Rekha Khandia - Genetic Mutations

Author Information

Rekha Khandia is affiliated with the Department of Biochemistry and Genetics at Barkatullah University in Bhopal, MP, India. With a significant presence in the field of genetics, Rekha Khandia has made substantial contributions through her research work.

Research Contributions

Rekha Khandia has an extensive research portfolio with a focus on genetic studies, including the analysis of codon usage in various genes, the effects of drugs on cancer cell metastasis, and the molecular docking approaches against SARS-CoV-2. Her recent work has delved into the challenges posed by COVID-19 variants and the strategies to counter them. Additionally, her research spans the fields of neurodegeneration, tumor suppressor genes, primary immunodeficiencies, and the identification of cellular receptors for bacterial toxins.

Aliases

Rekha Khandia is also known by the aliases R Khandia and R. Khandia.

Publication and Citation Metrics

Metric	Value
Citation Count	5521
H-index	28
Paper Count	94

Publications:

Codon Usage Analysis of Pro-Apoptotic Bim Gene Isoforms.

DOI: 10.3233/jad-215691

Year: 2022

Evaluating the Effects of Hypotensive Drug Valsartan on Angiogenesis and Associated Breast Ductal Carcinoma Cell Metastasis

DOI: 10.3923/ijp.2022.817.825

Year: 2022

Emergence of SARS-CoV-2 Omicron (B.1.1.529) variant, salient features, high global health concerns and strategies to counter it amid ongoing COVID-19 pandemic

DOI: 10.1016/j.envres.2022.112816

Year: 2022

Twin combination of Omicron and Delta variants triggering a tsunami wave of ever high surges in COVID‐19 cases: A challenging global threat with a special focus on the Indian subcontinent

DOI: 10.1002/jmv.27585

Year: 2022

In silico analysis for the repurposing of broad-spectrum antiviral drugs against multiple targets from SARS-CoV-2: A molecular docking and ADMET approach

DOI: 10.21203/rs.3.rs-1242644/v1

Year: 2022

Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition)1

DOI: 10.1080/15548627.2020.1797280

Year: 2021

Leucine encoding codon TTG shows an inverse relationship with GC content in genes involved in neurodegeneration with iron accumulation.

DOI: 10.31083/j.jin2004092

Year: 2021

Insight into Codon Utilization Pattern of Tumor Suppressor Gene EPB41L3 from Different Mammalian Species Indicates Dominant Role of Selection Force

DOI: 10.3390/cancers13112739

Year: 2021

Identification of other Cellular Receptors for Edema Factor of Bacillus anthracis by Independent Inhibition of Protective Antigen Evidenced by Inhibition of Embryo Growth and Angiogenesis.

DOI: 10.22092/ARI.2021.355959.1756

Year: 2021

Genes Common in Primary Immunodeficiencies and Cancer Display Overrepresentation of Codon CTG and Dominant Role of Selection Pressure in Shaping Codon Usage

DOI: 10.3390/biomedicines9081001

Year: 2021

How Does Oxford Nanopore Sequencing Detect Genetic Mutations?

Why Study CNVs?

What are Copy Number Variations (CNVs)?

Are There Potential Treatments Targeting Genetic Mutations?

What is Mutagenesis?

What Are the Limitations of Sanger Sequencing?

What Role Does Biotechnology Play in Agriculture?

Are There Any FDA-Approved Medications Specifically Designed for Genetic Mutations?

What are the types of inherited mutations?

How is the Delta F508 Mutation Diagnosed?

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