Quantitative Trait Loci
Concept
Vocabulary Service
Overview
subject area of
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A 3-bp deletion in the HBS1L-MYB intergenic region on chromosome 6q23 is associated with HbF expression Journal Articles
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A coding and non-coding transcriptomic perspective on the genomics of human metabolic disease Journal Articles
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A genome-wide association study in Europeans and South Asians identifies five new loci for coronary artery disease Journal Articles
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A long noncoding RNA from the HBS1L-MYB intergenic region on chr6q23 regulates human fetal hemoglobin expression Journal Articles
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A principal component regression based genome wide analysis approach reveals the presence of a novel QTL on BTA7 for MAP resistance in holstein cattle Journal Articles
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Analytical strategies to include the X‐chromosome in variance heterogeneity analyses: Evidence for trait‐specific polygenic variance structure Journal Articles
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Association of breast cancer risk in BRCA1 and BRCA2 mutation carriers with genetic variants showing differential allelic expression: identification of a modifier of breast cancer risk at locus 11q22.3 Journal Articles
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BCL11A is a major HbF quantitative trait locus in three different populations with β-hemoglobinopathies Journal Articles
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CRISPRi screens reveal a DNA methylation-mediated 3D genome dependent causal mechanism in prostate cancer Journal Articles
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Causes and Consequences of Genetic Background Effects Illuminated by Integrative Genomic Analysis Journal Articles
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Contribution of Large Region Joint Associations to Complex Traits Genetics Journal Articles
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Correction of chromosomal mutation and random integration in embryonic stem cells with helper-dependent adenoviral vectors Journal Articles
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Dynamic interaction between fetal adversity and a genetic score reflecting dopamine function on developmental outcomes at 36 months Journal Articles
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Fetal globin gene inducers: novel agents and new potential Journal Articles
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Fetal hemoglobin in sickle cell anemia: Molecular characterization of the unusually high fetal hemoglobin phenotype in African Americans Journal Articles
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Fetal hemoglobin in sickle cell anemia: Saudi patients from the Southwestern province have similar HBB haplotypes but higher HbF levels than African Americans Journal Articles
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Gene-centric Meta-analysis in 87,736 Individuals of European Ancestry Identifies Multiple Blood-Pressure-Related Loci Journal Articles
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Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits Journal Articles
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Genome-Wide Association Meta-analysis of Neuropathologic Features of Alzheimer's Disease and Related Dementias Journal Articles
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Genome-wide association and linkage identify modifier loci of lung disease severity in cystic fibrosis at 11p13 and 20q13.2 Journal Articles
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Genome-wide association and transcriptome studies identify target genes and risk loci for breast cancer Journal Articles
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Genome-wide germline correlates of the epigenetic landscape of prostate cancer Journal Articles
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Genome-wide linkage analysis of systolic blood pressure slope using the Genetic Analysis Workshop 13 data sets Journal Articles
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Identification of Genetic Loci Underlying the Phenotypic Constructs of Autism Spectrum Disorders Journal Articles
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Identification of QTLs Associated with Virulence Related Traits and Drug Resistance in Cryptococcus neoformans Journal Articles
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Integrative Genetic Variation, DNA Methylation, and Gene Expression
Analysis of Escitalopram and Aripiprazole Treatment Outcomes in Depression: A
CAN-BIND-1 Study Journal Articles
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K45R variant of squalene synthase increases total cholesterol levels in two study samples from a French Canadian population Journal Articles
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Large meta-analysis of genome-wide association studies identifies five loci for lean body mass Journal Articles
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Large-Scale Gene-Centric Meta-analysis across 32 Studies Identifies Multiple Lipid Loci Journal Articles
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Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation Journal Articles
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Meta-analysis of SNPs involved in variance heterogeneity using Levene’s test for equal variances Journal Articles
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Multi-ancestry GWAS of the electrocardiographic PR interval identifies 202 loci underlying cardiac conduction Journal Articles
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Multi-ethnic genome-wide association study for atrial fibrillation Journal Articles
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Multilocus sequence analyses reveal extensive diversity and multiple origins of fluconazole resistance in Candida tropicalis from tropical China Journal Articles
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New alcohol-related genes suggest shared genetic mechanisms with neuropsychiatric disorders Journal Articles
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On the Use of Variance per Genotype as a Tool to Identify Quantitative Trait Interaction Effects: A Report from the Women's Genome Health Study Journal Articles
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Penetrance of Polygenic Obesity Susceptibility Loci across the Body Mass Index Distribution Journal Articles
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Ranking and characterization of established BMI and lipid associated loci as candidates for gene-environment interactions Journal Articles
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Risk Alleles in/near ADCY5, ADRA2A, CDKAL1, CDKN2A/B, GRB10, and TCF7L2 Elevate Plasma Glucose Levels at Birth and in Early Childhood: Results from the FAMILY Study Journal Articles
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SNPs in the bovine IL-10 receptor are associated with somatic cell score in Canadian dairy bulls Journal Articles
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Susceptibility to chronic pain following nerve injury is genetically affected by CACNG2 Journal Articles
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The LASSO and Sparse Least Squares Regression Methods for SNP Selection in Predicting Quantitative Traits Journal Articles
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The association of HBG2, BCL11A, and HMIP polymorphisms with fetal hemoglobin and clinical phenotype in Iraqi Kurds with sickle cell disease Journal Articles
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The genetic basis of asymptomatic codon 8 frame‐shift (HBB:c25_26delAA) β0‐thalassaemia homozygotes Journal Articles
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Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies Journal Articles
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eQTL Set–Based Association Analysis Identifies Novel Susceptibility Loci for Barrett Esophagus and Esophageal Adenocarcinoma Journal Articles
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α+-Thalassemia Trait Caused by a Frameshift Mutation in Exon 2 of the α2-Globin Gene [HBA2 c.244delT] Journal Articles