majid mojarrad

About majid mojarrad

majid mojarrad, With an exceptional h-index of 22 and a recent h-index of 19 (since 2020), a distinguished researcher at Mashhad University of Medical Sciences,

His recent articles reflect a diverse array of research interests and contributions to the field:

Design principles of a novel construct for HBB gene-editing and investigation of its gene-targeting efficiency in HEK293 cells

Characterizing Homozygous Variants in Bardet-Biedl Syndrome-Associated Genes Within Iranian Families: Unveiling a Founder Variant in BBS2, c.471G>A

Bi-allelic genetic variants in the translational GTPases GTPBP1 and GTPBP2 cause a distinct identical neurodevelopmental syndrome

Wortmannin Inhibits Cell Growth and Induces Apoptosis in Colorectal Cancer Cells by Suppressing the PI3K/AKT Pathway.

Identification of a novel mutation of PDGFC gene in a girl with non-syndromic cleft lip and palate

CRISPR-Based Fluorescent Reporter (CBFR) Assay for Sensitive, Specific, Inexpensive, and Visual Detection of a Specific EGFR Exon 19 Deletion in NSCLC

Recent Advances in CRISPR/Cas9 Delivery Approaches for Therapeutic Gene Editing of Stem Cells

New advancements in CRISPR based gene therapy of Duchenne muscular dystrophy

majid mojarrad Information

University

Position

Department of Medical Genetics School of Medicine

Citations(all)

1652

Citations(since 2020)

1280

Cited By

799

hIndex(all)

22

hIndex(since 2020)

19

i10Index(all)

53

i10Index(since 2020)

39

Email

University Profile Page

Mashhad University of Medical Sciences

Google Scholar

View Google Scholar Profile

Top articles of majid mojarrad

Title

Journal

Author(s)

Publication Date

Design principles of a novel construct for HBB gene-editing and investigation of its gene-targeting efficiency in HEK293 cells

Molecular Biotechnology

Malihe Lotfi

Atefeh Ashouri

Majid Mojarrad

Sina Mozaffari-Jovin

Mohammad Reza Abbaszadegan

2024/3

Characterizing Homozygous Variants in Bardet-Biedl Syndrome-Associated Genes Within Iranian Families: Unveiling a Founder Variant in BBS2, c.471G>A

Biochemical Genetics

Masoumeh Heidari Feizabadi

Masoome Alerasool

Atieh Eslahi

Emran Esmaeilzadeh

Mohammad Yahya Vahidi Mehrjardi

...

2024/2/26

Bi-allelic genetic variants in the translational GTPases GTPBP1 and GTPBP2 cause a distinct identical neurodevelopmental syndrome

The American Journal of Human Genetics

Vincenzo Salpietro

Reza Maroofian

Maha S Zaki

Jamie Wangen

Andrea Ciolfi

...

2024/1/4

Wortmannin Inhibits Cell Growth and Induces Apoptosis in Colorectal Cancer Cells by Suppressing the PI3K/AKT Pathway.

Anti-cancer Agents in Medicinal Chemistry

Nastaran Bani

Farzad Rahmani

Neda Shakour

Forouzan Amerizadeh

Ghazaleh Khalili-Tanha

...

2024/4/4

Identification of a novel mutation of PDGFC gene in a girl with non-syndromic cleft lip and palate

Gene

Maryam Rahnama

Tahereh Movahedi

Atieh Eslahi

Nasrin Kaseb-Mojaver

Masoome Alerasool

...

2024/3/2

CRISPR-Based Fluorescent Reporter (CBFR) Assay for Sensitive, Specific, Inexpensive, and Visual Detection of a Specific EGFR Exon 19 Deletion in NSCLC

Molecular Biotechnology

Pouya Salehipour

Mojdeh Mahdiannasser

Ghazal Sedaghat Shayegan

Kimia Shankaie

Mina Tabrizi

...

2023/5

Recent Advances in CRISPR/Cas9 Delivery Approaches for Therapeutic Gene Editing of Stem Cells

Malihe Lotfi

Dorsa Morshedi Rad

Samaneh Sharif Mashhadi

Atefeh Ashouri

Majid Mojarrad

...

2023/11

New advancements in CRISPR based gene therapy of Duchenne muscular dystrophy

Atieh Eslahi

Farzaneh Alizadeh

Amir Avan

Gordon A Ferns

Meysam Moghbeli

...

2023/3/11

Investigation of genetic variants causing Bardet–Biedl syndrome in Iranian families: Identification of a founder mutation in BBS2, p. T157T

Masoumeh Heidari Feizabadi

Masoome Alerasool

Atieh Eslahi

Emran Esmaeilzadeh

Mohammad Yahya Vahidi Mehrjardi

...

2023/10/18

Identification of a Rare Mutation in the SRD5A2 Gene in an Iranian Family with Sex Development Disorder

Journal of Sciences, Islamic Republic of Iran

Atiyeh Ataei

Peyman Eshraghi

Atiyeh Eslahi

Zeinab Khazaei

Masoome Alerasool

...

2023/3/1

Isolation of plasma small extracellular vesicles by an optimized size-exclusion chromatography-based method for clinical applications

Journal of Drug Delivery Science and Technology

Samaneh Sharif

Sina Mozaffari-Jovin

Farzaneh Alizadeh

Majid Mojarrad

Hossein Baharvand

...

2023/9/1

Cannabis sativa ethanolic extract demonstrated significant anti-tumor effects associated with elevated expression of AXIN1 protein in glioblastoma U87-MG cell line

Gene Reports

Fatemeh Esfandiary

Aliakbar Rajabzadeh

Majid Mojarrad

Amir Delavar

Mohammad Soukhtanloo

2023/3/1

Broadening the phenotypic and molecular spectrum of FINCA syndrome: Biallelic NHLRC2 variants in 15 novel individuals

European Journal of Human Genetics

Henrike L Sczakiel

Max Zhao

Brigitte Wollert-Wulf

Magdalena Danyel

Nadja Ehmke

...

2023/8

Design of a rapid electrochemical biosensor based on MXene/Pt/C nanocomposite and DNA/RNA hybridization for the detection of COVID-19

Talanta

Monireh Bolourinezhad

Majid Rezayi

Zahra Meshkat

Saman Soleimanpour

Majid Mojarrad

...

2023/12/1

Lunapark deficiency leads to an autosomal recessive neurodevelopmental phenotype with a degenerative course, epilepsy and distinct brain anomalies

Brain Communications

Andrea Accogli

Maha S Zaki

Mohammed Al-Owain

Mansour Y Otaif

Adam Jackson

...

2023

Production of Duchenne muscular dystrophy cellular model using CRISPR-Cas9 exon deletion strategy

Molecular and Cellular Biochemistry

Farzaneh Alizadeh

Yousef Jafari Abraghan

Shima Farrokhi

Yasamin Yousefi

Yeganeh Mirahmadi

...

2023/6/8

Generation of Zebrafish Models of Human Retinitis Pigmentosa Diseases Using CRISPR/Cas9-Mediated Gene Editing System

Molecular Biotechnology

Farzaneh Mirzaei

Atiyeh Eslahi

Sareh Karimi

Farzaneh Alizadeh

Arash Salmaninejad

...

2023/11/19

MicroRNA-96: A therapeutic and diagnostic tumor marker

Hamid Reza Rahimi

Majid Mojarrad

Meysam Moghbeli

2022/1

Sensitive and specific clinically diagnosis of SARS-CoV-2 employing a novel biosensor based on boron nitride quantum dots/flower-like gold nanostructures signal amplification

Biosensors and Bioelectronics

Behnaz Hatamluyi

Majid Rezayi

Saeid Amel Jamehdar

Kobra Salimian Rizi

Majid Mojarrad

...

2022/7/1

CFTR mutations causing congenital unilateral absence of the vas deferens (CUAVD) and congenital absence of the uterus (CAU) in a consanguineous family

Asian Journal of Andrology

Mahdieh Daliri Ghouchanatigh

Ranjha Khan

Majid Mojarrad

Uzma Hameed

Muhammad Zubair

...

2022/7/1

See List of Professors in majid mojarrad University(Mashhad University of Medical Sciences)