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PreviewIssue DateTitleAuthor(s)
2012Genetic variation in the 15q25 nicotinic acetylcholine receptor gene cluster (CHRNA5-CHRNA3-CHRNB4) interacts with maternal self-reported smoking status during pregnancy to influence birth weightTyrrell, J.; Huikari, V.; Christie, J.; Cavadino, A.; Bakker, R.; Brion, M.; Geller, F.; Paternoster, L.; Myhre, R.; Potter, C.; Johnson, P.; Ebrahim, S.; Feenstra, B.; Hartikainen, A.; Hattersley, A.; Hofman, A.; Kaakinen, M.; Lowe, L.; Magnus, P.; McConnachie, A.; et al.
2012Observation of anisotropy in the galactic cosmic-ray arrival directions at 400 TeV with IceCubeAbbasi, R.; Abdou, Y.; Abu-Zayyad, T.; Ackermann, M.; Adams, J.; Aguilar, J.A.; Ahlers, M.; Allen, M.M.; Altmann, D.; Andeen, K.; Auffenberg, J.; Bai, X.; Baker, M.; Barwick, S.W.; Bay, R.; Bazo Alba, J.L.; Beattie, K.; Beatty, J.J.; Bechet, S.; Becker, J.K.; et al.
2012Phenotype and polyp landscape in serrated polyposis syndrome: a series of 100 patients from genetics clinicsRosty, C.; Buchanan, D.; Walsh, M.; Pearson, S.; Pavluk, E.; Walters, R.; Clendenning, M.; Spring, K.; Jenkins, M.; Win, A.; Hopper, J.; Sweet, K.; Frankel, W.; Aronson, M.; Gallinger, S.; Goldblatt, J.; Woodall, S.; Arnold, J.; Walker, N.; Jass, J.; et al.
2012Combined search for the Standard Model Higgs boson using up to 4.9 fb−¹ of pp collision data at √s = 7 TeV with the ATLAS detector at the LHCATLAS Collaboration; Aad, G.; Abbott, B.; Abdallah, J.; Abdel Khalek, S.; Abdelalim, A.; Abdesselam, A.; Abdinov, O.; Abi, B.; Abolins, M.; AbouZeid, O.; Abramowicz, H.; Abreu, H.; Acerbi, E.; Acharya, B.; Adamczyk, L.; Adams, D.; Addy, T.; Aderholz, M.; Adomeit, S.; et al.
2012Somatic histone H3 alterations in pediatric diffuse intrinsic pontine gliomas and non-brainstem glioblastomasWu, G.; Broniscer, A.; McEachron, T.; Lu, C.; Paugh, B.; Becksfort, J.; Qu, C.; Ding, L.; Huether, R.; Parker, M.; Zhang, J.; Gajjar, A.; Dyer, M.; Mullighan, C.; Gilbertson, R.; Mardis, E.; Wilson, R.; Downing, J.; Ellison, D.; Zhang, J.; et al.
2012Loss-of-function germline GATA2 mutations in patients with MDS/AML or MonoMAC syndrome and primary lymphedema reveal a key role for GATA2 in the lymphatic vasculatureKazenwadel, J.; Secker, G.; Liu, Y.; Rosenfeld, J.; Wildin, R.; Cuellar-Rodriguez, J.; Hsu, A.; Dyack, S.; Fernandez, C.; Chong, C.; Babic, M.; Bardy, P.; Shimamura, A.; Zhang, M.; Walsh, T.; Holland, S.; Hickstein, D.; Horwitz, M.; Hahn, C.; Scott, H.; et al.
2012Disability-adjusted life years (DALYs) for 291 diseases and injuries in 21 regions, 1990-2010: a systematic analysis for the Global Burden of Disease Study 2010Murray, C.; Vos, T.; Lozano, R.; Naghavi, M.; Flaxman, A.; Michaud, C.; Ezzati, M.; Shibuya, K.; Salomon, J.; Abdalla, S.; Aboyans, V.; Abraham, J.; Ackerman, I.; Aggarwal, R.; Ahn, S.; Ali, M.; Alvarado, M.; Anderson, H.; Anderson, L.; Andrews, K.; et al.
2012KCNQ2 encephalopathy: Emerging phenotype of a neonatal epileptic encephalopathyWeckhuysen, S.; Mandelstam, S.; Suls, A.; Audenaert, D.; Deconinck, T.; Claes, L.; Deprez, L.; Smets, K.; Hristova, D.; Yordanova, I.; Jordanova, A.; Ceulemans, B.; Jansen, A.; Hasaerts, D.; Roelens, F.; Lagae, L.; Yendle, S.; Stanley, T.; Heron, S.; Mulley, J.; et al.
2012Common variants at 12q15 and 12q24 are associated with infant head circumferenceTaal, H.; St Pourcain, B.; Thiering, E.; Das, S.; Mook-Kanamori, D.; Warrington, N.; Kaakinen, M.; Kreiner-Møller, E.; Bradfield, J.; Freathy, R.; Geller, F.; Guxens, M.; Cousminer, D.; Kerkhof, M.; Timpson, N.; Arfan Ikram, M.; Beilin, L.; Bønnelykke, K.; Buxton, J.; Charoen, P.; et al.
2012A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistancePalmer, L.; Manning, A.K.; Hivert M-, F.; Scott, R.A.; Grimsby, J.L.; Bouatia-Naji, N.; Chen, H.; Rybin, D.; Liu C-, T.; Bielak, L.F.; Prokopenko, I.; Amin, N.; Barnes, D.; Cadby, G.; Hottenga J-, J.; Ingelsson, E.; Jackson, A.U.; Johnson, T.; Kanoni, S.; Ladenvall, C.; et al.