All Stories

  1. Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels
  2. Metabolomic Identification of a Novel Pathway of Blood Pressure Regulation Involving HexadecanedioateNovelty and Significance
  3. Erratum: A rare variant in APOC3 is associated with plasma triglyceride and VLDL levels in Europeans
  4. Genetics of skin color variation in Europeans: genome-wide association studies with functional follow-up
  5. Decreasing initial telomere length in humans intergenerationally understates age‐associated telomere shortening
  6. Paternal age and telomere length in twins: the germ stem cell selection paradigm
  7. Metabolomic study of carotid–femoral pulse-wave velocity in women
  8. The Genetic Architecture of the Human Immune System: A Bioresource for Autoimmunity and Disease Pathogenesis
  9. Age- and Sex-Specific Causal Effects of Adiposity on Cardiovascular Risk Factors
  10. DCAF4, a novel gene associated with leucocyte telomere length
  11. A rare variant in APOC3 is associated with plasma triglyceride and VLDL levels in Europeans
  12. Association of vitamin D status with arterial blood pressure and hypertension risk: a mendelian randomisation study
  13. Circulating Proteomic Signatures of Chronological Age
  14. Novel Approach Identifies SNPs in SLC2A10 and KCNK9 with Evidence for Parent-of-Origin Effect on Body Mass Index
  15. Association of adiponectin and leptin with relative telomere length in seven independent cohorts including 11,448 participants
  16. Salt-inducible kinase 3, SIK3, is a new gene associated with hearing
  17. Parent-of-origin-specific allelic associations among 106 genomic loci for age at menarche
  18. Genomics of ageing in twins
  19. Genome-Wide Association Study Identifies Variants in Casein Kinase II ( CSNK2A2 ) to be Associated With Leukocyte Telomere Length in a Punjabi Sikh Diabetic Cohort
  20. Lipidomics Profiling and Risk of Cardiovascular Disease in the Prospective Population-Based Bruneck Study
  21. Low copy number of the salivary amylase gene predisposes to obesity
  22. Estimating telomere length from whole genome sequence data
  23. The Rate of Nonallelic Homologous Recombination in Males Is Highly Variable, Correlated between Monozygotic Twins and Independent of Age
  24. Gender and telomere length: Systematic review and meta-analysis
  25. Interaction between allelic variations in vitamin D receptor and retinoid X receptor genes on metabolic traits
  26. Glycans Are a Novel Biomarker of Chronological and Biological Ages
  27. Glycosylation of Immunoglobulin G: Role of Genetic and Epigenetic Influences
  28. Telomere length in circulating leukocytes is associated with lung function and disease
  29. Heritability analyses show visit-to-visit blood pressure variability reflects different pathological phenotypes in younger and older adults
  30. Inference of the Genetic Architecture Underlying BMI and Height with the Use of 20,240 Sibling Pairs
  31. Common variants associated with plasma triglycerides and risk for coronary artery disease
  32. Discovery and refinement of loci associated with lipid levels
  33. Meta-Analysis of Genome-Wide Association Studies Identifies Six New Loci for Serum Calcium Concentrations
  34. Genome Wide Association Analysis of a Founder Population Identified TAF3 as a Gene for MCHC in Humans
  35. The Role of Adiposity in Cardiometabolic Traits: A Mendelian Randomization Analysis
  36. Causal metabolomic pathways to osteoporosis in elderly women
  37. Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture
  38. Association of Adiposity Genetic Variants With Menarche Timing in 92,105 Women of European Descent
  39. Identification of seven loci affecting mean telomere length and their association with disease
  40. Meta-analysis of telomere length in 19 713 subjects reveals high heritability, stronger maternal inheritance and a paternal age effect
  41. A genome-wide association study of early menopause and the combined impact of identified variants
  42. Genome-wide association analyses identify 18 new loci associated with serum urate concentrations
  43. Understanding coronary artery disease using twin studies: Table 1
  44. Genome-wide meta-analysis points to CTC1 and ZNF676 as genes regulating telomere homeostasis in humans
  45. Gene-centric meta-analyses of 108 912 individuals confirm known body mass index loci and reveal three novel signals
  46. FTO genotype is associated with phenotypic variability of body mass index
  47. Large-scale association analyses identify new loci influencing glycemic traits and provide insight into the underlying biological pathways
  48. Genome-wide meta-analysis of common variant differences between men and women
  49. A Genome-Wide Association Meta-Analysis of Circulating Sex Hormone–Binding Globulin Reveals Multiple Loci Implicated in Sex Steroid Hormone Regulation
  50. Six Novel Susceptibility Loci for Early-Onset Androgenetic Alopecia and Their Unexpected Association with Common Diseases
  51. Differential profile analysis of urinary cytokines in patients with overactive bladder: comment
  52. Genome-wide association and functional studies identify theDOT1Lgene to be involved in cartilage thickness and hip osteoarthritis
  53. Epigenome-Wide Scans Identify Differentially Methylated Regions for Age and Age-Related Phenotypes in a Healthy Ageing Population
  54. Meta-analyses identify 13 loci associated with age at menopause and highlight DNA repair and immune pathways
  55. Meta-analysis of genome-wide association studies identifies three new risk loci for atopic dermatitis
  56. New gene functions in megakaryopoiesis and platelet formation
  57. Physical Activity Attenuates the Influence of FTO Variants on Obesity Risk: A Meta-Analysis of 218,166 Adults and 19,268 Children
  58. Erratum: Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution
  59. A Genome-Wide Screen for Interactions Reveals a New Locus on 4p15 Modifying the Effect of Waist-to-Hip Ratio on Total Cholesterol
  60. Genome-wide association and large-scale follow up identifies 16 new loci influencing lung function
  61. Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure
  62. Human metabolic individuality in biomedical and pharmaceutical research
  63. Genome-wide association analysis of coffee drinking suggests association with CYP1A1/CYP1A2 and NRCAM
  64. Large Scale Replication Study of the Association between HLA Class II/BTNL2 Variants and Osteoarthritis of the Knee in European-Descent Populations
  65. Multiple Loci Are Associated with White Blood Cell Phenotypes
  66. Genetic variation near IRS1 associates with reduced adiposity and an impaired metabolic profile
  67. A Comprehensive Evaluation of Potential Lung Function Associated Genes in the SpiroMeta General Population Sample
  68. Eight Common Genetic Variants Associated with Serum DHEAS Levels Suggest a Key Role in Ageing Mechanisms
  69. Genome-wide association and genetic functional studies identify autism susceptibility candidate 2 gene ( AUTS2 ) in the regulation of alcohol consumption
  70. Genetic architecture of circulating lipid levels
  71. Genomic inflation factors under polygenic inheritance
  72. Association of genetic variation with systolic and diastolic blood pressure among African Americans: the Candidate Gene Association Resource study
  73. Common Genetic Determinants of Vitamin D Insufficiency: A Genome-Wide Association Study
  74. Contributors
  75. A polymorphism associated with entrepreneurship: evidence from dopamine receptor candidate genes
  76. Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies
  77. Genome-Wide Association Study Identifies Two Novel Regions at 11p15.5-p13 and 1p31 with Major Impact on Acute-Phase Serum Amyloid A
  78. Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution
  79. Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index
  80. Hundreds of variants clustered in genomic loci and biological pathways affect human height
  81. A Common Variant in the Telomerase RNA Component Is Associated with Short Telomere Length
  82. Leukocyte telomere length and marital status among middle-aged adults
  83. Genetic variation in the SMAD3 gene is associated with hip and knee osteoarthritis
  84. Biological, clinical and population relevance of 95 loci for blood lipids
  85. IRF4 Variants Have Age-Specific Effects on Nevus Count and Predispose to Melanoma
  86. Common genetic determinants of vitamin D insufficiency: a genome-wide association study
  87. Erratum: New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk
  88. Genome-wide association identifies OBFC1 as a locus involved in human leukocyte telomere biology
  89. Sequence variants at CHRNB3–CHRNA6 and CYP2A6 affect smoking behavior
  90. Common variants near TERC are associated with mean telomere length
  91. New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk
  92. Quantitative Trait Loci for CD4:CD8 Lymphocyte Ratio Are Associated with Risk of Type 1 Diabetes and HIV-1 Immune Control
  93. Genome-wide association study identifies five loci associated with lung function
  94. A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium
  95. Correction: Genome-Wide Association Scan Meta-Analysis Identifies Three Loci Influencing Adiposity and Fat Distribution
  96. Genome-Wide Association Scan Meta-Analysis Identifies Three Loci Influencing Adiposity and Fat Distribution
  97. An obesogenic postnatal environment is more important than the fetal environment for the development of adult adiposity: a study of female twins
  98. Meta-Analysis of 28,141 Individuals Identifies Common Variants within Five New Loci That Influence Uric Acid Concentrations
  99. A genome-wide association study identifies a novel locus on chromosome 18q12.2 influencing white cell telomere length
  100. Bivariate genetic modelling of the response to an oral glucose tolerance challenge: A gene × environment interaction approach
  101. Six new loci associated with body mass index highlight a neuronal influence on body weight regulation
  102. Correction: Lifelong Reduction of LDL-Cholesterol Related to a Common Variant in the LDL-Receptor Gene Decreases the Risk of Coronary Artery Disease—A Mendelian Randomisation Study
  103. Lifelong Reduction of LDL-Cholesterol Related to a Common Variant in the LDL-Receptor Gene Decreases the Risk of Coronary Artery Disease—A Mendelian Randomisation Study
  104. Arachidonate 5-lipoxygenase (5-LO) promoter genotype and risk of myocardial infarction: A case–control study
  105. The novel genetic variant predisposing to coronary artery disease in the region of the PSRC1 and CELSR2 genes on chromosome 1 associates with serum cholesterol
  106. Lack of association of genetic variants in the LRP8 gene with familial and sporadic myocardial infarction
  107. A regulatory SNP of the BICD1 gene contributes to telomere length variation in humans
  108. Common variants near MC4R are associated with fat mass, weight and risk of obesity
  109. Genome-wide association analysis identifies 20 loci that influence adult height
  110. Repeated Replication and a Prospective Meta-Analysis of the Association Between Chromosome 9p21.3 and Coronary Artery Disease
  111. Localization of type 1 diabetes susceptibility to the MHC class I genes HLA-B and HLA-A
  112. Association scan of 14,500 nonsynonymous SNPs in four diseases identifies autoimmunity variants
  113. Association analysis of IL-12B and IL-23R polymorphisms in myocardial infarction
  114. LGALS2 functional variant rs7291467 is not associated with susceptibility to myocardial infarction in Caucasians
  115. Genomewide Association Analysis of Coronary Artery Disease
  116. Replication of Genome-Wide Association Signals in UK Samples Reveals Risk Loci for Type 2 Diabetes
  117. Leukotriene B 4 production in healthy subjects carrying variants of the arachidonate 5-lipoxygenase-activating protein gene associated with a risk of myocardial infarction
  118. Enhanced linkage of a locus on chromosome 2 to premature coronary artery disease in the absence of hypercholesterolemia
  119. Mapping of a Major Locus that Determines Telomere Length in Humans
  120. A gene for familial isolated chronic nail candidiasis maps to chromosome 11p12–q12.1
  121. NF1 gene analysis based on DHPLC
  122. Hereditary gingival fibromatosis (HGF) with hypertrichosis is unlinked to the HGF1 and HGF2 loci
  123. Assignment of a locus for autosomal dominant idiopathic scoliosis (IS) to human chromosome 17p11
  124. Identification of a novel NOG gene mutation (P35S) in an Italian family with symphalangism
  125. Identification of a novel NOG gene mutation (P35S) in an Italian family with symphalangism
  126. Mapping of a new autosomal dominant nonsyndromic hearing loss locus (DFNA30) to chromosome 15q25-26
  127. Identification of novel RP2 mutations in a subset of X-linked retinitis pigmentosa families and prediction of new domains
  128. Three novel mutations causing a truncated protein within the RP2 gene in Italian families with X-linked retinitis pigmentosa
  129. Mutation analysis of the RPGR gene reveals novel mutations in south European patients with X-linked retinitis pigmentosa
  130. Localization of a Gene for Familial Patella Aplasia-Hypoplasia (PTLAH) to Chromosome 17q21–22
  131. A Novel Mutation (R271X) in the Myotubularin Gene Causes a Severe Miotubular Myopathy
  132. A single-nucleotide polymorphism in the human bone morphogenetic protein-4 (BMP 4) gene
  133. First‐trimester prenatal diagnosis of Ellis–van Creveld syndrome using linked microsatellite markers
  134. First-trimester prenatal diagnosis of Ellis–van Creveld syndrome using linked microsatellite markers
  135. Two new missense mutations (A105T and C110G) in the Norrin gene in two Italian families with Norrie disease and familial exudative vitreoretinopathy