Alpha 2.0
Login Register
» Authors » Farkhondeh Behjati

Farkhondeh Behjati

Explore the profile of Farkhondeh Behjati including associated specialties, affiliations and a list of published articles. Areas
Snapshot
Articles 50
Citations 891
Followers 0
Related Specialties
Genetics
General Medicine
Molecular Biology
Top 10 Co-Authors
Hossein Najmabadi
Kimia Kahrizi
Saghar Ghasemi Firouzabadi
Roxana Kariminejad
Elahe Keyhani
Andreas Tzschach
Hossein Darvish
Masoud Garshasbi
Seyedeh Sedigheh Abedini
Yousef Shafeghati
Published In
Rep Biochem Mol Biol
Gene
Int J Mol Cell Med
Hum Genet
Indian J Hum Genet
Affiliations
Soon will be listed here.
Recent Articles
1.
Novel splicing variant and gonadal mosaicism in DYRK1A gene identified by whole-genome sequencing in multiplex autism spectrum disorder families
Agha Gholizadeh M, Behjati F, Ghasemi Firouzabadi S, Heidari E, Razmara E, Almadani N, et al.
Neurogenetics . 2024 Jul; 25(4):377-391. PMID: 38976082
Autism spectrum disorder (ASD) is a complex neurodevelopmental condition with considerable genetic heterogeneity. The disorder is clinically diagnosed based on DSM-5 criteria, featuring deficits in social communication and interaction, along...
2.
Exploring the Genetic Causality of Discordant Phenotypes in Familial Apparently Balanced Translocation Cases Using Whole Exome Sequencing
Aristidou C, Theodosiou A, Alexandrou A, Papaevripidou I, Evangelidou P, Kosmaidou-Aravidou Z, et al.
Genes (Basel) . 2023 Jan; 14(1). PMID: 36672823
Familial apparently balanced translocations (ABTs) are usually not associated with a phenotype; however, rarely, ABTs segregate with discordant phenotypes in family members carrying identical rearrangements. The current study was a...
3.
Expression of ERBB gene family in females with breast cancer and its correlation with clinicopathological characteristics of the disease
Soosanabadi M, Ghahfarokhi A, Pourghazi F, Ehtesham N, Mirfakhraie R, Atanesyan L, et al.
Mol Biol Rep . 2022 Jun; 49(9):8547-8553. PMID: 35763181
Background: Breast cancer (BC) is the most prevalent and fatal cancer in women. Given that there are very few studies investigating the overexpression of four members of ERBB genes, we...
4.
The Relationship between Copy Number Variation, Protein Expression, and Angiogenesis in Sporadic Breast Cancer
Rahimi M, Behjati F, Hamid Reza K, Karimlou M, Keyhani E
Rep Biochem Mol Biol . 2020 Aug; 9(1):40-49. PMID: 32821750
Background: is a protooncogene that encodes for the KIT oncoprotein, which is a transmembrane tyrosine kinase growth factor receptor that holds a critical role in a variety of normal physiological...
5.
Whole-Exome Sequencing Identifies Three Candidate Homozygous Variants in a Consanguineous Iranian Family with Autism Spectrum Disorder and Skeletal Problems
Valilou S, Alavi A, Pashaei M, Ghasemi Firouzabadi S, Shafeghati Y, Nozari A, et al.
Mol Syndromol . 2020 Jul; 11(2):62-72. PMID: 32655337
Autism spectrum disorder (ASD) is characterized by 3 core symptoms with impaired social communication, repetitive behavior, and/or restricted interests in early childhood. As a complex neurodevelopmental disorder (NDD), the phenotype...
6.
Bi-allelic Mutations in ALDH5A1 is associated with succinic semialdehyde dehydrogenase deficiency and severe intellectual disability
Fattahi M, Bushehri A, Alavi A, Asghariazar V, Nozari A, Ghasemi Firouzabadi S, et al.
Gene . 2020 Jul; :144918. PMID: 32621952
Homozygous mutations of ALDH5A1 have been reportedly associated with Succinic semialdehyde dehydrogenase deficiency (SSADHD) that affects gamma-aminobutyric acid (GABA) catabolism and evinces a wide range of clinical phenotype from mild...
7.
Investigation of Aneusomy of Chromosome 21 in the Micronuclei of 13 Patients with Early Onset Alzheimer's Disease Using Fluorescence in Situ Hybridization: A Pilot Study
Biglari S, Kamali K, Banihashemi S, Faal Sezavari A, Aghajanpour-Mir S, Behjati F
Rep Biochem Mol Biol . 2020 Jun; 8(4):446-453. PMID: 32582804
Background: Alzheimer's disease is one of the most common neurodegenerative and dementia disorders in people between the ages of 30 and 65. When symptoms appear in this age group, the...
8.
Application of Multiplex Ligation-Dependent Probe Amplification in Determining the Copy Number Alterations of Gene Family Members in Invasive Ductal Breast Carcinoma
Soosanabadi M, Mirfakhraie R, Atanesyan L, Biglarian A, Aghakhani Moghadam F, Rahimi M, et al.
Rep Biochem Mol Biol . 2019 Jul; 8(1):91-101. PMID: 31334294
Background: The aim of this study was to assess the usability of multiplex ligation-dependent probe amplification (MLPA) for copy number determination of gene family members () in invasive breast carcinoma...
9.
Combination of Genetics and Nanotechnology for Down Syndrome Modification: A Potential Hypothesis and Review of the Literature
Tafazoli A, Behjati F, Farhud D, Abbaszadegan M
Iran J Public Health . 2019 Jun; 48(3):371-378. PMID: 31223563
Down syndrome (DS) is one of the most prevalent genetic disorders in humans. The use of new approaches in genetic engineering and nanotechnology methods in combination with natural cellular phenomenon...
10.
Investigation of Chromosomal Abnormalities and Microdeletion/ Microduplication(s) in Fifty Iranian Patients with Multiple Congenital Anomalies
Mohammadzadeh A, Akbaroghli S, Aghaei-Moghadam E, Mahdieh N, Badv R, Jamali P, et al.
Cell J . 2019 Jun; 21(3):337-349. PMID: 31210441
Objective: Major birth defects are inborn structural or functional anomalies with long-term disability and adverse impacts on individuals, families, health-care systems, and societies. Approximately 20% of birth defects are due...