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Results 1-10 of 11 (Search time: 0.003 seconds).
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PreviewIssue DateTitleAuthor(s)
201117-alpha-hydroxyprogesterone caproate for the prevention of adverse neonatal outcome in multiple pregnancies: A randomized controlled trialLim, A.; Schuit, E.; Bloemenkamp, K.; Bernardus, R.; Duvekot, J.; Erwich, J.; van Eyck, J.; Groenwold, R.; Hasaart, T.; Hummel, P.; Kars, M.; Kwee, A.; van Oirschot, C.; van Pampus, M.; Papatsonis, D.; Porath, M.; Spaanderman, M.; Willekes, C.; Wilpshaar, J.; Mol, B.; 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.
2011Association of genetic variation with systolic and diastolic blood pressure among African Americans: the Candidate Gene Association Resource StudyFox, E.; Young, J.; Li, Y.; Dreisbach, A.; Keating, B.; Musani, S.; Liu, K.; Morrison, A.; Ganesh, S.; Kutlar, A.; Ramachandran, V.; Polak, J.; Fabsitz, R.; Dries, D.; Farlow, D.; Redline, S.; Adeyemo, A.; Hirschorn, J.; Sun, Y.; Wyatt, S.; 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.
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.
2011A genome-wide significant linkage for severe depression on chromosome 3: the depression network studyBreen, G.; Webb, B.; Butler, A.; van den Oord, E.; Tozzi, F.; Craddock, N.; Gill, M.; Korszun, A.; Maier, W.; Middleton, L.; Mors, O.; Owen, M.; Cohen-Woods, S.; Perry, J.; Galwey, N.; Upmanyu, R.; Craig, I.; Lewis, C.; Ng, M.; Brewster, S.; 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.
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.
2011Identification of SOX3 as an XX male sex reversal gene in mice and humansSutton, E.; Hughes, J.; White, S.; Sekido, R.; Tan, J.; Arboleda, V.; Rogers, N.; Knower, K.; Rowley, L.; Eyre, H.; Rizzoti, K.; McAninch, D.; Golcalves, J.; Slee, J.; Turbitt, E.; Bruno, D.; Bengtsson, H.; Harley, V.; Vilain, E.; Sinclair, A.; et al.
2011Genomewide association scan of suicidal thoughts and behaviour in major depressionSchosser, A.; Butler, A.; Ising, M.; Perroud, N.; Uher, R.; Ng, M.; Cohen-Woods, S.; Craddock, N.; Owen, M.; Korszun, A.; Jones, L.; Jones, I.; Gill, M.; Rice, J.; Maier, W.; Mors, O.; Rietschel, M.; Lucae, S.; Binder, E.; Preisig, M.; et al.; Domschke, K.

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