Quantitative Trait Loci
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MTNR1B G24E Variant Associates With BMI and Fasting Plasma Glucose in the General Population in Studies of 22,142 Europeans Academic Article
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TCF7L2 Variation Predicts Hyperglycemia Incidence in a French General Population Academic Article
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A 3-bp deletion in the HBS1L-MYB intergenic region on chromosome 6q23 is associated with HbF expression Academic Article
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A coding and non-coding transcriptomic perspective on the genomics of human metabolic disease Academic Article
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A genome-wide association study in Europeans and South Asians identifies five new loci for coronary artery disease Academic Article
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A long noncoding RNA from the HBS1L-MYB intergenic region on chr6q23 regulates human fetal hemoglobin expression Academic Article
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Analytical strategies to include the X‐chromosome in variance heterogeneity analyses: Evidence for trait‐specific polygenic variance structure Academic Article
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Association Analysis Indicates That a Variant GATA-Binding Site in the PIK3CB Promoter Is a Cis-Acting Expression Quantitative Trait Locus for This Gene and Attenuates Insulin Resistance in Obese Children Academic Article
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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 Academic Article
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BCL11A is a major HbF quantitative trait locus in three different populations with β-hemoglobinopathies Academic Article
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Causes and Consequences of Genetic Background Effects Illuminated by Integrative Genomic Analysis Academic Article
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Common variants near MC4R are associated with fat mass, weight and risk of obesity Academic Article
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Contribution of Large Region Joint Associations to Complex Traits Genetics Academic Article
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Correction of chromosomal mutation and random integration in embryonic stem cells with helper-dependent adenoviral vectors Academic Article
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Dynamic interaction between fetal adversity and a genetic score reflecting dopamine function on developmental outcomes at 36 months Academic Article
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Fetal globin gene inducers: novel agents and new potential Academic Article
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Fetal hemoglobin in sickle cell anemia: Molecular characterization of the unusually high fetal hemoglobin phenotype in African Americans Academic Article
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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 Academic Article
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Gene-centric Meta-analysis in 87,736 Individuals of European Ancestry Identifies Multiple Blood-Pressure-Related Loci Academic Article
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Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits Academic Article
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Genome-Wide Association Meta-analysis of Neuropathologic Features of Alzheimer's Disease and Related Dementias Academic Article
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Genome-wide association and linkage identify modifier loci of lung disease severity in cystic fibrosis at 11p13 and 20q13.2 Academic Article
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Genome-wide association study for early-onset and morbid adult obesity identifies three new risk loci in European populations Academic Article
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Genome-wide linkage analysis of systolic blood pressure slope using the Genetic Analysis Workshop 13 data sets Academic Article
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Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture Academic Article
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Identification of Genetic Loci Underlying the Phenotypic Constructs of Autism Spectrum Disorders Academic Article
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Identification of QTLs Associated with Virulence Related Traits and Drug Resistance in Cryptococcus neoformans Academic Article
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Impact of Type 2 Diabetes Susceptibility Variants on Quantitative Glycemic Traits Reveals Mechanistic Heterogeneity Academic Article
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K45R variant of squalene synthase increases total cholesterol levels in two study samples from a French Canadian population Academic Article
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Large meta-analysis of genome-wide association studies identifies five loci for lean body mass Academic Article
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Large-Scale Gene-Centric Meta-analysis across 32 Studies Identifies Multiple Lipid Loci Academic Article
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Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation Academic Article
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Meta-analysis of SNPs involved in variance heterogeneity using Levene’s test for equal variances Academic Article
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Multi-ancestry GWAS of the electrocardiographic PR interval identifies 202 loci underlying cardiac conduction Academic Article
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Multi-ethnic genome-wide association study for atrial fibrillation Academic Article
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Multilocus sequence analyses reveal extensive diversity and multiple origins of fluconazole resistance in Candida tropicalis from tropical China Academic Article
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New alcohol-related genes suggest shared genetic mechanisms with neuropsychiatric disorders Academic Article
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New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk Academic Article
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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 Academic Article
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Penetrance of Polygenic Obesity Susceptibility Loci across the Body Mass Index Distribution Academic Article
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Probability genotype imputation method and integrated weighted lasso for QTL identification Academic Article
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Ranking and characterization of established BMI and lipid associated loci as candidates for gene-environment interactions Academic Article
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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 Academic Article
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Susceptibility to chronic pain following nerve injury is genetically affected by CACNG2 Academic Article
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The LASSO and Sparse Least Squares Regression Methods for SNP Selection in Predicting Quantitative Traits Academic Article
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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 Academic Article
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The genetic basis of asymptomatic codon 8 frame-shift (HBB:c25_26delAA) β0-thalassaemia homozygotes Academic Article
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Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies Academic Article
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α+-Thalassemia Trait Caused by a Frameshift Mutation in Exon 2 of the α2-Globin Gene [HBA2 c.244delT] Academic Article