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Cortical structure and the risk for Alzheimer’s disease: a bidirectional Mendelian randomization study



Genetic meta-analysis of diagnosed Alzheimer’s disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing



Serum calcium and 25-hydroxyvitamin D in relation to longevity, cardiovascular disease and cancer: a Mendelian randomization study.



A survey of functional dyspepsia in 361,360 individuals: Phenotypic and genetic cross-disease analyses.



Education Attainment, Intelligence and COVID-19: A Mendelian Randomization Study



Homocysteine and female fertility, pregnancy loss and offspring birthweight: a two-sample Mendelian randomization study



Genetic association study of childhood aggression across raters, instruments, and age



New and sex-specific migraine susceptibility loci identified from a multiethnic genome-wide meta-analysis



Genetic investigation of fibromuscular dysplasia identifies risk loci and shared genetics with common cardiovascular diseases.



Cortical structure and the risk for Alzheimer’s disease: a bidirectional Mendelian randomization study



Haploinsufficiency of the Attention-Deficit/Hyperactivity Disorder Risk Gene St3gal3 in Mice Causes Alterations in Cognition and Expression of Genes Involved in Myelination and Sialylation



Circulating Alpha-Tocopherol Levels, Bone Mineral Density, and Fracture: Mendelian Randomization Study



Population-scale analysis of common and rare genetic variation associated with hearing loss in adults



The genetic architecture of age-related hearing impairment revealed by genome-wide association analysis



A large multiethnic GWAS meta-analysis of cataract identifies new risk loci and sex-specific effects



Genetic meta-analysis of twin birth weight shows high genetic correlation with singleton birth weight



Investigating the genetic and environmental basis of head micromovements during MRI



Causal effects of education on chronic kidney disease: a Mendelian randomization study



Genomic Risk Score for Melanoma in a Prospective Study of Older Individuals.



Cannabis Use and the Risk of Cardiovascular Diseases: A Mendelian Randomization Study



Exploring Polygenic Contributors to Subgroups of Comorbid Conditions in Atism Spectrum Disorder



Eleven genomic loci affect plasma levels of chronic inflammation marker soluble urokinase-type plasminogen activator receptor



Model-based assessment of replicability for genome-wide association meta-analysis



Genetic investigation of fibromuscular dysplasia identifies risk loci and shared genetics with common cardiovascular diseases



Variation in the SERPINA6/SERPINA1 locus alters morning plasma cortisol, hepatic corticosteroid binding globulin expression, gene expression in peripheral tissues, and risk of cardiovascular disease



Polyunsaturated fatty acids and risk of Alzheimer’s disease: a Mendelian randomization study



Variants in the fetal genome near pro-inflammatory cytokine genes on 2q13 associate with gestational duration



Genetic meta-analysis of diagnosed Alzheimer’s disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing



Thyroid Function and Dysfunction in Relation to 16 Cardiovascular Diseases: A Mendelian Randomization Study


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10.1080/15592294.2019.1590085

Epigenome-wide association study reveals methylation pathways associated with childhood allergic sensitization



Genetic variation in PLEKHG1 is associated with white matter hyperintensities (n = 11,226)



Identification of common genetic risk variants for autism spectrum disorder



Integrative Genome-Wide Association Studies of eQTL and GWAS Data for Gout Disease Susceptibility



Genetic meta-analysis of diagnosed Alzheimer’s disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing



Genetic Association Study of Childhood Aggression across raters, instruments and age



A Potential Role for the STXBP5-AS1 Gene in Adult ADHD Symptoms



Multivariate genome-wide analyses of the well-being spectrum



A genome-wide association study identifies that the GDF5 and COL27A1 genes are associated with knee pain in UK Biobank (N = 171, 516)


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10.1093/cdn/nzz037.P15-008-19

Associations of Lipid-related SNPs with Circulating Phylloquinone Are Proportional with Triglycerides (P15-008-19).



Common genetic variation indicates separate etiologies for periventricular and deep white matter hyperintensities



The protective effect of club cell secretory protein (CC-16) on COPD risk and progression: a Mendelian randomisation study



Multi-trait genome-wide association meta-analysis of dietary intake identifies new loci and genetic and functional links with metabolic traits



HDAC9 is implicated in atherosclerotic aortic calcification and affects vascular smooth muscle cell phenotype


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10.1158/1538-7445.AM2019-LB-174

Abstract LB-174: Genome-wide association meta-analysis identifies novelGP2gene risk variants for pancreatic cancer in the Japanese population



Genetic Ancestry Markers and Difference in A1c Between African American and White in the Diabetes Prevention Program



Systolic Blood Pressure and Risk of Valvular Heart Disease: A Mendelian Randomization Study.



Genetic predisposition to increased serum calcium, bone mineral density, and fracture risk in individuals with normal calcium levels: mendelian randomisation study



Genome-wide association meta-analysis for early age-related macular degeneration highlights novel loci and insights for advanced disease


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