Search details
1.
Homozygous Missense Variants in NTNG2, Encoding a Presynaptic Netrin-G2 Adhesion Protein, Lead to a Distinct Neurodevelopmental Disorder.
Am J Hum Genet
; 105(5): 1048-1056, 2019 11 07.
Article
in English
| MEDLINE | ID: mdl-31668703
2.
Biallelic variants in ZNF142 lead to a syndromic neurodevelopmental disorder.
Clin Genet
; 102(2): 98-109, 2022 08.
Article
in English
| MEDLINE | ID: mdl-35616059
3.
Novel variants underlying autosomal recessive neurodevelopmental disorders with intellectual disability in Iranian consanguineous families.
J Clin Lab Anal
; 36(2): e24241, 2022 Feb.
Article
in English
| MEDLINE | ID: mdl-35019165
4.
Molecular biomarkers in diabetes mellitus (DM).
Med J Islam Repub Iran
; 34: 28, 2020.
Article
in English
| MEDLINE | ID: mdl-32617267
5.
Defective phosphatidylethanolamine biosynthesis leads to a broad ataxia-spasticity spectrum.
Brain
; 144(3): e30, 2021 04 12.
Article
in English
| MEDLINE | ID: mdl-33454747
6.
Type 1 early infantile epileptic encephalopathy: A case report and literature review.
Mol Genet Genomic Med
; 12(2): e2412, 2024 Feb.
Article
in English
| MEDLINE | ID: mdl-38400608
7.
Evaluation of Rap1GAP and EPAC1 Gene Expression in Endometriosis Disease.
Adv Biomed Res
; 12: 101, 2023.
Article
in English
| MEDLINE | ID: mdl-37288024
8.
Interaction of dietary patterns with rs28362491 on severity of coronary artery stenosis in patients undergoing coronary angiography.
Sci Rep
; 13(1): 14608, 2023 09 05.
Article
in English
| MEDLINE | ID: mdl-37669998
9.
Association of NFKB1 gene polymorphism (rs28362491) with cardiometabolic risk factor in patients undergoing coronary angiography.
J Cardiovasc Thorac Res
; 15(3): 161-167, 2023.
Article
in English
| MEDLINE | ID: mdl-38028716
10.
Plasma miR-21 as a potential predictor in prediabetic individuals with a positive family history of type 2 diabetes mellitus.
Physiol Rep
; 10(2): e15163, 2022 01.
Article
in English
| MEDLINE | ID: mdl-35076188
11.
Evaluation of NF1 and RASA1 gene expression in endometriosis.
Eur J Obstet Gynecol Reprod Biol X
; 15: 100152, 2022 Aug.
Article
in English
| MEDLINE | ID: mdl-35586752
12.
Joint effects of paraoxonase 1 rs662 polymorphism and vitamins C/E intake on coronary artery disease severity (Gensini and SYNTAX scores) and lipid profile in patients undergoing coronary angiography.
Front Nutr
; 9: 1097411, 2022.
Article
in English
| MEDLINE | ID: mdl-36817064
13.
The association of the paraoxonase 1 Q192R polymorphism with coronary artery disease (CAD) and cardiometabolic risk factors in Iranian patients suspected of CAD.
Front Cardiovasc Med
; 9: 1037940, 2022.
Article
in English
| MEDLINE | ID: mdl-36741829
14.
Circulating microRNA-122, microRNA-126-3p and microRNA-146a are associated with inflammation in patients with pre-diabetes and type 2 diabetes mellitus: A case control study.
PLoS One
; 16(6): e0251697, 2021.
Article
in English
| MEDLINE | ID: mdl-34077450
15.
A Novel PCNT Frame Shift Variant (c.7511delA) Causing Osteodysplastic Primordial Dwarfism of Majewski Type 2 (MOPD II).
Front Pediatr
; 8: 340, 2020.
Article
in English
| MEDLINE | ID: mdl-32671003
16.
Circulating miR-15a and miR-222 as Potential Biomarkers of Type 2 Diabetes.
Diabetes Metab Syndr Obes
; 13: 3461-3469, 2020.
Article
in English
| MEDLINE | ID: mdl-33061506
17.
Evaluation of miR-181b and miR-126-5p expression levels in T2DM patients compared to healthy individuals: Relationship with NF-κB gene expression.
Endocrinol Diabetes Nutr (Engl Ed)
; 67(7): 454-460, 2020.
Article
in English, Spanish
| MEDLINE | ID: mdl-31948856
18.
Effects of synbiotic supplementation on gut microbiome, serum level of TNF-α, and expression of microRNA-126 and microRNA-146a in patients with type 2 diabetes mellitus: study protocol for a double-blind controlled randomized clinical trial.
Trials
; 21(1): 324, 2020 Apr 14.
Article
in English
| MEDLINE | ID: mdl-32290852
19.
Exome-wide copy number variation analysis identifies a COL9A1 in frame deletion that is associated with hearing loss.
Eur J Med Genet
; 62(10): 103724, 2019 Oct.
Article
in English
| MEDLINE | ID: mdl-31315069
20.
Recessive mutations in ATP8A2 cause severe hypotonia, cognitive impairment, hyperkinetic movement disorders and progressive optic atrophy.
Orphanet J Rare Dis
; 13(1): 86, 2018 05 31.
Article
in English
| MEDLINE | ID: mdl-30012219