Moazzeni H[au] - Search Results

Year	Number of Results
2012	2
2013	1
2014	1
2015	1
2016	1
2017	2
2019	3
2020	6
2021	3
2022	3
2023	1
2024	1

1

Insights into the regulatory molecules involved in glaucoma pathogenesis.

Moazzeni H, Khani M, Elahi E. Moazzeni H, et al. Am J Med Genet C Semin Med Genet. 2020 Sep;184(3):782-827. doi: 10.1002/ajmg.c.31833. Epub 2020 Sep 16. Am J Med Genet C Semin Med Genet. 2020. PMID: 32935930 Review.

2

MicroRNAs that target RGS5.

Banaei-Esfahani A, Moazzeni H, Nosar PN, Amin S, Arefian E, Soleimani M, Yazdani S, Elahi E. Banaei-Esfahani A, et al. Among authors: moazzeni h. Iran J Basic Med Sci. 2015 Feb;18(2):108-14. Iran J Basic Med Sci. 2015. PMID: 25810883 Free PMC article.

3

Identification of UBA1 as the causative gene of an X-linked non-Kennedy spinal-bulbar muscular atrophy.

Khani M, Nafissi S, Shamshiri H, Moazzeni H, Taheri H, Sadeghi M, Salehi N, Chitsazian F, Elahi E. Khani M, et al. Among authors: moazzeni h. Eur J Neurol. 2022 Dec;29(12):3556-3563. doi: 10.1111/ene.15528. Epub 2022 Sep 13. Eur J Neurol. 2022. PMID: 35996994

4

Identification of RNF13 as cause of recessively inherited ALS in a multi-case pedigree.

Khani M, Nafissi S, Shamshiri H, Moazzeni H, Taheri H, Elahi E. Khani M, et al. Among authors: moazzeni h. J Med Genet. 2022 Jul 25:jmedgenet-2022-108645. doi: 10.1136/jmg-2022-108645. Online ahead of print. J Med Genet. 2022. PMID: 35879052

5

Description of combined ARHSP/JALS phenotype in some patients with SPG11 mutations.

Khani M, Shamshiri H, Fatehi F, Rohani M, Haghi Ashtiani B, Akhoundi FH, Alavi A, Moazzeni H, Taheri H, Ghani MT, Javanparast L, Hashemi SS, Haji-Seyed-Javadi R, Heidari M, Nafissi S, Elahi E. Khani M, et al. Among authors: moazzeni h. Mol Genet Genomic Med. 2020 Jul;8(7):e1240. doi: 10.1002/mgg3.1240. Epub 2020 May 8. Mol Genet Genomic Med. 2020. PMID: 32383541 Free PMC article.

6

Minimal climate change impacts on the geographic distribution of Nepeta glomerulosa, medicinal species endemic to southwestern and central Asia.

Karami S, Ejtehadi H, Moazzeni H, Vaezi J, Behroozian M. Karami S, et al. Among authors: moazzeni h. Sci Rep. 2022 Nov 18;12(1):19893. doi: 10.1038/s41598-022-24524-8. Sci Rep. 2022. PMID: 36400923 Free PMC article.

7

BVVL/ FL: features caused by SLC52A3 mutations; WDFY4 and TNFSF13B may be novel causative genes.

Khani M, Shamshiri H, Taheri H, Hardy J, Bras JT, Carmona S, Moazzeni H, Alavi A, Heshmati A, Taghizadeh P, Nilipour Y, Ghazanfari T, Shahabi M, Okhovat AA, Rohani M, Valle G, Boostani R, Abdi S, Eshghi S, Nafissi S, Elahi E. Khani M, et al. Among authors: moazzeni h. Neurobiol Aging. 2021 Mar;99:102.e1-102.e10. doi: 10.1016/j.neurobiolaging.2020.09.021. Epub 2020 Oct 5. Neurobiol Aging. 2021. PMID: 33189404

8

A case of adult onset Sandhoff disease that mimics Brown-Vialetto-Van Laere syndrome.

Khani M, Shamshiri H, Moazzeni H, Taheri H, Ahmadieh H, Alavi A, Farboodi N, Nafissi S, Elahi E. Khani M, et al. Among authors: moazzeni h. Neuromuscul Disord. 2021 Jun;31(6):528-531. doi: 10.1016/j.nmd.2021.03.003. Epub 2021 Mar 8. Neuromuscul Disord. 2021. PMID: 33824075

9

Underestimated diversity in high elevations of a global biodiversity hotspot: two new endemic species of Aethionema (Brassicaceae) from the alpine zone of Iran.

Moazzeni H, Mahmoodi M, Jafari M, Schneeweiss GM, Noroozi J. Moazzeni H, et al. Front Plant Sci. 2023 May 26;14:1182073. doi: 10.3389/fpls.2023.1182073. eCollection 2023. Front Plant Sci. 2023. PMID: 37304726 Free PMC article.

10

Identification of genes involved in glaucoma pathogenesis using combined network analysis and empirical studies.

Moazzeni H, Mirrahimi M, Moghadam A, Banaei-Esfahani A, Yazdani S, Elahi E. Moazzeni H, et al. Hum Mol Genet. 2019 Nov 1;28(21):3637-3663. doi: 10.1093/hmg/ddz222. Hum Mol Genet. 2019. PMID: 31518395

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