| Deep sequencing reveals 50 novel genes for recessive cognitive disorders H Najmabadi, H Hu, M Garshasbi, T Zemojtel, SS Abedini, W Chen, ... Nature 478 (7367), 57-63, 2011 | 1045 | 2011 |
| Homozygosity mapping in consanguineous families reveals extreme heterogeneity of non-syndromic autosomal recessive mental retardation and identifies 8 novel gene loci H Najmabadi, MM Motazacker, M Garshasbi, K Kahrizi, A Tzschach, ... Human genetics 121, 43-48, 2007 | 150 | 2007 |
| A clinical and molecular genetic study of 112 Iranian families with primary microcephaly H Darvish, S Esmaeeli-Nieh, GB Monajemi, M Mohseni, ... Journal of medical genetics, 2010 | 120 | 2010 |
| Mutation of the conserved polyadenosine RNA binding protein, ZC3H14/dNab2, impairs neural function in Drosophila and humans CH Pak, M Garshasbi, K Kahrizi, C Gross, LH Apponi, JJ Noto, SM Kelly, ... Proceedings of the National Academy of Sciences 108 (30), 12390-12395, 2011 | 97 | 2011 |
| Alginate/chitosan hydrogel containing olfactory ectomesenchymal stem cells for sciatic nerve tissue engineering M Salehi, Z Bagher, SK Kamrava, A Ehterami, R Alizadeh, M Farhadi, ... Journal of cellular physiology 234 (9), 15357-15368, 2019 | 91 | 2019 |
| Autosomal recessive mental retardation: homozygosity mapping identifies 27 single linkage intervals, at least 14 novel loci and several mutation hotspots AW Kuss, M Garshasbi, K Kahrizi, A Tzschach, F Behjati, H Darvish, ... Human genetics 129, 141-148, 2011 | 74 | 2011 |
| Differentiation of human mesenchymal stem cells (MSC) to dopaminergic neurons: A comparison between Wharton’s Jelly and olfactory mucosa as sources of MSCs R Alizadeh, Z Bagher, SK Kamrava, M Falah, HG Hamidabadi, ... Journal of chemical neuroanatomy 96, 126-133, 2019 | 72 | 2019 |
| A novel nonsense mutation in TUSC3 is responsible for non‐syndromic autosomal recessive mental retardation in a consanguineous Iranian family M Garshasbi, K Kahrizi, M Hosseini, L Nouri Vahid, M Falah, S Hemmati, ... American journal of medical genetics Part A 155 (8), 1976-1980, 2011 | 65 | 2011 |
| Human olfactory stem cells: As a promising source of dopaminergic neuron-like cells for treatment of Parkinson's disease R Alizadeh, SK Kamrava, Z Bagher, M Farhadi, M Falah, F Moradi, ... Neuroscience letters 696, 52-59, 2019 | 39 | 2019 |
| Differentiation of neural crest stem cells from nasal mucosa into motor neuron-like cells Z Bagher, SK Kamrava, R Alizadeh, M Farhadi, M Absalan, M Falah, ... Journal of chemical neuroanatomy 92, 35-40, 2018 | 39 | 2018 |
| Expression levels of the BAK1 and BCL2 genes highlight the role of apoptosis in age-related hearing impairment M Falah, M Najafi, M Houshmand, M Farhadi Clinical interventions in aging, 1003-1008, 2016 | 26 | 2016 |
| Association of genetic variations in the mitochondrial DNA control region with presbycusis M Falah, M Farhadi, SK Kamrava, S Mahmoudian, A Daneshi, M Balali, ... Clinical interventions in aging, 459-465, 2017 | 22 | 2017 |
| Identification of a critical novel mutation in the exon 1 of androgen receptor gene in 2 brothers with complete androgen insensitivity syndrome R Radpour, M Falah, A Aslani, XY Zhong, A Saleki Journal of andrology 30 (3), 230-232, 2009 | 22 | 2009 |
| The potential role for use of mitochondrial DNA copy number as predictive biomarker in presbycusis M Falah, M Houshmand, M Najafi, M Balali, S Mahmoudian, A Asghari, ... Therapeutics and Clinical Risk Management, 1573-1578, 2016 | 19 | 2016 |
| Novel nucleotide changes in mutational analysis of mitochondrial 12SrRNA gene in patients with nonsyndromic and aminoglycoside-induced hearing loss MA Dowlati, P Derakhshandeh-Peykar, M Houshmand, M Farhadi, ... Molecular biology reports 40, 2689-2695, 2013 | 17 | 2013 |
| Role of GJB2 and GJB6 in Iranian Nonsyndromic Hearing Impairment: From Molecular Analysis to Literature Reviews M Falah, M Houshmand, M Balali, A Asghari, Z Bagher, R Alizadeh, ... Fetal and Pediatric Pathology 39 (1), 1-12, 2020 | 15 | 2020 |
| Chromosome abnormality rate among Iranian patients with idiopathic mental retardation from consanguineous marriages F Behjati, SG Firouzabadi, K Kahrizi, R Kariminejad, I Bagherizadeh, ... Archives of Medical Science 7 (2), 321-325, 2011 | 14 | 2011 |
| The genetic landscape and possible therapeutics of neurofibromatosis type 2 MA Ghalavand, A Asghari, M Farhadi, F Taghizadeh-Hesary, M Garshasbi, ... Cancer Cell International 23 (1), 1-27, 2023 | 13 | 2023 |
| Novel phenotype and genotype spectrum of NARS2 and literature review of previous mutations M Vafaee-Shahi, M Farhadi, E Razmara, S Morovvati, S Ghasemi, ... Irish Journal of Medical Science (1971-) 191 (4), 1877-1890, 2022 | 13 | 2022 |
| The anticipation and inheritance pattern of c. 487A> G mutation in the GJB2 gene M Falah, M Houshmand, S Mahmoudian, H Emamdjomeh, Y Ghavami, ... ARCHIVES OF IRANIAN MEDICINE 15 (1), 49-51, 2012 | 13 | 2012 |
Mohammad FarhadiENT and Head&Neck Research Center, Iran University of Medical Sciences在 iums.ac.ir 的电子邮件经过验证
