Mohammad Yahya Vahidi Mehrjardi
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Explore the profile of Mohammad Yahya Vahidi Mehrjardi including associated specialties, affiliations and a list of published articles.
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Citations
314
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Recent Articles
11.
Darabi Z, Seyed Hosseini S, Sarebanhassanabadi M, Jambarsang S, Vahidi Mehrjardi M, Hosseinzadeh M, et al.
Sci Rep
. 2023 Sep;
13(1):14608.
PMID: 37669998
Coronary artery disease (CAD) is one of the most important cardiovascular diseases. Lifestyle and genetic factors play important roles in the development of CAD. The aim of the study is...
12.
Dehghanian M, Yarahmadi G, Sandoghsaz R, Khodadadian A, Shamsi F, Vahidi Mehrjardi M
Adv Biomed Res
. 2023 Jun;
12:101.
PMID: 37288024
Background: Endometriosis is a female reproductive system disease in which the endometrial tissue is found in other women's organs. Various factors are effective in the development of endometriosis, and because...
13.
Darand M, Salehi-Abargouei A, Vahidi Mehrjardi M, Feizi A, Seyedhossaini S, Askari G
Front Nutr
. 2023 Feb;
9:1097411.
PMID: 36817064
Introduction: Considering the emergence of the concept of personalized nutrition in recent years and its importance in the treatment of diseases, the purpose of this study was to investigate the...
14.
Darand M, Salehi-Abargouei A, Vahidi Mehrjardi M, Feizi A, Seyedhossaini S, Askari G
Front Cardiovasc Med
. 2023 Feb;
9:1037940.
PMID: 36741829
Introduction: The present study aimed to investigate the association of the paraoxonase 1 (PON1) Q192R polymorphism with coronary artery disease (CAD) and cardiometabolic risk factors in Iranian patients suspected of...
15.
Yarahmadi G, Dehghanian M, Sandoghsaz R, Savaee M, Shamsi F, Vahidi Mehrjardi M
Eur J Obstet Gynecol Reprod Biol X
. 2022 Dec;
17:100173.
PMID: 36506347
[This corrects the article DOI: 10.1016/j.eurox.2022.100152.].
16.
Yarahmadi G, Fazeli J, Dehghanian M, Vahidi Mehrjardi M, Javaheri A, Kalantar S
Eur J Obstet Gynecol Reprod Biol
. 2022 Aug;
277:12-15.
PMID: 35970002
Background: Endometriosis is a common gynecological condition with a substantial economic burden on society. It is known that both genetic and environmental factors are contributing to the phenotypic development of...
17.
Kaiyrzhanov R, Perry L, Rocca C, Zaki M, Hosny H, Moreno C, et al.
Ann Clin Transl Neurol
. 2022 Jul;
9(9):1465-1474.
PMID: 35869884
Ultra-rare biallelic pathogenic variants in geranylgeranyl diphosphate synthase 1 (GGPS1) have recently been associated with muscular dystrophy/hearing loss/ovarian insufficiency syndrome. Here, we describe 11 affected individuals from four unpublished families...
18.
Christensen M, Levy A, Mohammadi N, Niceta M, Kaiyrzhanov R, Dentici M, et al.
Clin Genet
. 2022 May;
102(2):98-109.
PMID: 35616059
Biallelic variants of the gene encoding for the zinc-finger protein 142 (ZNF142) have recently been associated with intellectual disability (ID), speech impairment, seizures, and movement disorders in nine individuals from...
19.
Yarahmadi G, Dehghanian M, Sandoghsaz R, Savaee M, Shamsi F, Vahidi Mehrjardi M
Eur J Obstet Gynecol Reprod Biol X
. 2022 May;
15:100152.
PMID: 35586752
Background: Endometrios affecting 6-10% of women of reproductive ages around the globe. Important pathways, including the MAPK and PI3K / Akt pathways, have been identified in the disease. The NF1...
20.
Yazdanpanah Z, Kazemipour N, Kalantar S, Vahidi Mehrjardi M
Physiol Rep
. 2022 Jan;
10(2):e15163.
PMID: 35076188
Type 2 diabetes mellitus (T2DM) is a heritable metabolic perturbation, rapidly growing across the world. Primary recognition of susceptible individuals with a family history of type 2 diabetes (FHD) in...