Works matching IS 03406717 AND DT 2014 AND VI 133 AND IP 9
Results: 11
HLA alleles associated with the adaptive immune response to smallpox vaccine: a replication study.
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- Human Genetics, 2014, v. 133, n. 9, p. 1083, doi. 10.1007/s00439-014-1449-x
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- Article
Validated context-dependent associations of coronary heart disease risk with genotype variation in the chromosome 9p21 region: the Atherosclerosis Risk in Communities study.
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- Human Genetics, 2014, v. 133, n. 9, p. 1105, doi. 10.1007/s00439-014-1451-3
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Identification of methylation quantitative trait loci (mQTLs) influencing promoter DNA methylation of alcohol dependence risk genes.
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- Human Genetics, 2014, v. 133, n. 9, p. 1093, doi. 10.1007/s00439-014-1452-2
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- Article
A genetic association study detects haplotypes associated with obstructive heart defects.
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- Human Genetics, 2014, v. 133, n. 9, p. 1127, doi. 10.1007/s00439-014-1453-1
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- Article
A single codon insertion in PICALM is associated with development of familial subvalvular aortic stenosis in Newfoundland dogs.
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- Human Genetics, 2014, v. 133, n. 9, p. 1139, doi. 10.1007/s00439-014-1454-0
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- Article
Opposite effects on facial morphology due to gene dosage sensitivity.
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- Human Genetics, 2014, v. 133, n. 9, p. 1117, doi. 10.1007/s00439-014-1455-z
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- Article
Hennekam syndrome can be caused by FAT4 mutations and be allelic to Van Maldergem syndrome.
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- Human Genetics, 2014, v. 133, n. 9, p. 1161, doi. 10.1007/s00439-014-1456-y
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- Article
Mitochondrial DNA copy number in peripheral blood cells declines with age and is associated with general health among elderly.
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- Human Genetics, 2014, v. 133, n. 9, p. 1149, doi. 10.1007/s00439-014-1458-9
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- Article
The population genomic landscape of human genetic structure, admixture history and local adaptation in Peninsular Malaysia.
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- Human Genetics, 2014, v. 133, n. 9, p. 1169, doi. 10.1007/s00439-014-1459-8
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- Article
Host genetics and viral load in primary HIV-1 infection: clear evidence for gene by sex interactions.
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- Human Genetics, 2014, v. 133, n. 9, p. 1187, doi. 10.1007/s00439-014-1465-x
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- Article
Amniotic fluid RNA gene expression profiling provides insights into the phenotype of Turner syndrome.
- Published in:
- Human Genetics, 2014, v. 133, n. 9, p. 1075, doi. 10.1007/s00439-014-1448-y
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- Article