Eskandar Taghizadeh
Ahvaz Jundishapur University of Medical Sciences
H-index: 12
Asia-Iran
Top articles of Eskandar Taghizadeh
Title | Journal | Author(s) | Publication Date |
|---|---|---|---|
Integrative bioinformatics analysis of miRNA and mRNA expression profiles identified some potential biomarkers for breast cancer | Egyptian Journal of Medical Human Genetics | Seyed Masoud Rezaeijo Monireh Rezaei Arash Poursheikhani Shima Mohammadkhani Naieme Goharifar | 2023/10/19 |
Long non-coding RNA GAS5 rs145204276 indel polymorphism and cancer risk: A systemic and meta-analysis review | Authorea Preprints | Arash Poursheikhani Vahid Reza Askari Eskandar Taghizadeh Negin Nokhandani Arash Salmaninejad | 2023/8/29 |
The role of miRNAs in the diagnosis and treatment of male infertility: a review study | Roya Sinaei Khosro Jamebozorgi Hossein Mirshekarpour Hossein Poormasoumi Amirhossein Mahdizadeh | 2023/6/24 | |
The influence of CDKAL1 (rs7754840) gene polymorphism on susceptibility to gestational diabetes mellitus in pregnant women: A systematic review and meta-analysis | Amir Hossein Mahdizade Seyed Sobhan Bahreiny Mohammad-Navid Bastani Mohammad Reza Dabbagh Mojtaba Aghaei | 2023/10/31 | |
Cellular and molecular aspects of managing familial hypercholesterolemia: recent and emerging therapeutic approaches | Forough Taheri Eskandar Taghizadeh Fatemeh Baniamerian Daryoush Rostami Ahmad Rozeian | 2022/9/1 | |
Genetics of familial combined hyperlipidemia (FCHL) disorder: an update | Eskandar Taghizadeh Najmeh Farahani Rajab Mardani Forough Taheri Hassan Taghizadeh | 2022/4/1 | |
The role of efferocytosis in neuro-degenerative diseases | Forough Taheri Eskandar Taghizadeh Jamshid Gholizadeh Navashenaq Mehdi Rezaee Seyed Mohammad Gheibihayat | 2022/3 | |
Abnormal angiogenesis associated with HIF-1α/VEGF signaling pathway in recurrent miscarriage along with therapeutic goals | Eskandar Taghizadeh Khalil Tazik Forough Taheri Ghazal Shayankia Seyed Mohammad Gheibihayat | 2022/3/1 | |
Effect of diabetes on efferocytosis process | Ali Mahmoudi Ali Ahmadizad Firouzjaei Jamshid Gholizadeh Navashenaq Eskandar Taghizadeh Majid Darroudi | 2022/7/28 | |
Breast cancer prediction with transcriptome profiling using feature selection and machine learning methods | BMC bioinformatics | Eskandar Taghizadeh Sahel Heydarheydari Alihossein Saberi Shabnam JafarpoorNesheli Seyed Masoud Rezaeijo | 2022/10/1 |
CD47 functionalization of nanoparticles as a poly (ethylene glycol) alternative: a novel approach to improve drug delivery | Noushin R Vandchali Fatemeh Moadab Eskandar Taghizadeh Amir Tajbakhsh Seyed M Gheibihayat | 2021/11/1 | |
LncRNAs as putative biomarkers and therapeutic targets for Parkinson’s disease | Eskandar Taghizadeh Seyed Mohammad Gheibihayat Forough Taheri Seyed Mohammadreza Afshani Najmeh Farahani | 2021/10 | |
A novel variant in iranian patient with cystinuria: a case report | Iranian Journal of Public Health | Ali Mardi Hamed Heidary Seyyed Mohammad Mousavi Ghasem Khazaei Eskandar Taghizadeh | 2021/9 |
Epigenetic aspects of multiple sclerosis and future therapeutic options | Khosro Jamebozorgi Daryoush Rostami Hosein Pormasoumi Eskandar Taghizadeh George E Barreto | 2021/1/2 | |
Secondary findings from whole-exome sequencing data in families with familial combined hyperlipidemia (FCHL) | Egyptian Journal of Medical Human Genetics | Mana Zakeri Mohammad Sadegh Safaiee Forough Taheri Eskandar Taghizadeh Gordon A Ferns | 2021/12 |
Limb-girdle Muscular Dystrophy and Therapy: Insights into Cell and Gene-based Approaches. | Forough Taheri Eskandar Taghizadeh Mohammad JR Pour Daryoush Rostami Pedram G Renani | 2020/1/1 | |
Molecular pathways, screening and follow-up of colorectal carcinogenesis: An overview | Eskandar Taghizadeh Seyed MG Hayat Rhonda J Rosengren Daryoush Rostami Hamed Abdolkarimi | 2020/6/1 | |
A novel variant in LPL gene is associated with familial combined hyperlipidemia | Biofactors | Eskandar Taghizadeh Majid Ghayour‐Mobarhan Gordon A Ferns Alireza Pasdar | 2020/1 |
A novel variant in C5ORF42 gene is associated with Joubert syndrome | Molecular Biology Reports | Rajab Mardani Eskandar Taghizadeh Forough Taheri Mohammadali Raeisi Mohammad Reza Karimzadeh | 2020/5 |
A novel mutation in USF1 gene is associated with familial combined hyperlipidemia | IUBMB life | Eskandar Taghizadeh Farzaneh Mirzaei Nazanin Jalilian Majid Ghayour Mobarhan Gordon A Ferns | 2020/4 |
Co-Authors
