| Whole exome sequencing identifies both nuclear and mitochondrial variations in an Iranian family with non-syndromic hearing loss S Khatami, H Rokni-Zadeh, N Mohsen-Pour, A Biglari, M Changi-Ashtiani, ... Mitochondrion 46, 321-325, 2019 | 16 | 2019 |
| Phytochemical screening and Cytotoxicity assessment of Plantago lanceolata L. root extracts on Colorectal cancer cell lines and Brine shrimp larvae and determination of the … AS Samaneh Rahamouz-Haghighi, Khadijeh Bagheri , Mahdi Tavakkolizadeh, Neda ... South African Journal of Botany 149, Pages 740-747, 2022 | 15 | 2022 |
| Chromosome 9 inversion: pathogenic or benign? A comprehensive systematic review of all clinical reports N Mohsen-Pour, T Talebi, N Naderi, MH Moghadam, M Maleki, ... Current Molecular Medicine 22 (5), 385-400, 2022 | 13 | 2022 |
| Whole-exome sequencing identified compound heterozygous variants in the TTN gene causing Salih myopathy with dilated cardiomyopathy in an Iranian family M Mahdavi, N Mohsen-Pour, M Maleki, M Hesami, N Naderi, ... Cardiology in the Young 32 (9), 1462-1467, 2022 | 9 | 2022 |
| The association between in vitro fertilization and intracytoplasmic sperm injection treatment and the risk of congenital heart defects T Talebi, N Mohsen-Pour, M Hesami, M Maleki, S Kalayinia The Journal of Maternal-Fetal & Neonatal Medicine 35 (25), 7471-7485, 2022 | 7 | 2022 |
| in vitro Evaluation of Cytotoxicity and Antibacterial Activities of Ribwort Plantain (Plantago Lanceolata L.) Root Fractions and Phytochemical Analysis by Gas Chromatography … SA Rahamouz-Haghighi, Samaneh , Bagheri Khadujeh, Mohsen-Pour Neda Archives of Razi Institute 77, 2131-2143, 2022 | 6 | 2022 |
| In silico analysis of GATA4 variants demonstrates main contribution to congenital heart disease S Abbasi, N Mohsen-Pour, N Naderi, S Rahimi, M Maleki, S Kalayinia Journal of Cardiovascular and Thoracic Research 13 (4), 336, 2021 | 4 | 2021 |
| Quantitative determination of apigenin, catalpol, and gallic acid in total extracts from different parts of plantago species by high-performance liquid chromatography S Rahamouz-Haghighi, K Bagheri, N Mohsen-Pour, A Sharafi Avicenna Journal of Pharmaceutical Research 2 (2), 49-54, 2021 | 3 | 2021 |
| Whole exome sequencing revealed a novel GJB1 pathogenic variant and a rare BSCL2 mutation in two Iranian large pedigrees with multiple affected cases of Charcot-Marie-Tooth N Mohsenpour, H Roknizadeh, M Maghbooli, M Changi-Ashtiani, ... International Journal of Molecular and Cellular Medicine 8 (3), 169, 2019 | 3 | 2019 |
| Comparison of the Effect of Duloxetine and Imipramine in the Treatment of Patients with Diarrhea Dominant Irritable Bowel Syndrome S Jafari, SK Mahani, N Mohsen-Pour J Adv Med Biomed Res 32 (150), 33-40, 2024 | | 2024 |
| A novel heterozygous missense MYH7 mutation potentially causes an autosomal dominant form of myosin storage myopathy with dilated cardiomyopathy MMSK Niloofar Naderi, Neda Mohsen-Pour, Yalda Nilipour, Maryam Pourirahim BMC Cardiovascular Disorders 23, 487, 2023 | | 2023 |
| Toxicity Assessment of Euphorbia esula L. Extracts on HCT116, SW480, HEK293 Cell Lines, Artemia salina Larvae, and Its Bactericidal Effects S Rahamouz-Haghighi, N Mohsen-Pour Journal of Genetic Resources 9 (2), 123-132, 2023 | | 2023 |
| Whole-exome sequencing reveals a likely pathogenic LMNA variant causing hypertrophic cardiomyopathy KS 1. Mahdavi M, Mohsen-Pour N, Maleki M, Ghasemi S, Tabib A, Houshmand G ... Lab Med, 2023 | | 2023 |
| Whole-Exome Sequencing Revealed a Pathogenic Nonsense Variant in the SLC19A2 Gene in an Iranian Family with Thiamine-Responsive Megaloblastic Anemia N Mohsen-Pour, N Naderi, S Ghasemi, M Hesami, M Maleki, S Kalayinia Laboratory Medicine 53 (6), 640-650, 2022 | | 2022 |
