Dr. Maghsood Mehri

Faculty of Medicine-Assistant Professor of Medical Genetics

Research Interests

Keep in touch

-mehri.m129@gmail.com--

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Citations

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Publications and Conferences

Title of Article / Authors / Journal

Publication Year

Identification of the potential pathogenicity of a VUS in the ASL gene associated with argininosuccinic aciduria in an Iranian family

Elaheh Hasani, Maryam Naghinejad, Sima Mansoori Derakhshan, Akbar Amirfiroozy, Maghsood Mehri, Mahmoud Shekari Khaniani

Molecular Biology Reports

2025-08-25T07:21:37.082Z

Evaluation of miR-27a-5p and miR-449a as potential serum biomarkers for breast cancer: a combined bioinformatics and experimental study

Tahereh Barati, Zohreh Mirzaei, Amir Ebrahimi, Mahmoud Shekari Khaniani, Solmaz Hashemi, Maghsood Mehri, Sima Mansoori Derakhshan

Molecular Biology Reports

2025-06-13T07:18:36.123Z

The known structural variations in hearing loss and their diagnostic approaches: a comprehensive review

Maryam Naghinejad, Sepideh Parvizpour, Mahmoud Shekari Khaniani, Maghsood Mehri, Sima Mansoori Derakhshan, Akbar Amirfiroozy

Molecular Biology Reports

2025-01-17T07:07:43.526Z

Acute myeloid leukemia with unreported translocation (x; 3)(q24; p13): A case report

Nasrin Gholami, Amirreza Khalaji, Maghsood Mehri, Saba Mehrtabar, Elham Habibzade

Clinical Case Reports

2024-02-20T06:58:33.238Z

Genetic Diagnosis of Pyruvate Kinase Deficiency in Undiagnosed Iranian Patients with Severe Hemolytic Anemia, using Whole Exome Sequencing

Jafar Mehrabi Sisakht, Maghsood Mehri, Hossein Najmabadi, Azita Azarkeivan, Maryam Neishabury

Archives of Iranian medicine

2022-10-01T06:56:41.699Z

The first case of BENTA disease (B cell expansion with NF-κB and T cell anergy) from Iran

Maryam Neishabury, Azita Azarkeivan, Maghsood Mehri, Hossein Najmabadi, Taher Cheraghi

Journal of Clinical Immunology

2021-05-01T05:53:41.619Z

Novel variants in Iranian individuals suspected to have inherited red blood cell disorders, including bone marrow failure syndromes

Maryam Neishabury, Maghsood Mehri, Zohreh Fattahi, Hossein Najmabadi, Azita Azarkeivan

haematologica

2020-01-01T06:50:11.469Z

Novel mutations in mitochondrial carrier family gene SLC25A38, causing congenital sideroblastic anemia in Iranian families, identified by whole exome sequencing

Maghsood Mehri, Maryam Zarin, Fariba Ardalani, Hossein Najmabadi, Azita Azarkeivan, Maryam Neishabury

Blood Cells, Molecules, and Diseases

2018-07-01T03:17:37.232Z

Pharmacogenetic study on the effect of rivastigmine on PS2 and APOE genes in Iranian Alzheimer patients

M Zamani, M Mehri, A Kollaee, P Yenki, M Ghaffarpor, MH Harirchian, M Shahbazi

Dementia and geriatric cognitive disorders extra

2011-06-29T11:10:42.848Z