Mansoor Salehi

About Mansoor Salehi

Mansoor Salehi, With an exceptional h-index of 29 and a recent h-index of 21 (since 2020), a distinguished researcher at Isfahan University of Medical Sciences, specializes in the field of Medical Genetics.

His recent articles reflect a diverse array of research interests and contributions to the field:

CTNS Mutations Causing Autosomal Recessive Cystinosis in a Subset of Iranian Population: Report of Two New Variants

Whole Exome Sequencing and Whole Genome Sequencing for Investigation of the Genetic Basis of Obesity: A Rapid Review

Assessment of circulating miRNA-218, miRNA-222, and miRNA-146 as biomarkers of polycystic ovary syndrome in epileptic patients receiving valproic acid

GLIS2 and CCND1 expression levels in breast cancer patients

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

Investigation of the Relationship between Genetic Polymorphisms in GSTM1 and GSTT1 Genes and Susceptibility to Lung Functional Abnormalities in Workers Exposed to Air …

Retinitis pigmentosa: A Case Report with Thr17Arg as a Novel Mutation in RHO Gene.

Evaluation of the association between centrosome amplification in tumor tissue of breast cancer patients and changes in the expression of CETN1 and CNTROB genes

Mansoor Salehi Information

University

Position

1.Department of Genetics and Molecular Biology Medical School

Citations(all)

2864

Citations(since 2020)

1667

Cited By

1944

hIndex(all)

29

hIndex(since 2020)

21

i10Index(all)

85

i10Index(since 2020)

51

Email

University Profile Page

Google Scholar

Mansoor Salehi Skills & Research Interests

Medical Genetics

Top articles of Mansoor Salehi

CTNS Mutations Causing Autosomal Recessive Cystinosis in a Subset of Iranian Population: Report of Two New Variants

Advanced Biomedical Research

2024/1/1

Whole Exome Sequencing and Whole Genome Sequencing for Investigation of the Genetic Basis of Obesity: A Rapid Review

Bahrain Medical Bulletin

2021/10/1

Assessment of circulating miRNA-218, miRNA-222, and miRNA-146 as biomarkers of polycystic ovary syndrome in epileptic patients receiving valproic acid

Biomedical Research and Therapy

2023

GLIS2 and CCND1 expression levels in breast cancer patients

Breast Disease

2023

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

Egyptian Journal of Medical Human Genetics

2023

Investigation of the Relationship between Genetic Polymorphisms in GSTM1 and GSTT1 Genes and Susceptibility to Lung Functional Abnormalities in Workers Exposed to Air …

Journal of Environmental Health and Sustainable Development

2022/3/15

Retinitis pigmentosa: A Case Report with Thr17Arg as a Novel Mutation in RHO Gene.

Journal of Epigenetics

2022/3

Evaluation of the association between centrosome amplification in tumor tissue of breast cancer patients and changes in the expression of CETN1 and CNTROB genes

Gene Reports

2022/3/1

An experimental in silico study on COVID‐19: Response of neutrophil‐related genes to antibiotics

Health Science Reports

2022/3

Mohammad Kazemi
Mohammad Kazemi

H-Index: 12

Mansoor Salehi
Mansoor Salehi

H-Index: 16

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

Molecular Genetics & Genomic Medicine

2023/2

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

Journal of Research in Medical Sciences

2022/1/1

miR-574, miR-499, miR-125b, miR-106a, and miR-9 potentially target TGFBR-1 and TGFBR-2 genes involving in Inflammatory Response Pathway: potential novel biomarkers for Chronic …

Pathology-Research and Practice

2022/10/1

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)

2022/7

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

Case Reports in Ophthalmological Medicine

2022/7/21

A novel mutation in GJC2 associated with hypomyelinating leukodystrophy type 2 disorder.

Genomics & Informatics

2022/6/3

A novel NR0B1 mutation correlated with X-linked adrenal hypoplasia congenital (AHC)

Gene Reports

2022/3/18

Dysregulation of RNA interference components in COVID-19 patients

BMC Research Notes

2021/12

Clinical and genetic profile of children with unexplained intellectual disability/developmental delay and epilepsy

Epilepsy Research

2021/11/1

A glance at glioblastoma molecular culprits through in-silico analysis

Gene Reports

2021/6/1

Nima Hemmat
Nima Hemmat

H-Index: 7

Mansoor Salehi
Mansoor Salehi

H-Index: 16

Identification and prediction of common molecular culprits between psoriasis and melanoma via bioinformatical analysis

Gene Reports

2021/4/15

Mansoor Salehi
Mansoor Salehi

H-Index: 16

See List of Professors in Mansoor Salehi University(Isfahan University of Medical Sciences)