NO.

Article

Authors

Year

Journal

۱

Determination of Fetal Abnormalities in Pregnancies Leading to Legal Abortion in Golestan Province (۲۰۱۸-۱۹)

A Mehrara, A Mirfazeli, MJ Golalipour

۲۰۲۳

Journal of Gorgan University of Medical Sciences

۲

Curcumin can improve ecstasy-induced hippocampal damage in rat

Z Nazari, K Bahrehbar, H Sepehri, MJ Golalipour

۲۰۲۳

Toxicology and Environmental Health Sciences

۳

Dysregulation of long non-coding RNA Rian expression in the brain of memory-impaired diabetic mice

R Safari, N Sanchooli, MJ Golalipour, H Sepehri, M Golalipour

۲۰۲۳

۴

Effect of induced diabetes on morphometric indexes of the cerebellar cortex and gene expression in C۵۷BL mice

S Sharifi, M Golalipour, S Ghafari, R Safari, MJ Golalipour

۲۰۲۳

Iranian Journal of Basic Medical Sciences

۵

Gestational diabetes mellitus increased the number of dopaminergic neurons in the olfactory bulb of rat offspring

Z Nazari, K Bahrehbar, S Ghafari, MJ Golalipour

۲۰۲۳

Iranian Journal of Basic Medical Sciences

۶

An overview of miRNAs role in neurofibromatosis type ۲
 

N Rezaie, T Khosravi, A Vahidi, M Oladnabi

۲۰۲۳

Health Biotechnology and Biopharma (HBB)

۷

The Molecular Pathogenesis, Diagnostic Criteria, Symptoms, Clinical Manifestations, and Gene-Based Therapeutic Approaches in Neurofibromatosis

F Shahraki, M Oladnabi

۲۰۲۳

Journal of Gorgan University of Medical Sciences

۸

Whole exome sequencing identifies a novel variant in the COL۱۲A۱ gene in a family with Ullrich congenital muscular dystrophy ۲

Karim Naghipoor, Teymoor Khosravi, Morteza Oladnabi

۲۰۲۳

۹

Frequency of c.۳۵delG Mutation in GJB۲ gene in Patients with Autosomal Recessive Non-Syndromic Hearing Loss of Five Ethnic Groups in Golestan, Iran

M Hajilari, A Sharifinya, T Khosravi, A Kianmehr, MH Taziki, A Khosravi, ...

۲۰۲۳

International Journal of Pediatrics

۱۰

A novel biallelic ۱۹-bp deletion in the IL۱۰RB gene caused infant-onset inflammatory bowel disease in a consanguineous family: a molecular docking simulation study and …
 

Farzaneh Motallebi,Zainab M Al Sudani,Fatemeh Vaghefi,Teymoor Khosravi ...

۲۰۲۴

Molecular Biology Reports

۱۱

Hearing Loss Among Families with ۲ and More Affected Members in Golestan Province, Iran: A Cross-Sectional Study of ۳۲۰ Families

Zainab M. Al Sudani , Teymoor Khosravi

۲۰۲۴

The Journal of International Advanced Otology

۱۲

In silico analysis of mutation spectrum of Ehlers–Danlos, osteogenesis imperfecta, and cutis laxa overlapping phenotypes in Iranian population

Teymoor Khosravi, Karim Naghipoor, Fatemeh Vaghefi, Ali Mohammad Falahati

۲۰۲۴

Egyptian Journal of Medical Human Genetics

۱۳

Effects of Interleukin-۱۰ (-۱۰۸۲/-۸۱۹) and Interleukin-۶ (-۱۷۴) Gene Polymorphisms on Corpus Callosum Changes in Women with Multiple Sclerosis

M Abolghazi, M Shahbazi, MJ Golalipour

۲۰۲۴

Journal of Gorgan University of Medical Sciences

۱۴

Impact of Mild Gestational Diabetes Mellitus on Maternal and Fetal Liver Histopathological Alterations

SA Khales, A Mafinezhad, M Golalipour, G Roshandel, S Ghafari, ...

۲۰۲۴

Journal of the Anatomical Society of India

۱۵

Prevalence of Neural Tube Defects Following Flour Fortification with Folic Acid in North Iran
 

M Barzegar, G Veghari, N Kaviany, E Golalipour, MJ Golalipour

۲۰۲۴

IJ Pediatrics

۱۶

Congenital Malformations of the Digestive System in Northern Iran (۲۰۱۸-۱۹).

SA Khales, MA Vakili, MJ Golalipour

۲۰۲۴

Iranian Journal of Neonatology

۱۷

Effect of mild gestational diabetes mellitus on histological, ultrastructural, and quantitative morphometric alterations of rat fetal liver

SA Khales, A Mafinezhad, M Golalipour, G Roshandel, S Ghafari, ...

۲۰۲۴

ranian Journal of Basic Medical Sciences

۱۸

Second report of TEDC۱-related microcephaly caused by a novel biallelic mutation in an Iranian consanguineous family

A Sarli, ZM Al Sudani, F Vaghefi, F Motallebi, T Khosravi, N Rezaie, ..

۲۰۲۴

Molecular Biology Reports

۱۹

To what extent does ChatGPT understand genetics?
 

T Khosravi, ZM Al Sudani, M Oladnabi

۲۰۲۴

Innovations in Education and Teaching International

۲۰

The Role of Genetic Counseling in the Prevention of Intellectual Disability and Deafness: Two Common Disabilities in Iran
 

F Shahraki, M Oladnabi

۲۰۲۴

Journal of Gorgan University of Medical Sciences

۲۱

A comprehensive in silico analysis of mutation spectrum of maple syrup urine disease (MSUD) genes in Iranian population
 

Nahid Rezaie,Saeedeh Sadat Ghazanfari,Teymoor Khosravi,Fatemeh Vaghefi

۲۰۲۴

Molecular Biology Research Communications

۲۲

A Rare Combination of Compound Heterozygous Mutations in PAH Gene in Three Unrelated Consanguineous Iranian Families with Classical Phenylketonuria

Arian Rahimzadeh,Teymoor Khosravi,Farzaneh Motallebi ,Zainab M. Al Sudani ...

۲۰۲۴

Advanced Biomedical Research

۲۳

Identification of Novel and Known Genetic Variants Associated with Hereditary Hearing Loss in Iranian Families Using Whole Exome Sequencing
 

Nahid Rezaie,Nader Mansour Samaei

۲۰۲۴

Molecular Biology Reports