All Stories

  1. Scalable and accurate rare-variant association tests for whole genome sequencing time-to-event analysis in large biobanks
  2. LACE-UP: An ensemble machine-learning method for health subtype classification on multidimensional binary data
  3. Accurate and efficient method for computing polygenic risk scores for common diseases and traits
  4. Genetic Variant Set-Based Tests Using the Generalized Berk–Jones Statistic With Application to a Genome-Wide Association Study of Breast Cancer
  5. Epigenome-wide association study reveals methylation pathways associated with childhood allergic sensitization
  6. DNA methylation in blood as a mediator of the association of mid-childhood body mass index with cardio-metabolic risk score in early adolescence
  7. Metastable DNA methylation sites associated with longitudinal lung function decline and aging in humans: an epigenome-wide study in the NAS and KORA cohorts
  8. A Geometric Perspective on the Power of Principal Component Association Tests in Multiple Phenotype Studies
  9. Cumulative lifetime maternal stress and epigenome-wide placental DNA methylation in the PRISM cohort
  10. Robust analysis of secondary phenotypes in case-control genetic association studies
  11. Test for rare variants by environment interactions in sequencing association studies