Lavanya Ravichandran
Ida Scudder Road
Vellore, TN, India
Vellore, TN, India
Last Updated: 09/26/2026
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Found 12 publications
Advocating Targeted Sequential Screening over Whole Exome Sequencing in 21-Hydroxylase Deficiency.
Journal: Indian journal of pediatrics
Published: June 07, 2024
A Novel Large Deletion in the EVER1 Gene in a Family With Epidermodysplasia Verruciformis From India.
Journal: The American Journal of dermatopathology
Published: April 04, 2024
Clinical, Hormonal, and Genetic Spectrum of 46 XY Disorders of Sexual Development (DSD) Patients.
Journal: Indian journal of pediatrics
Published: February 10, 2024
High carrier frequency of CYP21A2 gene mutations in Southern India - underscoring the need for genetic testing in Congenital Adrenal Hyperplasia.
Journal: Endocrine
Published: November 04, 2023
Congenital Adrenal Hyperplasia - A Comprehensive Review of Genetic Studies on 21-Hydroxylase Deficiency from India.
Journal: Indian journal of endocrinology and metabolism
Published: July 13, 2023
The BRCA mutation spectrum among breast and ovarian cancers in India: highlighting the need to screen BRCA1 185delAG among South Indians.
Journal: European journal of human genetics : EJHG
Published: June 30, 2023
Clinical Features of Unrecognized Congenital Adrenal Hyperplasia Due to 17α-hydroxylase Deficiency Since Adolescence: A Case Report.
Journal: Journal of the ASEAN Federation of Endocrine Societies
Published: September 11, 2022
Allele-specific and multiplex PCR based tools for cost-effective and comprehensive genetic testing in Congenital Adrenal Hyperplasia.
Journal: MethodsX
Published: November 26, 2021
Genetic Heterogeneity and Challenges in the Management of Permanent Neonatal Diabetes Mellitus: A Single-Centre Study from South India.
Journal: Indian journal of endocrinology and metabolism
Published: October 02, 2021
Allele-specific PCR and Next-generation sequencing based genetic screening for Congenital Adrenal Hyperplasia in India.
Journal: European journal of medical genetics
Published: August 10, 2021
WFS1 Gene-associated Diabetes Phenotypes and Identification of a Founder Mutation in Southern India.
WFS1 Gene-associated Diabetes Phenotypes and Identification of a Founder Mutation in Southern India.
Journal: The Journal of clinical endocrinology and metabolism
Published: July 19, 2021
Epitope-based immunoinformatics approach on RNA-dependent RNA polymerase (RdRp) protein complex of Nipah virus (NiV).
Journal: Journal of cellular biochemistry
Published: August 03, 2018
Showing 1-12 of 12
Last Updated: 09/26/2026