|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
|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 (1), 43-48, 2007
|Survival rate of gastric and esophageal cancers in Ardabil province, North-West of Iran|
F Samadi, ED NASR, AR SAJADI, MH DERAKHSHAN, R Malekzadeh, ...
ARCHIVES OF IRANIAN MEDICINE 10 (1), 32-37, 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 47 (12), 823-828, 2010
|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 (2), 141-148, 2011
|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
|Cancer incidence and mortality in Ardabil: Report of an ongoing population-based cancer registry in Iran, 2004-2006|
M Babaei, H Jaafarzadeh, AR Sadjadi, F Samadi, A Yazdanbod, M Fallah, ...
Iranian Journal of Public Health, 35-45, 2009
|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
|The immunologic response to anti-hepatitis B vaccination among medical students of Guilan University of Medical Sciences, Guilan, Iran|
GF Mansour, MS FALAH, SR JAAFAR, F JOUKAR, M Arami, EA ALE, ...
HEPATITIS MONTHLY 6 (2), 63-66, 2006
|Prevalence of hepatitis B surface antigen and hepatitis C virus antibody and their risk factors among Guilan's volunteer blood donors (1998-2003)|
GF MANSOUR, MS FALAH, R Jafarshad, F Joukar, A Salari, ZR TAVAF
HEPATITIS MONTHLY 7 (4), 239-241, 2007
|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
|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
|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
|Causes of catastrophic failure of high Mn steel utilized as crusher overlaying shields|
INTERNATIONAL JOURNAL OF ENGINEERING 21 (1), 55-64, 2008
|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 11, 1003, 2016
|Seroprevalence of hepatitis B and C among residents of Guilan Nursing Home|
GF MANSOUR, MS FALAH, SR JAAFAR, F Joukar, TA POUR, ...
HEPATITIS MONTHLY 7 (3), 139-141, 2007
|Epidemiology of malaria in Hamadan province during a 20-year period (1980-2001)|
M FALAH, A MIRAARAB, F JAMALIAN, A Ghaderi, AA ZOU
JOURNAL OF KERMANSHAH UNIVERSITY OF MEDICAL SCIENCES (BEHBOOD) 7 (2), 36-44, 2003
|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
|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 12, 1573, 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 (3), 2689-2695, 2013