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Gandham Sri Lakshmi Bhavani (Gandham SriLakshmi Bhavani, Gandham Sl Bhavani, Gandham Srilakshmi Bhavani)

Scopus Author ID ORCID

Publication Activity (10 Years)

Years Active: 2020-2023
Publications (10 Years): 5

Top Topics

Duchenne Muscular Dystrophy

Intellectual Disability

Dna Methylation

Top Venues

American journal of medical genetics. Part A

Indian journal of pediatrics

Journal of human genetics

Kasturba Medical College

Kasturba Medical College Manipal (PHD)

This page only lists publications with an associated author ORCID identifier.

Affiliation History

Kasturba Medical College Feb 1o 2018

India

Assistant Professor :: Medical Genetics

Education History

Kasturba Medical College Manipal Nov 28o 2012 - Oct 13o 2017

India

PHD :: Medical Genetics

Publications

Swathi Sunil Rao, Gandham Sri Lakshmi Bhavani, Anil B Jalan, Rathika Damodara Shenoy
Nuclear Mitochondrial Disorder Due to a Variant in NAXE in Two Unrelated Indian Children. Indian journal of pediatrics (2023)
Swati Singh, Prince Jacob, Siddaramappa Jagdish Patil, Mamta Muranjan, Hitesh Shah, Katta Mohan Girisha, Gandham Sri Lakshmi Bhavani
Indian patients with CHST3-related chondrodysplasia with congenital joint dislocations. American journal of medical genetics. Part A (2023)
Prajna Udupa, Debasish Kumar Ghosh, Neethukrishna Kausthubham, Hitesh Shah, Sandip Bartakke, Ashwin B Dalal, Katta M Girisha, Gandham Sri Lakshmi Bhavani
Genome sequencing identifies a large non-coding region deletion of SNX10 causing autosomal recessive osteopetrosis. Journal of human genetics (2022)
Prince Jacob, Gandham Sri Lakshmi Bhavani, Hitesh Shah, Chelna Galada, Sheela Nampoothiri, Nutan Kamath, Shubha Rao Phadke, Mamta Muranjan, Chaitanya A Datar, Anju Shukla, Katta Mohan Girisha
Pseudoachondroplasia: Phenotype and genotype in 11 Indian patients. American journal of medical genetics. Part A (2021)
Dhanya Lakshmi Narayanan, Greeshma Purushothama, Gandham Sri Lakshmi Bhavani, Anju Shukla
Burn-McKeown syndrome with biallelic promoter type 2 deletion in TXNL4A in two siblings. American journal of medical genetics. Part A 182 (6) (2020)