Shayan Khalili Alashti

A passionate and accomplished researcher with a strong background in Medical Genetics, Microbiology, and a proven track record of contributing to various publications. My expertise encompasses skills in molecular and cellular genetics, systems biology, bioinformatics, and NGS. Seeking to leverage expertise in neurological diseases, gene editing, and infertility genetics to make a meaningful impact in the field of medical sciences.

Living in : Iran

Gender : MaleRace : No Response

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Academic Profile

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Educations

Human GeneticsMaster'sShiraz University of Medical Sciences2020-08-31 Iran

Supervisor's name :Dr. Majid Fardaei

Title :

CRISPR/Cas9 knock‐in toward creating a Rett syndrome cell model with a synonymous mutation in the MECP2 gene

Work Experiences

Molecular Genetic Clinic

at Bayan Gene Pars

I am currently working in this role

Conferences

Your Presentation Title :

CRISPR workshop at Tehran University of Medical Sciences, Tehran, Iran

Conference Name :CRISPR workshop

Iran

2020

Your Presentation Title :

International Congress of Isfahan 020, Isfahan, Iran

Conference Name :Biomedical Sciences

Iran

2020

Journal Publications

Publication Title :

CRISPR/Cas9 knock‐in toward creating a Rett syndrome cell model with a synonymous mutation in the MECP2 geneFirst author

Journal :

Journal of Gene Medicine

Link :

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Publication Title :

Recurrent pregnancy loss in the female with a heterozygous mutation in KHDC3L geneSecond author

Journal :

Gene Reports

Link :

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Publication Title :

Escherichia coli cytosine deaminase: Structural and biotechnological aspectsFourth author

Journal :

Biotechnology and Applied Biochemistry

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Publication Title :

Exploration of the influence of KHDC3L gene knock-out by CRISPR/Cas9 technology on PEG3 promoterSecond author

Link :

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Publication Title :

Two novel mutations in the MECP2 gene in patients with Rett syndromeFirst author

Journal :

Gene

Link :

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Publication Title :

A Meta-Analysis of Microarray Datasets to Identify Biological Regulatory Networks in Alzheimer's DiseaseCorresponding author

Journal :

Frontiers in Genetics

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Publication Title :

The FOXG1-related syndrome with two novel mutations in the FOXG1 geneFirst author

Journal :

Gene Reports

Link :

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Research Keywords

bioinformatic

systems biology

crispr

Molecular Genetic

medical genetic

NIPT

Microarray analysis

Next generation sequencing

Awards

First Rank Student in UniversityMaster

References

Majid Fardaei

mfardaei@gmail.com

Majid Yavarian

majid.yavarian@gmail.com