Alireza Pasdar
Overview
Explore the profile of Alireza Pasdar including associated specialties, affiliations and a list of published articles.
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Articles
101
Citations
1046
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Recent Articles
1.
Ardehaie R, Eslahi A, Alerasool M, Rad E, Shoeibi N, Sedaghat M, et al.
Clin Genet
. 2025 Jan;
107(3):300-310.
PMID: 39761966
Inherited retinal diseases (IRDs) may have significant diagnostic challenges due to their genetic complexity and diverse inheritance patterns. Advanced genotyping tools like exome sequencing (ES) offer promising opportunities for identifying...
2.
Azimi S, Sadegh Nia H, Bahrami N, Dargahi H, Jamaati H, Pasdar A, et al.
Tanaffos
. 2024 Dec;
23(1):58-64.
PMID: 39703445
Background: Cancer is a disease caused by manifestation and abnormal gene expression. Many of the genes that inhibit cancer by the microRNAs. The aim of this study was to investigate...
3.
Shamshiri A, Amerizadeh F, Navaei Z, Pasdar A
Iran J Public Health
. 2024 Dec;
53(11):2440-2450.
PMID: 39619899
Background: Background: Hepatitis virus infections are among the serious emerging health issues. They are the primary causes of cirrhosis and hepatocellular carcinoma. Growing evidence shows a link between certain genomic...
4.
Mirinezhad M, Bana H, Aghsizadeh M, Mohammadi M, Ghazizadeh H, Dabagh A, et al.
Cardiovasc Hematol Agents Med Chem
. 2024 Nov;
PMID: 39506439
Background: Premature menopause (PM) is defined as the end of ovulation before the age of 40 years, a condition commonly referred to as primary ovarian insufficiency. It has been shown...
5.
Alerasool M, Eslahi A, Vona B, Kahaei M, Mojaver N, Rajati M, et al.
Clin Genet
. 2024 Aug;
106(6):693-701.
PMID: 39107234
Hearing loss is one of the most prevalent genetic disorders in humans. Locus and allelic heterogeneity cause fundamental challenges in hearing loss genetic diagnosis and management of patients and their...
6.
Mirinezhad M, Aghasizadeh M, Ghazizadeh H, Hemmatpur A, Mashhadi M, Khedmatgozar H, et al.
Cardiovasc Hematol Disord Drug Targets
. 2024 Jun;
24(2):98-109.
PMID: 38910412
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 investigated the possible association...
7.
Rahpeyma M, Sabermoghaddam A, Kiarudi M, Aghabozorgi A, Pasdar A
J Curr Ophthalmol
. 2024 Apr;
35(3):216-225.
PMID: 38681684
Purpose: To look for causative genetic mutations in a series of Iranian families with strabismus. In addition, we systematically reviewed all the published articles regarding the role of genetic variations...
8.
Mirinezhad M, Aghsizadeh M, Fazl Mashhadi M, Moazedi S, Mohammadi Bajgiran M, Ghazizadeh H, et al.
Int J Fertil Steril
. 2024 Feb;
18(2):100-107.
PMID: 38368511
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 disorders. This is the...
9.
Mirinezhad M, Aghsizadeh M, Ghazizadeh H, Ghoflchi S, Bidary M, Naghipour A, et al.
BMC Womens Health
. 2024 Feb;
24(1):91.
PMID: 38311764
Background And Aim: premature ovarian insufficiency (POI) is defined as the menopause before 40 years of age, and its prevalence is reported to be two-fold higher in Iranian women than...
10.
Ghadamgahi S, Hosseinzadeh L, Ardalan Khales S, Nassiri M, Alidoust M, Etemadrezaei S, et al.
Iran J Med Sci
. 2023 Dec;
48(6):551-562.
PMID: 38094285
Background: Despite suggesting many genetic risk markers as the outcome of Genome-wide association studies (GWAS) for breast cancer, replicating the results in different populations has remained the main issue. In...