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Sirenomelia: two case reports

Journal of medical case reports, 2021-04, Vol.15 (1), p.217-4, Article 217

2021

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Novel Mutations in the MKKS, BBS7, and ALMS1 Genes in Iranian Children with Clinically Suspected Bardet–Biedl Syndrome

Case reports in ophthalmological medicine, 2022-07, Vol.2022, p.1-6

2022

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Identification of disease-causing genes using microarray data mining and Gene Ontology

BMC medical genomics, 2011-01, Vol.4 (1), p.12-12, Article 12

2011

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A homozygous NOP14 variant is likely to cause recurrent pregnancy loss

Journal of human genetics, 2018-04, Vol.63 (4), p.425-430

2018

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Clinical Trial: CYP2D6 Related Dose Escalation of Tamoxifen in Breast Cancer Patients With Iranian Ethnic Background Resulted in Increased Concentrations of Tamoxifen and Its Metabolites

Frontiers in pharmacology, 2019-05, Vol.10, p.530-530

2019

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A Novel Mutation in the VPS13B Gene in a Cohen Syndrome Patient with Positive Antiphospholipid Antibodies

Case reports in immunology, 2021, Vol.2021, p.1-3

2021

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Effects of ABCG2 C421A and ABCG2 G34A genetic polymorphisms on clinical outcome and response to imatinib mesylate, in Iranian chronic myeloid leukemia patients

The Egyptian journal of medical human genetics, 2023-12, Vol.24 (1), p.1

2023

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A novel homozygous mutation in HSF4 causing autosomal recessive congenital cataract

Journal of human genetics, 2016-02, Vol.61 (2), p.177-179

2016

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Promising effect of rapamycin on multiple sclerosis

Multiple sclerosis and related disorders, 2018-11, Vol.26, p.40-45

2018

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GJB2 mutations causing autosomal recessive non-syndromic hearing loss (ARNSHL) in two Iranian populations: Report of two novel variants

International journal of pediatric otorhinolaryngology, 2018-04, Vol.107, p.121-126

2018

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Distribution of CYP2D6 polymorphism in the Middle Eastern region

Journal of research in medical sciences, 2019-01, Vol.24 (1), p.61-61

2019

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Dysregulation of RNA interference components in COVID-19 patients

BMC research notes, 2021-10, Vol.14 (1), p.401-401, Article 401

2021

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Novel mutations of PCCA and PCCB genes found by whole-exome sequencing related to propionic acidemia patients

European Journal of Biological Research, 2022-11, Vol.12 (4), p.294-306

2022

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A Novel Cadherin 23 Variant for Hereditary Hearing Loss Reveals Additional Support for a DFNB12 Nonsyndromic Phenotype of CDH23

Audiology & neurotology, 2020, Vol.25 (5), p.258-262

2020

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A Novel Pathogenic Variant in the CABP2 Gene Causes Severe Nonsyndromic Hearing Loss in a Consanguineous Iranian Family

Audiology & neurotology, 2019, Vol.24 (5), p.258-263

2019

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A comprehensive reference for BRCA1/2 genes pathogenic variants in Iran: published, unpublished and novel

Familial cancer, 2022-04, Vol.21 (2), p.137-142

2022

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New long noncoding RNA biomarkers and ceRNA networks on miR-616-3p in colorectal cancer: Bioinformatics-based studyNew long noncoding RNA biomarkers and ceRNA networks on miR-616-3p in colorectal cancer: Bioinformatics-based study

Journal of research in medical sciences, 2024-01, Vol.29 (1), p.10-10

2024

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Study of The Correlation between miR-106a, miR-125b, and miR-330 on Multiple Sclerosis Patients by Targeting TNFSF4 and SP1 in NF-кb/TNF-α Pathway: A Case-Control Study

Cell journal (Yakhteh), 2022-07, Vol.24 (7), p.403-409

2022

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Causative variants linked with limb girdle muscular dystrophy in an Iranian population: 6 novel variants

Molecular genetics & genomic medicine, 2023-02, Vol.11 (2), p.e2101-n/a

2023

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A novel homozygous DPH1 mutation causes intellectual disability and unique craniofacial features

Journal of human genetics, 2018-04, Vol.63 (4), p.487-491

2018

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The Relationship between VDR Gene Polymorphisms Bsm1 and Apa1 with Breast Cancer Risk

Global medical genetics, 2024-01, Vol.11 (1), p.69-75

2024

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Investigation of the Impact of Foretinib on AURKA and AURKB Expression in T98 Glioblastoma Cell Line

Research in molecular medicine, 2019-09, Vol.7 (1), p.1-7

2019

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Expression Profiles of IGF1, EGF, and FGF2 Genes in Patients With Prostate Cancer in Isfahan Province, Iran

Research in molecular medicine, 2019-09, Vol.7 (2), p.39-44

2019

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RORA and Autism in The Isfahan Population: Is There An Epigenetic Relationship

Cell journal (Yakhteh), 2017, Vol.18 (4), p.540-546

2017

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Constructing a novel competing Endogenous RNAs network based on NR3C1 and X-linked inhibitor of apoptosis protein genes reveals potential prognostic biomarkers in colorectal cancer

Journal of research in medical sciences, 2022-01, Vol.27 (1), p.71-71

2022

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Sirenomelia: two case reports

Novel Mutations in the MKKS, BBS7, and ALMS1 Genes in Iranian Children with Clinically Suspected Bardet–Biedl Syndrome

Identification of disease-causing genes using microarray data mining and Gene Ontology

A homozygous NOP14 variant is likely to cause recurrent pregnancy loss

Clinical Trial: CYP2D6 Related Dose Escalation of Tamoxifen in Breast Cancer Patients With Iranian Ethnic Background Resulted in Increased Concentrations of Tamoxifen and Its Metabolites

A Novel Mutation in the VPS13B Gene in a Cohen Syndrome Patient with Positive Antiphospholipid Antibodies

Effects of ABCG2 C421A and ABCG2 G34A genetic polymorphisms on clinical outcome and response to imatinib mesylate, in Iranian chronic myeloid leukemia patients

A novel homozygous mutation in HSF4 causing autosomal recessive congenital cataract

Promising effect of rapamycin on multiple sclerosis

GJB2 mutations causing autosomal recessive non-syndromic hearing loss (ARNSHL) in two Iranian populations: Report of two novel variants

Distribution of CYP2D6 polymorphism in the Middle Eastern region

Dysregulation of RNA interference components in COVID-19 patients

Novel mutations of PCCA and PCCB genes found by whole-exome sequencing related to propionic acidemia patients

A Novel Cadherin 23 Variant for Hereditary Hearing Loss Reveals Additional Support for a DFNB12 Nonsyndromic Phenotype of CDH23

A Novel Pathogenic Variant in the CABP2 Gene Causes Severe Nonsyndromic Hearing Loss in a Consanguineous Iranian Family

A comprehensive reference for BRCA1/2 genes pathogenic variants in Iran: published, unpublished and novel

New long noncoding RNA biomarkers and ceRNA networks on miR-616-3p in colorectal cancer: Bioinformatics-based studyNew long noncoding RNA biomarkers and ceRNA networks on miR-616-3p in colorectal cancer: Bioinformatics-based study

Study of The Correlation between miR-106a, miR-125b, and miR-330 on Multiple Sclerosis Patients by Targeting TNFSF4 and SP1 in NF-кb/TNF-α Pathway: A Case-Control Study

Causative variants linked with limb girdle muscular dystrophy in an Iranian population: 6 novel variants

A novel homozygous DPH1 mutation causes intellectual disability and unique craniofacial features

The Relationship between VDR Gene Polymorphisms Bsm1 and Apa1 with Breast Cancer Risk

Investigation of the Impact of Foretinib on AURKA and AURKB Expression in T98 Glioblastoma Cell Line

Expression Profiles of IGF1, EGF, and FGF2 Genes in Patients With Prostate Cancer in Isfahan Province, Iran

RORA and Autism in The Isfahan Population: Is There An Epigenetic Relationship

Constructing a novel competing Endogenous RNAs network based on NR3C1 and X-linked inhibitor of apoptosis protein genes reveals potential prognostic biomarkers in colorectal cancer

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