Personal profile
Research interests
Hereditary anemias, rare disorders
Experience
Assistant Professor, Medical Genetics Oct 2022 till date
Fingerprint
Dive into the research topics where Vivekananda Bhat is active. These topic labels come from the works of this person. Together they form a unique fingerprint.
- 1 Similar Profiles
Collaborations and top research areas from the last five years
Recent external collaboration on country/territory level. Dive into details by clicking on the dots or
-
A novel homozygous in-frame deletion variant in TPRKB causing Galloway-Mowat syndrome 5
Kaur, N., Shirsat, K., Bhat, V., Yeole, M., Farooqui, S., Limaye, S., Radhakrishnan, P., Siddiqui, S., Narayanan, D. L., Shenoy, R. & Shukla, A., 12-2026, In: Neurogenetics. 27, 1, 15.Research output: Contribution to journal › Article › peer-review
-
Further delineation of defects in MRPS2 causing human OXPHOS deficiency and early developmental abnormalities in zebrafish
Kandettu, A., Yeole, M., Sekar, H., Garapati, K., Kaur, N., Anand, A., Hegde, P., Nair, K., Medishetti, R., Bhat, V., Radhakrishnan, P., Mundkur, S. C., Shrikiran, H. A., Pandey, A., Sevilimedu, A., Chakrabarty, S. & Shukla, A., 2025, (Accepted/In press) In: European Journal of Human Genetics. 33, 11, p. 1451-1461 11 p., 16080.Research output: Contribution to journal › Article › peer-review
Open Access1 Link opens in a new tab Citation (Scopus) -
Report of a novel UBA2 variant causing Aplasia Cutis Congenita with Ectrodactyly syndrome (ACCES) in an Indian family
Shirodkar, A. N., Akhil, K. A., Bhat, V., Shah, H., Shukla, A. & Periyasamy, R., 01-07-2025, In: Clinical Dysmorphology. 34, 3, p. 102-106 5 p., 10.1097/MCD.0000000000000520.Research output: Contribution to journal › Article › peer-review
Open Access -
AUTS2 variant in a child diagnosed with autism spectrum disorder and intellectual disability disorder, a case report
Vardhan, A., Kamath, A., Soman, S., Nagaraj, A. K. M., Bhat, V. & Vishwanath, R., 07-2024, In: Indian Journal of Psychiatry. 66, 7, p. 673-675 3 p.Research output: Contribution to journal › Letter › peer-review
-
Bi-Allelic Splicing Variant, c.153-2A > C in TOMM7 Is Associated With Leigh Syndrome
Yeole, M., Majethia, P., Siddiqui, S., Girisha, K., Shukla, A., Radhakrishnan, P. & Bhat, V., 2024, (Accepted/In press) In: American Journal of Medical Genetics, Part A. 197, 2, e63892.Research output: Contribution to journal › Article › peer-review
3 Link opens in a new tab Citations (Scopus)