| A Form of the Metabolic Syndrome Associated with Mutations in DYRK1B AR Keramati, M Fathzadeh, GW Go, R Singh, M Choi, S Faramarzi, ... New England Journal of Medicine 370 (20), 1909-1919, 2014 | 130 | 2014 |
| Rare Nonconservative LRP6 Mutations Are Associated with Metabolic Syndrome R Singh, E Smith, M Fathzadeh, W Liu, GW Go, L Subrahmanyan, ... Human mutation 34 (9), 1221-1225, 2013 | 78 | 2013 |
| Epidemiological and clinical study of Phenylketonuria (PKU) disease in the National Screening Program of Neonates, Fars province, Southern Iran S Senemar, H Ganjekarimi, M Fathzadeh, B Tarami, M Bazrgar Iranian Journal of Public Health 38 (2), 58-64, 2009 | 43 | 2009 |
| Mutations in the histone modifier PRDM6 are associated with isolated nonsyndromic patent ductus arteriosus N Li, L Subrahmanyan, E Smith, X Yu, S Zaidi, M Choi, S Mane, ... The American Journal of Human Genetics 98 (6), 1082-1091, 2016 | 42 | 2016 |
| Apolipoprotein E polymorphism in Southern Iran: E4 allele in the lowest reported amounts M Bazrgar, M Karimi, M Fathzadeh, S Senemar, F Peiravian, A Shojaee, ... Molecular biology reports 35, 495-499, 2008 | 42 | 2008 |
| Genetic counseling in southern Iran: consanguinity and reason for referral M Fathzadeh, MA Babaie Bigi, M Bazrgar, M Yavarian, HR Tabatabaee, ... Journal of genetic counseling 17, 472-479, 2008 | 41 | 2008 |
| FAM13A affects body fat distribution and adipocyte function M Fathzadeh, J Li, A Rao, N Cook, I Chennamsetty, M Seldin, X Zhou, ... Nature communications 11 (1), 1465, 2020 | 39 | 2020 |
| Nat1 deficiency is associated with mitochondrial dysfunction and exercise intolerance in mice I Chennamsetty, M Coronado, K Contrepois, MP Keller, I Carcamo-Orive, ... Cell reports 17 (2), 527-540, 2016 | 38 | 2016 |
| CELA2A mutations predispose to early-onset atherosclerosis and metabolic syndrome and affect plasma insulin and platelet activation F Esteghamat, JS Broughton, E Smith, R Cardone, T Tyagi, M Guerra, ... Nature genetics 51 (8), 1233-1243, 2019 | 29 | 2019 |
| Dyrk1b promotes hepatic lipogenesis by bypassing canonical insulin signaling and directly activating mTORC2 in mice N Bhat, A Narayanan, M Fathzadeh, M Kahn, D Zhang, L Goedeke, ... The Journal of clinical investigation 132 (3), 2022 | 22 | 2022 |
| The protective effect of transcription factor 7-like 2 risk allele rs7903146 against elevated fasting plasma triglyceride in type 2 diabetes: a meta-analysis S Wang, K Song, R Srivastava, M Fathzadeh, N Li, A Mani Journal of diabetes research 2015, 2015 | 17 | 2015 |
| Apolipoprotein E gene polymorphism and left ventricular function in Iranian patients with thalassemia major M Bazrgar, M Karimi, F Peiravian, M Fathzadeh Haematologica 92 (2), 256-257, 2007 | 10 | 2007 |
| Epidemiological Study of T4, T3 and TSH Mean Concentrations in Four Iranian Populations M Fathzadeh, Y Seyedna, DD Farhud, H Khazali, M Sheidai Iranian Journal of Public Health 34, 1-2, 2005 | 9 | 2005 |
| The Human Arylamine N-Acetyltransferase Type 2 Gene: Genomics and Cardiometabolic Risk M Fathzadeh, DW Hein, JW Knowles ARYLAMINE N-ACETYLTRANSFERASES IN HEALTH AND DISEASE: From Pharmacogenetics …, 2018 | 5 | 2018 |
| Dyrk1b promotes autophagy during skeletal muscle differentiation by upregulating 4e-bp1 N Bhat, A Narayanan, M Fathzadeh, K Shah, M Dianatpour, MD Abou Ziki, ... Cellular signalling 90, 110186, 2022 | 4 | 2022 |
| Predictive Value of Cardiovascular Risk Factors for Risk Assessment in Cohort of Shiraz Heart Study M Fathzadeh, MJ ZIBAEINEZHAD, BMA BABAEI, SH KHOSROUPANAH, ... INTERNATIONAL CARDIOVASCULAR RESEARCH JOURNAL 4 (1), 8-13, 2010 | 4 | 2010 |
| Genetic and non-genetic abnormalities in children with cousin and non-cousin parents M Fathzadeh, N Hadi, MA Babaeebeigi, M Bazrgar, M Darboee, ... Journal of Researches Medical Science 3 (4), 95-102, 2005 | 4 | 2005 |
| Correlation between left ventricular dysfunction with hematological parameters and Iron chelation in β-thalassemia major M Bazregar, F Peiravian, M Karimi, M Fathzadeh JOURNAL OF MEDICAL RESEARCH (JMR) 3 (1), 48-57, 2004 | 4 | 2004 |
| Frequency of cystathionine b-synthase 844ins 68 polymorphism in southern Iraninan population S SENEMAR, M FATHZADEH, M BAZREGAR, M DOROUDCHI, ... IRANIAN JOURNAL OF BIOLOGY 20 (2), 225-232, 2007 | 3 | 2007 |
| Dyrk1b is a key Regulatory Kinase Integrating Fgf, Shh and mTORC1 signaling in Skeletal Muscle Development and Homeostasis N Bhat, A Narayanan, M Fathzadeh, A Srivastava, A Mani bioRxiv, 2020.04. 22.055947, 2020 | 1 | 2020 |
Masood BazrgarGenetics Department, Royan Institute, Tehran, Iran.Email verificata su royaninstitute.org
