Pages that link to "Q34583438"
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The following pages link to WHAP: haplotype-based association analysis (Q34583438):
Displaying 50 items.
- High-density SNP screening of the major histocompatibility complex in systemic lupus erythematosus demonstrates strong evidence for independent susceptibility regions (Q21092448) (← links)
- Common variants within MECP2 confer risk of systemic lupus erythematosus (Q21144341) (← links)
- Calpain-5 gene variants are associated with diastolic blood pressure and cholesterol levels (Q21261445) (← links)
- Gene-environment interactions in the development of combined type ADHD: evidence for a synapse-based model (Q24298427) (← links)
- Sex-specific association of depression and a haplotype in leukotriene A4 hydrolase gene (Q24615583) (← links)
- Association scan of 14,500 nonsynonymous SNPs in four diseases identifies autoimmunity variants (Q24646663) (← links)
- TRAF1-C5 as a risk locus for rheumatoid arthritis--a genomewide study (Q24657292) (← links)
- The association of common polymorphisms in the QPCT gene with bone mineral density in the Chinese population (Q28239988) (← links)
- Admixture mapping in lupus identifies multiple functional variants within IFIH1 associated with apoptosis, inflammation, and autoantibody production (Q28486228) (← links)
- Identification of two independent risk factors for lupus within the MHC in United Kingdom families (Q30837981) (← links)
- Likelihood-based association analysis for nuclear families and unrelated subjects with missing genotype data (Q31151241) (← links)
- A case-control study of rheumatoid arthritis identifies an associated single nucleotide polymorphism in the NCF4 gene, supporting a role for the NADPH-oxidase complex in autoimmunity (Q33300467) (← links)
- DNA sequence variants in the LOXL1 gene are associated with pseudoexfoliation glaucoma in a U.S. clinic-based population with broad ethnic diversity (Q33318569) (← links)
- Osteopontin and systemic lupus erythematosus association: a probable gene-gender interaction (Q33323356) (← links)
- Fine mapping of the psoriasis susceptibility locus PSORS1 supports HLA-C as the susceptibility gene in the Han Chinese population (Q33325907) (← links)
- Specificity of the STAT4 genetic association for severe disease manifestations of systemic lupus erythematosus (Q33339386) (← links)
- SNPAnalyzer 2.0: a web-based integrated workbench for linkage disequilibrium analysis and association analysis. (Q33345613) (← links)
- Novel association of ABO histo-blood group antigen with soluble ICAM-1: results of a genome-wide association study of 6,578 women (Q33349442) (← links)
- Novel association of HK1 with glycated hemoglobin in a non-diabetic population: a genome-wide evaluation of 14,618 participants in the Women's Genome Health Study (Q33394569) (← links)
- Evaluation of TRAF6 in a large multiancestral lupus cohort (Q33399089) (← links)
- Variations in the NBN/NBS1 gene and the risk of breast cancer in non-BRCA1/2 French Canadian families with high risk of breast cancer (Q33467074) (← links)
- Targeting 160 candidate genes for blood pressure regulation with a genome-wide genotyping array (Q33475633) (← links)
- Association between protective and deleterious HLA alleles with multiple sclerosis in Central East Sardinia (Q33490625) (← links)
- Conditional analysis of the major histocompatibility complex in rheumatoid arthritis (Q33519303) (← links)
- Reduced expression of integrin alphavbeta8 is associated with brain arteriovenous malformation pathogenesis (Q33597272) (← links)
- Haplotype association analysis of combining unrelated case-control and triads with consideration of population stratification (Q33641229) (← links)
- Blood biomarker levels to aid discovery of cancer-related single-nucleotide polymorphisms: kallikreins and prostate cancer (Q33833602) (← links)
- Evidence for a role of the NOS1AP (CAPON) gene in schizophrenia and its clinical dimensions: an association study in a South American population isolate. (Q33846861) (← links)
- Genome-wide association analysis of soluble ICAM-1 concentration reveals novel associations at the NFKBIK, PNPLA3, RELA, and SH2B3 loci (Q33885956) (← links)
- Efficacy of vitamin D3-fortified-yogurt drink on anthropometric, metabolic, inflammatory and oxidative stress biomarkers according to vitamin D receptor gene polymorphisms in type 2 diabetic patients: a study protocol for a randomized [...] (Q33940070) (← links)
- Using an uncertainty-coding matrix in Bayesian regression models for haplotype-specific risk detection in family association studies (Q33971149) (← links)
- Polymorphisms at the Microseminoprotein-beta locus associated with physiologic variation in beta-microseminoprotein and prostate-specific antigen levels (Q34158465) (← links)
- DASH: a method for identical-by-descent haplotype mapping uncovers association with recent variation (Q34188020) (← links)
- Human longevity and 11p15.5: a study in 1321 centenarians (Q34327320) (← links)
- SLC22A1-ABCB1 haplotype profiles predict imatinib pharmacokinetics in Asian patients with chronic myeloid leukemia (Q34525644) (← links)
- Common genetic variations in CLOCK transcription factor are associated with nonalcoholic fatty liver disease (Q34604846) (← links)
- A broad analysis of IL1 polymorphism and rheumatoid arthritis. (Q34788695) (← links)
- Diplotyper: diplotype-based association analysis (Q34789910) (← links)
- KCNJ6 is associated with adult alcohol dependence and involved in gene × early life stress interactions in adolescent alcohol drinking (Q34820222) (← links)
- Evaluation of imputation-based association in and around the integrin-alpha-M (ITGAM) gene and replication of robust association between a non-synonymous functional variant within ITGAM and systemic lupus erythematosus (SLE). (Q34917266) (← links)
- PTPN22 association in systemic lupus erythematosus (SLE) with respect to individual ancestry and clinical sub-phenotypes (Q34946314) (← links)
- Evaluation of the TREX1 gene in a large multi-ancestral lupus cohort (Q35022304) (← links)
- Fine mapping of a region of chromosome 11q13 reveals multiple independent loci associated with risk of prostate cancer (Q35056055) (← links)
- Genetic determinants of chronic obstructive pulmonary disease in South Indian male smokers (Q35108447) (← links)
- Genome-wide association study of theta band event-related oscillations identifies serotonin receptor gene HTR7 influencing risk of alcohol dependence (Q35116111) (← links)
- Uncoupling the roles of HLA-DRB1 and HLA-DRB5 genes in multiple sclerosis (Q35137159) (← links)
- Association of PPP2CA polymorphisms with systemic lupus erythematosus susceptibility in multiple ethnic groups (Q35184749) (← links)
- Population analysis of vitamin D receptor polymorphisms and the role of genetic ancestry in an admixed population. (Q35199924) (← links)
- Influence of SLCO1B3 haplotype-tag SNPs on docetaxel disposition in Chinese nasopharyngeal cancer patients (Q36036384) (← links)
- HYST: a hybrid set-based test for genome-wide association studies, with application to protein-protein interaction-based association analysis (Q36439328) (← links)