Meghna Singh
Overview
Explore the profile of Meghna Singh including associated specialties, affiliations and a list of published articles.
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Articles
38
Citations
360
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Recent Articles
1.
Mallick R, Kumari R, Bahurupi Y, M A, Aravindan N, Singh M
Cureus
. 2024 Aug;
16(7):e63950.
PMID: 39105010
Introduction Adolescence is a critical period known for presenting specific challenges in disease treatment and health promotion. Studies have highlighted that increased nutritional awareness is associated with healthier eating habits,...
2.
Raghuwanshi B, Ahuja K, Sharma G, Sharma K, Singh M, Yadav A, et al.
Cureus
. 2024 Jul;
16(6):e62476.
PMID: 39015862
Introduction: The determination of one's blood group is dictated by the inheritance-based diversity in the presence or absence of RBC antigens on the surface. Extended Rhesus (Rh) antigens are the...
3.
Saxena V, Singh M
Indian J Community Med
. 2024 Jan;
48(6):817-822.
PMID: 38249708
Approximately one-quarter of the world's population is suffering from anemia, out of which 12.7% of men suffer from anemia around the globe. In India, anemia is a moderate public health...
4.
Bangera A, Singh M, Godse K, Patil S
Qatar Med J
. 2023 Nov;
2023(2):16.
PMID: 38025326
: A frequent condition known as chronic urticaria (CU) is characterized by the appearance of wheals, angioedema, or both. CU lowers the quality of life and may also result in...
5.
Krishnamurthy P, Mulvey M, Gowda K, Singh M, Venkatesan N, Syam S, et al.
Front Public Health
. 2023 Oct;
11:1177634.
PMID: 37900017
Objectives: India's Covid-19 vaccination campaign engaged frontline workers (FLWs) to encourage vaccination among vulnerable segments of society. The FLWs report encountering a variety of barriers to vaccination and are often...
6.
Singh M, Spendlove S, Wei A, Bondhus L, Nava A, de L Vitorino F, et al.
Hum Genet
. 2023 Oct;
142(12):1705-1720.
PMID: 37861717
Arboleda-Tham Syndrome (ARTHS) is a rare genetic disorder caused by heterozygous, de novo mutations in Lysine(K) acetyltransferase 6A (KAT6A). ARTHS is clinically heterogeneous and characterized by several common features, including...
7.
Singh M, Spendlove S, Wei A, Bondhus L, Nava A, de L Vitorino F, et al.
bioRxiv
. 2023 Aug;
PMID: 37577627
Arboleda-Tham Syndrome (ARTHS) is a rare genetic disorder caused by heterozygous, truncating mutations in . ARTHS is clinically heterogeneous and characterized by several common features including intellectual disability, developmental and...
8.
Gautam D, Dolma K, Khandelwal B, Gupta M, Singh M, Mahboob T, et al.
PeerJ
. 2023 Aug;
11:e15590.
PMID: 37529215
The biosynthesis of nanoparticles using the green route is an effective strategy in nanotechnology that provides a cost-effective and environmentally friendly alternative to physical and chemical methods. This study aims...
9.
Lin I, Wei A, Awamleh Z, Singh M, Ning A, Herrera A, et al.
JCI Insight
. 2023 Apr;
8(10).
PMID: 37053013
ASXL1 (additional sex combs-like 1) plays key roles in epigenetic regulation of early developmental gene expression. De novo protein-truncating mutations in ASXL1 cause Bohring-Opitz syndrome (BOS; OMIM #605039), a rare...
10.
Zavadil J, Singh M, Robertson E, Clark L, Snaman J, McNeil M, et al.
J Pediatr
. 2023 Mar;
257:113393.
PMID: 36940869
Our institution's annual bereaved family event was modified to a virtual format during the COVID-19 pandemic. While necessary to comply with physical distancing directives, the transition also provided greater accessibility...