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203,952 studies31 sourcesUpdated 44 min ago

Human genetics

961 studies23 in 7 days555 in 30 days

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961 studies

  1. Transfusion-related costs in anemic myelofibrosis patients treated with JAK inhibitors in Germany
    M Krammer, C Iwamoto, FS Nikitas +5
    The European Journal of Public HealthPeer-reviewedCC BY-NC 4.0Full textHuman geneticsPMCEurope PMC
  2. Research hotspots and evolution trends of human amniotic fluid stem cells: A cite space bibliometric analysis based on WoSCC and PubMed.
    Huanying Lou, Zheng Wang, Shuai Zhang +3
    MedicinePeer-reviewedCC BYFull textHuman geneticsEurope PMC
  3. Activation of Platelet Caspase-1 and P-Selectin Over-Expression in Sickle Cell Disease Patients: An Involvement of NLRP3 Inflammasome?
    Livia Claude, Frédéric Martino, Lydiane Mordier +6
    Journal of cellular and molecular medicinePeer-reviewedCC BYFull textHuman geneticsEurope PMC
  4. Mesenchymal Stromal Cells for Heart Diseases: Current Perspective and Future Directions
    Miłosz Andrzej Zajączkowski, Milena Deptuła-Knioła, Małgorzata Zawrzykraj-Motylińska +3
    BiomoleculesPeer-reviewedCC BY 4.0Full textHuman geneticsCrossrefEurope PMC
  5. Targeting Redox Homeostasis with Arvanil Is Preferentially Cytotoxic to Glioma Stem Cells
    Kazuki Nakamura, Senri Takenouchi, Yurika Nakagawa-Saito +8
    International Journal of Molecular SciencesPeer-reviewedCC BY 4.0Full textHuman geneticsCrossrefEurope PMC
  6. Progesterone Receptor Expression in Different Regions of Glioblastoma Multiforme and in an In Vitro Model
    Donata Szubert, Klaudyna Kojder, Dariusz Jeżewski +8
    International Journal of Molecular SciencesPeer-reviewedCC BY 4.0Full textHuman geneticsCrossrefEurope PMC
  7. Reduced DDB2 Expression Is Associated with Temozolomide Resistance in Glioblastoma Cells
    Inés Grávalos-Cano, Teresa Morales-Ruiz, Rafael R. Ariza +2
    International Journal of Molecular SciencesPeer-reviewedCC BY 4.0Full textHuman geneticsCrossrefEurope PMC
  8. Cooperative Repression of γ-Globin by LYAR and NONO
    Dongliang Wu, Wenbing Shangguan, Xiaoning Wang +11
    Journal of Biological ChemistryPeer-reviewedCC BY 4.0Human geneticsCrossref
  9. DALYs for rare disease surveillance: real-world SMA burden in Belgium during 2018–2024
    A Noppe, M Jagut, J Haagsma +3
    The European Journal of Public HealthPeer-reviewedCC BY-NC 4.0Full textHuman geneticsPMCEurope PMC
  10. Diffuse Leptomeningeal Glioneuronal Tumor With Initial Diagnosis of Pilocytic Astrocytoma With Anaplasia: A Case Study
    Anita Zhou, Joseph Carmicheal, Jie Chen +1
    Clinical case reportsPeer-reviewedCC BY-NC-NDFull textHuman geneticsEurope PMCDOAJ
  11. The future of brain tumor treatment: integrating platelet-based liquid biopsy, advanced drug delivery systems, and eicosanoid inhibition
    Sara Di Berardino, Marta Zarà, Huzaifa Ali Ahfaz +2
    Frontiers in pharmacologyPeer-reviewedCC BYFull textHuman geneticsEurope PMCCrossref
  12. Hereditary angioedema in Latin America: international recommendations, expert consensus, and reported implementation barriers
    Guillermo Arturo Guidos-Fogelbach, Andrea Aida Velasco-Medina, Freya Helena Campos-Romero +32
    Frontiers in pharmacologyPeer-reviewedCC BYFull textHuman geneticsEurope PMCCrossref
  13. Garadacimab in Hereditary Angioedema: Modeling Suggests Sustained Improvements in Attack-Free Probability and Quality of Life Over 5 Years.
    Philip H Li, F Ida Hsu, Emel Aygören-Pürsün +7
    Clinical and translational sciencePeer-reviewedCC BY-NCFull textHuman geneticsEurope PMC
  14. Tumor Treating Fields Enhance Temozolomide-Associated Growth Suppression in Glioblastoma Cells and Patient-Derived Organoids Through Cell-Cycle Blockade, Apoptosis, and SMAD-Associated Signaling.
    Haiping Zhu, Yingbo Hou, Xuetao Li +14
    CNS neuroscience & therapeuticsPeer-reviewedCC BYFull textHuman geneticsEurope PMC
  15. Early Mortality in Patients with Biopsy-Only Glioblastoma: Clinical, Radiological and Molecular Predictors from a Retrospective Cohort
    Massimiliano Domenico Rizzaro, Giulio Bertani, Claudia Fanizzi +9
    Journal of clinical medicinePeer-reviewedCC BYFull textHuman geneticsEurope PMCCrossref
  16. CT Features of Sickle Cell Disease-Associated Pulmonary Hypertension
    Nouran Waleed Molla, Sarah Sewaralthahab, Razan Abdulrahman Alotaibi +5
    Journal of clinical medicinePeer-reviewedCC BYFull textHuman geneticsEurope PMCCrossref
  17. Uptake of sickle cell screening among sexually active unmarried young adults in Gulu City, northern Uganda: a community-based cross-sectional study
    Daniel Kitamirike Bwamiki, James Nelson Okema, Samuel Ochola Lunyuta +7
    Scientific ReportsPeer-reviewedCC BY 4.0Full textHuman geneticsCrossref
  18. Human genetics implicates a BACH2–NRF2 axis in fetal haemoglobin activation
    C. Guo, Uma P. Arora, Xiaoheng Cheng +51
    NaturePeer-reviewedCC BYFull text11 citedHuman geneticsOpenAlex
  19. Cross-Cancer Characterization of CAMK2A Reveals Its Favorable Prognostic Association and Neuronal Signature Enrichment in Glioma.
    Yimin Pan, Changwu Wu, Jun Tan +2
    BiomedicinesPeer-reviewedCC BYFull textHuman geneticsEurope PMC
  20. The Same, but Different: Shared Hallmarks and Divergent Drivers in Adult, Pediatric and Canine Glioma.
    R Timothy Bentley, Sagar M Utturkar, Harish Kothandaraman +6
    Current oncology (Toronto, Ont.)Peer-reviewedCC BYFull textHuman geneticsEurope PMC
  21. Quantitative Fetal Hemoglobin Measurement: GazelleTM Point-of-Care Electrophoresis versus Standard HPLC Methodology
    T. N. Williams, R. Connon, R. Muhindo +20
    medRxivPreprintCC BYFull textHuman geneticsmedRxiv
  22. Prediction of ROR1 and CAV1 expression from whole-exome sequencing of tumor tissue and plasma cfDNA to infer the efficacy of B013 plus nab-paclitaxel in triple-negative breast cancer
    M. Jiang, D. Zhang, Y.-C. Hsueh +18
    medRxivPreprintAll rights reservedFull textHuman geneticsmedRxiv
  23. Overcoming a diagnostic blindspot: Identifying balanced translocations in Mendelian rare disease cohorts
    T. R. Jammihal, K. Szot, M. Kaur +5
    medRxivPreprintCC BYFull textHuman geneticsmedRxiv
  24. Rare coding variation implicates thirteen genes in bipolar disorder across 232,536 individuals from global populations
    C. Liao, R. Ye, J. M. Sealock +39
    medRxivPreprintCC BYFull textHuman geneticsmedRxiv
  25. Perceptions, knowledge, and attitudes toward genetics among psychiatric patients and their relatives: A systematic review and a meta-analysis
    Pauline Bressin, Souleiman El Balkhi, Chahrazed El Hamel +4
    Genetics in MedicinePeer-reviewedCC BYFull text2 citedHuman geneticsHAL