Majid Fardaei
Majid Fardaei
Associate Professor of Human Genetics
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Three proteins, MBNL, MBLL and MBXL, co-localize in vivo with nuclear foci of expanded-repeat transcripts in DM1 and DM2 cells
M Fardaei, MT Rogers, HM Thorpe, K Larkin, MG Hamshere, PS Harper, ...
Human molecular genetics 11 (7), 805-814, 2002
In vivo co-localisation of MBNL protein with DMPK expanded-repeat transcripts
M Fardaei, K Larkin, JD Brook, MG Hamshere
Nucleic acids research 29 (13), 2766-2771, 2001
Muscleblind-like proteins: similarities and differences in normal and myotonic dystrophy muscle
I Holt, V Jacquemin, M Fardaei, CA Sewry, GS Butler-Browne, D Furling, ...
The American journal of pathology 174 (1), 216-227, 2009
Myotonic dystrophy—a multigene disorder
K Larkin, M Fardaei
Brain research bulletin 56 (3-4), 389-395, 2001
The genetics of recurrent hydatidiform moles: new insights and lessons from a comprehensive analysis of 113 patients
NMP Nguyen, Y Khawajkie, N Mechtouf, M Rezaei, M Breguet, ...
Modern Pathology 31 (7), 1116-1130, 2018
Auricular or body acupuncture: which one is more effective in reducing abdominal fat mass in Iranian men with obesity: a randomized clinical trial
M Darbandi, S Darbandi, AA Owji, P Mokarram, MG Mobarhan, M Fardaei, ...
Journal of Diabetes & Metabolic Disorders 13, 1-7, 2014
Effect of MIND diet intervention on cognitive performance and brain structure in healthy obese women: a randomized controlled trial
G Arjmand, M Abbas-Zadeh, MH Eftekhari
Scientific Reports 12 (1), 2871, 2022
Association of FTO rs9939609 polymorphism with serum leptin, insulin, adiponectin, and lipid profile in overweight adults
M Mehrdad, S Doaei, M Gholamalizadeh, M Fardaei, M Fararouei, ...
Adipocyte 9 (1), 51-56, 2020
Two novel mutations in the KHDC3L gene in Asian patients with recurrent hydatidiform mole
M Rezaei, NMP Nguyen, L Foroughinia, P Dash, F Ahmadpour, IC Verma, ...
Human genome variation 3 (1), 1-5, 2016
Clinical and genetic-epigenetic aspects of recurrent hydatidiform mole: a review of literature
N Moein-Vaziri, J Fallahi, B Namavar-Jahromi, M Fardaei, M Momtahan, ...
Taiwanese Journal of Obstetrics and Gynecology 57 (1), 1-6, 2018
Effects of auricular acupressure combined with low-calorie diet on the leptin hormone in obese and overweight Iranian individuals
M Darbandi, S Darbandi, MG Mobarhan, AA Owji, B Zhao, K Iraji, H Abdi, ...
Acupuncture in Medicine 30 (3), 208-213, 2012
The genomic architecture of NLRP7 is Alu rich and predisposes to disease-associated large deletions
R Reddy, NMP Nguyen, G Sarrabay, M Rezaei, MCG Rivas, A Kavasoglu, ...
European Journal of Human Genetics 24 (10), 1445-1452, 2016
Enhancing stability of destabilized green fluorescent protein using chimeric mRNA containing human beta-globin 5′ and 3′ untranslated regions
S Adibzadeh, M Fardaei, MA Takhshid, MR Miri, GR Dehbidi, A Farhadi, ...
Avicenna Journal of Medical Biotechnology 11 (1), 112, 2019
A novel mutation in NLRP7 related to recurrent hydatidiform mole and reproductive failure
J Fallahi, V Razban, M Momtahan, M Akbarzadeh-Jahromi, ...
International journal of fertility & sterility 13 (2), 135, 2019
VSX1 and SOD1 Mutation Screening in Patients with Keratoconus in the South of Iran
M Nejabat, P Naghash, H Dastsooz, S Mohammadi, M Alipour, M Fardaei
Journal of ophthalmic & vision research 12 (2), 135, 2017
Novel pathogenic variants in NLRP7, NLRP5, and PADI6 in patients with recurrent hydatidiform moles and reproductive failure
M Rezaei, B Suresh, E Bereke, Z Hadipour, M Aguinaga, J Qian, R Bagga, ...
Clinical Genetics 99 (6), 823-828, 2021
High dietary inflammatory index (DII) scores increase odds of overweight in adults with rs9939609 polymorphism of FTO gene
M Mehrdad, F Vahid, N Shivappa, JR Hébert, M Fardaei, MH Eftekhari
Clinical Nutrition ESPEN 42, 221-226, 2021
The association between FTO rs9939609 gene polymorphism and anthropometric indices in adults
M Mehrdad, M Fardaei, M Fararouei, MH Eftekhari
Journal of physiological anthropology 39, 1-7, 2020
A case report: Autosomal recessive microcephaly caused by a novel mutation in MCPH1 gene
S Ghafouri-Fard, M Fardaei, M Gholami, M Miryounesi
Gene 571 (1), 149-150, 2015
A Novel Mutation in ERCC8 Gene Causing Cockayne Syndrome
M Taghdiri, H Dastsooz, M Fardaei, S Mohammadi, MA Farazi Fard, ...
Frontiers in pediatrics 5, 169, 2017
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