Torkamandi S - Search Results

1

Association of CpG-SNP and 3'UTR-SNP of WFS1 with the Risk of Type 2 Diabetes Mellitus in an Iranian Population.

Torkamandi S, Bastami M, Ghaedi H, Tarighi S, Shokri F, Javadi A, Mirfakhraie R, Omrani MD. Torkamandi S, et al. Int J Mol Cell Med. 2017 Fall;6(4):197-203. doi: 10.22088/BUMS.6.4.197. Epub 2017 Nov 21. Int J Mol Cell Med. 2017. PMID: 29988211 Free PMC article.

2

Variation in the miRNA-433 binding site of FGF20 is a risk factor for Parkinson's disease in Iranian population.

Haghnejad L, Emamalizadeh B, Jamshidi J, Bidoki AZ, Ghaedi H, Ahmadi E, Abdollahi S, Shahmohammadibeni N, Taghavi S, Fazeli A, Motallebi M, Zarneh AE, Mohammadihosseinabad S, Abbaszadegan MR, Torkamandi S, Gavenaroudi MA, Pedram N, Shahidi GA, Tafakhori A, Darvish H, Movafagh A. Haghnejad L, et al. Among authors: torkamandi s. J Neurol Sci. 2015 Aug 15;355(1-2):72-4. doi: 10.1016/j.jns.2015.05.020. Epub 2015 May 27. J Neurol Sci. 2015. PMID: 26070653

3

MAP3K1 May be a Promising Susceptibility Gene for Type 2 Diabetes Mellitus in an Iranian Population.

Torkamandi S, Bastami M, Ghaedi H, Moghadam F, Mirfakhraie R, Omrani MD. Torkamandi S, et al. Int J Mol Cell Med. 2016 Summer;5(3):134-140. Epub 2016 Aug 21. Int J Mol Cell Med. 2016. PMID: 27942499 Free PMC article.

4

A Novel Splicesite Mutation in the EDAR Gene Causes Severe Autosomal Recessive Hypohydrotic (Anhidrotic) Ectodermal Dysplasia in an Iranian Family.

Torkamandi S, Gholami M, Mohammadi-Asl J, Rezaie S, Zaimy MA, Omrani MD. Torkamandi S, et al. Int J Mol Cell Med. 2016 Fall;5(4):260-263. Epub 2016 Oct 23. Int J Mol Cell Med. 2016. PMID: 28357203 Free PMC article.

5

Association of MiR-146a Expression and Type 2 Diabetes Mellitus: A Meta-Analysis.

Alipoor B, Ghaedi H, Meshkani R, Torkamandi S, Saffari S, Iranpour M, Omrani MD. Alipoor B, et al. Among authors: torkamandi s. Int J Mol Cell Med. 2017 Summer;6(3):156-163. doi: 10.22088/acadpub.BUMS.6.3.156. Epub 2017 Aug 14. Int J Mol Cell Med. 2017. PMID: 29682487 Free PMC article. Review.

6

Genotype-phenotype associations in hereditary spastic paraplegia: a systematic review and meta-analysis on 13,570 patients.

Erfanian Omidvar M, Torkamandi S, Rezaei S, Alipoor B, Omrani MD, Darvish H, Ghaedi H. Erfanian Omidvar M, et al. Among authors: torkamandi s. J Neurol. 2021 Jun;268(6):2065-2082. doi: 10.1007/s00415-019-09633-1. Epub 2019 Nov 19. J Neurol. 2021. PMID: 31745725 Review.

7

The novel homozygous p.Asn197_Ser201del mutation in BTD gene is associated with profound biotinidase deficiency in an Iranian consanguineous family.

Torkamandi S, Rezaei S, Mirfakhraie R, Golmohamadi S, Gholami M. Torkamandi S, et al. Mol Biol Rep. 2020 May;47(5):4021-4027. doi: 10.1007/s11033-020-05424-4. Epub 2020 Apr 12. Mol Biol Rep. 2020. PMID: 32281057

8

A homozygous missense mutation of WFS1 gene causes Wolfram's syndrome without hearing loss in an Iranian family (a report of clinical heterogeneity).

Torkamandi S, Rezaei S, Mirfakhraie R, Bayat S, Piltan S, Gholami M. Torkamandi S, et al. J Clin Lab Anal. 2020 Aug;34(8):e23358. doi: 10.1002/jcla.23358. Epub 2020 May 17. J Clin Lab Anal. 2020. PMID: 32419160 Free PMC article.

9

Whole exome sequencing identified two homozygous ALMS1 mutations in an Iranian family with Alström syndrome.

Torkamandi S, Rezaei S, Mirfakhraei R, Askari M, Piltan S, Gholami M. Torkamandi S, et al. Gene. 2020 Feb 15;727:144228. doi: 10.1016/j.gene.2019.144228. Epub 2019 Oct 26. Gene. 2020. PMID: 31669637

10

Matrix metalloproteinases (MMPs) family gene polymorphisms and the risk of multiple sclerosis: systematic review and meta-analysis.

Mohammadhosayni M, Khosrojerdi A, Lorian K, Aslani S, Imani D, Razi B, Babaie F, Torkamandi S. Mohammadhosayni M, et al. Among authors: torkamandi s. BMC Neurol. 2020 May 29;20(1):218. doi: 10.1186/s12883-020-01804-2. BMC Neurol. 2020. PMID: 32471473 Free PMC article.

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