Genetics & genomics
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3,279 studies
- Genetic Insights Into Protective Effects of GLP-1 Receptor Agonists on Stroke and Alzheimer Disease Across Ancestries
- How does the efficiency of Nanopore compare to Illumina sequencing in tracking the spread of aquatic invasive species?
- Unveiling the Genomic Landscape of Pseudorasbora parva, the Most Invasive Freshwater Fish Worldwide: A Key Step Towards Understanding Invasion Dynamics
- Comparing patients’ perceptions and cognitive and emotional responses to pretest cancer genetic services delivered via chatbot vs standard of care: Findings from the BRIDGE trial
- MinD-like ATPase FlhG synchronizes flagellation and cell division in spirochetes
- Combining pro-resolving therapy with cyclosporine A restores immune homeostasis and reduces toxicity in autoimmune bone marrow failure
- Pangenome-resolved polymorphic transposable elements reveal human regulatory evolution in action
- Integrated transcriptomic analysis identifies Paternally Expressed Gene 10 as a novel candidate biomarker associated with aggressive features in liposarcoma
- Transcriptional adaptation influences buffering among essential paralog gene families
- Disease relevance and replicability of deep learning gene expression prediction
- Linkage disequilibrium - equivalence of the correlation and probability approaches
- Snurportin-1 maintains muscle niche integrity and myogenic progenitor homeostasis
- Mapping the response of primary human chondrocytes to an osteoarthritis-relevant stimulus by single-cell RNA sequencing
- MOD-scTWAS: Leveraging gene co-expression for single-cell transcriptome-wide association studies
- SCAR: Controlled mutations, ancient DNA damage, and fragmentation of fasta and fastq sequences
- Alcohol Use Disorder and Smoking-Associated Molecular Alterations in Human Prefrontal Cortex in Single Nucleus (sn) RNA-Seq
- Evolutionary dynamics of the insertion sequence IS6110 in the Mycobacterium tuberculosis complex
- Large language model-based bibliometric evaluation of population descriptors in human genetics
- Mitigating biases of rescaling in forward-in-time population genetic simulations
- Targeted CRISPRi screening reveals unexpected resilience across the RNA polymerase III transcriptome
- Mechanism-selective deep mutational scanning distinguishes ERCC2 disease phenotypes
- OPA1 controls mitochondrial dysfunction-driven liver fibrosis in MASLD
- Temporal control of mitochondrial mutagenesis reveals the fate of mtDNA mutations with age
- A single-nuclei multiomics resource across four brain regions prioritises human neural cell types influencing brain-related traits
- EMMA: an R/Bioconductor package to automate tracking of metadata in functional enrichment analyses