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  • Transcriptomic and epigenomic dynamics associated with development of human iPSC-derived GABAergic interneurons
  • Rare variants in MYH15 modify amyotrophic lateral sclerosis risk
  • KBP interacts with SCG10, linking Goldberg-Shprintzen syndrome to microtubule dynamics and neuronal differentiation
  • Validity of polygenic risk scores: are we measuring what we think we are?
  • Loss of Tsc2 in radial glia models the brain pathology of tuberous sclerosis complex in the mouse
  • Maternal BMI at the start of pregnancy and offspring epigenome-wide DNA methylation: findings from the pregnancy and childhood epigenetics (PACE) consortium
  • Fine-mapping, novel loci identification, and SNP association transferability in a genome-wide association study of QRS duration in African Americans
  • Discovery of novel heart rate-associated loci using the Exome Chip.
  • Genetically predicted longer telomere length is associated with increased risk of B-cell lymphoma subtypes
  • Identification of genetic modifiers of age-at-onset for familial Parkinson's disease.