Noroozi R - Search Results

1

Association of ANRIL gene polymorphisms with prostate cancer and benign prostatic hyperplasia in an Iranian population.

Taheri M, Pouresmaeili F, Omrani MD, Habibi M, Sarrafzadeh S, Noroozi R, Rakhshan A, Sayad A, Ghafouri-Fard S. Taheri M, et al. Among authors: noroozi r. Biomark Med. 2017 May;11(5):413-422. doi: 10.2217/bmm-2016-0378. Biomark Med. 2017. PMID: 28621612

2

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: noroozi r. Gene. 2017 Jan 5;596:119-122. doi: 10.1016/j.gene.2016.10.019. Epub 2016 Oct 14. Gene. 2017. PMID: 27751813

3

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: noroozi r. 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

4

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: noroozi r. 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

5

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. Among authors: noroozi r. Gene. 2017 May 20;613:20-24. doi: 10.1016/j.gene.2017.02.031. Epub 2017 Mar 1. Gene. 2017. PMID: 28259691

6

Myxovirus resistance protein A (MxA) polymorphism is associated with IFNβ response in Iranian multiple sclerosis patients.

Sayad A, Ghafouri-Fard S, Omrani MD, Noroozi R, Taheri M. Sayad A, et al. Among authors: noroozi r. Neurol Sci. 2017 Jun;38(6):1093-1099. doi: 10.1007/s10072-017-2935-4. Epub 2017 Apr 6. Neurol Sci. 2017. PMID: 28386647

7

Association study of the vesicular monoamine transporter 1 (VMAT1) gene with autism in an Iranian population.

Noroozi R, Ghafouri-Fard S, Omrani MD, Habibi M, Sayad A, Taheri M. Noroozi R, et al. Gene. 2017 Aug 20;625:10-14. doi: 10.1016/j.gene.2017.05.003. Epub 2017 May 2. Gene. 2017. PMID: 28476685

8

ANRIL Genetic Variants in Iranian Breast Cancer Patients.

Khorshidi HR, Taheri M, Noroozi R, Sarrafzadeh S, Sayad A, Ghafouri-Fard S. Khorshidi HR, et al. Among authors: noroozi r. Cell J. 2017 Spring;19(Suppl 1):72-78. doi: 10.22074/cellj.2017.4496. Epub 2017 May 17. Cell J. 2017. PMID: 28580310 Free PMC article.

9

Retinoic acid-related orphan receptor alpha (RORA) variants and risk of breast cancer.

Taheri M, Omrani MD, Noroozi R, Ghafouri-Fard S, Sayad A. Taheri M, et al. Among authors: noroozi r. Breast Dis. 2017;37(1):21-25. doi: 10.3233/BD-160248. Breast Dis. 2017. PMID: 28598825

10

Retinoic acid-related orphan receptor alpha (RORA) variants are associated with autism spectrum disorder.

Sayad A, Noroozi R, Omrani MD, Taheri M, Ghafouri-Fard S. Sayad A, et al. Among authors: noroozi r. Metab Brain Dis. 2017 Oct;32(5):1595-1601. doi: 10.1007/s11011-017-0049-6. Epub 2017 Jun 12. Metab Brain Dis. 2017. PMID: 28608249

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