Literature DB >> 33712060

Genetic and molecular biology of autism spectrum disorder among Middle East population: a review.

Zahra Rahmani1, Mohammad Reza Fayyazi Bordbar2, Mohsen Dibaj3, Maliheh Alimardani4,5, Meysam Moghbeli6.   

Abstract

BACKGROUND: Autism spectrum disorder (ASD) is a neurodevelopmental disease, characterized by impaired social communication, executive dysfunction, and abnormal perceptual processing. It is more frequent among males. All of these clinical manifestations are associated with atypical neural development. Various genetic and environmental risk factors are involved in the etiology of autism. Genetic assessment is essential for the early detection and intervention which can improve social communications and reduce abnormal behaviors. Although, there is a noticeable ASD incidence in Middle East countries, there is still a lack of knowledge about the genetic and molecular biology of ASD among this population to introduce efficient diagnostic and prognostic methods. MAIN BODY: In the present review, we have summarized all of the genes which have been associated with ASD progression among Middle East population. We have also categorized the reported genes based on their cell and molecular functions.
CONCLUSIONS: This review clarifies the genetic and molecular biology of ASD among Middle East population and paves the way of introducing an efficient population based panel of genetic markers for the early detection and management of ASD in Middle East countries.

Entities:  

Keywords:  Autism; Diagnosis; Genetic; Middle East; Prognosis; Risk factor

Mesh:

Year:  2021        PMID: 33712060      PMCID: PMC7953769          DOI: 10.1186/s40246-021-00319-2

Source DB:  PubMed          Journal:  Hum Genomics        ISSN: 1473-9542            Impact factor:   4.639


  106 in total

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2.  The efficacy of interferon-beta therapy in multiple sclerosis patients: investigation of the RORA gene as a predictive biomarker.

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Journal:  Pharmacogenomics J       Date:  2019-10-24       Impact factor: 3.550

Review 3.  Genetic Variation across Phenotypic Severity of Autism.

Authors:  Claudio Toma
Journal:  Trends Genet       Date:  2020-02-06       Impact factor: 11.639

4.  Association of angiotensin-converting enzyme (ACE) gene polymorphism with elevated serum ACE activity and major depression in an Iranian population.

Authors:  Negar Firouzabadi; Massoumeh Shafiei; Ehsan Bahramali; Soltan Ahmed Ebrahimi; Hooman Bakhshandeh; Nader Tajik
Journal:  Psychiatry Res       Date:  2012-06-09       Impact factor: 3.222

Review 5.  Signaling by the angiotensin-converting enzyme.

Authors:  Ingrid Fleming
Journal:  Circ Res       Date:  2006-04-14       Impact factor: 17.367

Review 6.  Genetics and biology of vitamin D receptor polymorphisms.

Authors:  André G Uitterlinden; Yue Fang; Joyce B J Van Meurs; Huibert A P Pols; Johannes P T M Van Leeuwen
Journal:  Gene       Date:  2004-09-01       Impact factor: 3.688

Review 7.  The Oxytocin Receptor: From Intracellular Signaling to Behavior.

Authors:  Benjamin Jurek; Inga D Neumann
Journal:  Physiol Rev       Date:  2018-07-01       Impact factor: 37.312

Review 8.  The Balance of Th17 versus Treg Cells in Autoimmunity.

Authors:  Gap Ryol Lee
Journal:  Int J Mol Sci       Date:  2018-03-03       Impact factor: 5.923

9.  Genomic and epigenetic evidence for oxytocin receptor deficiency in autism.

Authors:  Simon G Gregory; Jessica J Connelly; Aaron J Towers; Jessica Johnson; Dhani Biscocho; Christina A Markunas; Carla Lintas; Ruth K Abramson; Harry H Wright; Peter Ellis; Cordelia F Langford; Gordon Worley; G Robert Delong; Susan K Murphy; Michael L Cuccaro; Antonello Persico; Margaret A Pericak-Vance
Journal:  BMC Med       Date:  2009-10-22       Impact factor: 8.775

Review 10.  Adolescence/adult onset MTHFR deficiency may manifest as isolated and treatable distinct neuro-psychiatric syndromes.

Authors:  Ana Gales; Marion Masingue; Stephanie Millecamps; Stephane Giraudier; Laure Grosliere; Claude Adam; Claudio Salim; Vincent Navarro; Yann Nadjar
Journal:  Orphanet J Rare Dis       Date:  2018-02-01       Impact factor: 4.123

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  3 in total

1.  The oxytocin receptor gene polymorphism rs2268491 and serum oxytocin alterations are indicative of autism spectrum disorder: A case-control paediatric study in Iraq with personalized medicine implications.

Authors:  Zainab Al-Ali; Akeel Abed Yasseen; Arafat Al-Dujailli; Ahmed Jafar Al-Karaqully; Katherine Ann McAllister; Alaa Salah Jumaah
Journal:  PLoS One       Date:  2022-03-22       Impact factor: 3.240

Review 2.  Modelling Autism Spectrum Disorder (ASD) and Attention-Deficit/Hyperactivity Disorder (ADHD) Using Mice and Zebrafish.

Authors:  Godfried Dougnon; Hideaki Matsui
Journal:  Int J Mol Sci       Date:  2022-07-07       Impact factor: 6.208

3.  SNP-PCR genotyping links alterations in the GABAA receptor (GABRG3: rs208129) and RELN (rs73670) genes to autism spectrum disorder among peadiatric Iraqi Arabs.

Authors:  Zainab A Ali; Akeel A Yasseen; Katherine A McAllister; Arafat Al-Dujailli; Ahmed J Al-Karaqully; Alaa S Jumaah
Journal:  Mol Biol Rep       Date:  2022-04-11       Impact factor: 2.742

  3 in total

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