Works matching IS 03406717 AND DT 2014 AND VI 133 AND IP 5
Results: 20
A genome-wide association study of prostate cancer in West African men.
- Published in:
- Human Genetics, 2014, v. 133, n. 5, p. 509, doi. 10.1007/s00439-013-1387-z
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- Publication type:
- Article
Significant associations of CHRNA2 and CHRNA6 with nicotine dependence in European American and African American populations.
- Published in:
- Human Genetics, 2014, v. 133, n. 5, p. 575, doi. 10.1007/s00439-013-1398-9
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- Publication type:
- Article
Identification of BACH2 as a susceptibility gene for Graves' disease in the Chinese Han population based on a three-stage genome-wide association study.
- Published in:
- Human Genetics, 2014, v. 133, n. 5, p. 661, doi. 10.1007/s00439-013-1404-2
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- Publication type:
- Article
Does variation in NIPA2 contribute to genetic generalized epilepsy?
- Published in:
- 2014
- By:
- Publication type:
- Letter
Exploring the genetic architecture of alcohol dependence in African-Americans via analysis of a genomewide set of common variants.
- Published in:
- Human Genetics, 2014, v. 133, n. 5, p. 617, doi. 10.1007/s00439-013-1399-8
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- Publication type:
- Article
Natural and orthogonal model for estimating gene-gene interactions applied to cutaneous melanoma.
- Published in:
- Human Genetics, 2014, v. 133, n. 5, p. 559, doi. 10.1007/s00439-013-1392-2
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- Publication type:
- Article
Improving genetic risk prediction by leveraging pleiotropy.
- Published in:
- Human Genetics, 2014, v. 133, n. 5, p. 639, doi. 10.1007/s00439-013-1401-5
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- Publication type:
- Article
COOH-terminal collagen Q ( COLQ) mutants causing human deficiency of endplate acetylcholinesterase impair the interaction of ColQ with proteins of the basal lamina.
- Published in:
- Human Genetics, 2014, v. 133, n. 5, p. 599, doi. 10.1007/s00439-013-1391-3
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- Publication type:
- Article
A genome-wide association study on copy-number variation identifies a 11q11 loss as a candidate susceptibility variant for colorectal cancer.
- Published in:
- Human Genetics, 2014, v. 133, n. 5, p. 525, doi. 10.1007/s00439-013-1390-4
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- Publication type:
- Article
Erratum to: RET and NRG1 interplay in Hirschsprung disease.
- Published in:
- 2014
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- Publication type:
- Erratum
X-linked congenital ptosis and associated intellectual disability, short stature, microcephaly, cleft palate, digital and genital abnormalities define novel Xq25q26 duplication syndrome.
- Published in:
- Human Genetics, 2014, v. 133, n. 5, p. 625, doi. 10.1007/s00439-013-1403-3
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- Publication type:
- Article
Case-control association study of polymorphisms in the voltage-gated sodium channel genes SCN1A, SCN2A, SCN3A, SCN1B, and SCN2B and epilepsy.
- Published in:
- Human Genetics, 2014, v. 133, n. 5, p. 651, doi. 10.1007/s00439-013-1405-1
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- Publication type:
- Article
Gene-gene and gene-environment interactions in ulcerative colitis.
- Published in:
- Human Genetics, 2014, v. 133, n. 5, p. 547, doi. 10.1007/s00439-013-1395-z
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- Publication type:
- Article
Comparative-high resolution melting: a novel method of simultaneous screening for small mutations and copy number variations.
- Published in:
- Human Genetics, 2014, v. 133, n. 5, p. 535, doi. 10.1007/s00439-013-1393-1
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- Publication type:
- Article
Common DNA variants predict tall stature in Europeans.
- Published in:
- Human Genetics, 2014, v. 133, n. 5, p. 587, doi. 10.1007/s00439-013-1394-0
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- Publication type:
- Article
Genome-wide association study of subtype-specific epithelial ovarian cancer risk alleles using pooled DNA.
- Published in:
- Human Genetics, 2014, v. 133, n. 5, p. 481, doi. 10.1007/s00439-013-1383-3
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- Publication type:
- Article
Erratum to: A genome-wide association study of prostate cancer in West African men.
- Published in:
- 2014
- By:
- Publication type:
- Erratum
NIPA2 mutations are correlative with childhood absence epilepsy in the Han Chinese population.
- Published in:
- 2014
- By:
- Publication type:
- Letter
BRG1 variant rs1122608 on chromosome 19p13.2 confers protection against stroke and regulates expression of pre-mRNA-splicing factor SFRS3.
- Published in:
- Human Genetics, 2014, v. 133, n. 5, p. 499, doi. 10.1007/s00439-013-1389-x
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- Publication type:
- Article
The genetic basis of pulmonary arterial hypertension.
- Published in:
- Human Genetics, 2014, v. 133, n. 5, p. 471, doi. 10.1007/s00439-014-1419-3
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- Publication type:
- Article