Core Scientific Domain
Craniosynostosis & Genetics
Pioneering research into the molecular basis of craniosynostosis in Asian Indian children, identifying novel mutations in FGFR genes and correlating them with radiological findings and SPECT imaging.
Specialized Sub-Domains & Methodologies
FGFR1-4 Gene Mutations
Nuclear Imaging Correlations
Genetic Engineering
Surgical Outcome Prediction
Key Research Publications in Craniosynostosis & Genetics
View All (106) →2014Journal Article
Role of 99mTc- ECD SPECT in the management of children with craniosynostosis
Biomed Res Int
2015Journal Article
Novel mutation detection of fibroblast growth factor receptor 1 (FGFR1) gene, FGFR2IIIa, FGFR2IIIb, FGFR2IIIc, FGFR3, FGFR4 gene for craniosynostosis: A prospective study in Asian Indian patient
J Pediatr Neurosci
2013Journal Article
Study of environmental and genetic factors in children with craniosynostosis: A case-control study
J Pediatr Neurosci
2014Journal Article
Strengthening molecular genetics and training in craniosynostosis: The need of the hour
J Neurosci Rural Pract
2013Journal Article
Potential therapeutic strategies and its application in correcting birth defects, craniosynostosis, neurological disorders and other diseases
J Metab Syndr
2012Conference Paper
To compare the various imaging modalities in the diagnosis and management of children with craniosynostosis
J Nucl Med