Farzad Hashemi-Gorji

I am researcher of Human Genetics.

Living in : Iran

Gender : MaleRace : Middle Eastern

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Academic Profile

Posts

Contact Information

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Educations

GeneticsMaster'sIslamic Azad University Tehran Science & Research Branch2008-12-31 Iran

Supervisor's name :Dr. Noori-dalooii

Title :

Molecular identification of the most prevalent mutations of glucose-6-phosphate dehydrogenase (G6PD) in Fars and Isfahan of Iran

Cell And Molecular BiologyBachelor'sIslamic Azad University Tonekabon2006-01-31 Iran

Work Experiences

Research Assistant

at Genomic Research Center

I am currently working in this role

Research Assistant

at Pasteur institute of Iran

Start : 31-Dec-2009

End : 31-Mar-2011

English Scores

TOEFL31-Dec-2015

82/120Total

Reading :

20/30

Listening :

20/30

Speaking :

20/30

Writing :

22/30

GRE General03-Jul-2023

285/340Total

Verbal Reasoning :

141/170

Quantitative Reasoning :

140/170

Analytical Writing :

4/6

Journal Publications

Publication Title :

Alopecia areata-like pattern of baldness: the most recent update and the expansion of novel phenotype and genotype in the CTNNB1 geneCorresponding author

Journal :

Neurological Sciences

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Publication Title :

BRAT1–related disorders: phenotypic spectrum and phenotype-genotype correlations from 97 patientsCorresponding author

Journal :

European Journal of Human Genetics

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Publication Title :

Gnathodiaphyseal dysplasia with a novel genetic variant in a large family from IranThird author

Journal :

Molecular genetics & genomic medicine

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Publication Title :

Analysis of Cytogenetic Abnormalities in Iranian Patients with Syndromic Autism Spectrum Disorder: A Case SeriesThird author

Journal :

Iranian Journal of Child Neurology

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Publication Title :

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

Journal :

Neurological Sciences

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Publication Title :

Delineating the expanding phenotype of HERC2‐related disorders: The impact of biallelic loss of function versus missense variationCorresponding author

Journal :

Clinical Genetics

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Publication Title :

A novel SRD5A2 mutation in an Iranian family with sex development disorderFirst author

Journal :

Andrologia

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Publication Title :

Novel mutation in the MED23 gene for intellectual disability: A case report and literature reviewFirst author

Journal :

Clinical Case Reports

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References

Reza Mirfakhraie

reza_mirfakhraie@yahoo.com

Mohammad Miryounesi

miryounesi@gmail.com

Vahid Reza Yassaee

v.yassaee-grc@sbmu.ac.ir