Hossein Darvish
Hossein Darvish
medical genetics
Verified email at sbmu.ac.ir
TitleCited byYear
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, 2011
The Sac1 Domain of SYNJ1 Identified Mutated in a Family with Early‐Onset Progressive Parkinsonism with Generalized Seizures
CE Krebs, S Karkheiran, JC Powell, M Cao, V Makarov, H Darvish, ...
Human mutation 34 (9), 1200-1207, 2013
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
Identification of a nonsense mutation in the very low-density lipoprotein receptor gene (VLDLR) in an Iranian family with dysequilibrium syndrome
LA Moheb, A Tzschach, M Garshasbi, K Kahrizi, H Darvish, Y Heshmati, ...
European journal of human genetics 16 (2), 270, 2008
Detection of copy number changes in genes associated with Parkinson's disease in Iranian patients
H Darvish, A Movafagh, MD Omrani, SG Firouzabadi, E Azargashb, ...
Neuroscience letters 551, 75-78, 2013
Evolutionary trend of exceptionally long human core promoter short tandem repeats
M Ohadi, S Mohammadparast, H Darvish
Gene 507 (1), 61-67, 2012
Glutamate receptor, metabotropic 7 (GRM7) gene variations and susceptibility to autism: A case–control study
R Noroozi, M Taheri, A Movafagh, R Mirfakhraie, G Solgi, A Sayad, ...
Autism Research 9 (11), 1161-1168, 2016
Core promoter STRs: novel mechanism for inter-individual variation in gene expression in humans
A Heidari, ZNS Fam, E Esmaeilzadeh-Gharehdaghi, M Banan, ...
Gene 492 (1), 195-198, 2012
A clinical and molecular genetic study of 50 families with autosomal recessive parkinsonism revealed known and novel gene mutations
S Taghavi, R Chaouni, A Tafakhori, LJ Azcona, SG Firouzabadi, ...
Molecular neurobiology 55 (4), 3477-3489, 2018
Variation in the miRNA-433 binding site of FGF20 is a risk factor for Parkinson's disease in Iranian population
L Haghnejad, B Emamalizadeh, J Jamshidi, AZ Bidoki, H Ghaedi, ...
Journal of the neurological sciences 355 (1-2), 72-74, 2015
Mutations in the histamine N-methyltransferase gene, HNMT, are associated with nonsyndromic autosomal recessive intellectual disability
A Heidari, C Tongsook, R Najafipour, L Musante, N Vasli, M Garshasbi, ...
Human molecular genetics 24 (20), 5697-5710, 2015
Core promoter short tandem repeats as evolutionary switch codes for primate speciation
M Ohadi, E Valipour, S Ghadimi‐Haddadan, P Namdar‐Aligoodarzi, ...
American journal of primatology 77 (1), 34-43, 2015
Biased homozygous haplotypes across the human caveolin 1 upstream purine complex in Parkinson’s disease
H Darvish, A Heidari, S Hosseinkhani, A Movafagh, A Khaligh, J Jamshidi, ...
Journal of Molecular Neuroscience 51 (2), 389-393, 2013
Novel evidence of the involvement of calreticulin in major psychiatric disorders
M Ohadi, A Mirabzadeh, E Esmaeilzadeh-Gharehdaghi, M Rezazadeh, ...
Progress in Neuro-Psychopharmacology and Biological Psychiatry 37 (2), 276-281, 2012
Exceptional human core promoter nucleotide compositions
H Darvish, MO Nabi, SG Firouzabadi, M Karimlou, A Heidari, ...
Gene 475 (2), 79-86, 2011
RIT2, a susceptibility gene for Parkinson's disease in Iranian population.
B Emamalizadeh, A Movafagh, M Akbari, S Kazeminasab, A Fazeli, ...
Neurobiology of aging 35 (12), e27, 2014
Fragile X syndrome screening of families with consanguineous and non-consanguineous parents in the Iranian population
AR Pouya, SS Abedini, N Mansoorian, F Behjati, N Nikzat, M Mohseni, ...
European journal of medical genetics 52 (4), 170-173, 2009
Identification of a Large DNAJB2 Deletion in a Family with Spinal Muscular Atrophy and Parkinsonism
E Sanchez, H Darvish, R Mesias, S Taghavi, SG Firouzabadi, RH Walker, ...
Human mutation 37 (11), 1180-1189, 2016
HLA‐DRA is associated with Parkinson's disease in Iranian population
J Jamshidi, A Movafagh, B Emamalizadeh, A Zare Bidoki, A Manafi, ...
International journal of immunogenetics 41 (6), 508-511, 2014
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