Askari M - Search Results

1

Integrative Bioinformatics Analysis: Unraveling Variant Signatures and Single-Nucleotide Polymorphism Markers Associated with 5-FU-Based Chemotherapy Resistance in Colorectal Cancer Patients.

Askari M, Mirzaei E, Navapour L, Karimpour M, Rejali L, Sarirchi S, Nazemalhosseini-Mojarad E, Nobili S, Cava C, Sadeghi A, Fatemi N. Askari M, et al. J Gastrointest Cancer. 2024 Dec;55(4):1607-1619. doi: 10.1007/s12029-024-01102-x. Epub 2024 Sep 6. J Gastrointest Cancer. 2024. PMID: 39240276

2

A systematic review and meta-analysis for the association of the insulin-like growth factor1 pathway genetic polymorphisms with colorectal cancer susceptibility.

Cheraghpour M, Askari M, Tierling S, Shojaee S, Sadeghi A, Ketabi Moghadam P, Khazdouz M, Asadzadeh Aghdaei H, Piroozkhah M, Nazemalhosseini-Mojarad E, Fatemi N. Cheraghpour M, et al. Among authors: askari m. Front Oncol. 2023 May 22;13:1168942. doi: 10.3389/fonc.2023.1168942. eCollection 2023. Front Oncol. 2023. PMID: 37284192 Free PMC article.

3

A novel missense variant in CDK5RAP2 associated with non-obstructive azoospermia.

Rahimian M, Askari M, Salehi N, Riccio A, Jaafarinia M, Almadani N, Totonchi M. Rahimian M, et al. Among authors: askari m. Taiwan J Obstet Gynecol. 2023 Nov;62(6):830-837. doi: 10.1016/j.tjog.2023.03.015. Taiwan J Obstet Gynecol. 2023. PMID: 38008501 Free article.

4

Prediction and interpretation of rare missense variant in OTOG associated with hearing loss.

Askari M, Moradi Z, Mohammadi M, Lagzian M, Asgharzade S. Askari M, et al. Genomics. 2021 Jul;113(4):2793-2799. doi: 10.1016/j.ygeno.2021.06.012. Epub 2021 Jun 9. Genomics. 2021. PMID: 34118384 Free article.

5

A rare frameshift mutation in SYCP1 is associated with human male infertility.

Nabi S, Askari M, Rezaei-Gazik M, Salehi N, Almadani N, Tahamtani Y, Totonchi M. Nabi S, et al. Among authors: askari m. Mol Hum Reprod. 2022 Apr 1;28(4):gaac009. doi: 10.1093/molehr/gaac009. Mol Hum Reprod. 2022. PMID: 35377450

6

A novel missense variant in PNLDC1 associated with nonobstructive azoospermia.

Rahimian M, Askari M, Salehi N, Jaafarinia M, Forouzanfar M, Almadani N, Riccio A, Totonchi M. Rahimian M, et al. Among authors: askari m. J Genet. 2024;103:28. J Genet. 2024. PMID: 39223739 Free article.

7

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. Among authors: askari m. Gene. 2020 Feb 15;727:144228. doi: 10.1016/j.gene.2019.144228. Epub 2019 Oct 26. Gene. 2020. PMID: 31669637

8

Novel MYO15A variants are associated with hearing loss in the two Iranian pedigrees.

Khatami S, Askari M, Bahreini F, Hashemzadeh-Chaleshtori M, Hematian S, Asgharzade S. Khatami S, et al. Among authors: askari m. BMC Med Genet. 2020 Nov 18;21(1):226. doi: 10.1186/s12881-020-01168-x. BMC Med Genet. 2020. PMID: 33208113 Free PMC article.

9

A missense mutation in NR5A1 causing female to male sex reversal: A case report.

Askari M, Rastari M, Seresht-Ahmadi M, McElreavey K, Bashamboo A, Razzaghy-Azar M, Totonchi M. Askari M, et al. Andrologia. 2020 Jul;52(6):e13585. doi: 10.1111/and.13585. Epub 2020 Apr 9. Andrologia. 2020. PMID: 32271476

10

Identification of a missense variant in CLDN2 in obstructive azoospermia.

Askari M, Karamzadeh R, Ansari-Pour N, Karimi-Jafari MH, Almadani N, Sadighi Gilani MA, Gourabi H, Vosough Taghi Dizaj A, Mohseni Meybodi A, Sadeghi M, Bashamboo A, McElreavey K, Totonchi M. Askari M, et al. J Hum Genet. 2019 Oct;64(10):1023-1032. doi: 10.1038/s10038-019-0642-0. Epub 2019 Jul 18. J Hum Genet. 2019. PMID: 31320686

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