- Genomic inflation factors under polygenic inheritance
[作者：Yang, J; Weedon, MN; Purcell, S; Lettre, G; Estrada, K; Willer, CJ; Smith, AV; Ingelsson, E; O'Connell, JR; Mangino, M; Magi, R; Madden, PA; Heath, AC; Nyholt, DR; Martin, NG; Montgomery, GW; Frayling, TM; Hirschhorn, JN; McCarthy, MI; Goddard, ME; Visscher, PM,期刊：European Journal of Human Genetics, 页码：807-812 , 文章类型： Article，,卷期：2011年19-7]
- Population structure, including population stratification and cryptic relatedness, can cause spurious associations in genome-wide association studies (GWAS). Usually, the scaled median or mean test statistic for associat...
- Genetic architecture of circulating lipid levels
[作者：Demirkan, A; Amin, N; Isaacs, A; Jarvelin, MR; Whitfield, JB; Wichmann, HE; Kyvik, KO; Rudan, I; Gieger, C; Hicks, AA; Johansson, A; Hottenga, JJ; Smith, JJ; Wild, SH; Pedersen, NL; Willemsen, G; Mangino, M; Hayward, C; Uitterlinden, AG; Hofman, A; Witteman, J; Montgomery, GW; Pietilainen, KH; Rantanen, T; Kaprio, J; Doring, A; Pramstaller, PP; Gyllensten, U; de Geus, EJC; Penninx, BW; Wilson, JF; Rivadeneria, F; Magnusson, PKE; Boomsma, DI; Spector, T; Campbell, H; Hoehne, B; Martin, NG; Oostra, BA; McCarthy, M; Peltonen-Palotie, L; Aulchenko, Y; Visscher, PM; Ripatti, S; Janssens, ACJW; van Duijn, CM,期刊：European Journal of Human Genetics, 页码：813-819 , 文章类型： Article，,卷期：2011年19-7]
- Serum concentrations of low-density lipoprotein cholesterol (LDL-C), high-density lipoprotein cholesterol (HDL-C), triglycerides (TGs) and total cholesterol (TC) are important heritable risk factors for cardiovascular di...
- A novel autosomal dominant condition consisting of congenital heart defects and low atrial rhythm maps to chromosome 9q
[作者：van de Meerakker, JBA; van Engelen, K; Mathijssen, IB; Deprez, RHLD; Lam, J; Wilde, AAM; Baars, MJH; Mannens, MMAM; Mulder, BJM; Moorman, AFM; Postma, AV,期刊：European Journal of Human Genetics, 页码：820-826 , 文章类型： Article，,卷期：2011年19-7]
- Congenital heart defects (CHDs) occur mostly sporadic, but familial CHD cases have been reported. Mutations in several genes, including NKX2.5, GATA4 and NOTCH1, were identified in families and patients with CHD, but the...
- The GENCODE exome: sequencing the complete human exome
[作者：Coffey, AJ; Kokocinski, F; Calafato, MS; Scott, CE; Palta, P; Drury, E; Joyce, CJ; LeProust, EM; Harrow, J; Hunt, S; Lehesjoki, AE; Turner, DJ; Hubbard, TJ; Palotie, A,期刊：European Journal of Human Genetics, 页码：827-831 , 文章类型： Article，,卷期：2011年19-7]
- Sequencing the coding regions, the exome, of the human genome is one of the major current strategies to identify low frequency and rare variants associated with human disease traits. So far, the most widely used commerci...
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