Genetics and genomic medicine in Iran

B Behnam, M Zakeri - Molecular Genetics & Genomic Medicine, 2019 - Wiley Online Library
1 BACKGROUND Iran (Persia; officially the Islamic Republic of Iran), is the 18th most
populous country (with over 81 million individuals) in the world (www. amar. org. ir). Iran is …

[HTML][HTML] Association between Genetic Variants Linked to Premature Ovarian Insufficiency and Inflammatory Markers: A Cross-Sectional Study

MR Mirinezhad, M Aghsizadeh… - … Journal of Fertility & …, 2024 - ncbi.nlm.nih.gov
Background: Premature menopause (PM) is the cessation of ovarian function before age 40.
PM women are more likely to have cardiovascular diseases (CVDs), diabetes, and mental …

[PDF][PDF] Genotype-Phenotype Correlation for Cystic Fibrosis According to Registry Center of Cystic Fibrosis.

M Rafeey, M Jabarpoor-Bonyadi, L Vahedi - Crescent Journal of Medical & …, 2020 - sid.ir
Objectives: The present study aimed to investigate the correlation of genotype-phenotype in
patients with cystic fibrosis (CF) in the Azeri-Turkish population, Iran. Materials and Methods …

Hematological Indices and Genetic Variants of Premature Ovarian Insufficiency: Machine Learning Approaches

MR Mirinezhad, M Aghasizadeh… - Cardiovascular & …, 2024 - benthamdirect.com
Background: Premature Ovarian Insufficiency (POI) is associated with infertility. Little is
known about the potential circulating biomarkers that could be used to predict POI. We have …

Association between the rs2241883 polymorphism of the fatty acid‐binding protein‐1 (FABP1) gene and obesity in a population of MASHAD study cohort

M Valizadeh, M Aghasizadeh, F Shaghi… - … Genetics & Genomic …, 2023 - Wiley Online Library
Abstract Background and Aims The fatty acid‐binding proteins (FABPs) gene
polymorphisms are related to several metabolic properties. We investigated the association …

[PDF][PDF] Prevalence of Cystic Fibrosis Trans-membrane Conductance Regulator Gene common mutations in children with cystic fibrosis in Isfahan, Iran

M Reisi, M Behnam, SJ Sayedi, F Salimi, P Kargar… - Int J Pediatr, 2019 - academia.edu
Background: Cystic fibrosis (CF) is the most common lethal genetic disorder of Cystic
Fibrosis Trans-membrane Conductance (CFTR) Regulator gene mutations. We aimed to …

[HTML][HTML] Clinical manifestation, laboratory findings, and outcome of children with cystic fibrosis over a 10-year period in South Iran

F Ziyaee, SM Dehghani, S Hosseini… - Egyptian Pediatric …, 2020 - Springer
Background Cystic fibrosis (CF) is a monogenic hereditary disease with diverse
complications, which substantially reduce the quality of life and longevity of patients. With …

[HTML][HTML] Novel CFTR mutations in two Iranian families with severe cystic fibrosis

M Mohseni, M Razzaghmanesh, EP Mehr… - Iranian biomedical …, 2016 - ncbi.nlm.nih.gov
Background: Cystic fibrosis (CF) is a common autosomal recessive disorder that affects
many body systems and is produced by mutations in the cystic fibrosis transmembrane …

Identification of a mutation in the novel compound heterozygous CFTR in a Chinese family with cystic fibrosis

H Shao, J Hua, Q Wu, X Li, M Zhang… - Canadian …, 2020 - Wiley Online Library
Cystic fibrosis (CF) is one of the most common autosomal recessive disorders among
Caucasians of Northern European descent but is uncommon in the Chinese population …

Following the Trace of HVS II Mitochondrial region within the nine Iranian ethnic groups based on genetic population analysis

A Shasttiri, M Moridi, A Safari, SHA Raza… - Biochemical …, 2022 - Springer
The Iranian gene pool is seen as an important human genetic resource for investigating the
region connecting Mesopotamia and the Iranian plateau. The main objective of this study …