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Journal of Cellular Biochemistry|November 13, 2018
Epitope-based immunoinformatics approach on RNA-dependent RNA polymerase (RdRp) protein complex of Nipah virus (NiV)Lavanya Ravichandran, Arthi Venkatesan, J Febin Prabhu Dass
Indian Journal of Endocrinology and Metabolism|June 24, 2024
Congenital Adrenal Hyperplasia - A Comprehensive Review of Genetic Studies on 21-Hydroxylase Deficiency from IndiaLavanya Ravichandran, Hesarghatta S Asha, Sarah Mathai, et al.
Indian Dermatology Online Journal|February 23, 2026
Online Survey on Perceptions and Practices of Hair Oiling Among Diverse Demographics in the Southern States of IndiaSenkadhir Vendhan, Shekhar Neema, Lavanya Ravichandran, et al.
Heart Asia|June 22, 2016
Non-alcoholic fatty liver disease and outcomes in persons with acute coronary syndromes: insights from the GRACE-ALT analysisLavanya Ravichandran, Shaun G Goodman, Andrew T Yan, et al.
Methodsx|June 27, 2022
Allele-specific and multiplex PCR based tools for cost-effective and comprehensive genetic testing in Congenital Adrenal HyperplasiaLavanya Ravichandran, Deny Varghese, Parthiban R, et al.
Indian Journal of Pediatrics|May 18, 2024
Clinical, Hormonal, and Genetic Spectrum of 46 XY Disorders of Sexual Development (DSD) PatientsRajan Palui, Lavanya Ravichandran, Sadishkumar Kamalanathan, et al.
Journal of Obstetrics and Gynaecology Canada : JOGC = Journal D'Obstetrique Et Gynecologie Du Canada : JOGC|October 11, 2020
Incidence, Intrapartum Risk Factors, and Prognosis of Neonatal Hypoxic-Ischemic Encephalopathy Among Infants Born at 35 Weeks Gestation or MoreLavanya Ravichandran, Victoria M Allen, Alexander C Allen, et al.
Indian Journal of Endocrinology and Metabolism|June 6, 2022
Genetic Heterogeneity and Challenges in the Management of Permanent Neonatal Diabetes Mellitus: A Single-Centre Study from South IndiaSophy Korula, Lavanya Ravichandran, Praveen G Paul, et al.
Journal of the ASEAN Federation of Endocrine Societies|December 4, 2023
Clinical Features of Unrecognized Congenital Adrenal Hyperplasia Due to 17α-hydroxylase Deficiency Since Adolescence: A Case ReportK G Rashmi, Lavanya Ravichandran, Ayan Roy, et al.
Endocrine|March 5, 2024
High carrier frequency of CYP21A2 gene mutations in Southern India - underscoring the need for genetic testing in Congenital Adrenal HyperplasiaLavanya Ravichandran, Shriti Paul, Rekha A, et al.
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