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1. Whole genome sequencing identifies associations for nonsyndromic sagittal craniosynostosis with the intergenic region of BMP2 and noncoding RNA gene LINC01428

2. Whole genome sequencing identifies associations for nonsyndromic sagittal craniosynostosis with the intergenic region of BMP2 and noncoding RNA gene LINC01428

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3. Family‐based association of HLA‐DRB1 and DQB1 alleles and haplotypes in a group of Iranian Type 1 diabetes children.

4. High Resolution Haplotype Analyses of Classical HLA Genes in Families With Multiple Sclerosis Highlights the Role of HLA-DP Alleles in Disease Susceptibility

5. Causal inference in genetic trio studies

6. Investigation of previously implicated genetic variants in chronic tic disorders: a transmission disequilibrium test approach

7. Family-based analysis of -675 4G/5G polymorphism in the PAI-1 gene of polycystic ovary syndrome in Chinese population.

8. ASH1L may contribute to the risk of Tourette syndrome: Combination of family‐based analysis and case–control study.

9. ASH1L may contribute to the risk of Tourette syndrome: Combination of family‐based analysis and case–control study

10. Detecting gene–environment interactions in human birth defects: Study designs and statistical methods

11. Two tSNPs in BRIP1 are associated with breast cancer during TDT analysis

12. Two tSNPs in BRIP1 are associated with breast cancer during TDT analysis.

13. SNAP25 MnlI 多态性与儿童注意缺陷 多动障碍关联性的 meta 分析.

14. Candidate-gene association analysis for a continuous phenotype with a spike at zero using parent-offspring trios.

15. Genome‐wide association analysis of autism identified multiple loci that have been reported as strong signals for neuropsychiatric disorders.

16. Statistical Analysis of GWAS

18. Genetic associations and parent-of-origin effects of PVRL1 in non-syndromic cleft lip with or without cleft palate across multiple ethnic populations.

19. Genotype Correlation Analysis Reveals Pathway-Based Functional Disequilibrium and Potential Epistasis in the Human Interactome

20. NTN1 gene was risk to non‐syndromic cleft lip only among Han Chinese population.

25. Association Analysis in Family Designs

26. Association between Tourette Syndrome and the Dopamine D3 Receptor Gene Rs6280

29. FUT2 Variants Confer Susceptibility to Familial Otitis Media.

30. Family-based study of association between MAFB gene polymorphisms and NSCL/P among Western Han Chinese population.

31. Weighted Transmission Disequilibrium Test for Family Trio Association Design.

32. Family-based analysis of GGT1 and HNF1A gene polymorphisms in patients with polycystic ovary syndrome.

38. Genetics of Atopic Eczema

42. Transmission Based Conditional Logistic Model for Testing Main and Interaction Effects

45. Genetic association tests when a nuisance parameter is not identifiable under no association.

46. Lack of association between SLC5A7 polymorphisms and Tourette syndrome in a Chinese Han population.

47. Gene Mapping in Admixed Families: A Cautionary Note on the Interpretation of the Transmission Disequilibrium Test and a Possible Solution.

49. Association of MICA and HLA‐B alleles with leprosy in two endemic populations in Brazil

50. Causal inference in genetic trio studies