All Stories

  1. Cis-trans divergence in the regulatory architectures of MYBL2 and MYB underlies distinct transcriptional networks in immunometabolic traits
  2. Genetic regulation of B cell receptor signaling pathway: Insights from expression quantitative trait locus analysis using a mixed model
  3. Deciphering the Genetic Complexity of Classical Hodgkin Lymphoma: Insights and Effective Strategies
  4. Bayesian colocalization of GWAS and eQTL signals reveals cell type-specific genes and regulatory variants for susceptibility to subtypes of ischemic stroke
  5. Genetic Association of Diagnostic Traits of Metabolic Syndrome with Lysosomal Pathways: Insights from Target Gene Enrichment Analysis
  6. Enrichment of Spatial eGenes Colocalized with Type 2 Diabetes Mellitus Genome-Wide Association Study Signals in the Lysosomal Pathway
  7. Identification and Interpretation of eQTL and eGenes for Hodgkin Lymphoma Susceptibility
  8. Towards the Genetic Architecture of Complex Gene Expression Traits: Challenges and Prospects for eQTL Mapping in Humans
  9. Meet the Section Editor
  10. Underestimation of Heritability across the Molecular Layers of the Gene Expression Process
  11. Regulatory Nucleotide Sequence Signals for Expression of the Genes Encoding Ribosomal Proteins
  12. Expression Quantitative Trait Loci for ALMS1 and Their Influence on the Symptoms of Alstrom Syndrome
  13. Association of Apolipoprotein E With Intracerebral Hemorrhage Risk by Race/Ethnicity
  14. Bayesian Inference for Mixed Model-Based Genome-Wide Analysis of Expression Quantitative Trait Loci by Gibbs Sampling
  15. Genetic variation in PLEKHG1 is associated with white matter hyperintensities (n = 11,226)
  16. Genetic and lifestyle risk factors for MRI-defined brain infarcts in a population-based setting
  17. Atrial fibrillation genetic risk differentiates cardioembolic stroke from other stroke subtypes
  18. Genome-Wide Expression Quantitative Trait Loci Analysis Using Mixed Models
  19. Polymorphisms of MTHFR, eNOS, ACE, AGT, ApoE, PON1, PDE4D, and Ischemic Stroke: Meta-Analysis
  20. Genome-wide association study for genetic variants related with maximal voluntary ventilation reveals two novel genomic signals associated with lung function
  21. Association Between Telomere Length and Risk of Cancer and Non-Neoplastic Diseases
  22. Common Expression Quantitative Trait Loci Shared by Histone Genes
  23. Expression quantitative trait loci for PI3K/AKT pathway
  24. Strong cis-acting expression quantitative trait loci for the genes encoding SNHG5 and PEX6
  25. Genetic variants in CETP increase risk of intracerebral hemorrhage
  26. Genome-wide identification of expression quantitative trait loci for human telomerase
  27. Best Linear Unbiased Prediction of Individual Polygenic Susceptibility to Sporadic Vascular Dementia
  28. Analytical Models For Genetics of Human Traits Influenced By Sex
  29. Genome-wide association study reveals sex-specific selection signals against autosomal nucleotide variants
  30. Genome-wide meta-analysis of cerebral white matter hyperintensities in patients with stroke
  31. Genetic association of marbling score with intragenic nucleotide variants at selection signals of the bovine genome
  32. Differential promoter activity by nucleotide substitution at a type 2 diabetes genome‐wide association study signal upstream of the wolframin gene
  33. Transcriptional Downregulation by Nucleotide Substitution with the Minor Allele of rs3760776 Located in the Promoter of FUT6 Gene
  34. A mixed model reduces spurious genetic associations produced by population stratification in genome-wide association studies
  35. Age- and gender-dependent heterogeneous proportion of variation explained by SNPs in quantitative traits reflecting human health
  36. Recommendations From the International Stroke Genetics Consortium, Part 1
  37. Recommendations From the International Stroke Genetics Consortium, Part 2
  38. Statistical power for identifying nucleotide markers associated with quantitative traits in genome-wide association analysis using a mixed model
  39. Profile of Differential Promoter Activity by Nucleotide Substitution at GWAS Signals For Multiple Sclerosis
  40. Genomic Heritability of Bovine Growth Using a Mixed Model
  41. Identification of contemporary selection signatures using composite log likelihood and their associations with marbling score in Korean cattle
  42. Genetic Relationships of Carcass Traits with Retail Cut Productivity of Hanwoo Cattle
  43. Identification of Functional Haplotypes in the Promoter Region of the LST1 Gene
  44. Functional investigation of a venous thromboembolism GWAS signal in a promoter region of coagulation factor XI gene
  45. Replicated association of single‐nucleotide marker on chromosome 6 with bovine yearling weight using a mixed model analysis
  46. Underestimation of heritability using a mixed model with a polygenic covariance structure in a genome-wide association study for complex traits
  47. IL-6 attenuates trimethyltin-induced cognitive dysfunction via activation of JAK2/STAT3, M1 mAChR and ERK signaling network
  48. Identification of functional nucleotide and haplotype variants in the promoter of the CEBPE gene
  49. Complex genetic susceptibility to vascular dementia and an evidence for its underlying genetic factors associated with memory and associative learning
  50. Down-Regulation of Survivin by Nemadipine-A Sensitizes Cancer Cells to TRAIL-Induced Apoptosis
  51. Empirical Statistical Power for Testing Multilocus Genotypic Effects under Unbalanced Designs Using a Gibbs Sampler
  52. Genetic associations with C‐reactive protein level and white blood cell count in the KARE study
  53. Association of bovine fatty acid composition with novel missense nucleotide polymorphism in the thyroid hormone–responsive (THRSP) gene
  54. Genetic association of the gene encoding RPGRIP1L with susceptibility to vascular dementia
  55. Genetic architecture for susceptibility to gout in the KARE cohort study
  56. Lack of common genetic factors for susceptibility to vascular dementia and Alzheimer's disease
  57. Association of glycosylated hemoglobin with the gene encoding CDKAL1 in the Korean Association Resource (KARE) study
  58. Functions of intronic nucleotide variants in the gene encoding pleckstrin homology like domain beta 2 (PHLDB2) on susceptibility to vascular dementia
  59. Association of bovine fatty acid composition with missense nucleotide polymorphism in exon7 of peroxisome proliferator‐activated receptor gamma gene
  60. Genetic association of Phosphodiesterase 1B (PDE1B) with carcass traits in Korean cattle
  61. Fatty acid composition of beef is associated with exonic nucleotide variants of the gene encoding FASN
  62. Heterogeneous genetic associations of nucleotide sequence variants with bone mineral density by gender
  63. Association of bovine carcass phenotypes with genes in an adaptive thermogenesis pathway
  64. Genetic dissection of susceptibility to vascular dementia
  65. Association of intronic sequence variant in the gene encoding spleen tyrosine kinase with susceptibility to vascular dementia
  66. Genome‐wide association study reveals five nucleotide sequence variants for carcass traits in beef cattle
  67. Heterogeneity of genetic associations of CDKAL1 and HHEX with susceptibility of type 2 diabetes mellitus by gender
  68. A strong synergistic epistasis between FAM134B and TNFRSF19 on the susceptibility to vascular dementia
  69. Multilocus genotypic association with vascular dementia by multifactor dimensionality reduction and entropy-based estimation
  70. A national survey on the allelic, genotypic, and haplotypic distribution of PRNP insertion and deletion polymorphisms in Korean cattle
  71. Optimal designs for estimating and testing interaction among multiple loci in complex traits by a Gibbs sampler
  72. Promoter sequence variants of LIGHT are associated with female vascular dementia
  73. Haplotype analysis revealed a genetic influence of osteopontin on large artery atherosclerosis
  74. In silico Comparative Analysis of DNA and Amino Acid Sequences for Prion Protein Gene
  75. The dopamine D4 receptor polymorphism affects the canine fearfulness
  76. An Interactive Association of Common Sequence Variants in the Neuropeptide Y Gene With Susceptibility to Ischemic Stroke
  77. Estimation of epistasis among finite polygenic loci for complex traits with a mixed model using Gibbs sampling
  78. The Gene Encoding Transforming Growth Factor β1 Confers Risk of Ischemic Stroke and Vascular Dementia
  79. Klotho is a genetic risk factor for ischemic stroke caused by cardioembolism in Korean females
  80. Sequence variants of ACE, AGT, AT1R, and PAI-1 as genetic risk factors for vascular dementia
  81. Haplotype analysis of single nucleotide polymorphisms in VEGF gene for vascular dementia
  82. Analysis of the SREBF2 gene as a genetic risk factor for vascular dementia
  83. Polymorphism at 3′ UTR +28 of the prion-like protein gene is associated with sporadic Creutzfeldt–Jakob disease
  84. Single nucleotide variants in the β2-adrenergic and β3-adrenergic receptor genes explained 18.3% of adolescent obesity variation
  85. Allelic and haplotypic diversity of HLA‐A, ‐B, ‐C, ‐DRB1, and ‐DQB1 genes in the Korean population
  86. Selection Bias in Quantitative Trait Loci Mapping
  87. Identification of variants in cyclin D1 (CCND1) and B-Cell CLL/lymphoma 2 (BCL2)
  88. PROTECTION AGAINST KAINATE NEUROTOXICITY BY PYRROLIDINE DITHIOCARBAMATE
  89. Genetic antagonism between body weight and milk production in beef cattle1
  90. What Holds the Future of Quantitative Genetics? - A Review
  91. Dual effects of dextromethorphan on cocaine-induced conditioned place preference in mice
  92. A global survey of haplotype frequencies and linkage disequilibrium at the DRD2 locus
  93. Multiplicative Factors for Estimation of Daily Milk and Component Yields from Single Morning or Afternoon Tests