SciGenom Labs (India)

Recent papers from SciGenom Labs (India)

1. After the First Crisis Response: Testing GPT-4o Safety Persistence in Long Conversations: A Synthetic Safety Evaluation Motivated by Raine v. OpenAI2026
2. The Sustainability of Robusta Coffee Under Global Change—A ReviewSustainable Development · 2026
3. Clinical, Biochemical, and Molecular Spectrum of Pseudohypoaldosteronism Type 1B in Indian Children: A Multicentric Case SeriesClinical Endocrinology · 2026
4. Validation of a Genome-Wide Polygenic Score for Coronary Artery Disease in South AsiansJournal of the American College of Cardiology · 2020
5. Consensus recommendations for technical standardization of flow cytometric measurable residual disease assessment in B ‐cell acute lymphoblastic leukemia: A report from The Cytometry Society, IndiaCytometry Part B Clinical Cytometry · 2026
6. Abstract LT05: How EGFR Mutations Shape Lung Cancer in Never-SmokersCancer Research · 2026
7. Plasma separation by recycled squeeze flow of a single blood dropletBiomicrofluidics · 2026
8. Association of VDR haplotypes with vitamin D status: a comparative pilot study identifying the F−t combination as a risk factor in South IndiaBMJ connections. · 2026
9. Metatranscriptomic Insights into Microbial Responses of a Bacterial Consortium from Activated Sludge at the Zeekoegat Wastewater Treatment Plant to Perfluorooctane Sulfonate and Perfluorooctanoic AcidWater · 2026
10. Progressive Supranuclear Palsy in India: Insights from a Large Multicenter Clinical Cohort (Project PAIR ‐ PSP )Movement Disorders Clinical Practice · 2026
11. Child Neurology: Expanding the LGI1 SpectrumNeurology · 2026
12. Genomic elucidation of hybridization between Liberica and excelsa coffee and its implications for coffee crop developmentScientific Reports · 2026
13. MC4R-related monogenic obesity in children: insights from 2 casesAnnals of Pediatric Endocrinology & Metabolism · 2026
14. Pediatric Ciliopathy Linked to TULP3 Variant—A Case ReportJournal of Molecular Pathology · 2026
15. Diverse and rare candidate MODY gene variants were identified in one-fifth of a Bangladeshi cohort with nonobese, nonautoimmune youth-onset diabetesScientific Reports · 2026
16. Clinical Impact of Integrating RNA-Based Next-Generation Sequencing Into the Diagnostic Evaluation of Soft Tissue Sarcomas: Insights From a Single-Center Multidisciplinary WorkflowSHILAP Revista de lepidopterología · 2026
17. Factors influencing inconclusive sex chromosomal aneuploidies results on non-invasive prenatal testingWadia Journal of Women and Child Health · 2026
18. Association of Bassoon ( BSN ) Gene Mutations With Gait and Motor Impairments in Parkinson's DiseaseEuropean Journal of Neuroscience · 2026
19. Incidental Identification of Molar Pregnancy During Maternal Cell Contamination TestingJournal of Fetal Medicine · 2026
20. The Inheritance Puzzle: A Case of Dual Genetic Kidney Disease.2026