Niken Satiti Nur Handayani - Genetic Mutations

Author Information

Niken Satiti Nur Handayani is affiliated with the Laboratory of Genetics and Breeding, Faculty of Biology, Universitas Gadjah Mada, Yogyakarta, Indonesia. She has made significant contributions to the field of genetics, particularly in the study of genetic mutations and their implications in various conditions such as thalassemia and nasopharyngeal carcinoma.

Research Contributions

Niken Satiti Nur Handayani's research primarily focuses on the molecular and haematological characteristics of genetic mutations. Her studies include detailed analyses of alpha-thalassemia deletions, splice-site and frameshift mutations of the β-globin gene, and the use of DNA barcoding for species identification. Additionally, she has explored the expression profiles of genes in response to infections and the genetic basis for biofilm formation in bacteria. Her work is pivotal for understanding genetic disorders and improving diagnostic techniques.

Aliases

Niken Satiti Nur Handayani is also known by other names including Niken Handayani and Niken Satuti Nur Handayani.

Publication and Citation Metrics

Metric	Value
Citation Count	109
h-Index	6
Paper Count	49

Publications:

Molecular and Haematological Characteristics of alpha-Thalassemia Deletions in Yogyakarta Special Region, Indonesia.

DOI: 10.52547/rbmb.10.3.346

Year: 2021

Splice-site and Frameshift Mutations of β-Globin Gene Found in Thalassemia Carrier Screening in Yogyakarta Special Region, Indonesia

DOI: 10.18585/INABJ.V13I1.1406

Year: 2021

The Use of DNA Barcoding and Phylogenetic Analysis to Improve Identification of Usnea spp. Based on ITS rDNA

DOI: 10.22146/JTBB.58635

Year: 2021

The Distribution of M2 Macrophage and Treg in Nasopharyngeal Carcinoma Tumor Tissue and the Correlation with TNM Status and Clinical Stage.

DOI: 10.31557/APJCP.2021.22.11.3447

Year: 2021

Insertion of cellulase gene in yeast expression vector (pYY1 and pWYH257 Plasmid) as a candidate for cellulosic ethanol-producing strain

DOI: 10.13057/BIODIV/D220532

Year: 2021

Detection of HBB:c.92+5G>C and HBB:c.108delC mutations in β-thalassemia carriers using high-resolution melting analysis

DOI: 10.1007/s11033-020-05625-x

Year: 2020

Physiological, biochemical and HSP70 and HSP90 gene expression profiles of tropical abalone Haliotis squamata in response to Vibrio alginolyticus infection

DOI: 10.22146/IJBIOTECH.51322

Year: 2020

Comparison Between Three Molecular Diagnostics for the Identification of Heterozygous Hemoglobin E.

DOI: 10.3923/pjbs.2020.17.26

Year: 2020

Kajian Molekular Tarsius sp. Pada Gen Penyandi Cytochrome Oxidase Sub-unit 2 Mitokondria

DOI: 10.24002/biota.v15i1.2653

Year: 2019

Differences among clinical isolates of Pseudomonas aeruginosa in their capability of forming biofilms and their susceptibility to antibiotics

DOI: 10.13057/BIODIV/D200538

Year: 2019

What is the Future of Genetic Research?

Can Genetic Mutations be Prevented or Repaired?

What is Phylogenetic Analysis?

How are Genetic Mutations Detected?

What is the Future of Genetic Data Analysis?

Which Genes Are Affected by Asbestos-Induced Mutations?

How Do Nucleotide Mutations Occur?

How is Data Collected in Populace Genomics?

What Are Some Common Developmental Disorders Linked to Genetic Mutations?

How Do Genetic Mutations Cause Developmental Disorders?

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