Neda Kamal

Neda kamal main current project is "investigations towards human genome variation and rare genetic diseases." She also has a strong interest in targeted genome editing and CRISPR .

Living in : Iran

Gender : FemaleRace : Middle Eastern

0Followers 0Following

Academic Profile

Posts

Contact Information

-Email

NedaKamalApplyChance Link

Educations

Human GeneticsMaster'sShiraz University of Medical Sciences2022-09-15 Iran

Title :

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

Molecular And Cellular BiologyBachelor'sIslamic Azad University Tehran Medical Sciences2017-09-15 Iran

Conferences

Your Presentation Title :

Autism Spectrum Disorder

Conference Name :behavior problems

Iran

2021

Your Presentation Title :

Mitochondrial genome editing

Conference Name :gene therapy

Iran

2020

Journal Publications

Publication Title :

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

Journal :

Gene

Link :

View Link

Publication Title :

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

Journal :

European Journal of Medical Genetics

Link :

View Link

Publication Title :

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

Journal :

Annals of Human Genetics

Link :

View Link

Publication Title :

Phenotypic spectrum of autosomal recessive Keratitis-Ichthyosis-Deafness Syndrome (KIDAR) due to mutations in AP1B1Fourth author

Journal :

European Journal of Medical Genetics

Link :

View Link

Publication Title :

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

Journal :

Journal of Genetics

Link :

View Link

Publication Title :

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

Journal :

European Journal of Medical Genetics

Link :

View Link

Publication Title :

A novel nonsense variant in the ATL3 gene is associated with disturbed pain sensitivity, numbness of distal limbs and muscle weaknessFourth author

Journal :

Annals of Human Genetics

Link :

View Link

Publication Title :

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

Journal :

European Journal of Medical Genetics

Link :

View Link

Awards

First Rank Student in UniversityMaster

28th Rank 28th Rank 2019-08-31