GenVec

Recent papers from GenVec

1. HLA allelic variation and COVID-19 severity in a Kuwait-based population: a high-resolution immunogenetic studyFrontiers in Immunology · 2026
2. A Second Pathogenic Protein, PolyGN2C‐iso2, Reveals a Dual‐Protein Pathology in Neuronal Intranuclear Inclusion DiseaseAdvanced Science · 2026
3. Angiogenesis Gene TherapyCirculation · 1999
4. Wellens’ Sign and Syndrome Detected With the Home Use of a Novel 12-Lead ElectrocardiogramJACC Case Reports · 2026
5. Feasibility Pilot to Expand Exome Sequencing Access for Children With Nonsyndromic Neurodevelopmental DisordersPediatric Neurology · 2026
6. Delineating the clinical and molecular spectrum of the neurodevelopmental disorder associated with SETGenetics in Medicine · 2026
7. Autologous skeletal myoblasts transplanted to ischemia-damaged myocardium in humansJournal of the American College of Cardiology · 2003
8. Biallelic inactivating variants in the chromatin remodeler DMAP1 cause a syndromic neurodevelopmental disorderJournal of Clinical Investigation · 2026
9. Scanner‐Independent Calibrations of Handheld Near‐Infrared Spectra for Robust Quality Assessment of Vanilla PodsJournal of Food Quality · 2026
10. CIRAN D5.2 Guidelines for public engagement and dialogue2025
11. Sensitivity of HiFi long-read genome sequencing for difficult-to-detect pathogenic variants when applied to real-world clinical laboratory samplesThe American Journal of Human Genetics · 2026
12. Phenotypic Discordance in Monozygotic Twins with a CDH2 VariantEuropean Journal of Medical Genetics · 2026
13. Challenges and opportunities for the use of telehealth in rare disease diagnosis, treatment, research, and education: key opinion leader interviews by the IRDiRC telehealth task forceTherapeutic Advances in Rare Disease · 2026
14. Genetically Significant Hereditary Mutations Associated with Breast and Ovarian Cancer among Ukrainian WomenCytology and Genetics · 2026
15. Toward self-validating ECG Systems: A personalized, uncertainty-aware approach for detecting and estimating lead misplacementJournal of Electrocardiology · 2026
16. Clinical, in vitro, and in vivo evidence of WAPL as a novel cohesinopathy gene and phenotypic driver of 10q22.3q23.2 genomic disorder2026
17. A novel spliceosomopathy caused by de novo SF3B3 variantsGenome Medicine · 2026
18. Multiscore, a gene ranker powered by artificial intelligence and real-world clinical data, shows high sensitivity for the molecular diagnosis of Mendelian disorders in nearly 10,000 exomes and genomesHuman Genetics · 2026
19. Primary ovarian insufficiency diagnosis, treatment, and sequelae: current evidenceCurrent Opinion in Obstetrics & Gynecology · 2026
20. Plasma proteomics biomarkers for predicting anti‐tuberculosis drug‐induced liver injury: A comprehensive assessmentBritish Journal of Clinical Pharmacology · 2026