Pages that link to "Q53282374"

The following pages link to A new multimarker test for family-based association studies. (Q53282374):

Displaying 29 items.

• SNP set association analysis for familial data (Q30564362) (← links)
• Family-based association tests for sequence data, and comparisons with population-based association tests (Q30587122) (← links)
• A comparative analysis of family-based and population-based association tests using whole genome sequence data (Q30879700) (← links)
• Detecting rare variants for quantitative traits using nuclear families (Q31065205) (← links)
• Transmission and decorrelation methods for detecting rare variants using sequencing data from related individuals (Q31149251) (← links)
• Parsing the effects of individual SNPs in candidate genes with family data. (Q33517592) (← links)
• Statistical challenges for genome-wide association studies of suicidality using family data (Q33571903) (← links)
• An omnibus test for family-based association studies with multiple SNPs and multiple phenotypes (Q33869573) (← links)
• Finding disease variants in Mendelian disorders by using sequence data: methods and applications (Q34089812) (← links)
• A noise-reduction GWAS analysis implicates altered regulation of neurite outgrowth and guidance in autism (Q34557745) (← links)
• Rare variant analysis for family-based design (Q34558081) (← links)
• Complex pedigrees in the sequencing era: to track transmissions or decorrelate? (Q34743725) (← links)
• A multi-SNP association test for complex diseases incorporating an optimal P-value threshold algorithm in nuclear families (Q35610202) (← links)
• Ordered-subset analysis (OSA) for family-based association mapping of complex traits (Q36970064) (← links)
• Nominal association with CHRNA4 variants and nicotine dependence (Q37055419) (← links)
• Further examination of the candidate genes in chromosome 12p13 locus for late-onset Alzheimer disease (Q37083853) (← links)
• Family-based methods for linkage and association analysis (Q37115908) (← links)
• Multiple superoxide dismutase 1/splicing factor serine alanine 15 variants are associated with the development and progression of diabetic nephropathy: the Diabetes Control and Complications Trial/Epidemiology of Diabetes Interventions and Complicat (Q37127488) (← links)
• Blocking approach for identification of rare variants in family-based association studies (Q37509918) (← links)
• Latent class model with familial dependence to address heterogeneity in complex diseases: adapting the approach to family-based association studies (Q37724218) (← links)
• Association between the oxytocin receptor (OXTR) gene and children's social cognition at 18 months (Q39177599) (← links)
• A combined linkage and association strategy identifies a variant near the GSTP1 gene associated with BMI in the Mexican population. (Q40459546) (← links)
• TNFSF10/TRAIL regulates human T4 effector memory lymphocyte radiosensitivity and predicts radiation-induced acute and subacute dermatitis (Q40996284) (← links)
• Contrasting linkage disequilibrium as a multilocus family-based association test (Q44741578) (← links)
• The use of haplotypes in the identification of interaction between SNPs (Q45251995) (← links)
• Detecting multi-way epistasis in family-based association studies (Q47958819) (← links)
• Association test with the principal component analysis in case-parents studies (Q50882823) (← links)
• Distribution of the number of false discoveries in large-scale family-based association testing with application to the association between PTPN1 and hypertension and obesity (Q51620660) (← links)
• Sex-specific effect of IL9 polymorphisms on lung function and polysensitization (Q51631367) (← links)