Pages that link to "Q55035893"
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The following pages link to Counterpoint: bias from population stratification is not a major threat to the validity of conclusions from epidemiological studies of common polymorphisms and cancer. (Q55035893):
Displaying 50 items.
- Local literature bias in genetic epidemiology: an empirical evaluation of the Chinese literature (Q21563436) (← links)
- The use of racial, ethnic, and ancestral categories in human genetics research (Q22066114) (← links)
- Control of confounding of genetic associations in stratified populations (Q22337167) (← links)
- Ethnic background and genetic variation in the evaluation of cancer risk: a systematic review (Q24288685) (← links)
- Genetic structure, self-identified race/ethnicity, and confounding in case-control association studies (Q24530649) (← links)
- Lactase persistence-related genetic variant: population substructure and health outcomes (Q24601219) (← links)
- Measuring European population stratification with microarray genotype data (Q24682611) (← links)
- The impact of genetic research on our understanding of normal cognitive ageing: 1995 to 2009 (Q28259199) (← links)
- Clustered environments and randomized genes: a fundamental distinction between conventional and genetic epidemiology (Q28756441) (← links)
- Assessing the probability that a positive report is false: an approach for molecular epidemiology studies (Q29616285) (← links)
- Review and evaluation of methods correcting for population stratification with a focus on underlying statistical principles (Q30492697) (← links)
- Comprehensive analysis of 5-aminolevulinic acid dehydrogenase (ALAD) variants and renal cell carcinoma risk among individuals exposed to lead (Q31025638) (← links)
- An evaluation of power and type I error of single-nucleotide polymorphism transmission/disequilibrium-based statistical methods under different family structures, missing parental data, and population stratification (Q31084618) (← links)
- Role of single nucleotide polymorphisms of KIF1B gene in HBV-associated viral hepatitis (Q31101549) (← links)
- Family-based versus unrelated case-control designs for genetic associations (Q33253242) (← links)
- Correction of population stratification in large multi-ethnic association studies (Q33314841) (← links)
- The M235T polymorphism in the AGT gene and CHD risk: evidence of a Hardy-Weinberg equilibrium violation and publication bias in a meta-analysis (Q33346323) (← links)
- Population substructure and control selection in genome-wide association studies (Q33348644) (← links)
- 118 SNPs of folate-related genes and risks of spina bifida and conotruncal heart defects (Q33459545) (← links)
- An analysis of growth, differentiation and apoptosis genes with risk of renal cancer (Q33482168) (← links)
- Analysis of SNPs and haplotypes in vitamin D pathway genes and renal cancer risk (Q33503237) (← links)
- Armitage's trend test for genome-wide association analysis: one-sided or two-sided? (Q33519304) (← links)
- Minireview: the molecular and genomic basis for prostate cancer health disparities (Q33633160) (← links)
- Interaction between 5-HTTLPR and BDNF Val66Met polymorphisms on HPA axis reactivity in preschoolers (Q33653447) (← links)
- Variants in blood pressure genes and the risk of renal cell carcinoma (Q33759665) (← links)
- Environmental exposures, nitric oxide synthase genes, and exhaled nitric oxide in asthmatic children (Q33801295) (← links)
- Association between a germline OCA2 polymorphism at chromosome 15q13.1 and estrogen receptor-negative breast cancer survival (Q33828680) (← links)
- Antifibrotic effects of CXCL9 and its receptor CXCR3 in livers of mice and humans (Q33943907) (← links)
- Recent developments in genomewide association scans: a workshop summary and review (Q34021104) (← links)
- Assessing sources of inconsistencies in genotypes and their effects on genome-wide association studies with HapMap samples. (Q34083227) (← links)
- A hybrid design for studying genetic influences on risk of diseases with onset early in life (Q34114547) (← links)
- Exogenous visual orienting is associated with specific neurotransmitter genetic markers: a population-based genetic association study (Q34163247) (← links)
- Genome-wide association studies of cancer (Q34193988) (← links)
- Large-scale SNP analysis reveals clustered and continuous patterns of human genetic variation (Q34432345) (← links)
- Population genetic structure and origins of Native Hawaiians in the multiethnic cohort study (Q34473598) (← links)
- CYP1A1/2 haplotypes and lung cancer and assessment of confounding by population stratification (Q34477176) (← links)
- Self-reported ethnicity, genetic structure and the impact of population stratification in a multiethnic study (Q34669917) (← links)
- Hemophilic siblings with chronic hepatitis C: Familial aggregation of spontaneous and treatment-related viral clearance (Q34914406) (← links)
- A Klothoβ variant mediates protein stability and associates with colon transit in irritable bowel syndrome with diarrhea (Q35028313) (← links)
- Integrating epidemiology and genetic association: the challenge of gene-environment interaction (Q35038043) (← links)
- Comprehensive evaluation of one-carbon metabolism pathway gene variants and renal cell cancer risk (Q35409934) (← links)
- Molecular genetic studies of gene identification for osteoporosis: a 2004 update (Q35691688) (← links)
- The chromosome 2p21 region harbors a complex genetic architecture for association with risk for renal cell carcinoma (Q35750240) (← links)
- Drug-gene interactions between genetic polymorphisms and antihypertensive therapy (Q35859028) (← links)
- Admixture-matched case-control study: a practical approach for genetic association studies in admixed populations (Q36338286) (← links)
- Analysis of genetically complex epilepsies. (Q36344238) (← links)
- The maternal HLA-G 1597ΔC null mutation is associated with increased risk of pre-eclampsia and reduced HLA-G expression during pregnancy in African-American women (Q36629793) (← links)
- Investigating the complex genetic architecture of ankle-brachial index, a measure of peripheral arterial disease, in non-Hispanic whites (Q36699490) (← links)
- Nicotinic acetylcholine receptor beta2 subunit gene implicated in a systems-based candidate gene study of smoking cessation (Q36851620) (← links)
- Innate immunogenetics: a tool for exploring new frontiers of host defence (Q36889564) (← links)