Works matching IS 03406717 AND DT 2011 AND VI 129 AND IP 2
Results: 10
Genetic risk sum score comprised of common polygenic variation is associated with body mass index.
- Published in:
- Human Genetics, 2011, v. 129, n. 2, p. 221, doi. 10.1007/s00439-010-0917-1
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- Article
Genome-wide linkage and peak-wide association study of obesity-related quantitative traits in Caribbean Hispanics.
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- Human Genetics, 2011, v. 129, n. 2, p. 209, doi. 10.1007/s00439-010-0916-2
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- Article
Identification and experimental validation of G protein alpha inhibiting activity polypeptide 2 (GNAI2) as a microRNA-138 target in tongue squamous cell carcinoma.
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- Human Genetics, 2011, v. 129, n. 2, p. 189, doi. 10.1007/s00439-010-0915-3
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- Article
Conditional meta-analysis stratifying on detailed HLA genotypes identifies a novel type 1 diabetes locus around TCF19 in the MHC.
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- Human Genetics, 2011, v. 129, n. 2, p. 161, doi. 10.1007/s00439-010-0908-2
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- Article
Autosomal recessive mental retardation: homozygosity mapping identifies 27 single linkage intervals, at least 14 novel loci and several mutation hotspots.
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- Human Genetics, 2011, v. 129, n. 2, p. 141, doi. 10.1007/s00439-010-0907-3
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- Article
Molecular cloning of two novel mucin-like genes in the disease-susceptibility locus for diffuse panbronchiolitis.
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- Human Genetics, 2011, v. 129, n. 2, p. 117, doi. 10.1007/s00439-010-0906-4
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- Article
AKT1 polymorphisms are associated with risk for metabolic syndrome.
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- Human Genetics, 2011, v. 129, n. 2, p. 129, doi. 10.1007/s00439-010-0910-8
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- Article
Modifier locus of the skeletal muscle involvement in Emery-Dreifuss muscular dystrophy.
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- Human Genetics, 2011, v. 129, n. 2, p. 149, doi. 10.1007/s00439-010-0909-1
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- Article
Uncovering hidden variance: pair-wise SNP analysis accounts for additional variance in nicotine dependence.
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- Human Genetics, 2011, v. 129, n. 2, p. 177, doi. 10.1007/s00439-010-0911-7
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- Article
High resolution mapping of OCA2 intragenic rearrangements and identification of a founder effect associated with a deletion in Polish albino patients.
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- Human Genetics, 2011, v. 129, n. 2, p. 199, doi. 10.1007/s00439-010-0913-5
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- Article