Works matching IS 07410395 AND DT 2008 AND VI 32 AND IP 6
Results: 12
Erratum.
- Published in:
- Genetic Epidemiology, 2008, v. 32, n. 6, p. 586, doi. 10.1002/gepi.20332
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- Publication type:
- Article
Simple association analysis combining data from trios/sibships and unrelated controls.
- Published in:
- Genetic Epidemiology, 2008, v. 32, n. 6, p. 520, doi. 10.1002/gepi.20325
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- Publication type:
- Article
Fragile X-associated primary ovarian insufficiency: evidence for additional genetic contributions to severity.
- Published in:
- Genetic Epidemiology, 2008, v. 32, n. 6, p. 553, doi. 10.1002/gepi.20329
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- Publication type:
- Article
On multiple-testing correction in genome-wide association studies.
- Published in:
- Genetic Epidemiology, 2008, v. 32, n. 6, p. 567, doi. 10.1002/gepi.20331
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- Publication type:
- Article
Calculation of IBD probabilities with dense SNP or sequence data.
- Published in:
- Genetic Epidemiology, 2008, v. 32, n. 6, p. 513, doi. 10.1002/gepi.20324
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- Publication type:
- Article
Does strong linkage disequilibrium guarantee redundant association results?
- Published in:
- Genetic Epidemiology, 2008, v. 32, n. 6, p. 546, doi. 10.1002/gepi.20328
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- Publication type:
- Article
Analysis of multiple SNPs in a candidate gene or region.
- Published in:
- Genetic Epidemiology, 2008, v. 32, n. 6, p. 560, doi. 10.1002/gepi.20330
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- Publication type:
- Article
CLUMPHAP: a simple tool for performing haplotype-based association analysis.
- Published in:
- Genetic Epidemiology, 2008, v. 32, n. 6, p. 539, doi. 10.1002/gepi.20327
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- Publication type:
- Article
Inference from genome-wide association studies using a novel Markov model.
- Published in:
- Genetic Epidemiology, 2008, v. 32, n. 6, p. 497, doi. 10.1002/gepi.20322
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- Publication type:
- Article
Quantifying the contribution of genetic variants for survival phenotypes.
- Published in:
- Genetic Epidemiology, 2008, v. 32, n. 6, p. 574, doi. 10.1002/gepi.20333
- By:
- Publication type:
- Article
Enhanced detection of genetic association of hypertensive heart disease by analysis of latent phenotypes.
- Published in:
- Genetic Epidemiology, 2008, v. 32, n. 6, p. 528, doi. 10.1002/gepi.20326
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- Publication type:
- Article
Differential parental transmission of markers in RUNX2 among cleft case-parent trios from four populations.
- Published in:
- Genetic Epidemiology, 2008, v. 32, n. 6, p. 505, doi. 10.1002/gepi.20323
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- Publication type:
- Article