Pages that link to "Q33654995"
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The following pages link to Genevar: a database and Java application for the analysis and visualization of SNP-gene associations in eQTL studies (Q33654995):
Displayed 50 items.
- Identification of IGF1, SLC4A4, WWOX, and SFMBT1 as hypertension susceptibility genes in Han Chinese with a genome-wide gene-based association study (Q21134736) (← links)
- Ensembl 2014 (Q24567767) (← links)
- An allele of IKZF1 (Ikaros) conferring susceptibility to childhood acute lymphoblastic leukemia protects against type 1 diabetes (Q24612348) (← links)
- Identification of multiple genetic susceptibility loci in Takayasu arteritis (Q24632711) (← links)
- Connecting SNPs in Diabetes: A Spatial Analysis of Meta-GWAS Loci (Q26802073) (← links)
- Disease mechanisms in rheumatology--tools and pathways: defining functional genetic variants in autoimmune diseases (Q27005017) (← links)
- Genome-wide association study identifies a PSMD3 variant associated with neutropenia in interferon-based therapy for chronic hepatitis C (Q28254011) (← links)
- A novel sarcoidosis risk locus for Europeans on chromosome 11q13.1 (Q28271903) (← links)
- Genetic variants in GPR126 are associated with adolescent idiopathic scoliosis (Q28290491) (← links)
- Expression of phosphofructokinase in skeletal muscle is influenced by genetic variation and associated with insulin sensitivity (Q28303350) (← links)
- A 3'-UTR Polymorphism in Soluble Epoxide Hydrolase Gene Is Associated with Acute Rejection in Renal Transplant Recipients (Q28384776) (← links)
- Common variants near ABCA1, AFAP1 and GMDS confer risk of primary open-angle glaucoma (Q28394939) (← links)
- Novel genetic locus implicated for HIV-1 acquisition with putative regulatory links to HIV replication and infectivity: a genome-wide association study (Q28544526) (← links)
- Susceptibility loci associated with specific and shared subtypes of lymphoid malignancies (Q28943260) (← links)
- A genome-wide association study identifies multiple susceptibility loci for chronic lymphocytic leukemia (Q28943318) (← links)
- A meta-analysis of Hodgkin lymphoma reveals 19p13.3 TCF3 as a novel susceptibility locus (Q28943487) (← links)
- Identification of two new loci at IL23R and RAB32 that influence susceptibility to leprosy (Q28943497) (← links)
- Functional variants in NFKBIE and RTKN2 involved in activation of the NF-κB pathway are associated with rheumatoid arthritis in Japanese (Q28943519) (← links)
- Large-scale genotyping identifies 41 new loci associated with breast cancer risk (Q29416989) (← links)
- Variants near TERT and TERC influencing telomere length are associated with high-grade glioma risk (Q29417088) (← links)
- Evidence of new risk genetic factor to systemic lupus erythematosus: the UBASH3A gene. (Q30009882) (← links)
- Whole-genome sequence-based analysis of thyroid function. (Q30316724) (← links)
- A genome-wide association study of chronic otitis media with effusion and recurrent otitis media identifies a novel susceptibility locus on chromosome 2 (Q30409304) (← links)
- Cis-acting polymorphisms affect complex traits through modifications of microRNA regulation pathways (Q30416926) (← links)
- Association between risk of oral precancer and genetic variations in microRNA and related processing genes. (Q30487016) (← links)
- Identification of genetic modifiers of age-at-onset for familial Parkinson's disease (Q30833988) (← links)
- A genome-wide survey for SNPs altering microRNA seed sites identifies functional candidates in GWAS. (Q31034509) (← links)
- Genetic association study of adiposity and melanocortin-4 receptor (MC4R) common variants: replication and functional characterization of non-coding regions (Q33599821) (← links)
- Genetic predictors of risk and resilience in psychiatric disorders: a cross-disorder genome-wide association study of functional impairment in major depressive disorder, bipolar disorder, and schizophrenia (Q33603700) (← links)
- Mapping eQTLs with RNA-seq reveals novel susceptibility genes, non-coding RNAs and alternative-splicing events in systemic lupus erythematosus (Q33614670) (← links)
- A replication study confirms the association of GWAS-identified SNPs at MICB and PLCE1 in Thai patients with dengue shock syndrome (Q33647936) (← links)
- Single Nucleotide Polymorphisms Associated with MicroRNA Regulation. (Q33649524) (← links)
- BMI prediction within a Korean population (Q33862122) (← links)
- Genetic variation in DNA repair pathways and risk of non-Hodgkin's lymphoma (Q33882519) (← links)
- Genome-wide association meta-analysis of human longevity identifies a novel locus conferring survival beyond 90 years of age. (Q33920700) (← links)
- Maps of open chromatin guide the functional follow-up of genome-wide association signals: application to hematological traits (Q33954469) (← links)
- An interaction between Nrf2 polymorphisms and smoking status affects annual decline in FEV1: a longitudinal retrospective cohort study (Q33966503) (← links)
- Genome-wide association study in Chinese men identifies two new prostate cancer risk loci at 9q31.2 and 19q13.4. (Q33977740) (← links)
- ADAM19 and HTR4 variants and pulmonary function: Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium Targeted Sequencing Study (Q34060246) (← links)
- Genome-wide association study of sexual maturation in males and females highlights a role for body mass and menarche loci in male puberty. (Q34209068) (← links)
- Patterns of cis regulatory variation in diverse human populations (Q34244935) (← links)
- Genome-wide association study identifies multiple susceptibility loci for pancreatic cancer (Q34314018) (← links)
- Novel locus including FGF21 is associated with dietary macronutrient intake (Q34325630) (← links)
- Human genomic regions with exceptionally high levels of population differentiation identified from 911 whole-genome sequences (Q34342301) (← links)
- Identification of CAD candidate genes in GWAS loci and their expression in vascular cells (Q34344282) (← links)
- The complex SNP and CNV genetic architecture of the increased risk of congenital heart defects in Down syndrome. (Q34352054) (← links)
- A meta-analysis of genome-wide association studies of follicular lymphoma (Q34425597) (← links)
- Ankylosing spondylitis is associated with the anthrax toxin receptor 2 gene (ANTXR2). (Q34431607) (← links)
- Association of genetic variation in IKZF1, ARID5B, and CEBPE and surrogates for early-life infections with the risk of acute lymphoblastic leukemia in Hispanic children (Q34466695) (← links)
- Melanoma risk loci as determinants of melanoma recurrence and survival (Q34493237) (← links)