GGenetics Read More Is enhancer-driven gene regulation all wrapped up?September 17, 2025 Symmons, O. et al. The Shh topological domain facilitates the action of remote enhancers by reducing the effects…
GGenetics Read More Regulatory genome annotation | Nature Reviews GeneticsSeptember 17, 2025 Gerstein, M. B. et al. Architecture of the human regulatory network derived from ENCODE data. Nature 489, 91–100…
GGenetics Read More The Solve-RD Solvathons as a pan-European interdisciplinary collaboration to diagnose patients with rare diseaseSeptember 15, 2025 School of Computation, Information and Technology, Technical University of Munich, Garching, Germany Vicente A. Yépez, Rebeka Luknárová, Felix Brechtmann, Leon Kraß, Shubhankar…
GGenetics Read More Decomposition of phenotypic heterogeneity in autism reveals underlying genetic programsSeptember 15, 2025 Identifying the structures of autism phenotypes To best reflect the complexity of presentations across autistic individuals, we identified…
GGenetics Read More Uncovering the multivariate genetic architecture of frailty with genomic structural equation modelingSeptember 14, 2025 Fogg, C. et al. The dynamics of frailty development and progression in older adults in primary care in…
GGenetics Read More A genome-wide association analysis reveals new pathogenic pathways in goutSeptember 11, 2025 Kuo, C. F. et al. Global epidemiology of gout: prevalence, incidence and risk factors. Nat. Rev. Rheumatol. 11,…
GGenetics Read More Robust and accurate Bayesian inference of genome-wide genealogies for hundreds of genomesSeptember 9, 2025 An overview of the SINGER algorithm SINGER takes in phased WGS data and samples ARGs iteratively by adding…
GGenetics Read More Large-scale genome-wide analyses of stutteringSeptember 9, 2025 Yairi, E. & Ambrose, N. Epidemiology of stuttering: 21st century advances. J. Fluen. Disord. 38, 66–87 (2013). Article …
GGenetics Read More Methods and applications of in vivo CRISPR screeningSeptember 9, 2025 Auton, A. et al. A global reference for human genetic variation. Nature 526, 68–74 (2015). Article PubMed Google…
GGenetics Read More Multiancestry brain pQTL fine-mapping and integration with genome-wide association studies of 21 neurologic and psychiatric conditionsSeptember 9, 2025 Ethics Our study complies with all relevant ethical regulations and was approved by the institutional review boards at…
GGenetics Read More Single-nucleus chromatin accessibility profiling identifies cell types and functional variants contributing to major depressionSeptember 9, 2025 James, S. L. et al. Global, regional, and national incidence, prevalence, and years lived with disability for 354…