Masomeh Askari - Acad Ctr Educ Culture & Res ACECR, Royan Inst Reprod Biomed

基本信息

浏览量：0

职业迁徙

个人简介

暂无内容

研究兴趣

论文共 18 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

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

Masomeh Askari,Ebrahim Mirzaei,Leila Navapour,Mina Karimpour,Leili Rejali, Somayeh Sarirchi,Ehsan Nazemalhosseini-Mojarad,Stefania Nobili,Claudia Cava,Amir Sadeghi,Nayeralsadat Fatemi

JOURNAL OF GASTROINTESTINAL CANCERno. 4 (2024): 1607-1619

引用0浏览0WOS引用

A Novel Missense Variant in PNLDC1 Associated with Nonobstructive Azoospermia

Mouness Rahimian,Masomeh Askari,Najmeh Salehi,Mojtaba Jaafarinia,Mohsen Forouzanfar,Navid Almadani,Andrea Riccio,Mehdi Totonchi

Journal of Geneticsno. 2 (2024): 1-10

引用0浏览0WOS引用

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

Makan Cheraghpour,Masomeh Askari,Sascha Tierling,Sajad Shojaee,Amir Sadeghi,Pardis Ketabi Moghadam,Maryam Khazdouz,Hamid Asadzadeh Aghdaei,Moein Piroozkhah,Ehsan Nazemalhosseini-Mojarad,Nayeralsadat Fatemi

Frontiers in oncology (2023): 1168942

引用0浏览0WOS引用

A Novel Missense Variant in CDK5RAP2 Associated with Non-Obstructive Azoospermia

Mouness Rahimian,Masomeh Askari,Najmeh Salehi,Andrea Riccio,Mojtaba Jaafarinia,Navid Almadani,Mehdi Totonchi

Taiwanese Journal of Obstetrics and Gynecologyno. 6 (2023): 830-837

引用0浏览0WOS引用

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

Soheila Nabi,Masomeh Askari,Maryam Rezaei-Gazik,Najmeh Salehi,Navid Almadani,Yaser Tahamtani,Mehdi Totonchi

MOLECULAR HUMAN REPRODUCTION（2022）

引用5浏览0WOS引用

Prediction and Interpretation of Rare Missense Variant in OTOG Associated with Hearing Loss

Masomeh Askari,Zahra Moradi,Mahsa Mohammadi,Milad Lagzian,Samira Asgharzade

Genomics（2021）

引用1浏览0WOS引用

Targeted sequencing of CDH23 and GJB2 genes in an Iranian pedigree with Usher syndrome and non-syndromic hearing loss

Shahram Torkamandi,Sahar Bayat,Reza Mirfakhraie,Somaye Rezaei,Masomeh Askari,Samira Piltan,Milad Gholami

GENE REPORTS（2021）

引用0浏览0引用

Whole exome sequencing identified two homozygous ALMS1 mutations in an Iranian family with Alstrom syndrome

Shahram Torkamandi,Somaye Rezaei,Reza Mirfakhraei,Masomeh Askari,Samira Piltan,Milad Gholami

GENE（2020）

引用8浏览0WOS引用

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

Khatami Somayeh,Askari Masomeh,Bahreini Fatemeh,Hashemzadeh-Chaleshtori Morteza,Hematian Saeed,Asgharzade Samira

BMC Medical Genetics（2020）

引用2浏览0WOS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