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User profiles for Roshanak Jazayeri

Roshanak Jazayeri

Alborz university of medical sciences

Verified email at abzums.ac.ir

Cited by 104

[PDF] mpg.de

Effect of inbreeding on intellectual disability revisited by trio sequencing

…, F Sadeghinia, R Jazayeri… - Clinical …, 2019 - Wiley Online Library

In outbred Western populations, most individuals with intellectual disability (ID) are sporadic
cases, dominant de novo mutations (DNM) are frequent, and autosomal recessive ID (ARID) …

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[PDF] mdedge.com

[PDF][PDF] Investigation of the asporin gene polymorphism as a risk factor for knee osteoarthritis in Iran

R Jazayeri, M Qoreishi, HR Hoseinzadeh… - Am J …, 2013 - cdn.mdedge.com

Materials and Methods One hundred KOA patients (72 women, 28 men) were consecutively
enrolled in the clinic of the Akhtar Orthopedic Educational Hospital, which is affiliated with …

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[PDF] nsj.org.sa

Etiological characteristics of people with intellectual disability in Iran

R Jazayeri, SH Saberi, M Soleymanzadeh - Neurosciences Journal, 2010 - nsj.org.sa

OBJECTIVE: To describe the etiological characteristics of intellectual disability in one Iranian
center. METHODS: In a cross-sectional study, 64 cases with mental retardation (MR) were …

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[PDF] sid.ir

[PDF][PDF] Exome sequencing and linkage analysis identified novel candidate genes in recessive intellectual disability associated with ataxia

R Jazayeri, H Hu, Z Fattahi, L Musante, SS Abedini… - 2015 - sid.ir

Background: Intellectual disability (ID) is a neuro-developmental disorder which causes
considerable socio-economic problems. Some ID individuals are also affected by ataxia, and the …

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[PDF] cambridge.org

Allelic and Genotype Frequencies of CYP2B6∗ 2 (64C> T) and CYP2B6∗ 3 (777C> A) in Three Dominant Ethnicities of the Iranian Population

…, F Ghasemi, S Sheibaninia, R Jazayeri… - Genetics …, 2023 - cambridge.org

Background. Cytochrome P450 complex plays a key role in drug metabolism. CYP2B6 has
an essential part in Cytochrome P450 complex metabolism. This study aims to determine the …

[HTML] nih.gov

Familial hypercholesterolemia in an Iranian family due to a mutation in the APOE gene (first case report)

S Noorian, R Razmandeh, R Jazayeri - Journal of Diabetes & Metabolic …, 2022 - Springer

Familial Hypercholesterolemia is an autosomal, dominant genetic disorder associated with
premature cardiovascular disease (CVD). Mutations in the LDLR, APOB, and PCSK9 genes …

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[PDF] cambridge.org

Frequency of CYP2B6 Alleles in Major Iranian Ethnicities, Affecting Response to Efavirenz

P Mardi, B Tavakoli-Far, SS Nia, R Jazayeri… - Genetics …, 2022 - cambridge.org

Introduction. Efavirenz is an antihuman immunodeficiency virus (HIV) drug metabolized by
cytochrome P450 2B6 (CYP2B6) enzyme. Cytochrome P450 2B6 is an enzyme that in …

[PDF] academia.edu

[PDF][PDF] Research Article Allelic and Genotype Frequencies of CYP2B6 2 (64C> T) and CYP2B6

…, P Veis-Karami, F Ghasemi, S Sheibaninia, R Jazayeri… - 2023 - academia.edu

Background. Cytochrome P450 complex plays a key role in drug metabolism. CYP2B6 has
an essential part in Cytochrome P450 complex metabolism. Tis study aims to determine the …

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[HTML] brieflands.com

[HTML][HTML] Mutational Analysis of Mucopolysaccharidosis in Iranian Patients

…, S Farshidi, B Kamalidehghan, R Jazayeri… - Zahedan Journal of …, 2021 - brieflands.com

: Mucopolysaccharidosis (MPS) is a rare and heterogeneous metabolic disorder with wide
phenotypic distributions throughout the world. This study aimed to determine the genetic …