Reza Mirfakhraie - Genetic Mutations

Author Information

Reza Mirfakhraie is affiliated with the Department of Medical Genetics at the School of Medicine, Shahid Beheshti University of Medical Sciences, located in Tehran, Iran. His work is primarily focused on the field of genetics, with a particular interest in understanding the genetic basis of various diseases and conditions.

Research Contributions

Reza Mirfakhraie has made significant contributions to the field of genetics through his research on a wide range of topics. His recent work includes the study of circular RNAs as biomarkers for spermatogenesis defects and male infertility, the impact of CFAP44 expression on sperm motility, and the identification of novel mutations in the CTNNB1 gene related to intellectual disability. Additionally, he has explored the roles of FOXC1/FOXCUT/DANCR axis in triple negative breast cancer, investigated the immunomodulatory properties of mesenchymal stem cells in Graft Versus Host Disease management, and examined the emerging roles of long non-coding RNAs in uterine leiomyoma pathogenesis. His research also delves into genetic variants related to colorectal cancer, the role of CREBBP in preeclampsia, and genetic sequencing in Usher syndrome and non-syndromic hearing loss.

Aliases

Reza Mirfakhraie is also known by the aliases R Mirfakhraie and R. Mirfakhraie, which are used in various publications and academic references.

Publication and Citation Metrics

Metric	Count
Total Number of Papers	173
Total Citation Count	1595
h-index	22

Publications:

Circular RNAs: Novel Biomarkers in Spermatogenesis Defects and Male Infertility

DOI: 10.1007/s43032-022-00885-3

Year: 2022

Reduced expression of CFAP44 and CFAP44-AS1 may affect sperm motility and morphology.

DOI: 10.1111/and.14447

Year: 2022

Identification of a novel de novo mutation in the CTNNB1 gene in an Iranian patient with intellectual disability

DOI: 10.1007/s10072-022-05904-4

Year: 2022

The role of FOXC1/FOXCUT/DANCR axis in triple negative breast cancer: a bioinformatics and experimental approach.

DOI: 10.1007/s11033-021-07093-3

Year: 2022

Highlighting the interaction between immunomodulatory properties of mesenchymal stem cells and signaling pathways contribute to Graft Versus Host Disease management

DOI: 10.1016/j.trim.2021.101524

Year: 2022

Emerging Roles of Long Non-coding RNAs in Uterine Leiomyoma Pathogenesis: a Review

DOI: 10.1007/s43032-021-00571-w

Year: 2021

DACT1 variants and colorectal cancer

DOI: 10.1080/09674845.2021.1914919

Year: 2021

Long noncoding RNA LINC00978 acts as a potential diagnostic biomarker in patients with colorectal cancer.

DOI: 10.1016/j.yexmp.2021.104666

Year: 2021

CREB-binding protein (CREBBP) and preeclampsia: a new promising target gene.

DOI: 10.1007/s11033-021-06215-1

Year: 2021

Targeted sequencing of CDH23 and GJB2 genes in an Iranian pedigree with Usher syndrome and non-syndromic hearing loss

DOI: 10.1016/J.GENREP.2021.101149

Year: 2021

Can Genetic Disorders Affect Child Development?

Is Autism Spectrum Disorder Genetic?

What are the Current Therapeutic Innovations?

How is Hemoglobin Electrophoresis Used in Clinical Practice?

What are Mutant Crop Varieties?

How Do Epigenetics Influence Development?

Why are Induced Mutations Important in Research?

What is Gene Amplification?

How Does Biotechnology Impact Environmental Conservation?

How is the Regulatory Framework for Genetic Mutations in Agriculture?

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