SCOPUS 정보 검색 플랫폼

1
- 84938209461
- Exome sequencing in HFE C282Y homozygous men with extreme phenotypes identifies a GNPAT variant associated with severe iron overload
- McLaren CE, Emond MJ, Subramaniam VN, Phatak PD, Barton JC, Adams PC, et al. Exome sequencing in HFE C282Y homozygous men with extreme phenotypes identifies a GNPAT variant associated with severe iron overload. Hepatology 2015;62:429-439.
- (2015) Hepatology , vol.62 , pp. 429-439
- McLaren, C.E.¹ Emond, M.J.² Subramaniam, V.N.³ Phatak, P.D.⁴ Barton, J.C.⁵ Adams, P.C.⁶

2
- 82355169007
- Using extreme phenotype sampling to identify the rare causal variants of quantitative traits in association studies
- Li D, Lewinger JP, Gauderman WJ, Murcray CE, Conti D. Using extreme phenotype sampling to identify the rare causal variants of quantitative traits in association studies. Genet Epidemiol 2011;35:790-799.
- (2011) Genet Epidemiol , vol.35 , pp. 790-799
- Li, D.¹ Lewinger, J.P.² Gauderman, W.J.³ Murcray, C.E.⁴ Conti, D.⁵

3
- 84922962794
- Genome-wide association study identifies TF as a significant modifier gene of iron metabolism in HFE hemochromatosis
- de Tayrac M, Roth MP, Jouanolle AM, Coppin H, le Gac G, Piperno A, et al. Genome-wide association study identifies TF as a significant modifier gene of iron metabolism in HFE hemochromatosis. J Hepatol 2015;62:664-672.
- (2015) J Hepatol , vol.62 , pp. 664-672
- de Tayrac, M.¹ Roth, M.P.² Jouanolle, A.M.³ Coppin, H.⁴ le Gac, G.⁵ Piperno, A.⁶

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.