Detalhe da pesquisa
1.
Prognostic potential of circulating cell free mitochondrial DNA levels in COVID-19 patients.
Mol Biol Rep
; 50(12): 10249-10255, 2023 Dec.
Artigo
Inglês
| MEDLINE | ID: mdl-37934373
2.
A novel splice site mutation in the SDCCAG8 gene in an Iranian family with Bardet-Biedl syndrome.
Int Ophthalmol
; 41(2): 389-397, 2021 Feb.
Artigo
Inglês
| MEDLINE | ID: mdl-32926352
3.
Mutational analysis of CYP1B1 gene in Iranian pedigrees with glaucoma reveals known and novel mutations.
Int Ophthalmol
; 41(10): 3269-3276, 2021 Oct.
Artigo
Inglês
| MEDLINE | ID: mdl-34019190
4.
Features, genetics and their correlation in Jalili syndrome: a systematic review.
J Med Genet
; 56(6): 358-369, 2019 06.
Artigo
Inglês
| MEDLINE | ID: mdl-30705057
5.
RIT2: responsible and susceptible gene for neurological and psychiatric disorders.
Mol Genet Genomics
; 293(4): 785-792, 2018 Aug.
Artigo
Inglês
| MEDLINE | ID: mdl-29860660
6.
The human RIT2 core promoter short tandem repeat predominant allele is species-specific in length: a selective advantage for human evolution?
Mol Genet Genomics
; 292(3): 611-617, 2017 Jun.
Artigo
Inglês
| MEDLINE | ID: mdl-28214997
7.
A genetic variant in CAMKK2 gene is possibly associated with increased risk of bipolar disorder.
J Neural Transm (Vienna)
; 123(3): 323-8, 2016 Mar.
Artigo
Inglês
| MEDLINE | ID: mdl-26354101
8.
The analysis of association between SNCA, HUSEYO and CSMD1 gene variants and Parkinson's disease in Iranian population.
Neurol Sci
; 37(5): 731-6, 2016 May.
Artigo
Inglês
| MEDLINE | ID: mdl-26732583
9.
Association analysis of DISC1 gene polymorphisms with Attention-Deficit Hyperactivity Disorder in Iranian population.
Pak J Med Sci
; 31(5): 1162-6, 2015.
Artigo
Inglês
| MEDLINE | ID: mdl-26649006
10.
A novel mutation in the ALS2 gene in an iranian kurdish family with juvenile amyotrophic lateral sclerosis.
Amyotroph Lateral Scler Frontotemporal Degener
; 24(1-2): 148-151, 2023 Feb.
Artigo
Inglês
| MEDLINE | ID: mdl-35852402
11.
Association between leukocyte telomere length and COVID-19 severity.
Egypt J Med Hum Genet
; 24(1): 37, 2023.
Artigo
Inglês
| MEDLINE | ID: mdl-37273887
12.
The study of rs324420 (C385A) polymorphism of the FAAH gene of the endocannabinoid system in patients with epilepsy and ADHD.
Epilepsy Res
; 192: 107100, 2023 05.
Artigo
Inglês
| MEDLINE | ID: mdl-37018974
13.
Exhaled breath condensate efficacy to identify mutations in patients with lung cancer: A pilot study.
Nucleosides Nucleotides Nucleic Acids
; 41(4): 370-383, 2022.
Artigo
Inglês
| MEDLINE | ID: mdl-35249462
14.
An updated overview and classification of bioinformatics tools for MicroRNA analysis, which one to choose?
Comput Biol Med
; 134: 104544, 2021 07.
Artigo
Inglês
| MEDLINE | ID: mdl-34119921
15.
An interdependence between GAPVD1 gene polymorphism, expression level and response to interferon beta in patients with multiple sclerosis.
J Neuroimmunol
; 353: 577507, 2021 04 15.
Artigo
Inglês
| MEDLINE | ID: mdl-33548618
16.
Macromolecular biomarkers of chronic obstructive pulmonary disease in exhaled breath condensate.
Biomark Med
; 14(11): 1047-1063, 2020 07.
Artigo
Inglês
| MEDLINE | ID: mdl-32940079
17.
Tips for improving the quality and quantity of the extracted DNA from exhaled breath condensate samples.
Nucleosides Nucleotides Nucleic Acids
; 39(5): 688-698, 2020.
Artigo
Inglês
| MEDLINE | ID: mdl-31608776
18.
LRP8 (rs5177) and CEP85L (rs11756438) are contributed to schizophrenia susceptibility in Iranian population.
Psychiatr Genet
; 30(6): 162-165, 2020 12.
Artigo
Inglês
| MEDLINE | ID: mdl-33079740
19.
miR-504 expression level is increased in multiple sclerosis patients responder to interferon-beta.
J Neuroimmunol
; 342: 577212, 2020 Mar 07.
Artigo
Inglês
| MEDLINE | ID: mdl-32199199
20.
Connection of miR-185 and miR-320a expression levels with response to interferon-beta in multiple sclerosis patients.
Mult Scler Relat Disord
; 44: 102264, 2020 Sep.
Artigo
Inglês
| MEDLINE | ID: mdl-32554287