All Stories

  1. Haplotype analysis identifies functional elements in monoclonal gammopathy of unknown significance
  2. Deciphering the genetics and mechanisms of predisposition to multiple myeloma
  3. Vector integration and fate in the hemophilia dog liver multi-years following AAV-FVIII gene transfer
  4. Molecular evaluation and vector integration analysis of HCC complicating AAV gene therapy for hemophilia B
  5. Do GWAS-Identified Risk Variants for Chronic Lymphocytic Leukemia Influence Overall Patient Survival and Disease Progression?
  6. Validation and functional characterization of GWAS-identified variants for chronic lymphocytic leukemia: a CRuCIAL study
  7. Genome-wide meta-analysis of monoclonal gammopathy of undetermined significance (MGUS) identifies risk loci impacting IRF-6
  8. Correction: Prediction of clinical diagnosis of Alzheimer’s disease, vascular, mixed, and all-cause dementia by a polygenic risk score and APOE status in a community-based cohort prospectively followed over 17 years
  9. DNA Repair Gene Polymorphisms and Chromosomal Aberrations in Exposed Populations
  10. DNA repair gene polymorphisms and chromosomal aberrations in healthy, nonsmoking population
  11. Multiethnic genome‐wide association study of differentiated thyroid cancer in the EPITHYR consortium
  12. Familial Risks between Pernicious Anemia and Other Autoimmune Diseases in the Population of Sweden
  13. Familial risks between giant cell arteritis and Takayasu arteritis and other autoimmune diseases in the population of Sweden
  14. Familial associations for Addison’s disease and between Addison’s disease and other autoimmune diseases
  15. Familial associations between autoimmune hepatitis and primary biliary cholangitis and other autoimmune diseases
  16. Impact of genetic polymorphisms in kinetochore and spindle assembly genes on chromosomal aberration frequency in healthy humans
  17. Multiethnic genome-wide association study of differentiated thyroid cancer in the EPITHYR consortium
  18. Genomic imprinting analyses identify maternal effects as a cause of phenotypic variability in type 1 diabetes and rheumatoid arthritis
  19. Prediction of clinical diagnosis of Alzheimer’s disease, vascular, mixed, and all-cause dementia by a polygenic risk score and APOE status in a community-based cohort prospectively followed over 17 years
  20. Genome-wide study on uveal melanoma patients finds association to DNA repair gene TDP1
  21. Familial associations for rheumatoid autoimmune diseases
  22. Familial risks between Graves disease and Hashimoto thyroiditis and other autoimmune diseases in the population of Sweden
  23. Eight novel loci implicate shared genetic etiology in multiple myeloma, AL amyloidosis, and monoclonal gammopathy of unknown significance
  24. Genome-wide association meta-analyses and fine-mapping elucidate pathways influencing albuminuria
  25. Transcriptome-wide association study of multiple myeloma identifies candidate susceptibility genes
  26. Analysis of 153 115 patients with hematological malignancies refines the spectrum of familial risk
  27. Distinct pathways associated with chromosomal aberration frequency in a cohort exposed to genotoxic compounds compared to general population
  28. A catalog of genetic loci associated with kidney function from analyses of a million individuals
  29. Performance of individual and joint risk stratification by an environmental risk score and a genetic risk score in a colorectal cancer screening setting
  30. Genome-wide interaction and pathway-based identification of key regulators in multiple myeloma
  31. Genome-wide association study of monoclonal gammopathy of unknown significance (MGUS): comparison with multiple myeloma
  32. Author Correction: Identification of multiple risk loci and regulatory mechanisms influencing susceptibility to multiple myeloma
  33. Author Correction: Genome-wide association study of classical Hodgkin lymphoma identifies key regulators of disease susceptibility
  34. Genetic correlation between multiple myeloma and chronic lymphocytic leukaemia provides evidence for shared aetiology
  35. The involvement of the canonical Wnt-signaling receptor LRP5 and LRP6 gene variants with ADHD and sexual dimorphism: Association study and meta-analysis
  36. Genome-wide association study implicates immune dysfunction in the development of Hodgkin lymphoma
  37. 33rd Annual Meeting & Pre-Conference Programs of the Society for Immunotherapy of Cancer (SITC 2018)
  38. Clinical landscape of cancer metastases
  39. Genetic variation associated with chromosomal aberration frequency: A genome-wide association study
  40. Identification of multiple risk loci and regulatory mechanisms influencing susceptibility to multiple myeloma
  41. Familial risks of acute myeloid leukemia, myelodysplastic syndromes, and myeloproliferative neoplasms
  42. Genetic Risk Score Is Associated With Prevalence of Advanced Neoplasms in a Colorectal Cancer Screening Population
  43. Enrichment of B cell receptor signaling and epidermal growth factor receptor pathways in monoclonal gammopathy of undetermined significance: a genome-wide genetic interaction study
  44. Genome-wide association study of classical Hodgkin lymphoma identifies key regulators of disease susceptibility
  45. The impact of methylation quantitative trait loci (mQTLs) on active smoking-related DNA methylation changes
  46. Assessing the effect of obesity-related traits on multiple myeloma using a Mendelian randomisation approach
  47. Genomewide association study on monoclonal gammopathy of unknown significance (MGUS)
  48. Risk of Second Cancer in Hodgkin Lymphoma Survivors and Influence of Family History
  49. Genome-wide association analysis of chronic lymphocytic leukaemia, Hodgkin lymphoma and multiple myeloma identifies pleiotropic risk loci
  50. A genome-wide association study identifies risk loci for childhood acute lymphoblastic leukemia at 10q26.13 and 12q23.1
  51. Genome-wide association study identifies multiple susceptibility loci for multiple myeloma
  52. Evidence of Inbreeding in Hodgkin Lymphoma
  53. Runs of homozygosity and inbreeding in thyroid cancer
  54. Inbreeding and homozygosity in breast cancer survival
  55. The 9p21.3 risk of childhood acute lymphoblastic leukaemia is explained by a rare high-impact variant in CDKN2A
  56. Quantifying the heritability of testicular germ cell tumour using both population-based and genomic approaches
  57. Metastatic sites and survival in lung cancer
  58. Heritability estimates on Hodgkin’s lymphoma: a genomic- versus population-based approach
  59. Variation at 10p12.2 and 10p14 influences risk of childhood B-cell acute lymphoblastic leukemia and phenotype
  60. Variation at 3p24.1 and 6q23.3 influences the risk of Hodgkin’s lymphoma
  61. Comparison of survival of patients with metastases from known versus unknown primaries: survival in metastatic cancer
  62. Familial risks for childhood acute lymphocytic leukaemia in Sweden and Finland: far exceeding the effects of known germline variants
  63. Colorectal cancer patients: what do they die of?
  64. Death causes in breast cancer patients
  65. QTL explaining variation in production traits and udder health in the Danish Holstein population
  66. Determinants of unfavorable presentation of primary cutaneous melanoma
  67. Influence of family size and birth order on risk of cancer: a population-based study
  68. What Do Prostate Cancer Patients Die Of?
  69. Tumor location and patient characteristics of colon and rectal adenocarcinomas in relation to survival and TNM classes
  70. Auction price of Texel, Suffolk and German white-headed mutton rams: A genetic-statistical study
  71. Across-Family Marker-Assisted Selection Using Selective Genotyping Strategies in Dairy Cattle Breeding Schemes
  72. Effects of goat social rank on kid gender
  73. Confirmation of quantitative trait loci for somatic cell score on bovine chromosome 18 in the German Holstein
  74. Mapping of quantitative trait loci for lactation persistency traits in German Holstein dairy cattle
  75. Combined line-cross and half-sib QTL analysis of crosses between outbred lines
  76. Investigation of Obesity Candidate Genes On Porcine Fat Deposition Quantitative Trait Loci Regions
  77. New alleles in calpastatin gene are associated with meat quality traits in pigs1
  78. Multiple Quantitative Trait Loci Mapping With Cofactors and Application of Alternative Variants of the False Discovery Rate in an Enlarged Granddaughter Design
  79. Characterization of quantitative trait loci for growth and meat quality in a cross between commercial breeds of swine1
  80. The DGAT1 K232A Mutation Is Not Solely Responsible for the Milk Production Quantitative Trait Locus on the Bovine Chromosome 14
  81. Mapping of QTL for Body Conformation and Behavior in Cattle
  82. Combined analysis of data from two granddaughter designs: A simple strategy for QTL confirmation and increasing experimental power in dairy cattle
  83. Combined analysis of data from�two�granddaughter designs: A�simple strategy for QTL confirmation and increasing experimental power in�dairy cattle
  84. Quantitative Trait Loci Mapping of Functional Traits in the German Holstein Cattle Population
  85. Consensus and comprehensive linkage maps of bovine chromosome 24
  86. Mapping of the bovine blood group systems J, N′, R′, and Z show evidence for oligo-genetic inheritance
  87. Comparison of estimated breeding values, daughter yield deviations and de-regressed proofs within a whole genome scan for QTL
  88. A whole genome scan for differences in recombination rates among three Bos taurus breeds
  89. A mammary gland EST showing linkage disequilibrium to a milk production QTL on bovine Chromosome 14
  90. Comprehensive linkage map of bovine chromosome 11
  91. Comprehensive linkage map of bovine chromosome 27
  92. Consensus and comprehensive linkage maps of bovine chromosome 17
  93. Consensus and comprehensive linkage maps of bovine chromosome 25
  94. Consensus and comprehensive linkage maps of the bovine sex chromosomes
  95. A male bovine linkage map for the ADR granddaughter design
  96. A QTL for the degree of spotting in cattle shows synteny with the KIT locus on chromosome 6
  97. Bovine chromosome 4 workshop: consensus and comprehensive linkage maps