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Publications (42)
- Capturing India’s phenotypic diversity: Health insights from the GenomeIndia project Save
- Enhancing Diagnostic Precision in Non‐Immune Hydrops Fetalis: The Incremental Value of Whole Exome Sequencing—A Prospective Cohort Study Save
- Empowered Prenatal Choice-Making as a Simple Tool to Reduce Disease Burden in Severe Haemoglobinopathies by HBB Gene Variant Analysis, Prenatal Diagnosis and Genetic Counselling Save
- Assessing the Ethical Considerations in the Era of Advanced Prenatal Testing and Genetic Counselling – Clinicians’ Perspective Save
- Implementing Genetic Counseling for Rare Diseases in LMICs: Pediatric and Prenatal Perspectives from India Save
- Co-inheritance of hemoglobin D-Punjab and beta thalassemia: Familial case study highlighting the clinical relevance and the need for premarital screening Save
- Evaluating the Effectiveness of Quantitative Fluorescent Polymerase Chain Reaction as a Substitute or Complement to Conventional Karyotyping for Prenatal Diagnosis Save
- Revisiting ultrasonographic soft markers of aneuploidy: A thoughtful analysis in low‐risk and screening naïve Indian antenatal women Save
- Thalassemia major due to compound heterozygous Codon 8/9 (+G) mutation with Dutch beta° thalassemia deletion Save
- Comparing the diagnosis accuracy and efficacy of presepsin (sCD14) and nCD64 in neonatal sepsis: A systematic review and meta-analysis Save