New Nanoscale Genome Mapping Tool Pinpoints Causal Autoimmunity Variants
An Oxford-developed single-allele chromatin mapping platform called MCCv identifies causal noncoding variants in autoimmune disease and reveals that a neo-CTCF ...
An Oxford-developed single-allele chromatin mapping platform called MCCv identifies causal noncoding variants in autoimmune disease and reveals that a neo-CTCF ...
Researchers combined single nucleus RNA-sequencing with GWAS and UK Biobank data to show that an obesity-linked variant in SREBF1 allele-specifically ...
A six-model genome-wide association study of 239 maize inbred lines has identified 200 genetic variants linked to kernel fat content ...
A single-nucleus atlas of 5.6 million brain cells from 1,384 donors maps cell-type-specific genetic regulation underlying Alzheimer's disease, schizophrenia and ...
A new single-cell and spatial atlas of the developing human face identifies 56 cell states, hundreds of spatial patterning genes ...
A genome-wide association study in Han Chinese patients links a variant in the synaptic gene MCTP2 to greater improvement of ...
An integrated analysis of human genetics, patient-derived cell models and electronic health records has identified 19 Alzheimer's drug targets in ...
A single-cell chromatin accessibility atlas of the human intestine maps regulatory programs across 29 cell types and shows that Crohn's ...
An integrated genetic mapping study in a 530-line multi-parent maize population has prioritized four candidate genes controlling kernel number per ...
A new PLOS Genetics study shows that specific immune markers, particularly interleukin-6 rather than C-reactive protein, genetically mediate the links ...
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© 2025 Scienmag - Science Magazine