Prajnya Ranganath

Hyderabad, TG 500082, India

Last Updated: 09/26/2026

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Found 72 publications

CHFR gene variations: A novel cause for hereditary cancer predisposition?

CHFR gene variations: A novel cause for hereditary cancer predisposition?

Journal: Journal of genetics

Published: July 14, 2026

Correction to: Position Statement of the Indian Academy of Medical Genetics on Next Generation Sequencing-Based Testing for Rare Genetic Disorders.

Correction to: Position Statement of the Indian Academy of Medical Genetics on Next Generation Sequencing-Based Testing for Rare Genetic Disorders.

Journal: Indian journal of pediatrics

Published: July 12, 2026

Long-Term Outcomes of Enzyme Replacement Therapy in Indian Patients with Gaucher Disease - A Multicentric Study.

Long-Term Outcomes of Enzyme Replacement Therapy in Indian Patients with Gaucher Disease - A Multicentric Study.

Journal: Indian journal of pediatrics

Published: May 14, 2026

Clinical, biochemical and molecular spectrum of acute neuronopathic type 2 Gaucher disease from India.

Clinical, biochemical and molecular spectrum of acute neuronopathic type 2 Gaucher disease from India.

Journal: BMC pediatrics

Published: April 02, 2026

Position Statement of the Indian Academy of Medical Genetics on Cytogenetic and Molecular Cytogenetic Testing.

Position Statement of the Indian Academy of Medical Genetics on Cytogenetic and Molecular Cytogenetic Testing.

Journal: Indian journal of pediatrics

Published: February 22, 2026

Position Statement of the Indian Academy of Medical Genetics on Next Generation Sequencing-Based Testing for Rare Genetic Disorders.

Position Statement of the Indian Academy of Medical Genetics on Next Generation Sequencing-Based Testing for Rare Genetic Disorders.

Journal: Indian journal of pediatrics

Published: February 20, 2026

Slipped Capital Femoral Epiphysis in a Case of Hyperphosphatemic Familial Tumoral Calcinosis: A Case Report.

Slipped Capital Femoral Epiphysis in a Case of Hyperphosphatemic Familial Tumoral Calcinosis: A Case Report.

Journal: JBJS case connector

Published: October 16, 2025

Alexander Disease Due to a Homozygous GFAP Variant.

Alexander Disease Due to a Homozygous GFAP Variant.

Journal: Indian journal of pediatrics

Published: July 19, 2025

Experiences from inborn errors of immunity registry of India: A preliminary report.

Experiences from inborn errors of immunity registry of India: A preliminary report.

Journal: The Indian journal of medical research

Published: July 15, 2025

A Decade of Prenatal Genetic Diagnostics: Insights From 1949 Cases at a Medical Genetics Facility in South India.

A Decade of Prenatal Genetic Diagnostics: Insights From 1949 Cases at a Medical Genetics Facility in South India.

Journal: Prenatal diagnosis

Published: January 09, 2025

CEP72 Emerges as a Key Centriolar Satellite Protein in Health and Disease.

CEP72 Emerges as a Key Centriolar Satellite Protein in Health and Disease.

Journal: Cytoskeleton (Hoboken, N.J.)

Published: October 27, 2024

Reanalysis of Exome Sequencing Data in the Indian Undiagnosed Diseases Program: Improving Diagnostic Yield and Ending Diagnostic Odyssey.

Reanalysis of Exome Sequencing Data in the Indian Undiagnosed Diseases Program: Improving Diagnostic Yield and Ending Diagnostic Odyssey.

Journal: Clinical genetics

Published: October 14, 2024

Showing 1-12 of 72

Last Updated: 09/26/2026