Marzieh Mohseni

基本信息

浏览量：22

职业迁徙

个人简介

PhD of Medical Genetics, Research Assistant Professor, Genetics Research Center, USWR Tehran, Iran.

研究兴趣

论文共 79 篇作者统计合作学者相似作者

按年份排序按引用量排序主题筛选期刊级别筛选合作者筛选合作机构筛选

Unraveling the Genetic Landscape of Hearing Loss: A Comprehensive Study of Azeri Families in Ardabil, Iran

Marzieh Mohseni, Farzane Zare Ashrafi, Ehsan Abbaspour Rodbaneh, Haleh Mokabber, Maryam Vafaei, Ramiz Nobakht,Fatemeh Keshavarzi,Sanaz Arzhangi, Sara Arish, Zahra Nematollahi Azar, Kimia Kahrizi,Hossein Najmabadi,Behzad Davarnia

Molecular genetics & genomic medicineno. 2 (2025): e70080-e70080

引用0浏览0WOS引用

A Village in the Southeastern Region of Iran Harboring the C.716t>a (p.val239asp) Mutation in SLC26A4

Farzane Zare Ashrafi, Saeed Dorgaleleh, Raziye Rezvani Rezvandeh, Negar Kazemi, Nasrin Azizi,Masoud Edizadeh,Mohammad Hossein Azizi,Kimia Kahrizi,Hossein Najmabadi,Reza Najafipour,Marzieh Mohseni

ARCHIVES OF IRANIAN MEDICINE（2024）

引用0浏览0WOS引用

Genetic Analysis of 27 Y-STR Haplotypes in 11 Iranian Ethnic Groups

Somayeh Alinaghi,Marzieh Mohseni,Zohreh Fattahi,Maryam Beheshtian,Fatemeh Ghodratpour,Farzane Zare Ashrafi,Sanaz Arzhangi,Khadijeh Jalalvand,Reza Najafipour,Hamid Reza Khorram Khorshid,Kimia Kahrizi,Hossein Najmabadi

ARCHIVES OF IRANIAN MEDICINE（2024）

引用0浏览0WOS引用

Contribution of Genetic Variants in the Development of Familial Premature Coronary Artery Disease in a Cohort of Cardiac Patients

Sepideh Mehvari, Nahid Karimian Fathi,Sara Saki,Maryam Asadnezhad,Sanaz Arzhangi,Fatemeh Ghodratpour,Marzieh Mohseni,Farzane Zare Ashrafi,Saeed Sadeghian,Mohammadali Boroumand, Fatemeh Shokohizadeh, Elham Rostami, Rahnama Boroumand,Reza Najafipour,Reza Malekzadeh,Yasser Riazalhosseini,Mohammadreza Akbari,Mark Lathrop,Hossein Najmabadi,Kaveh Hosseini,Kimia Kahrizi

CLINICAL GENETICSno. 6 (2024): 611-619

引用1浏览0WOS引用

A Frameshift Variant in ANKRD24 Implicates Its Role in Human Non-Syndromic Hearing Loss

Negar Kazemi, Raziye Rezvani Rezvandeh,Farzane Zare Ashrafi,Ebrahim Shokouhian,Masoud Edizadeh, Kevin T. A. Booth,Kimia Kahrizi,Hossein Najmabadi,Marzieh Mohseni

Clinical geneticsno. 2 (2024): 214-218

引用0浏览0WOS引用

Implementation of an In-House Platform for Rapid Screening of SARS-CoV-2 Genome Variations

Farzane Zare Ashrafi,Marzieh Mohseni,Maryam Beheshtian,Zohreh Fattahi,Fatemeh Ghodratpour,Fatemeh Keshavarzi,Hanieh Behravan,Marzieh Kalhor,Khadijeh Jalalvand,Maryam Azad,Mahdieh Koshki,Ali Jafarpour,Azam Ghaziasadi,Alireza Abdollahi,Seyed Jalal Kiani,Angila Ataei-Pirkooh,Iman Rezaei Azhar,Farah Bokharaei-Salim,Mohammad Reza Haghshenas,Farhang Babamahmoodi,Zakiye Mokhames,Alireza Soleimani,Masood Ziaee,Davod Javanmard,Shokouh Ghafari,Akram Ezani,Alireza Ansari Moghaddam,Fariba Shahraki-Sanavi,Seyed Mohammad Hashemi Shahri,Azarakhsh Azaran,Farid Yousefi,Afagh Moattari,Mohsen Moghadami,Hamed Fakhim,Behrooz Ataei,Elahe Nasri,Vahdat Poortahmasebi,Mojtaba Varshochi,Ali Mojtahedi,Farid Jalilian,Mohammad Khazeni,Abdolvahab Moradi,Alijan Tabarraei,Ahmad Piroozmand,Yousef Yahyapour,Masoumeh Bayani,Amir Aboofazeli,Parsa Ghafari,Fariba Keramat,Mahsa Tavakoli,Tahmineh Jalali,Mohammad Hassan Pouriayevali,Mostafa Salehi-Vaziri,Hamid Reza Khorram Khorshid,Reza Najafipour,Reza Malekzadeh,Kimia Kahrizi,Seyed Mohammad Jazayeri,Hossein Najmabadi

ARCHIVES OF IRANIAN MEDICINEno. 2 (2023): 69-75

引用1浏览0WOS引用

Identification of a Homozygous Frameshift Mutation in the FGF3 Gene in a Consanguineous Iranian Family: First Report of Labyrinthine Aplasia, Microtia, and Microdontia Syndrome in Iran and Literature Review

Fereshteh Jamshidi,Ebrahim Shokouhian,Marzieh Mohseni,Kimia Kahrizi,Hossein Najmabadi,Mojgan Babanejad

Molecular Genetics & Genomic Medicine（2023）

引用1浏览0WOS引用

An Extended Iranian Family with Autosomal Dominant Non-syndromic Hearing Loss Associated with A Nonsense Mutation in the DIAPH1 Gene

Marzieh Mohseni, Yusuf Mohammadi,Farzane Zare Ashrafi,Fatemeh Ghodratpour,Khadijeh Jalalvand,Sanaz Arzhangi,Mojgan Babanejad,Mohammad Hossein Azizi,Kimia Kahrizi,Hossein Najmabadi

ARCHIVES OF IRANIAN MEDICINEno. 3 (2023): 176-180

引用1浏览0WOS引用

Targeted Next Generation Sequencing Revealed Novel Variants in the PKD1 and PKD2 Genes of Iranian Patients with Autosomal Dominant Polycystic Kidney Disease

Maryam Hosseinpour,Fariba Ardalani,Marzieh Mohseni,Maryam Beheshtian,Sanaz Arzhangi,Shahrzad Ossareh,Hossein Najmabadi,Ali Nobakht,Kimia Kahrizi,Behrooz Broumand

ARCHIVES OF IRANIAN MEDICINE（2022）

引用2浏览0WOS引用

Novel variants identified in the rare undiagnosed families

Farzane Zare Ashrafi,Fatemeh Peymani,Marzieh Mohseni,Sanaz Arzhangi,Mohammad R. Akbari,Hossein Najmabadi,Kimia Kahrizi

EUROPEAN JOURNAL OF HUMAN GENETICS（2022）

引用0浏览0引用

加载更多

作者统计

合作学者

合作机构

D-Core

合作者
学生
导师

暂无相似学者，你可以通过学者研究领域进行搜索筛选

数据免责声明

页面数据均来自互联网公开来源、合作出版商和通过AI技术自动分析结果，我们不对页面数据的有效性、准确性、正确性、可靠性、完整性和及时性做出任何承诺和保证。若有疑问，可以通过电子邮件方式联系我们：report@aminer.cn

研究员

论文共 79 篇作者统计合作学者相似作者