Vigneshwar Senthivel
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Explore the profile of Vigneshwar Senthivel including associated specialties, affiliations and a list of published articles.
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25
Citations
371
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Recent Articles
1.
Vatsyayan A, Mathur P, Bhoyar R, Imran M, Senthivel V, Divakar M, et al.
Cancer Causes Control
. 2025 Mar;
PMID: 40024972
Breast cancer is the most highly reported cancer in India. Genetic testing could help tackle the increasing cancer burden by enabling carriers obtain early diagnosis through increased surveillance, and help...
2.
Kumar M, Sharma S, Pandey S, Mammayil G, Pala Kuzhiyil A, Sreesh S, et al.
Mov Disord Clin Pract
. 2024 Nov;
12(2):185-195.
PMID: 39535360
Background: Wilson's disease (WD) results from pathogenic ATP7B gene variations, causing copper accumulation mainly in the liver, brain, and kidneys. Objectives: In India, despite studies on ATP7B variants, WD often...
3.
Vatsyayan A, Imran M, Bhardwaj J, Vr A, Agrawal S, Jyoti Saikia B, et al.
Endocrine
. 2024 Aug;
86(3):1178-1187.
PMID: 39112918
Purpose: Multiple Endocrine Neoplasia (MEN) is a group of familial cancer syndromes that encompasses several types of endocrine tumors differentiated by genetic mutations in RET, MEN1 and CDKN1B genes. Accurate...
4.
Bhoyar R, Jolly B, Vignesh H, Bhatt L, Senthivel V, Israni R, et al.
STAR Protoc
. 2024 Jul;
5(3):103020.
PMID: 39083382
Lumpy skin disease (LSD) is a viral disease predominantly affecting cattle caused by a poxvirus belonging to the capripoxvirus genus. Here, we present a protocol for next-generation sequencing of the...
5.
Senthivel V, Jolly B, Vr A, Bajaj A, Bhoyar R, Imran M, et al.
J Hum Genet
. 2024 Jun;
69(9):455-465.
PMID: 38890497
Cardiac channelopathies are a group of heritable disorders that affect the heart's electrical activity due to genetic variations present in genes coding for ion channels. With the advent of new...
6.
Gupta V, Jolly B, Bhoyar R, Divakar M, Jain A, Mishra A, et al.
Comput Biol Chem
. 2024 Jun;
112:108118.
PMID: 38878606
Mitochondrial disorders are a class of heterogeneous disorders caused by genetic variations in the mitochondrial genome (mtDNA) as well as the nuclear genome. The spectrum of mtDNA variants remains unexplored...
7.
Sivadas A, Sahana S, Jolly B, Bhoyar R, Jain A, Sharma D, et al.
BMJ Open Diabetes Res Care
. 2024 Mar;
12(2).
PMID: 38471670
Introduction: Genetic variants contribute to differential responses to non-insulin antidiabetic drugs (NIADs), and consequently to variable plasma glucose control. Optimal control of plasma glucose is paramount to minimizing type 2...
8.
Rophina M, Bhoyar R, Imran M, Senthivel V, Divakar M, Mishra A, et al.
Int J Immunogenet
. 2023 May;
50(3):134-143.
PMID: 37160415
Genetic variants in human platelet antigens (HPAs) considered allo- or auto antigens are associated with various disorders, including neonatal alloimmune thrombocytopenia, platelet transfusion refractoriness and post-transfusion purpura. Although global differences...
9.
Divakar M, Jain A, Bhoyar R, Senthivel V, Jolly B, Imran M, et al.
J Hum Genet
. 2023 Feb;
68(6):409-417.
PMID: 36813834
Structural variants contribute to genetic variability in human genomes and they can be presented in population-specific patterns. We aimed to understand the landscape of structural variants in the genomes of...
10.
Rophina M, Bhoyar R, Imran M, Senthivel V, Divakar M, Mishra A, et al.
HLA
. 2022 Dec;
101(3):262-269.
PMID: 36502377
Antibodies against human neutrophil antigens (HNAs) play a significant role in various clinical conditions such as neonatal alloimmune neutropenia, transfusion-related acute lung injury, and other nonhemolytic transfusion reactions. This study...