Dr. Maryam Rezazadeh

THE IMPACT OF INCREASE IN TASK COGNITIVE COMPLEXITY ON IRANIAN EFL LEARNERS’FLUENCY

International Journal of Language Learning and Applied Linguistics World

First Case Report of Costello Syndrome in the Azeri Turkish Population

ANNALS OF MEDICAL AND HEALTH SCIENCES RESEARCH

A single nucleotide polymorphism in the interferon regulatory factor 8 gene is associated with risk of AML in Iranian population

Ecological Genetics and Genomics

Analysis of CFTR Gene Variants and clinical presentations in Children with Diffuse Bronchiectasis and Unknown Etiology

Journal of Pediatric Perspectives

Report of Two Turner affected patients with dicentric X chromosome.

Research in Medicine: Journal of Research in Medical Sciences

Association between rs731236 (Taq1), rs1544410 (BsmI), and rs2228570 (FokI) polymorphisms of vitamin D receptor gene with autism spectrum disorder

Research in Medicine

Identification of key pathways and molecular players potentially involved in endometrial cancer metastasis through integrated bioinformatics analyses

BioImpacts: BI

miR-361-5p contributes to the pathogenesis of Alzheimer’s disease

Scientific Reports

Bioinformatics analysis for identifying hub genes in endometriosis and recurrent implantation failure: molecular pathways to enhanced IVF success

Middle East Fertility Society Journal

Exome sequencing reveals a novel de novo ARHGAP31 frameshift variant in a neurodevelopmental disorder: Structural and functional insights into RhoGAP domain loss

Gene Reports

Mutation screening of familial Mediterranean fever in the Azeri Turkish population: genotype-phenotype correlation and the clinical profile variability

Genetika

The assessment of health-related quality of life in scleroderma-interstitial lung disease

J Cardiothorac Med

The inhibitory effect of hsa-miR-330 replacement on the proliferation and migration of breast cancer Mcf-7 cells

Int. J. Womens Health

RUNX1 variant as a genetic predisposition factor for acute myeloid leukemia

Experimental and Molecular Pathology

Neurodevelopmental Outcome of Preterm Infants with Hypothyroidism

Zahedan Journal of Research in Medical Sciences

Complete Loss of Myelin protein zero (MPZ) in a patient with a late onset Charcot-Marie-Tooth (CMT)

Metabolic Brain Disease

Association of seven fundamental genetic polymorphisms in long noncoding RNA MALAT1, SOX2OT and H19 with recurrent miscarriage in Turkish-Azeri Iranian population

Human Gene

Expression analysis of inhibitory B7 family members in Alzheimer’s disease

Metabolic Brain Disease

Gene expression investigation of four key regulators of polyadenylation and alternative adenylation in the periphery of late-onset Alzheimer's disease patients

Gene

Compound heterozygous mutations in ADSL gene in a patient with autism spectrum disorder and epilepsy

Gene Reports

Association of CALHM1 gene polymorphism with late-onset Alzheimer disease

Middle East Journal of Medical Genetics

Loss of helicase C-terminal domain of SMARCAL1 protein associated with severe Schimke immuno-osseous dysplasia

Pathology-Research and Practice

A comprehensive review of the applications of RNA sequencing in celiac disease research

Gene

Neurotrophin growth factors and their receptors as promising blood biomarkers for Alzheimer’s Disease: A gene expression analysis study

Molecular Biology Reports

Gene expression patterns of CRYM and SIGLEC10 in Alzheimer's disease: potential early diagnostic indicators

Molecular Biology Reports

Molecular study of CFTR gene mutations in children with diffuse bronchiectasis with unknown etiology.

Investigating the expression of ERMN and LTN1 genes in patients with Schizophrenia

Evaluation of CKAMP59 and MicroRNA-185 expression in the peripheral blood of schizophrenia patients.

Study of the expression level of ZFP36 and MicroRNA-16 regulatory factors in patients with schizophrenia

Stress Granules in the mechanisms of action of anti-cancer medications: a systematic scoping review

Bioinformatics analysis of long non-coding RNA-associated competing endogenous RNA axes in olfactory epithelium in schizophrenia.

Shared lncRNAs in the pathogenesis of Alzheimer's and Parkinson's diseases : a scoping review

Investigation of gene expression profile of men with non-obstructive azoospermia, using RNA sequencing technique

Analysis of RNA-seq databases to identify candidate biomarkers for the diagnosis of schizophrenia and validation of their expression changes using q-PCR

Analysis of relation of HOT AIR and ANRIL lncRNA polymorphisms with Multiple Sclerosis

Investigating the expression of ERMN and LTN1 genes in patients with Multiple Sclerosis

Investigating the expression of RELN and DAB1 genes in patients with Multiple Sclerosis

Evaluation of ERMN and LTN1 expression in the peripheral blood of patients with autism spectrum disorders.

Investigation of lncRNA GAS5 and NR3C1 polymorphisms in patients with acute myeloid leukemia in north- west of Iran

Investigation of MEG3 and WT1 polymorphisms in patients with acute myeloid leukemia

Investigation of RUNX1 and BAALC polymorphisms in patients with acute myeloid leukemia

Investigating the relationship between miR-185, SHISA7 and BCAS4 expression as a ceRNA circuitry in Late onset Alzheimer's disease.

Investigating the relationship between miR-16 and TTP and ROQUIN expression with Late onset Alzheimer's disease.

Investigating the relationship between miR-361, ATAD1 and HOMER1 expression with Late onset Alzheimer's disease.

Evaluation of the relationship between NFκB 1-and NFκB2- gene expression in patients with sudden sensorineural hearing loss.

Isodicentric x chromosome and phenotype correlation of Turner’s syndrome.

Charcot-Marie-Tooth (CMT) genotype and phenotype correlation

Clinical and genetic features of PEHO and PEHO-Like syndromes: A scoping review

New Inside into Clinical Heterogeneity and Inheritance Diversity of FBLN5-related Cutis Laxa

DOCK8 immunodeficiency syndrome (DIDS) and job syndrome job