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203,952 studies31 sourcesUpdated 9 min ago

Human genetics

961 studies23 in 7 days555 in 30 days

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961 studies

  1. Comparative Cardiovascular Outcomes in Acalabrutinib vs. Zanubrutinib in B-Cell Malignancies: A TriNetX Data Study.
    Maan Awad, Sunanda Tah, Syed Ahmad +5
    Current oncology (Toronto, Ont.)Peer-reviewedCC BYFull textHuman geneticsEurope PMC
  2. EpiSignaLR: an open resource for genome-wide episignature analysis from methylation-aware short- and long-read sequencing
    S. B. Gibson, M. P. G. Zalusky, J. Goffena +20
    medRxivPreprintCC BY-NC-NDFull textHuman geneticsmedRxiv
  3. GWAS of Lyme disease identifies five loci and discovers a connection with post-infectious diseases
    S. Strausz, E. Romppanen, H. Haapaniemi +7
    medRxivPreprintCC BY-NC-NDFull textHuman geneticsmedRxiv
  4. Exome-based Preconception Carrier Screening for the Mexican Jewish Community; Yields and Implications
    R. Birnbaum, K. Lee, T. Metta-Harari +13
    medRxivPreprintAll rights reservedFull textHuman geneticsmedRxiv
  5. Insomnia and the genetic overlap of sleep with depression and anxiety: a genomic structural equation modelling study
    M. A. Sakiroglu, Y. Cicek, M. C. Celik +3
    medRxivPreprintCC BY-NC-NDFull textHuman geneticsmedRxiv
  6. Genetic ancestry shapes context-dependent immune regulation across Indigenous South American populations
    C. Choy, L. Vicuna, M. Patino +36
    medRxivPreprintCC BY-NC-NDFull textHuman geneticsmedRxiv
  7. Pulmonary Involvement in Chronic Lymphocytic Leukemia: A Structured Diagnostic Approach to Diffuse Infiltrates-A Case Report.
    Benoit Aguado, Florent Favard, Thomas Egenod +2
    EJHaemPeer-reviewedCC BY-NC-NDFull textHuman geneticsEurope PMC
  8. When Pain Crisis Turns Lethal: A Case Report of Fat Embolism Syndrome in Sickle Cell Disease
    Abrar J. Alwaheed
    Journal of Clinical MedicinePeer-reviewedCC BY 4.0Human geneticsCrossref
  9. Serum p-tau181 and p-tau217 levels in adolescents and adults with 5q spinal muscular atrophy.
    Caroline Deborah Stapf, Zeljko Uzelac, Louise Iterbeke +13
    Journal of neurologyPeer-reviewedCC BYFull textHuman geneticsEurope PMC
  10. Haemoptysis in chronic pulmonary vascular disease: a narrative review.
    Jan C Kamp, Brandon Budhram, Mitja Jevnikar +5
    European respiratory review : an official journal of the European Respiratory SocietyPeer-reviewedCC BYFull textHuman geneticsEurope PMC
  11. PCGF1 Promotes the Tumorigenesis of Malignancies Through Upregulating CCDC34 in Glioma.
    Yuanbing Chen, Jianbing Xiong, Ziran Ou +5
    Annals of clinical and translational neurologyPeer-reviewedCC BYFull textHuman geneticsEurope PMC
  12. USP7 inhibits FOXO1 activity in chronic lymphocytic leukaemia cells enhancing cell survival.
    Hassan N B Almuhanna, Jodie Hay, Michael W Moles +6
    Molecular oncologyPeer-reviewedCC BYFull textHuman geneticsEurope PMC
  13. Three-dimensional in vitro models for assessing temozolomide sensitivity in glioblastoma
    Andresa Hiromi Sakai, Marna Eliana Sakalem, Luiza Magosso Oliveira Rocha +7
    Frontiers in NeurosciencePeer-reviewedCC BY 4.0Full textHuman geneticsCrossrefPMC
  14. Audiological Phenotyping Evaluation in KBG Syndrome: Description of a Multicenter Review
    Laetitia Rhamati, Aurore Marcolla, Anne Marie Guerrot +20
    International Journal of Pediatric OtorhinolaryngologyPeer-reviewedLicence not stated3 citedHuman geneticsHAL
  15. Disruption of marrow microenvironments in chronic lymphocytic leukemia by high-resolution synchrotron micro-computed tomography
    In Kyu Lee, Yoshihiro Obata, Anthony D. Pomicter +6
    Communications MedicinePeer-reviewedCC BY 4.0Full textHuman geneticsCrossref
  16. Improving prenatal thalassemia carrier detection with a combined MCV and MCH strategy: a 24-year retrospective cohort study
    Han-Ying Chen, Shin-Yu Lin, Chih-En Li +3
    Scientific ReportsPeer-reviewedCC BY-NC-ND 4.0Full textHuman geneticsCrossref
  17. The growing repertoire of putative pathogen interaction genes in the Biomphalaria glabrata vs Schistosoma mansoni system
    Javier Calvelo, Stephanie R. Bollmann, Jacob A. Tennessen +1
    PLOS Neglected Tropical DiseasesPeer-reviewedCC BY 4.0Full textHuman geneticsPLOSPMCDOAJ
  18. Changes in bone density and metabolism marker levels in type I Gaucher's disease following annual zoledronic acid hydrate administration: A case report
    Hiroyuki Onuma, Naoki Haraguchi
    Bone ReportsPeer-reviewedCC BY 4.0Full textHuman geneticsPMC
  19. Diagnostic delay as a prognostic factor for non-response to treatment and relapse in Mexican pediatric patients with central nervous system tumors
    Juan-Carlos Pérez-De Marcos, Manuel Castillejos-López, Arnoldo Aquino-Gálvez +6
    Frontiers in pediatricsPeer-reviewedCC BYFull textHuman geneticsEurope PMCPMC
  20. Clinical analysis of abnormal hemoglobin detection results in northern Guangxi, China
    Weijia Yang, Xiangjun Wu, Qingyang Xie +1
    Molecular genetics and metabolism reportsPeer-reviewedCC BYFull textHuman geneticsEurope PMCEurope PMCPMC
  21. Off-Label Dextromethorphan/Bupropion for Emotional Lability Following Resection of an IDH-Mutant Astrocytoma: A Case Report.
    Olivia Hill, Riley Imlay, Ankit Chalia +4
    Healthcare (Basel, Switzerland)Peer-reviewedCC BYFull textHuman geneticsEurope PMC
  22. Genetic Modifiers of Age at Onset for Parkinson's Disease in European Populations
    The Global Parkinson's Genetics Program (GP2), E. Voss
    medRxivPreprintCC BYFull textHuman geneticsmedRxiv
  23. Measurable Residual Disease (MRD) Monitoring in Myeloproliferative Neoplasms
    Gary E. Markey, Stephen E. Langabeer
    CancersPeer-reviewedCC BY 4.0Human geneticsCrossref
  24. Pirtobrutinib for the Treatment of Therapy-Resistant Chronic Lymphatic Leukemia With CNS Localization.
    M E Roerink, A P Kater, S H Tonino +1
    Case reports in hematologyPeer-reviewedCC BYFull textHuman geneticsEurope PMC
  25. Machine learning predicts treatment response to nusinersen in non-sitter spinal muscular atrophy (SMA).
    Georgia Stimpson, Emer O'Reilly, Giorgia Coratti +10
    Journal of neuromuscular diseasesPeer-reviewedCC BYFull textHuman geneticsEurope PMC