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Yousef Daneshmandpour
Yousef Daneshmandpour
Department of Medical Genetics, Faculty of Medicine, Tabriz University of Medical Sciences, Tabriz
Bestätigte E-Mail-Adresse bei tbzmed.ac.ir
Titel
Zitiert von
Zitiert von
Jahr
MicroRNAs association with azoospermia, oligospermia, asthenozoospermia, and teratozoospermia: a systematic review
Y Daneshmandpour, Z Bahmanpour, H Hamzeiy, ...
Journal of assisted reproduction and genetics 37, 763-775, 2020
392020
Features, genetics and their correlation in Jalili syndrome: a systematic review
Y Daneshmandpour, H Darvish, F Pashazadeh, B Emamalizadeh
Journal of Medical Genetics 56 (6), 358-369, 2019
202019
Molecular insight into the therapeutic potential of long non-coding RNA-associated competing endogenous RNA axes in Alzheimer’s disease: a systematic scoping review
H Sabaie, N Amirinejad, MR Asadi, A Jalaiei, Y Daneshmandpour, ...
Frontiers in Aging Neuroscience 13, 742242, 2021
182021
An updated overview and classification of bioinformatics tools for MicroRNA analysis, which one to choose?
SS Mortazavi, Z Bahmanpour, Y Daneshmandpour, F Roudbari, ...
Computers in biology and medicine 134, 104544, 2021
182021
RIT2: responsible and susceptible gene for neurological and psychiatric disorders
Y Daneshmandpour, H Darvish, B Emamalizadeh
Molecular genetics and genomics 293, 785-792, 2018
172018
Long non-coding RNA-associated competing endogenous RNA axes in the olfactory epithelium in schizophrenia: a bioinformatics analysis
H Sabaie, M Mazaheri Moghaddam, M Mazaheri Moghaddam, ...
Scientific Reports 11 (1), 24497, 2021
122021
Mutational analysis of CYP1B1 gene in Iranian pedigrees with glaucoma reveals known and novel mutations
B Emamalizadeh, Y Daneshmandpour, S Kazeminasb, ...
International Ophthalmology 41 (10), 3269-3276, 2021
62021
A novel splice site mutation in the SDCCAG8 gene in an Iranian family with Bardet–Biedl syndrome
Z Bahmanpour, Y Daneshmandpour, S Kazeminasab, S Khalil Khalili, ...
International Ophthalmology 41, 389-397, 2021
62021
A new report of autoinflammation and PLCG2-associated antibody deficiency and immune dysregulation (APLAID) with a homozygous pattern from Iran
A Khabbazi, HR Kafshboran, MN Aghdam, JN Nojadeh, H Daghagh, ...
Immunology Letters 221, 27-32, 2020
62020
The comparative effect of magnetic activated cell sorting, density gradient centrifugation and swim up on assisted reproduction outcomes, sperm DNA fragmentation, and …
Y Daneshmandpour, F Pashazadeh, F Ansari, H Hosseinifard, M Nouri, ...
Meta Gene 22, 100607, 2019
62019
A novel mutation in the ALS2 gene in an iranian kurdish family with juvenile amyotrophic lateral sclerosis
Y Daneshmandpour, Z Bahmanpour, S Kazeminasab, ...
Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration 24 (1-2), 148-151, 2023
32023
Novel ABCD1 gene mutations in Iranian pedigrees with X-linked adrenoleukodystrophy
B Emamalizadeh, Y Daneshmandpour, A Tafakhori, S Ranji-Burachaloo, ...
Journal of Pediatric Endocrinology and Metabolism 32 (11), 1207-1215, 2019
22019
Homozygous mutation in CSF1R causes brain abnormalities, neurodegeneration, and dysosteosclerosis (BANDDOS)
H Daghagh, HR Kafshboran, Y Daneshmandpour, MN Aghdam, ...
BioImpacts: BI 13 (3), 183, 2023
12023
Lrp8 (rs5177) and cep85l (rs11756438) are contributed to schizophrenia susceptibility in iranian population
E Poursaei, Y Daneshmandpour, EA Moghadam, M Abolghasemi, ...
Psychiatric Genetics 30 (6), 162-165, 2020
12020
Genetic analysis of rs11038167, rs11038172 and rs835784 polymorphisms of the TSPAN18 gene in Iranian schizophrenia patients
P Shokraeian, Y Daneshmandpour, J Jamshidi, B Emamalizadeh, ...
Meta Gene 22, 100609, 2019
12019
MMP9 (RS20544) and ADCY2 (RS58502974) as susceptibility factors for schizophrenia in Iranian population
M Abolghasemi, Y Daneshmandpour, E Poursaei, J Jamshidi, ...
Meta Gene 26, 100810, 2020
2020
Molecular analysis of CTLA4 gene in patients with Behçet's disease from an Iranian Northwest Azeri population
S Abbaspour-Aghdam, M Ahmadi, S Aslani, Y Daneshmandpour, ...
Gene Reports 19, 100612, 2020
2020
The Analysis of expression level of UBE2B and CX3CR1 in sperm cell of infertile patients
Y Daneshmandpour
Tabriz University of Medical Sciences, Faculty of Medicine, 2019
2019
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