تالیفات و کارهای تحقیقاتی فاطمه نبیزاده
1. Nabizadeh, Fatemeh, Saeideh Momtaz, Maryam Ghanbari-Movahed, Farshad Qalekhani, Hadi Mohsenpour, Ina Yosifova Aneva, Anusha Bishayee, Mohammad Hosein Farzaei, and Anupam Bishayee. “Pediatric acute lymphoblastic leukemia management using multitargeting bioactive natural compounds: A systematic and critical review.” Pharmacological research (2022): 106116.
2. Koochakkhani, Shabnaz, Fatemeh Nabizadeh, Azim Nejatizadeh, and Ebrahim Eftekhar. “Association of methylenetetrahydrofolate reductase (MTHFR) and cystathionine β-synthase (CBS) genes promoter methylation pattern with the risk of essential hypertension.” Meta Gene 29 (2021): 100914.
3. Nabizadeh, Fatemeh, Shabnaz Koochakkhani, Hossein Farshidi, Zahra Farbood, Fatemeh Kharaee, Tasnim Eghbal Eftekhaari, Elaheh Farahbakhsh, Mahmood Khayatian, and Azim Nejatizadeh. “A Two-Single-Nucleotide Polymorphism Haplotype in Promoter Region of CYP11B2 Gene Affects Plasma Aldosterone Concentration: A Matched Case-Control Study.” Electronic Physician 12, no. 4 (2020).
4. Aghabozorgi, Amirsaeed Sabeti, Reyhane Ebrahimi, Alireza Bahiraee, Sadra Samavarchi Tehrani, Fatemeh Nabizadeh, Leila Setayesh, Reza Jafarzadeh-Esfehani, Gordon A. Ferns, Amir Avan, and Zahra Rashidi. “The genetic factors associated with Wnt signaling pathway in colorectal cancer.” Life Sciences 256 (2020): 118006.
5. Alimoradi, Elham, Fatemeh Nabizadeh, Farshad Qalekhani, and Reza Alibakhshi. “Whole-exome sequencing combined with in silico protein analysis identifies rare truncating variants in the TYR gene associated with oculocutaneous albinism IA (OCA1A) in an Iranian patient.” Gene Reports 36 (2024): 101933.
1. Nabizadeh, Fatemeh and Qalekhani, Farshad and Koochakkhani, Shabnaz, 2022, Bioinformatics-based Prediction of Recurrence in Tamoxifen-treated Patients with Estrogen Receptor-Positive Breast Cancer, The first international conference and the 10th National Bioinformatics Conference of Iran, Kish
2. Qalekhani, Farshad and Nabizadeh, Fatemeh, 2022, Pharmacoinformatics Study and High-Throughput Virtual Screening to Discover Effective Natural Compounds in Treatment of Erectile Dysfunction, The first international conference and the 10th National Bioinformatics Conference of Iran, Kish, https://civilica.com/doc/1473631/
3. Nabizadeh, Fatemeh and Nejatizadeh, Abdolazim and Shekari, Mohammad and Koochakkhani, Shabnaz and Allamehzadeh, Zeinab and Ahmadi, Banafsheh, 2018, A 3-year-old boy with lethargy, leg muscle degeneration, and mental retardation, The Third International and 15th National Genetics Congress, Tehran, https://civilica.com/doc/983916.
4. Koochakkhani, Shabnaz and Eftekhar, Ebrahim and Nabizadeh, Fatemeh and Nejatizadeh, Abdolazim, 2020, Assessment of MTHFR gene promoter methylation pattern in essential hypertensive patients, The fourth International and 16th National Genetics Congress, Tehran,https://civilica.com/doc/1195301.
5. Koochakkhani, Shabnaz and Shekari, Mohammad and Nejatizadeh, Abdolazim and Nabizadeh, Fatemeh and Allamehzadeh, Zeinab and Ahmadi, Banafsheh, 2018, Novel mutation in PNPLA1 gene, the causative defect in Lamellar Ichthyosis (LI), The Third International and 15th National Genetics Congress, Tehran, https://civilica.com/doc/983892.
6. Nabizadeh, Fatemeh, and Farshad Qalekhani, 2023, Unveiling the potential of NSAIDs to regulate a common oncomiR among various types of gastrointestinal cancer through a structural biology approach: an in-silico study, The First International Congress of Cancer Genomics (CGC2023)
7. TLR2 and TLR4 Genes Expression Analysis : A Hopeful Approach To Recognition Causes of Essential HypertensionMay 2018Conference: The Third International and 15th National Genetics CongressAt: Tehran, Iranian Genetics Society.
مشارکت در گرد آوری کتاب اطلس جامع بیماری های ژنتیکی در ایران، تحت نظر دانشگاه شهید چمران اهواز.