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Results 51-60 of 159 (Search time: 0.002 seconds).
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PreviewIssue DateTitleAuthor(s)
2013Identification Of KLHL41 mutations implicates BTB-Kelch-Mediated Ubiquitination as an alternate pathway to myofibrillar disruption in nemaline myopathyGupta, V.; Ravenscroft, G.; Shaheen, R.; Todd, E.; Swanson, L.; Shiina, M.; Ogata, K.; Hsu, C.; Clarke, N.; Darras, B.; Farrar, M.; Hashem, A.; Manton, N.; Muntoni, F.; North, K.; Sandaradura, S.; Nishino, I.; Hayashi, Y.; Sewry, C.; Thompson, E.; et al.
2012Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in womenPalmer, L.; Fox, C.S.; Liu, Y.; White, C.C.; Feitosa, M.; Smith, A.V.; Heard-Costa, N.; Lohman, K.; GIANT Consortium,; MAGIC Consortium,; GLGC Consortium,; Johnson, A.D.; Foster, M.C.; Greenawalt, D.M.; Griffin, P.; Ding, J.; Newman, A.B.; Tylavsky, F.; Miljkovic, I.; Kritchevsky, S.B.; et al.; Bray, M.
2012FTO genotype is associated with phenotypic variability of body mass indexYang, J.; Loos, R.; Powell, J.; Medland, S.; Speliotes, E.; Chasman, D.; Rose, L.; Thorleifsson, G.; Steinthorsdottir, V.; Mägi, R.; Waite, L.; Smith, A.; Yerges-Armstrong, L.; Monda, K.; Hadley, D.; Mahajan, A.; Li, G.; Kapur, K.; Vitart, V.; Huffman, J.; et al.
2010Genome-wide association study identifies five loci associated with lung functionRepapi, E.; Sayers, I.; Wain, L.; Burton, P.; Johnson, T.; Obeidat, M.; Zhao J-, H.; Ramasamy, A.; Zhai, G.; Vitart, V.; Huffman, J.; Igl, W.; Albrecht, E.; Deloukas, P.; Henderson, J.; Granell, R.; McArdle, W.; Rudnicka, A.; Wellcome Trust Case Control Consortium,; Barroso, I.; 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.
2013GWAS of 126,559 individuals identifies genetic variants associated with educational attainmentRietveld, C.; Medland, S.; Derringer, J.; Yang, J.; Esko, T.; Martin, N.; Westra, H.-J.; Shakhbazov, K.; Abdellaoui, A.; Agrawal, A.; Albrecht, E.; Alizadeh, B.; Amin, N.; Barnard, J.; Baumeister, S.; Benke, K.; Bielak, L.; Boatman, J.; Boyle, P.; Davies, G.; et al.
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.
2014Refining analyses of copy number variation identifies specific genes associated with developmental delayCoe, B.; Witherspoon, K.; Rosenfeld, J.; van Bon, B.; Vulto-van Silfhout, A.; Bosco, P.; Friend, K.; Baker, C.; Buono, S.; Vissers, L.; Schuurs-Hoeijmakers, J.; Hoischen, A.; Pfundt, R.; Krumm, N.; Carvill, G.; Li, D.; Amaral, D.; Brown, N.; Lockhart, P.; Scheffer, I.; et al.
2013Surgery versus physiotherapy for stress urinary incontinenceLabrie, J.; Berghmans, B.; Fischer, K.; Milani, F.; van der Wijk, I.; Smalbraak, D.; Vollebregt, A.; Schellart, R.; Graziosi, G.; van der Ploeg, J.; Brouns, J.; Tiersma, E.; Groenendijk, A.; Scholten, P.; Mol, B.; Blokhuis, E.; Adriaanse, A.; Schram, A.; Roovers, J.; Lagro-Janssen, A.; et al.
2013Genome-wide association and longitudinal analyses reveal genetic loci linking pubertal height growth, pubertal timing and childhood adiposityCousminer, D.; Berry, D.; Timpson, N.; Ang, W.; Thiering, E.; Byrne, E.; Taal, H.; Huikari, V.; Bradfield, J.; Kerkhof, M.; Groen-Blokhuis, M.; Kreiner-Møller, E.; Marinelli, M.; Holst, C.; Leinonen, J.; Perry, J.; Surakka, I.; Kettunen, J.; Anttila, V.; Kaakinen, M.; et al.

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