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74 results

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Page 1
Adiposity as a cause of cardiovascular disease: a Mendelian randomization study.
Hägg S, Fall T, Ploner A, Mägi R, Fischer K, Draisma HH, Kals M, de Vries PS, Dehghan A, Willems SM, Sarin AP, Kristiansson K, Nuotio ML, Havulinna AS, de Bruijn RF, Ikram MA, Kuningas M, Stricker BH, Franco OH, Benyamin B, Gieger C, Hall AS, Huikari V, Jula A, Järvelin MR, Kaakinen M, Kaprio J, Kobl M, Mangino M, Nelson CP, Palotie A, Samani NJ, Spector TD, Strachan DP, Tobin MD, Whitfield JB, Uitterlinden AG, Salomaa V, Syvänen AC, Kuulasmaa K, Magnusson PK, Esko T, Hofman A, de Geus EJ, Lind L, Giedraitis V, Perola M, Evans A, Ferrières J, Virtamo J, Kee F, Tregouet DA, Arveiler D, Amouyel P, Gianfagna F, Brambilla P, Ripatti S, van Duijn CM, Metspalu A, Prokopenko I, McCarthy MI, Pedersen NL, Ingelsson E; European Network for Genetic and Genomic Epidemiology Consortium. Hägg S, et al. Among authors: benyamin b. Int J Epidemiol. 2015 Apr;44(2):578-86. doi: 10.1093/ije/dyv094. Epub 2015 May 27. Int J Epidemiol. 2015. PMID: 26016847 Free PMC article.
Combined genome scans for body stature in 6,602 European twins: evidence for common Caucasian loci.
Perola M, Sammalisto S, Hiekkalinna T, Martin NG, Visscher PM, Montgomery GW, Benyamin B, Harris JR, Boomsma D, Willemsen G, Hottenga JJ, Christensen K, Kyvik KO, Sørensen TI, Pedersen NL, Magnusson PK, Spector TD, Widen E, Silventoinen K, Kaprio J, Palotie A, Peltonen L; GenomEUtwin Project. Perola M, et al. Among authors: benyamin b. PLoS Genet. 2007 Jun;3(6):e97. doi: 10.1371/journal.pgen.0030097. Epub 2007 May 2. PLoS Genet. 2007. PMID: 17559308 Free PMC article.
Multicenter dizygotic twin cohort study confirms two linkage susceptibility loci for body mass index at 3q29 and 7q36 and identifies three further potential novel loci.
Kettunen J, Perola M, Martin NG, Cornes BK, Wilson SG, Montgomery GW, Benyamin B, Harris JR, Boomsma D, Willemsen G, Hottenga JJ, Slagboom PE, Christensen K, Kyvik KO, Sørensen TI, Pedersen NL, Magnusson PK, Andrew T, Spector TD, Widen E, Silventoinen K, Kaprio J, Palotie A, Peltonen L; GenomEUtwin-project. Kettunen J, et al. Among authors: benyamin b. Int J Obes (Lond). 2009 Nov;33(11):1235-42. doi: 10.1038/ijo.2009.168. Epub 2009 Sep 1. Int J Obes (Lond). 2009. PMID: 19721450 Free PMC article.
Common variants in TMPRSS6 are associated with iron status and erythrocyte volume.
Benyamin B, Ferreira MA, Willemsen G, Gordon S, Middelberg RP, McEvoy BP, Hottenga JJ, Henders AK, Campbell MJ, Wallace L, Frazer IH, Heath AC, de Geus EJ, Nyholt DR, Visscher PM, Penninx BW, Boomsma DI, Martin NG, Montgomery GW, Whitfield JB. Benyamin B, et al. Nat Genet. 2009 Nov;41(11):1173-5. doi: 10.1038/ng.456. Epub 2009 Oct 11. Nat Genet. 2009. PMID: 19820699 Free PMC article.
Transferrin saturation and mortality.
Benyamin B, Montgomery GW, Martin NG, Whitfield JB. Benyamin B, et al. Clin Chem. 2011 Jun;57(6):921-3; author reply 923. doi: 10.1373/clinchem.2011.162784. Epub 2011 Feb 22. Clin Chem. 2011. PMID: 21343418 Free article. No abstract available.
GWAS of butyrylcholinesterase activity identifies four novel loci, independent effects within BCHE and secondary associations with metabolic risk factors.
Benyamin B, Middelberg RP, Lind PA, Valle AM, Gordon S, Nyholt DR, Medland SE, Henders AK, Heath AC, Madden PA, Visscher PM, O'Connor DT, Montgomery GW, Martin NG, Whitfield JB. Benyamin B, et al. Hum Mol Genet. 2011 Nov 15;20(22):4504-14. doi: 10.1093/hmg/ddr375. Epub 2011 Aug 23. Hum Mol Genet. 2011. PMID: 21862451 Free PMC article.
Loci affecting gamma-glutamyl transferase in adults and adolescents show age × SNP interaction and cardiometabolic disease associations.
Middelberg RP, Benyamin B, de Moor MH, Warrington NM, Gordon S, Henders AK, Medland SE, Nyholt DR, de Geus EJ, Hottenga JJ, Willemsen G, Beilin LJ, Mori TA, Wright MJ, Heath AC, Madden PA, Boomsma DI, Pennell CE, Montgomery GW, Martin NG, Whitfield JB. Middelberg RP, et al. Among authors: benyamin b. Hum Mol Genet. 2012 Jan 15;21(2):446-55. doi: 10.1093/hmg/ddr478. Epub 2011 Oct 18. Hum Mol Genet. 2012. PMID: 22010049 Free PMC article.
Childhood intelligence is heritable, highly polygenic and associated with FNBP1L.
Benyamin B, Pourcain B, Davis OS, Davies G, Hansell NK, Brion MJ, Kirkpatrick RM, Cents RA, Franić S, Miller MB, Haworth CM, Meaburn E, Price TS, Evans DM, Timpson N, Kemp J, Ring S, McArdle W, Medland SE, Yang J, Harris SE, Liewald DC, Scheet P, Xiao X, Hudziak JJ, de Geus EJ; Wellcome Trust Case Control Consortium 2 (WTCCC2); Jaddoe VW, Starr JM, Verhulst FC, Pennell C, Tiemeier H, Iacono WG, Palmer LJ, Montgomery GW, Martin NG, Boomsma DI, Posthuma D, McGue M, Wright MJ, Davey Smith G, Deary IJ, Plomin R, Visscher PM. Benyamin B, et al. Mol Psychiatry. 2014 Feb;19(2):253-8. doi: 10.1038/mp.2012.184. Epub 2013 Jan 29. Mol Psychiatry. 2014. PMID: 23358156 Free PMC article.
74 results