Works matching IS 03406717 AND DT 2013 AND VI 132 AND IP 2
Results: 11
Genome-wide investigation of gene-environment interactions in colorectal cancer.
- Published in:
- Human Genetics, 2013, v. 132, n. 2, p. 219, doi. 10.1007/s00439-012-1239-2
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- Article
Positive natural selection of TRIB2, a novel gene that influences visceral fat accumulation, in East Asia.
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- Human Genetics, 2013, v. 132, n. 2, p. 201, doi. 10.1007/s00439-012-1240-9
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- Article
The population genetics of the Jewish people.
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- Human Genetics, 2013, v. 132, n. 2, p. 119, doi. 10.1007/s00439-012-1235-6
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- Article
Comprehensive candidate gene study highlights UGT1A and BNC2 as new genes determining continuous skin color variation in Europeans.
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- Human Genetics, 2013, v. 132, n. 2, p. 147, doi. 10.1007/s00439-012-1232-9
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- Article
Suggestion of GLYAT gene underlying variation of bone size and body lean mass as revealed by a bivariate genome-wide association study.
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- Human Genetics, 2013, v. 132, n. 2, p. 189, doi. 10.1007/s00439-012-1236-5
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- Article
Assessment of systematic effects of methodological characteristics on candidate genetic associations.
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- Human Genetics, 2013, v. 132, n. 2, p. 167, doi. 10.1007/s00439-012-1237-4
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- Article
Exome-based linkage disequilibrium maps of individual genes: functional clustering and relationship to disease.
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- Human Genetics, 2013, v. 132, n. 2, p. 233, doi. 10.1007/s00439-012-1243-6
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- Article
Association between variants of EXT2 and type 2 diabetes: a replication and meta-analysis.
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- Human Genetics, 2013, v. 132, n. 2, p. 139, doi. 10.1007/s00439-012-1231-x
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- Article
A dominant-negative mutation of HSF2 associated with idiopathic azoospermia.
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- Human Genetics, 2013, v. 132, n. 2, p. 159, doi. 10.1007/s00439-012-1234-7
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- Article
Identity-by-descent-based heritability analysis in the Northern Finland Birth Cohort.
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- Human Genetics, 2013, v. 132, n. 2, p. 129, doi. 10.1007/s00439-012-1230-y
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- Article
Synergistical effect of 20-HETE and high salt on NKCC2 protein and blood pressure via ubiquitin-proteasome pathway.
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- Human Genetics, 2013, v. 132, n. 2, p. 179, doi. 10.1007/s00439-012-1238-3
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- Article