M J Nazemi Tabrizi - Genetic Mutations

Author Information

Mina Tabrizi is a distinguished researcher in the field of Genetics, currently affiliated with the Department of Medical Genetics at the School of Medicine, Tehran University of Medical Sciences, Tehran, Iran. Her research encompasses a wide range of topics within genetics, including gene expression, genetic mutations, and non-invasive prenatal diagnostics.

Research Contributions

Mina Tabrizi has made significant contributions to the field of genetics through her research on various topics such as hypoxia-related gene expression in brain tumors, androgen receptor mutations in sex development disorders, and the role of genes in schizophrenia. She has also explored innovative approaches in non-invasive prenatal diagnosis of Down syndrome and vaccine development against tuberculosis. Her work is characterized by its interdisciplinary approach, combining molecular genetics with clinical insights.

Aliases

Mina Tabrizi is also known by other names, including M J Nazemi Tabrizi and M Tabrizi. These aliases are often used interchangeably in academic publications and citations.

Publication and Citation Metrics

Metric	Value
Citation Count	1822
h-index	25
Paper Count	47

Publications:

Differential expression of hypoxia-related genes in primary brain tumors and correlation with clinicopathological data of patients.

DOI: 10.1016/j.wneu.2021.07.068

Year: 2021

In Memoriam Professor Dr. Javad Tavakkoly Bazzaz M.D., Ph.D. (1966 - 2020)

DOI: 10.5812/jhgg.120343

Year: 2021

Molecular investigation of mutations in androgen receptor and 5‐alpha‐reductase‐2 genes in 46,XY Disorders of Sex Development with normal testicular development

DOI: 10.1111/and.13250

Year: 2019

Catechol-O-methyltransferase gene expression in stress-induced and non-stress induced schizophrenia

DOI: 10.1097/YPG.0000000000000243

Year: 2019

Modified methylated DNA immunoprecipitation protocol for noninvasive prenatal diagnosis of Down syndrome

DOI: 10.1111/jog.13577

Year: 2018

Specific immune responses induced by multi-epitope DNA derived from Mycobacterium tuberculosis DosR antigens.

DOI: 10.1556/030.65.2018.019

Year: 2018

Healthy Adult LDL-C Bears Reverse Association with Serum IL-17A Levels

DOI: 10.2174/2213988501812010001

Year: 2018

Association of transcription factor 4 (TCF4) gene mRNA level with schizophrenia, its psychopathology, intelligence and cognitive impairments

DOI: 10.1080/01677063.2017.1396330

Year: 2017

Designing a Novel Multi-epitope DNA- Based Vaccine Against Tuberculosis: In Silico Approach

DOI: 10.5812/JJM.43950

Year: 2017

Very early onset inflammatory bowel disease: Investigation of the IL-10 signaling pathway in Iranian children.

DOI: 10.1016/j.ejmg.2017.08.016

Year: 2017

How Do Nucleotide Mutations Occur?

What is a Synonymous Mutation?

What Causes Sickle Cell Anemia?

How Do Inherited Mutations Occur?

What is Polyploidy?

What Are the Treatment Options for Hemophilia?

How are BRCA1 and BRCA2 Mutations Inherited?

How Do Genetic Mutations Cause Developmental Disorders?

How do Duplications Occur?

How Do Point Mutations Occur?

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