Agha Gholizadeh M - Search Results

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The X-ray Repair Cross-Complementing Group 1 Arg399Gln Genetic Polymorphism and Risk of Hepatocellular Carcinoma in an Iranian Population.

Bazgir A, Agha Gholizadeh M, Khosravi A, Mansour Samaei N. Bazgir A, et al. Among authors: agha gholizadeh m. Middle East J Dig Dis. 2018 Jan;10(1):40-44. doi: 10.15171/mejdd.2017.89. Epub 2018 Jan 10. Middle East J Dig Dis. 2018. PMID: 29682247 Free PMC article.

A Novel Frameshift Mutation in Abnormal Spindle-Like Microcephaly (ASPM) Gene in an Iranian Patient with Primary Microcephaly: A Case Report.

Bazgir A, Agha Gholizadeh M, Sarvar F, Pakzad Z. Bazgir A, et al. Among authors: agha gholizadeh m. Iran J Public Health. 2019 Nov;48(11):2074-2078. Iran J Public Health. 2019. PMID: 31970108 Free PMC article.

Novel splicing variant and gonadal mosaicism in DYRK1A gene identified by whole-genome sequencing in multiplex autism spectrum disorder families.

Agha Gholizadeh M, Behjati F, Ghasemi Firouzabadi S, Heidari E, Razmara E, Almadani N, Sharifi Zarchi A, Garshasbi M. Agha Gholizadeh M, et al. Neurogenetics. 2024 Oct;25(4):377-391. doi: 10.1007/s10048-024-00768-6. Epub 2024 Jul 8. Neurogenetics. 2024. PMID: 38976082

Identification of a Novel Homozygous GLS Gene Variant Associated with Developmental and Epileptic Encephalopathy (DEE) Type 71.

Bazgir A, Agha Gholizadeh M, Kahani SM, Tavasoli AR, Garshasbi M. Bazgir A, et al. Among authors: agha gholizadeh m. Neurogenetics. 2024 Jul;25(3):225-232. doi: 10.1007/s10048-024-00753-z. Epub 2024 Apr 15. Neurogenetics. 2024. PMID: 38622440

Association of Interleukin-28B Polymorphisms (rs12979860 C/T, rs12980275 A/G, rs8099917 T/G) and Risk of Hepatocellular Carcinoma in an Iranian Population.

Hajizadeh L, Samaei NM, Bazgir A, Agha Gholizadeh M, Khosravi A. Hajizadeh L, et al. Among authors: agha gholizadeh m. Middle East J Dig Dis. 2022 Jan;14(1):118-123. doi: 10.34172/mejdd.2022.264. Epub 2022 Jan 30. Middle East J Dig Dis. 2022. PMID: 36619736 Free PMC article.

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