Mohit Kumar Divakar
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Explore the profile of Mohit Kumar Divakar including associated specialties, affiliations and a list of published articles.
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26
Citations
521
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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.
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...
3.
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...
4.
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...
5.
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...
6.
Sivadas A, Rathore S, Sahana S, Jolly B, Bhoyar R, Jain A, et al.
Pharmacogenomics
. 2024 Mar;
25(3):147-160.
PMID: 38426301
The gene is highly polymorphic, causing large interindividual variability in the metabolism of several clinically important drugs. The authors investigated the diversity and distribution of alleles in Indians using whole...
7.
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...
8.
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...
9.
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...
10.
Bajaj A, Senthivel V, Bhoyar R, Jain A, Imran M, Rophina M, et al.
Hum Genomics
. 2022 Aug;
16(1):30.
PMID: 35932045
Background: The prevalence and genetic spectrum of cardiac channelopathies exhibit population-specific differences. We aimed to understand the spectrum of cardiac channelopathy-associated variations in India, which is characterised by a genetically...