Genome-wide association study identifies variants in TMPRSS6 associated with hemoglobin levels.
Genome-wide association study identifies variants in TMPRSS6 associated with hemoglobin levels.
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DOI:
10.1038/ng.462
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发表时间:
2009-11
期刊:
影响因子:
30.8
通讯作者:
Kooner, Jaspal S.
中科院分区:
文献类型:
--
作者:
Chambers, John C.;Zhang, Weihua;Li, Yun;Sehmi, Joban;Wass, Mark N.;Zabaneh, Delilah;Hoggart, Clive;Bayele, Henry;McCarthy, Mark I.;Peltonen, Leena;Freimer, Nelson B.;Srai, Surjit K.;Maxwell, Patrick H.;Sternberg, Michael J. E.;Ruokonen, Aimo;Abecasis, Goncalo;Jarvelin, Marjo-Riitta;Scott, James;Elliott, Paul;Kooner, Jaspal S.
We carried out a genome-wide association study of hemoglobin levels in 16,001 individuals of European and Indian Asian ancestry. The most closely associated SNP (rs855791) results in nonsynonymous (V736A) change in the serine protease domain of TMPRSS6 and a blood hemoglobin concentration 0.13 (95% CI 0.09–0.17) g/dl lower per copy of allele A (P = 1.6 × 10−13). Our findings suggest that TMPRSS6, a regulator of hepcidin synthesis and iron handling, is crucial in hemoglobin level maintenance.
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影响因子:
3.1
作者:
Ramsay, Andrew J.;Reid, Janet C.;Hooper, John D.
通讯作者:
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影响因子:
14.8
作者:
Kelley, Lawrence A.;Sternberg, Michael J. E.
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DOI:
10.1073/pnas.0711566105
发表时间:
2008-02-05
影响因子:
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作者:
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通讯作者:
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通讯作者:
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通讯作者:
Enns CA