How meaningful are heritability estimates of liability?
- Published in:
- Human Genetics, 2013, v. 132, n. 12, p. 1351, doi. 10.1007/s00439-013-1334-z
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- Publication type:
- Article
Works matching IS 03406717 AND DT 2013 AND VI 132 AND IP 12
Results: 12
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HLA-DPB1*04:01 allele is associated with non-obstructive azoospermia in Japanese patients.
- Published in:
- Human Genetics, 2013, v. 132, n. 12, p. 1405, doi. 10.1007/s00439-013-1347-7
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- Publication type:
- Article
3
Genome-wide copy number variation analysis of a Branchio-oto-renal syndrome cohort identifies a recombination hotspot and implicates new candidate genes.
- Published in:
- Human Genetics, 2013, v. 132, n. 12, p. 1339, doi. 10.1007/s00439-013-1338-8
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- Publication type:
- Article
4
A functional variant of pre-miRNA-196a2 confers risk for Behcet’s disease but not for Vogt–Koyanagi–Harada syndrome or AAU in ankylosing spondylitis.
- Published in:
- Human Genetics, 2013, v. 132, n. 12, p. 1395, doi. 10.1007/s00439-013-1346-8
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- Publication type:
- Article
5
Bayes’ rule, medical genetics and the wider world. A review of: the theory that would not die. How Bayes’ rule cracked the Enigma code, hunted down Russian submarines, and emerged triumphant from two centuries of controversy: by Sharon Bertsch McGrayne: New Haven, Yale University Press (2011; revised paperback edition 2012)
- Published in:
- 2013
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- Publication type:
- Book Review
6
Disorders with similar clinical phenotypes reveal underlying genetic interaction: SATB2 acts as an activator of the <i>UPF3B</i> gene.
- Published in:
- Human Genetics, 2013, v. 132, n. 12, p. 1383, doi. 10.1007/s00439-013-1345-9
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- Publication type:
- Article
7
A novel method for identifying nonlinear gene–environment interactions in case–control association studies.
- Published in:
- Human Genetics, 2013, v. 132, n. 12, p. 1413, doi. 10.1007/s00439-013-1350-z
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- Publication type:
- Article
8
Gene–smoking interactions in multiple Rho-GTPase pathway genes in an early-onset coronary artery disease cohort.
- Published in:
- Human Genetics, 2013, v. 132, n. 12, p. 1371, doi. 10.1007/s00439-013-1339-7
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- Publication type:
- Article
9
Genetics of healthy aging and longevity.
- Published in:
- Human Genetics, 2013, v. 132, n. 12, p. 1323, doi. 10.1007/s00439-013-1342-z
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- Publication type:
- Article
10
Erratum to: The success of pharmacogenomics in moving genetic association studies from bench to bedside: study design and implementation of precision medicine in the post-GWAS era.
- Published in:
- 2013
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- Publication type:
- Correction Notice
11
Variants in <i>BET1L</i> and <i>TNRC6B</i> associate with increasing fibroid volume and fibroid type among European Americans.
- Published in:
- Human Genetics, 2013, v. 132, n. 12, p. 1361, doi. 10.1007/s00439-013-1340-1
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- Publication type:
- Article
12
No evidence of interaction between known lipid-associated genetic variants and smoking in the multi-ethnic PAGE population.
- Published in:
- Human Genetics, 2013, v. 132, n. 12, p. 1427, doi. 10.1007/s00439-013-1375-3
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- Publication type:
- Article