Vivekananda Bhat
Overview
Explore the profile of Vivekananda Bhat including associated specialties, affiliations and a list of published articles.
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Articles
15
Citations
52
Followers
0
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Recent Articles
1.
Shirodkar A, Akhil K, Bhat V, Shah H, Shukla A, Periyasamy R
Clin Dysmorphol
. 2025 Mar;
PMID: 40073198
No abstract available.
2.
Rao L, Kothiwale V, Radhakrishnan P, Rangaswamy D, Shukla A, Bhat V
Indian J Nephrol
. 2024 Dec;
34(6):667-669.
PMID: 39649299
The cytosolic capping protein, Arp2/3 and myosin-I linker protein 2 or CARMIL2 plays an important role in T/B/NK cell function. Biallelic disease causing variants in CARMIL2 are known to cause...
3.
Kaur N, do Rosario M, Majethia P, Mascarenhas S, Rao L, Nair K, et al.
Am J Med Genet A
. 2024 Oct;
197(3):e63914.
PMID: 39470296
Several genetic disorders are associated with either a permanent deficit or a delay in central nervous system myelination. We investigated 24 unrelated families (25 individuals) with deficient myelination after clinical...
4.
Yeole M, Majethia P, Siddiqui S, Girisha K, Shukla A, Radhakrishnan P, et al.
Am J Med Genet A
. 2024 Sep;
197(2):e63892.
PMID: 39333057
Translocase of the outer mitochondrial membrane (TOMM) complex plays an important role in the transport of proteins from the cytoplasm into the mitochondria. TOMM7, one of the subunits of the...
5.
Vardhan A, Kamath A, Soman S, Nagaraj A, Bhat V, Vishwanath R
Indian J Psychiatry
. 2024 Sep;
66(7):673-675.
PMID: 39257499
No abstract available.
6.
Vasudeva A, Padavagodu Shivananda R, Handigodu Dugappa A, Bhat V
BMJ Case Rep
. 2024 Jun;
17(6).
PMID: 38839405
A third gravida with osteogenesis imperfecta (OI) type 1, in her 20s, was referred from the Medical Genetics department at 12+ weeks with a prenatal diagnosis of OI type 1...
7.
Majethia P, Kaur N, Mascarenhas S, Rao L, Pande S, Narayanan D, et al.
Clin Genet
. 2024 Feb;
105(6):639-654.
PMID: 38374498
The application of genomic technologies has led to unraveling of the complex genetic landscape of disorders of epilepsy, gaining insights into their underlying disease mechanisms, aiding precision medicine, and providing...
8.
Pande S, Majethia P, Nair K, Rao L, Mascarenhas S, Kaur N, et al.
Eur J Hum Genet
. 2023 Dec;
32(10):1291-1298.
PMID: 38114583
The contribution of de novo variants as a cause of intellectual disability (ID) is well established in several cohorts reported from the developed world. However, the genetic landscape as well...
9.
Chadaga K, Prabhu S, Bhat V, Sampathila N, Umakanth S, Upadya P S
SLAS Technol
. 2023 Sep;
28(6):393-410.
PMID: 37689365
The COVID-19 pandemic erupted at the beginning of 2020 and proved fatal, causing many casualties worldwide. Immediate and precise screening of affected patients is critical for disease control. COVID-19 is...
10.
Chadaga K, Prabhu S, Bhat V, Sampathila N, Umakanth S, Chadaga R
Ann Med
. 2023 Jul;
55(1):2233541.
PMID: 37436038
Objective: The persistent spread of SARS-CoV-2 makes diagnosis challenging because COVID-19 symptoms are hard to differentiate from those of other respiratory illnesses. The reverse transcription-polymerase chain reaction test is the...