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Genetics & genomics

3,213 studies179 in 7 days1,320 in 30 days

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3,213 studies

  1. Multi-modal in situ profiling of human cells using the AVITI24 platform characterizes single-cell responses to acute stress
    O. W. Lang, A. M. Gardner, C. M. Smugereski +3
    bioRxivPreprintCC BYFull textGenetics & genomicsbioRxiv
  2. A Chromosome Scale Genome Assembly for the Australian blue mussel Mytilus planulatus
    D. Kireta, D. E. Nerelli, A. Saco +5
    bioRxivPreprintCC BYFull textGenetics & genomicsbioRxiv
  3. Cellular context shapes the transcriptomic impact of somatic variants
    P. Sun, P. Jia, C. Lou +26
    bioRxivPreprintCC BY-NC-NDFull textGenetics & genomicsbioRxiv
  4. Tandem repeat variation shapes immune cell type-specific gene expression
    Hope A. Tanudisastro, Anna S. E. Cuomo, Ben Weisburd +55
    NaturePeer-reviewedLicence not stated14 citedGenetics & genomicsOpenAlex
  5. Rare and common genetic variants shape single-cell immune gene expression
    Anna S. E. Cuomo, Eleanor Spenceley, Hope A. Tanudisastro +41
    NaturePeer-reviewedCC BY-NC-ND33 citedGenetics & genomicsOpenAlex
  6. Robotic Ileocecal Resection for Crohn’s Disease Using Hugo RAS System
    Ana Cristina Silva, Pedro N. Brandão, Mónica Sampaio +1
    JSLS : Journal of the Society of Laparoscopic & Robotic SurgeonsPeer-reviewedLicence not statedFull textGenetics & genomicsPMC
  7. KaryoExplorer: an automated digital karyotyping pipeline with interactive visualizations
    Ugur Dura, Xavier Pastor Hostench, Peter Lichtner +2
    Briefings in Functional GenomicsPeer-reviewedCC BY-NC 4.0Full textGenetics & genomicsPMC
  8. Myoclonus, Dystonia, and Ataxia in U2AF2 ‐Related Neurodevelopmental Disorder
    Ana Luiza Viegas de Almeida, Renata Silva de Mendonça, Joemir Jábson da Conceição Brito +4
    Movement Disorders Clinical PracticePeer-reviewedLicence not statedFull textGenetics & genomicsPMC
  9. Thrombophilia-Related Gene Polymorphisms and Recurrent Miscarriages in Lebanese Population: A Case-Control Study.
    Ehssan Sharif-Askari, Khadija Atoui, Ola Srour +6
    Human mutationPeer-reviewedCC BYFull textGenetics & genomicsEurope PMCPMC
  10. Experimental benchmarking of in silico annotations at prostate cancer risk loci and hypothesis-generating cross-cancer prioritisation of ovarian risk variants.
    Wiaam Ahmed Al-Amili, Mohammed Ayyed Najm, Shatha Saadi Jumaah +1
    Genomics & informaticsPeer-reviewedCC BYFull textGenetics & genomicsEurope PMCPMC
  11. Genome-wide association study and haplotype characterization of bacterial kidney disease (BKD) resistance in Atlantic salmon (Salmo salar) across two generations
    Angela Astudillo, Ross Houston, Jean Paul Lhorente +1
    Frontiers in GeneticsPeer-reviewedCC BYFull textGenetics & genomicsDOAJ
  12. Machine‐Learning Models Trained on Genomic Summary Statistics Assess Extinction Risk and Recovery Potential of Bottlenecked Populations
    Johanna C. Winder, Jack N. Marsters, Thomas Birley +5
    Evolutionary ApplicationsPeer-reviewedCC BYFull textGenetics & genomicsDOAJ
  13. Occurrence of Yunnan Black-veined White Aporia goutellei (Oberthür, 1886) (Lepidoptera: Pieridae: Pierinae: Pierini) in Anjaw District of Arunachal Pradesh: a new addition to the Indian butterfly checklist
    Arun Pratap Singh
    Journal of Threatened TaxaPeer-reviewedCC BYFull textGenetics & genomicsDOAJ
  14. First record of interspecific mating between butterflies Athyma ranga and Tanaecia lepidea from Kerala, India
    Nishad Manathana, Konkada Manattayil Haneesh
    Journal of Threatened TaxaPeer-reviewedCC BYFull textGenetics & genomicsDOAJ
  15. End-To-End, Fully Automated Manufacturing of Hematopoietic Stem and Progenitor Cell Therapy Via CCR5-Targeted Integration
    Jack M.P. Castelli, Nowah Afangbedji, Sofia E. Luna +12
    bioRxivPreprintCC BYFull textGenetics & genomicsbioRxivPMC
  16. Increasing Awareness and Identification of Maturity-Onset Diabetes of the Young in a Pediatric Diabetes Program.
    Raymond J Kreienkamp, Jessica L Ruiz, Sarah Schlegel +5
    Pediatric quality & safetyPeer-reviewedCC BYFull textGenetics & genomicsEurope PMCPMC
  17. Exploring genetic variants in premature ovarian insufficiency: a cohort-based investigation of monogenic etiologies.
    Asma Sassi, Xavier Peyrassol, Martina Marangoni +8
    Journal of the Endocrine SocietyPeer-reviewedCC BYFull textGenetics & genomicsEurope PMCPMC
  18. Natural Variation in CYCLIC NUCLEOTIDE-GATED ION CHANNEL 16 Controls Fruit Weight in Tomato.
    Xiang Wang, Yixuan Huang, Huaiqi Miao +5
    Plant biotechnology journalPeer-reviewedCC BY-NCFull textGenetics & genomicsEurope PMCPMC
  19. Evolutionarily diverged on-switch for actin assembly in fungal endocytosis.
    Juliette Sebellin, Fabina Binth Kandiyoth, V T Bagyashree +7
    The Journal of cell biologyPeer-reviewedCC BYFull textGenetics & genomicsEurope PMCPMC
  20. Epigenomic Characterization of Fibroblasts in Darier Disease Identifies Cross-cell-type Regulatory Gene Signatures.
    Nuoqi Wang, Matthew Hunt, Monica Torres +2
    Acta dermato-venereologicaPeer-reviewedCC BYFull textGenetics & genomicsEurope PMCPMC
  21. pyTransRate: reference-free quality assessment of de novo transcriptome assemblies with current aligners and quantifiers
    Matthew MacManes
    arXivPreprintCC BY 4.0Full textBioinformatics & computational biologyGenetics & genomicsarXiv
  22. Variation in hypoxia tolerance is driven by evolutionary changes in gene regulation in the eastern oyster
    K. M. Eaton, R. V. Vaidya, J. La Peyre +3
    bioRxivPreprintAll rights reservedFull textGenetics & genomicsbioRxiv
  23. Characterisation of cis-regulatory elements and genome wide enhancer prediction in Heliconiini butterflies
    A. D. Ritchie, F. Cicconardi, S. H. Montgomery
    bioRxivPreprintCC BYFull textGenetics & genomicsbioRxiv
  24. Scalable variant-to-function screens using prime editing perturb-seq
    J. De Jonghe, M. Armas Reyes, C. Jamieson +3
    bioRxivPreprintCC BY-NC-NDFull textGenetics & genomicsbioRxiv
  25. Early-Onset Diabetes in Lahore and Kasur Districts of Punjab: A Hospital-Based Study
    Muhammad Khurram, Muhammad Sohail Afzal, Muhammad Tayyab +3
    Journal of Clinical MedicinePeer-reviewedCC BY 4.0Genetics & genomicsCrossref