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Hossein Darvish
Hossein Darvish
medical genetics
Verified email at sbmu.ac.ir
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Cited by
Cited by
Year
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
10212011
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
3702013
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
1222010
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, 3477-3489, 2018
742018
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
742011
Genotype–phenotype associations in hereditary spastic paraplegia: a systematic review and meta-analysis on 13,570 patients
M Erfanian Omidvar, S Torkamandi, S Rezaei, B Alipoor, MD Omrani, ...
Journal of neurology 268, 2065-2082, 2021
692021
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), 270-273, 2008
652008
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
562016
Defining the clinical, molecular and imaging spectrum of adaptor protein complex 4-associated hereditary spastic paraplegia
D Ebrahimi-Fakhari, J Teinert, R Behne, M Wimmer, A D'amore, ...
Brain 143 (10), 2929-2944, 2020
512020
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
452016
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
452013
Bi-allelic variants in RNF170 are associated with hereditary spastic paraplegia
M Wagner, DPS Osborn, I Gehweiler, M Nagel, U Ulmer, S Bakhtiari, ...
Nature communications 10 (1), 4790, 2019
432019
Identification of a large homozygous VPS13C deletion in a patient with early-onset Parkinsonism
H Darvish, P Bravo, A Tafakhori, LJ Azcona, S Ranji-Burachaloo, ...
Movement disorders: official journal of the Movement Disorder Society 33 (12 …, 2018
432018
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
402015
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
402015
PTRHD1 (C2orf79) mutations lead to autosomal‐recessive intellectual disability and parkinsonism
H Khodadadi, LJ Azcona, V Aghamollaii, MD Omrani, M Garshasbi, ...
Movement Disorders 32 (2), 287-291, 2017
362017
RIT2 Polymorphisms: Is There a Differential Association?
B Emamalizadeh, J Jamshidi, A Movafagh, M Ohadi, MS Khaniani, ...
Molecular neurobiology 54, 2234-2240, 2017
352017
Bi-allelic HPDL variants cause a neurodegenerative disease ranging from neonatal encephalopathy to adolescent-onset spastic paraplegia
RA Husain, M Grimmel, M Wagner, JC Hennings, C Marx, RG Feichtinger, ...
The American Journal of Human Genetics 107 (2), 364-373, 2020
342020
COL18A1 is a candidate eye iridocorneal angle-closure gene in humans
F Suri, S Yazdani, M Chapi, I Safari, P Rasooli, N Daftarian, ...
Human molecular genetics 27 (21), 3772-3786, 2018
342018
Evolutionary trend of exceptionally long human core promoter short tandem repeats
M Ohadi, S Mohammadparast, H Darvish
Gene 507 (1), 61-67, 2012
342012
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