Hossein Dehghani

ORCID: 0000-0002-9326-3621
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About
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Research Areas
  • Genomic variations and chromosomal abnormalities
  • Health and Well-being Studies
  • Cancer-related molecular mechanisms research
  • Autism Spectrum Disorder Research
  • Congenital heart defects research
  • Circular RNAs in diseases
  • Ophthalmology and Visual Health Research
  • Natural Antidiabetic Agents Studies
  • Hemoglobinopathies and Related Disorders
  • Genomics and Chromatin Dynamics
  • SARS-CoV-2 and COVID-19 Research
  • Psychological Well-being and Life Satisfaction
  • Genomics and Rare Diseases
  • COVID-19 Clinical Research Studies
  • Nerve injury and regeneration
  • COVID-19 and Mental Health
  • Reproductive System and Pregnancy
  • Vaccine Coverage and Hesitancy
  • Antimicrobial Peptides and Activities
  • COVID-19 Impact on Reproduction
  • Genetics and Neurodevelopmental Disorders
  • Cardiomyopathy and Myosin Studies
  • Muscle Physiology and Disorders
  • RNA Research and Splicing
  • Neurogenesis and neuroplasticity mechanisms

Birjand University of Medical Sciences
2018-2023

Zanjan University of Medical Sciences
2023

Social Welfare Department
2023

University of Social Welfare and Rehabilitation Sciences
2016-2018

Autism spectrum disorder (ASD) is a severe neurodevelopmental featuring impairment in verbal and non-verbal interactions, defects social stereotypic behaviors as well restricted interests. In recent times, the incidence of ASD growing at rapid pace. spite great endeavors devoted to explaining pathophysiology, its precise etiology remains unresolved. pathogenesis related different phenomena associated with immune system; however, mechanisms behind these potential contributing genes remain...

10.3389/fmolb.2021.754296 article EN cc-by Frontiers in Molecular Biosciences 2021-10-21

Schizophrenia (SCZ) is a severe mental disorder with an unknown pathophysiology. Brain-Derived Neurotrophic Factor (BDNF) neurotrophin that has been associated synapse plasticity, learning, and memory, as well neurodevelopment neuroprotection. The importance of neurodevelopmental neurotoxicity-related components in the pathophysiology SCZ highlighted research on neurobiology this disease. purpose to investigate significant expression two variables, tristetraprolin (TTP) miR-16, which are...

10.1186/s12888-022-04442-9 article EN cc-by BMC Psychiatry 2022-12-08

Background: Policy-makers in the Ministry of Health Care and Medical Education need to have knowledge concerning high-risk behaviors among medical students order positive changes educational system universities sciences. Objectives: To enquire into prevalence high risk students. Methods: A cross-sectional study was conducted on one largest Tehran, Iran. total 275 participated study. They filled out a self-developed questionnaire that covered both demographic characteristics items eight main...

10.5812/modernc.69327 article EN Modern Care Journal 2018-08-26

In our previous studies on the Iranian β-thalassemia (β-thal) patients, we identified an association between severity of β-thal phenotype and polymorphic palindromic site at 5' hypersensitive 4-locus control region (5'HS4-LCR) β-globin gene cluster. Furthermore, a linkage disequilibrium was observed this XmnI-HBG2 in patient population. Based data, it suggested that well-recognized phenotype-ameliorating role assigned to positive XmnI could be associated with its linked elements LCR. To...

10.1080/03630269.2016.1189931 article EN Hemoglobin 2016-07-03

Introduction: Considering the effectiveness of polymorphisms in occurrence respiratory diseases, it seems that these genetic variations viral and microbial receptors can be effective progression disease. The present study aimed to assess relationship between C-159T polymorphism CD14 gene promoter severity disease Covid-19 patients during 2020-2021. Method: subjects were randomly selected from referred for polymerase chain reaction (PCR) studied five groups: healthy, outpatient,...

10.32592/nkums.14.4.23 article EN cc-by-nc Journal of North Khorasan University of Medical Sciences 2022-11-29

Abstract Limb-girdle muscular dystrophy (LGMD) is a type of genetically heterogeneous disorders. The goal current training discovering novel mutations or deletion in an Iranian family with limb-girdle 2B patient by whole exome sequencing. Exome sequencing was completed, as well complete physical examinations the family. Then, silico studies have been done to discovery change that happened protein structure, associated DMD phenotype. On chromosome 2p13.2, there one new nonsense variant:...

10.21203/rs.3.rs-3281826/v1 preprint EN cc-by Research Square (Research Square) 2023-08-28

Background: The COVID-19 pandemic and its subsequent changes in the community lifestyle can be associated with problems complications. It seems very important to identify caused by accurately. Objectives: This study aimed investigate behavioral children due South Khorasan 2021. Methods: In this cross-sectional study, 312 were studied. Inclusion criteria included all under 12 years of age without apparent mental disorders chronic diseases affecting changes. Exclusion parental separation,...

10.5812/modernc.120820 article EN Modern Care Journal 2022-01-03
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