Babu Rao Vundinti

Publication Activity (10 Years)

Years Active: 2019-2023
Publications (10 Years): 12

Top Topics

Chronic Myeloid Leukemia

Mitochondrial Dna

Nitric Oxide Synthase

Top Venues

Molecular biology reports

Molecular human reproduction

BMC medical genomics

Annals of hematology

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

Publications

Vinayak Kulkarni, Selvaa Kumar Chellasamy, Somprakash Dhangar, Jagdeeshwar Ghatanatti, Babu Rao Vundinti
Comprehensive molecular analysis identifies eight novel variants in XY females with disorders of sex development. Molecular human reproduction 29 (2) (2023)
Anjali Shah, Chandan Kumar, Chandrakala Shanmukhaiah, Aruna Rajendran, Sangeeta Mudaliar, Susan Idicula-Thomas, Babu Rao Vundinti
Genomic and computational analysis of four novel variants of MPL gene in Congenital Amegakaryocytic Thrombocytopenia. Annals of hematology (2023)
Vinayak Kulkarni, Selvaa Kumar Chellasamy, Somprakash Dhangar, Jagdeeshwar Ghatanatti, Babu Rao Vundinti
Comprehensive molecular analysis identifies eight novel variants in XY females with disorders of sex development. Molecular human reproduction 29 (2) (2023)
Vinayak Kulkarni, Selvaa Kumar Chellasamy, Somprakash Dhangar, Jagdish Ghatanatti, Babu Rao Vundinti
Comprehensive molecular analysis identifies eight novel variants in XY females with disorders of sex development. Molecular human reproduction (2023)
Somprakash Dhangar, Purvi Panchal, Jagdeeshwar Ghatanatti, Jitendra Suralkar, Anjali Shah, Babu Rao Vundinti
Novel deletion of exon 3 in TYR gene causing Oculocutaneous albinism 1B in an Indian family along with intellectual disability associated with chromosomal copy number variations. BMC medical genomics 15 (1) (2022)
Somprakash Dhangar, Purvi Panchal, Jagdeeshwar Ghatanatti, Jitendra Suralkar, Anjali Shah, Babu Rao Vundinti
Correction to: Novel deletion of exon 3 in TYR gene causing Oculocutaneous albinism 1B in an Indian family along with intellectual disability associated with chromosomal copy number variations. BMC medical genomics 15 (1) (2022)
Nehakumari Maurya, Purvi Mohanty, Purvi Panchal, Chandrakala Shanmukhaiah, Babu Rao Vundinti
Over expression of mTOR gene predicts overall survival in myelodysplastic syndromes. Molecular biology reports (2022)
Merin George, Avani Solanki, Purvi Mohanty, Somprakash Dhangar, Aruna Rajendran, Sheila Mohan, Babu Rao Vundinti
Nitric oxide synthase-2 (NOS2) gene polymorphism c.1832C>T (Ser608Leu) associated with nitrosative stress in Fanconi anaemia. Molecular biology reports 48 (3) (2021)
Anjali Shah, Merin George, Somprakash Dhangar, Aruna Rajendran, Sheila Mohan, Babu Rao Vundinti
Severe telomere shortening in Fanconi anemia complementation group L. Molecular biology reports 48 (1) (2021)
Merin George, Avani Solanki, Niranjan Chavan, Aruna Rajendran, Revathi Raj, Sheila Mohan, Sandeep Nemani, Shailesh Kanvinde, Deendayalan Munirathnam, Sudha Rao, Nita Radhakrishnan, Harsha Prasada Lashkari, Radha Gulati Ghildhiyal, Mamta Manglani, Chandrakala Shanmukhaiah, Sunil Bhat, Sowmyashree Ramesh, Anchu Cherian, Pritesh Junagade, Babu Rao Vundinti
A comprehensive molecular study identified 12 complementation groups with 56 novel FANC gene variants in Indian Fanconi anemia subjects. Human mutation 42 (12) (2021)
Avani Solanki, Aruna Rajendran, Sheila Mohan, Revathy Raj, Babu Rao Vundinti
Mitochondrial DNA variations and mitochondrial dysfunction in Fanconi anemia. PloS one 15 (1) (2020)
Somprakash Dhangar, Vinay Shanbhag, Chandrakala Shanmukhaiah, Babu Rao Vundinti
Lack of association between functional polymorphism of DNA repair genes (XRCC1, XPD) and clinical response in Indian chronic myeloid leukemia patients. Molecular biology reports 46 (5) (2019)