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Hossein Jafari Khamirani

Hossein Jafari Khamirani currently works at the Comprehensive Medical Genetics Center, Shiraz University of Medical Sciences. His main current project is "investigations towards human genome variation and rare genetic diseases." He also has a strong interest in targeted genome editing and CRISPR delivery approaches.

Living in : Iran

Gender : MaleRace : Middle Eastern

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Academic Profile

Posts

Contact Information

-Email

HosseinJafariApplyChance Link

Educations

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

Supervisor's name :Alireza Dastgheib/ Mehdi Dianatpour/ Hossein Heli

Title :

Elimination of Beta 2 Microglobulin expression toward producing HLA class1 deficient cells by CRISPR/CAS9 system and utilizing polymeric nanoparticle as a delivery system for transfection to target cells in order to produce HLA Class I free cell lines

Molecular And Cell Biology And GeneticsBachelor'sUniversity of Isfahan2016-08-08 Iran

Work Experiences

Research assistant

at Medical Genetic Center

I am currently working in this role

Lab Supervisor

at Medical Genetic Center

I am currently working in this role

English Scores

TOEFL14-Apr-2023

101/120Total

Reading :

25/30

Listening :

25/30

Speaking :

26/30

Writing :

26/30

Conferences

Your Presentation Title :

Current and future perspectives of liquid biopsies in genomics-driven oncology

Conference Name :Medical and Human genetics

Iran

2019

Your Presentation Title :

Circular RNAs in cancer

Conference Name :Novel Insights in Genetics

Iran

2019

Journal Publications

Publication Title :

A pathogenic variant of TULP3 causes renal and hepatic fibrocystic diseaseFirst author

Journal :

Frontiers in Genetics

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Publication Title :

Phenotype of ST3GAL3 Deficient Patients: a Case and Review of the LiteratureFirst author

Journal :

European Journal of Medical Genetics

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Publication Title :

An analysis of inhibition of the severe acute respiratory syndrome coronavirus 2 RNA-dependent RNA polymerase by zinc ion: an in silico approachSecond author

Journal :

Future Virology

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Publication Title :

Clinical features of patients with Yin Yang 1 deficiency causing Gabriele‐de Vries syndrome: A new case and review of the literatureFirst author

Journal :

Annals of Human Genetics

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Publication Title :

Exome sequencing identified a de novo frameshift pathogenic variant of CTBP1 in an extremely rare case of HADDTSFirst author

Journal :

Journal of Genetics

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Publication Title :

Phenotypic spectrum of autosomal recessive Keratitis-Ichthyosis-Deafness Syndrome (KIDAR) due to mutations in AP1B1Second author

Journal :

European Journal of Medical Genetics

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Publication Title :

A novel non-sense mutation in TDP2 causes spinocerebellar ataxia autosomal recessive 23 accompanied by bilateral upward gaze; report of a case and review of the literatureSecond author

Journal :

European Journal of Medical Genetics

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Publication Title :

Clinical Features of Okur-Chung Neurodevelopmental Syndrome: Case Report and Literature ReviewFirst author

Journal :

Molecular Syndromology

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Publication Title :

A novel frameshift pathogenic variant in ST3GAL5 causing salt and pepper developmental regression syndrome (SPDRS): A case reportThird author

Journal :

Human Genome Variation

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Publication Title :

A novel PTRH2 missense mutation causing IMNEPD: a case reportFirst author

Journal :

Human Genome Variation

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Publication Title :

MCM2 mutation causes autosomal dominant nonsyndromic hearing loss (DFNA70): novel variant in the second familyFourth author

Journal :

Journal of Genetics

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Publication Title :

Genotypic and phenotypic spectrum of Myofibrillar Myopathy 7 as a result of Kyphoscoliosis Peptidase deficiency: The first description of a missense mutation in KY and literature reviewSecond author

Journal :

European Journal of Medical Genetics

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Publication Title :

A combination of two novels homozygous FCSK variants cause disorder of glycosylation with defective fucosylation: New patient and literature review.Third author

Journal :

European Journal of Medical Genetics

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Publication Title :

Recurrent Infections and Immunodeficiency Caused by Severe Pancytopenia Associated with a Novel Life-Threatening Mutation in Hypoxia-Upregulated Protein 1First author

Journal :

Immunological Investigations

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Publication Title :

NRXN3 mutations cause developmental delay, movement disorder, and behavioral problems: CRISPR edited cells based WES resultsSecond author

Journal :

Gene

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Publication Title :

ZNF142 mutation causes neurodevelopmental disorder with speech impairment and seizures: Novel variants and literature reviewSecond author

Journal :

European Journal of Medical Genetics

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Publication Title :

Intronic OTOF mutation causes an atypical splicing defect resulting in auditory neuropathy spectrum disorderSecond author

Journal :

Journal of Genetics

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Publication Title :

The third patient of ACACA-related acetyl-CoA carboxylase deficiency with seizure and literature reviewSecond author

Journal :

European Journal of Medical Genetics

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Publication Title :

Analysis of DYRK1B, PPARG, and CEBPB Expression Patterns in Adipose-Derived Stem Cells from Patients Carrying DYRK1B R102C and Healthy Individuals During AdipogenesisSecond author

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Publication Title :

LIMA1 Gene Knockout by CRISPR/Cas9 System Using Lentiviruses as an in Vitro Model for Reducing Cholesterol AbsorptionFourth author

Journal :

International Cardiovascular Research Journal

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Publication Title :

EPS8 variant causes deafness, autosomal recessive 102 (DFNB102) and literature reviewSecond author

Journal :

Human Genome Variation

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Awards

First Rank Student in UniversityMaster

KonkourArshad4th Rank 2016-06-06