Taheri M - Search Results

1

Emerging Role of Non-coding RNAs in Autism Spectrum Disorder.

Ghafouri-Fard S, Noroozi R, Brand S, Hussen BM, Eghtedarian R, Taheri M, Ebrahimzadeh K. Ghafouri-Fard S, et al. Among authors: taheri m. J Mol Neurosci. 2022 Feb;72(2):201-216. doi: 10.1007/s12031-021-01934-3. Epub 2021 Nov 12. J Mol Neurosci. 2022. PMID: 34767189 Review.

2

HLA genes as modifiers of response to IFN-β-1a therapy in relapsing-remitting multiple sclerosis.

Mazdeh M, Taheri M, Sayad A, Bahram S, Omrani MD, Movafagh A, Inoko H, Akbari MT, Noroozi R, Hajilooi M, Solgi G. Mazdeh M, et al. Among authors: taheri m. Pharmacogenomics. 2016 Apr;17(5):489-98. doi: 10.2217/pgs.16.2. Epub 2016 Mar 29. Pharmacogenomics. 2016. PMID: 27020477

3

Glutamate receptor, metabotropic 7 (GRM7) gene variations and susceptibility to autism: A case-control study.

Noroozi R, Taheri M, Movafagh A, Mirfakhraie R, Solgi G, Sayad A, Mazdeh M, Darvish H. Noroozi R, et al. Among authors: taheri m. Autism Res. 2016 Nov;9(11):1161-1168. doi: 10.1002/aur.1640. Epub 2016 Jun 17. Autism Res. 2016. PMID: 27312574

4

RAR-related orphan receptor A (RORA): A new susceptibility gene for multiple sclerosis.

Eftekharian MM, Noroozi R, Sayad A, Sarrafzadeh S, Toghi M, Azimi T, Komaki A, Mazdeh M, Inoko H, Taheri M, Mirfakhraie R. Eftekharian MM, et al. Among authors: taheri m. J Neurol Sci. 2016 Oct 15;369:259-262. doi: 10.1016/j.jns.2016.08.045. Epub 2016 Aug 24. J Neurol Sci. 2016. PMID: 27653902

5

FOXP3 gene variations and susceptibility to autism: A case-control study.

Safari MR, Ghafouri-Fard S, Noroozi R, Sayad A, Omrani MD, Komaki A, Eftekharian MM, Taheri M. Safari MR, et al. Among authors: taheri m. Gene. 2017 Jan 5;596:119-122. doi: 10.1016/j.gene.2016.10.019. Epub 2016 Oct 14. Gene. 2017. PMID: 27751813

6

Single nucleotide polymorphisms in the FOXP3 gene are associated with increased risk of relapsing-remitting multiple sclerosis.

Eftekharian MM, Sayad A, Omrani MD, Ghannad MS, Noroozi R, Mazdeh M, Mirfakhraie R, Movafagh A, Roshanaei G, Azimi T, Inoko H, Taheri M. Eftekharian MM, et al. Among authors: taheri m. Hum Antibodies. 2016;24(3-4):85-90. doi: 10.3233/HAB-160299. Hum Antibodies. 2016. PMID: 27792007

7

Synaptosome-Associated Protein 25 (SNAP25) Gene Association Analysis Revealed Risk Variants for ASD, in Iranian Population.

Safari MR, Omrani MD, Noroozi R, Sayad A, Sarrafzadeh S, Komaki A, Manjili FA, Mazdeh M, Ghaleiha A, Taheri M. Safari MR, et al. Among authors: taheri m. J Mol Neurosci. 2017 Mar;61(3):305-311. doi: 10.1007/s12031-016-0860-2. Epub 2016 Nov 26. J Mol Neurosci. 2017. PMID: 27888397

8

Ras-like without CAAX 2 (RIT2): a susceptibility gene for autism spectrum disorder.

Hamedani SY, Gharesouran J, Noroozi R, Sayad A, Omrani MD, Mir A, Afjeh SSA, Toghi M, Manoochehrabadi S, Ghafouri-Fard S, Taheri M. Hamedani SY, et al. Among authors: taheri m. Metab Brain Dis. 2017 Jun;32(3):751-755. doi: 10.1007/s11011-017-9969-4. Epub 2017 Feb 11. Metab Brain Dis. 2017. PMID: 28190241

9

Phospholipase D1 expression analysis in relapsing-remitting multiple sclerosis patients.

Eftekharian MM, Azimi T, Ghafouri-Fard S, Sayad A, Omrani MD, Sarrafzadeh S, Abbasalipourkabir R, Mazdeh M, Taheri M. Eftekharian MM, et al. Among authors: taheri m. Neurol Sci. 2017 May;38(5):865-872. doi: 10.1007/s10072-017-2857-1. Epub 2017 Feb 22. Neurol Sci. 2017. PMID: 28229303

10

HOTAIR genetic variants are associated with prostate cancer and benign prostate hyperplasia in an Iranian population.

Taheri M, Habibi M, Noroozi R, Rakhshan A, Sarrafzadeh S, Sayad A, Omrani MD, Ghafouri-Fard S. Taheri M, et al. Gene. 2017 May 20;613:20-24. doi: 10.1016/j.gene.2017.02.031. Epub 2017 Mar 1. Gene. 2017. PMID: 28259691

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