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Scientific Reports|January 24, 2020
Phenotypic and genotypic characterization of families with complex intellectual disability identified pathogenic genetic variations in known and novel disease genesHossein Darvish, Luis J Azcona, Abbas Tafakhori, et al.
International Journal of Molecular and Cellular Medicine|March 31, 2017
Analysis of Copy Number Variations in Patients with Autism Using Cytogenetic and MLPA Techniques: Report of 16p13.1p13.3 and 10q26.3 DuplicationsSaghar Ghasemi Firouzabadi, Roshanak Vameghi, Roxana Kariminejad, et al.
Molecular Neurobiology|November 1, 2016
Copy Number Variants in Patients with Autism and Additional Clinical Features: Report of VIPR2 Duplication and a Novel Microduplication SyndromeSaghar Ghasemi Firouzabadi, Roxana Kariminejad, Roshanak Vameghi, et al.
Genetic Testing and Molecular Biomarkers|July 21, 2017
Support for "Disease-Only" Genotypes and Excess of Homozygosity at the CYTH4 Primate-Specific GTTT-Repeat in SchizophreniaEhteram Khademi, Elham Alehabib, Ehsan Esmaili Shandiz, et al.
European Journal of Medical Genetics|January 17, 2016
c.376G>A mutation in WFS1 gene causes Wolfram syndrome without deafnessBehnam Safarpour Lima, Hamid Ghaedi, Narsis Daftarian, et al.
Journal of Neural Transmission (Vienna, Austria : 1996)|September 11, 2015
A genetic variant in CAMKK2 gene is possibly associated with increased risk of bipolar disorderMinoo Atakhorrami, Simin Rahimi-Aliabadi, Javad Jamshidi, et al.
Journal of Molecular Neuroscience : MN|May 4, 2013
Biased homozygous haplotypes across the human caveolin 1 upstream purine complex in Parkinson's diseaseHossein Darvish, Abolfazl Heidari, Saman Hosseinkhani, et al.
Journal of the Neurological Sciences|June 14, 2015
Variation in the miRNA-433 binding site of FGF20 is a risk factor for Parkinson's disease in Iranian populationLeyla Haghnejad, Babak Emamalizadeh, Javad Jamshidi, et al.
Neuroscience Letters|July 25, 2013
Detection of copy number changes in genes associated with Parkinson's disease in Iranian patientsHossein Darvish, Abolfazl Movafagh, Mir Davood Omrani, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|January 7, 2016
The analysis of association between SNCA, HUSEYO and CSMD1 gene variants and Parkinson's disease in Iranian populationNeda Shahmohammadibeni, Simin Rahimi-Aliabadi, Javad Jamshidi, et al.
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