.; Liang, J.; Kubala, M.; Hayashi, T.; Muser, D.; Pathak, M.; Kochar, A.; Castro, S.; Garcia, F.; Frankel, D.; Supple, G.; Schaller, R.; Lin, D.; Riley, M.; Deo, R.; Epstein, A.; Zado, E.; 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.
2011Genome-wide association analysis identifies variants associated with nonalcoholic fatty liver disease that have distinct effects on metabolic traitsSpeliotes, E.; Yerges-Armstrong, L.; Wu, J.; Hernaez, R.; Kim, L.; Palmer, C.; Gudnason, V.; Eiriksdottir, G.; Garcia, M.; Launer, L.; Nalls, M.; Clark, J.; Mitchell, B.; Shuldiner, A.; Butler, J.; Tomas, M.; Hoffmann, U.; Hwang, S.; Massaro, J.; O’Donnell, C.; et al.; McCarthy, M.I.
2018A genome-wide association study of diabetic kidney disease in subjects with type 2 diabetesVan Zuydam, N.R.; Ahlqvist, E.; Sandholm, N.; Deshmukh, H.; William Rayner, N.; Abdalla, M.; Ladenvall, C.; Ziemek, D.; Fauman, E.; Robertson, N.R.; McKeigue, P.M.; Valo, E.; Forsblom, C.; Harjutsalo, V.; Perna, A.; Rurali, E.; Loredana Marcovecchio, M.; Igo, R.P.; Salem, R.M.; Perico, N.; 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.
2012Common variants at 6q22 and 17q21 are associated with intracranial volumeIkram, M.; Fornage, M.; Smith, A.; Seshadri, S.; Schmidt, R.; Debette, S.; Vrooman, H.; Sigurdsson, S.; Ropele, S.; Taal, H.; Mook-Kanamori, D.; Coker, L.; Longstreth Jr, W.; Niessen, W.; DeStefano, A.; Beiser, A.; Zijdenbos, A.; Struchalin, M.; Jack Jr, C.; Rivadeneira, F.; et al.

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