Vamsi K. Yenamandra
Bengaluru, KA, India
Last Updated: 09/26/2026
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Found 30 publications
Dual Burden of Kidney Disease and Cognitive Impairment in the Longitudinal Aging Study in India-Diagnostic Assessment of Dementia-Cohort.
Journal: Kidney international reports
Published: December 21, 2025
DPYD genotyping in patients receiving capecitabine: an exploratory analysis from the D-TORCH study.
Journal: Frontiers in pharmacology
Published: October 25, 2025
Burden of MASLD and liver fibrosis: evidence from Phenome India cohort.
Journal: The Lancet regional health. Southeast Asia
Published: October 14, 2025
A Spontaneous Novel c.679dupG Mutation in the LOR Gene Resulting in Loricrin Keratoderma with Ichthyosis.
Journal: Dermatology practical & conceptual
Published: May 04, 2025
Pathogenic variants in PSENEN and NCSTN genes cause 'follicular' Dowling-Degos disease: Report of five unrelated Indian families.
Journal: Indian journal of dermatology, venereology and leprology
Published: November 21, 2024
Role of Patient Support Organizations and Collaborative Genomics Programs in Enabling Participatory Medicine for Rare Diseases in India: A Case Study of Autosomal Recessive Congenital Ichthyosis.
Journal: Indian dermatology online journal
Published: August 27, 2024
Bathing-suit ichthyosis: A rare but valuable entity for developing personalised pathogenesis-based therapies for autosomal recessive congenital ichthyosis.
Journal: Indian journal of dermatology, venereology and leprology
Published: June 28, 2024
Evolution of genome diagnostics in epidermolysis bullosa: Unveiling the power of next-generation sequencing.
Journal: Journal of the European Academy of Dermatology and Venereology : JEADV
Published: September 08, 2023
Mitochondrial calcium signaling mediated transcriptional regulation of keratin filaments is a critical determinant of melanogenesis.
Journal: bioRxiv : the preprint server for biology
Published: June 09, 2023
Oral Propranolol Therapy for Infantile Hemangioma: Long-term Follow-up.
Journal: Indian journal of pediatrics
Published: December 14, 2022
Functional genotype-phenotype associations in recessive dystrophic epidermolysis bullosa.
Journal: Journal of the American Academy of Dermatology
Published: October 03, 2022
Last Updated: 09/26/2026