| Biallelic variants in KIF14 cause intellectual disability with microcephaly P Makrythanasis, R Maroofian, A Stray-Pedersen, D Musaev, MS Zaki, ... European Journal of Human Genetics 26 (3), 330-339, 2018 | 67 | 2018 |
| Curcumin in tissue engineering: A traditional remedy for modern medicine N Ahangari, S Kargozar, M Ghayour‐Mobarhan, F Baino, A Pasdar, ... BioFactors 45 (2), 135-151, 2019 | 62 | 2019 |
| Circulating exosomal miRNAs in cardiovascular disease pathogenesis: New emerging hopes AS Aghabozorgi, N Ahangari, TE Eftekhaari, PN Torbati, A Bahiraee, ... Journal of cellular physiology 234 (12), 21796-21809, 2019 | 55 | 2019 |
| Cardiomyopathy with lethal arrhythmias associated with inactivation of KLHL24 C Hedberg-Oldfors, A Abramsson, DPS Osborn, O Danielsson, ... Human molecular genetics 28 (11), 1919-1929, 2019 | 40 | 2019 |
| Bi-allelic variants in HOPS complex subunit VPS41 cause cerebellar ataxia and abnormal membrane trafficking LE Sanderson, K Lanko, M Alsagob, R Almass, N Al-Ahmadi, M Najafi, ... Brain 144 (3), 769-780, 2021 | 36 | 2021 |
| Hereditary thrombophilia genetic variants in recurrent pregnancy loss N Ahangari, M Doosti, N Mousavifar, M Attaran, S Shahrokhzadeh, ... Archives of Gynecology and Obstetrics 300, 777-782, 2019 | 35 | 2019 |
| Expanding the clinical phenotype of IARS2-related mitochondrial disease B Vona, R Maroofian, E Bellacchio, M Najafi, K Thompson, A Alahmad, ... BMC Medical Genetics 19, 1-16, 2018 | 23 | 2018 |
| Personalised medicine in hypercholesterolaemia: the role of pharmacogenetics in statin therapy N Ahangari, M Doosti, M Ghayour Mobarhan, A Sahebkar, GA Ferns, ... Annals of Medicine 52 (8), 462-470, 2020 | 21 | 2020 |
| Brain monoamine vesicular transport disease caused by homozygous SLC18A2 variants: A study in 42 affected individuals K Saida, R Maroofian, T Sengoku, T Mitani, AT Pagnamenta, D Marafi, ... Genetics in Medicine 25 (1), 90-102, 2023 | 17 | 2023 |
| Molecular aspects of hypercholesterolemia treatment: current perspectives and hopes N Ahangari, M Ghayour Mobarhan, A Sahebkar, A Pasdar Annals of medicine 50 (4), 303-311, 2018 | 17 | 2018 |
| Genetic linkage analysis of DFNB4, DFNB28, DFNB93 loci in autosomal recessive non-syndromic hearing loss: evidence for digenic inheritance in GJB2 and GJB3 mutations M Naseri, M Akbarzadehlaleh, M Masoudi, N Ahangari, AAP Zonouzi, ... Iranian Journal of Public Health 47 (1), 95, 2018 | 15 | 2018 |
| The association between a Fatty Acid Binding Protein 1 (FABP1) gene polymorphism and serum lipid abnormalities in the MASHAD cohort study M Valizadeh, M Aghasizadeh, M Nemati, M Hashemi, ... Prostaglandins, Leukotrienes and Essential Fatty Acids 172, 102324, 2021 | 13 | 2021 |
| The effect of nanomicelle curcumin, sorafenib, and combination of the two on the cyclin D1 gene expression of the hepatocellular carcinoma cell line (HUH7) S Hosseini, J Chamani, M Sinichi, AM Bonakdar, Z Azad, N Ahangari, ... Iranian Journal of Basic Medical Sciences 22 (10), 1198, 2019 | 13 | 2019 |
| Diverse pattern of gap junction beta-2 and gap junction beta-4 genes mutations and lack of contribution of DFNB21, DFNB24, DFNB29, and DFNB42 loci in autosomal recessive … MA Laleh, M Naseri, AAP Zonouzi, AP Zonouzi, M Masoudi, N Ahangari, ... Journal of research in medical sciences: the official journal of Isfahan …, 2017 | 10 | 2017 |
| Genetic linkage analysis of DFNB3, DFNB9 and DFNB21 loci in GJB2 negative families with autosomal recessive non-syndromic hearing loss M Masoudi, N Ahangari, AAP Zonouzi, AP Zonouzi, A Nejatizadeh Iranian Journal of Public Health 45 (5), 680, 2016 | 10 | 2016 |
| A common ancestral Asn242Ser mutation in TMEM67 identified in multiple Iranian families with Joubert syndrome MR Dehghani, M Mojarad, E Ghayoor Karimiani, MY Vahidi Mehrjardi, ... Public health genomics 20 (3), 188-193, 2017 | 8 | 2017 |
| Congenital heart defects among Down syndrome patients: a clinical profiling AA Poursadegh Zonouzi, N Ahangari, S Rajai, A Poursadegh Zonouzi, ... Journal of Public Health 24, 57-63, 2016 | 7 | 2016 |
| Niemann-Pick Diseases: The Largest Iranian Cohort with Genetic Analysis S Hashemian, P Eshraghi, N Dilaver, H Galehdari, B Shalbafan, R Vakili, ... Iranian journal of child neurology 13 (2), 155, 2019 | 5 | 2019 |
| The clinical and genetic spectrum of autosomal-recessive TOR1A-related disorders A Saffari, T Lau, H Tajsharghi, EG Karimiani, A Kariminejad, S Efthymiou, ... Brain 146 (8), 3273-3288, 2023 | 4 | 2023 |
| Association between trace element status and depression in HTLV-1-infected patients: a retrospective cohort study S Darroudi, S Abolbashari, N Ahangari, M Tayefi, Z Khashyarmanesh, ... Biological Trace Element Research 191, 75-80, 2019 | 4 | 2019 |
Ehsan Ghayoor KarimianiConsultant Medical Geneticist, Hon. Lecturer at St George's, University of London.Verified email at sgul.ac.uk
