Author

Leila Emrahi

Observed names: L Emrahi, L. Emrahi

Institution: Iranian Legal Medicine Organization

Observed institutions: Tarbiat Modares University, Tabriz University of Medical Sciences, Sahlgrenska University Hospital, Iranian Legal Medicine Organization, University of Gothenburg

ORCID: 0000-0002-5952-6416

Observed ORCID: 0000-0002-5952-6416

OpenAlex ID: A5101980726

The various regulatory functions of long noncoding RNAs in apoptosis, cell cycle, and cellular senescence

2022 · Mohammad Heydarnezhad Asl, Faezeh Pasban Khelejani, et al. · Journal of Cellular Biochemistry · 59

Autosomal recessive cardiomyopathy and sudden cardiac death associated with variants in MYL3

2020 · Daniel Peter Sayer Osborn, Leila Emrahi, et al. · Genetics in Medicine · 37

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Vitamin D receptor gene polymorphisms in Iranian Azary patients with Behçet’s disease

2014 · S Kolahi, A Khabbazi, et al. · Scandinavian Journal of Rheumatology · 31

Motor neuron diseases caused by a novel VRK1 variant – A genotype/phenotype study

2019 · Maryam Sedghi, Ali‐Reza Moslemi, et al. · Annals of Clinical and Translational Neurology · 20

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Clinical utility of measuring expression levels of Stanniocalcin 2 in patients with colorectal cancer

2014 · Shahryar Hashemzadeh, Amir Ahmad Arabzadeh, et al. · Medical Oncology · 15

Spectrum of MYBPC3 Gene Mutations in Patients with Hypertrophic Cardiomyopathy, Reporting Two Novel Mutations from North-West of Iran

2016 · Leila Emrahi, Mehrnoush Tabrizi, et al. · Clinical Laboratory · 6

Whole Exome Sequencing Identified a Stop‐Gained Mutation in DYSF Gene Associated With Dysferlinopathy in an Iranian Family

2025 · Saba Baghshomali, Asiyeh Jebelli, et al. · International Journal of Genomics · 2

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Molecular analysis of vitamin D receptor gene polymorphisms rs2228570 (FokI) and rs1544410 (BsmI) in patients with Behcet's disease

2013 · Hamidreza Khodadadi, Alireza Khabazi, et al. · 2

Two rare variants in the MYBPC3 gene associated with familial hypertrophic cardiomyopathy

2021 · Leila Emrahi, Hassan Hosseinzadeh, et al. · Gene Reports · 1

Expression study of CYP19A1 gene in a cohort of Iranian leiomyoma patients

2017 · Leila Emrahi, Javad Behroozi, et al. · Egyptian Journal of Medical Human Genetics · 1

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Inter-chromosomal Effect in a Robertsonian Translocation (13;14) Carrier with a Child Affected by Down Syndrome: A Case Report

2026 · Sahra Sahraeean, Asiyeh Jebelli, et al. · Journal of Reproduction & Infertility

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Whole-exome sequencing identified a novel missense variant in the connexin 46 (GJA3) gene causing congenital cataract in an Iranian pedigree

2022 · Sanaz Ranjbarrad, Asiyeh Jebelli, et al. · Research Square

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New mutation in the NEBL gene in a family with Hypertrophic cardiomyopathy: Complexity of whole exome sequencing results interpretation

2021 · Leila Emrahi, Mehrnoush Toufan Tabrizi, et al. · Medical Journal of Tabriz University of Medical Sciences and Health Services

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MYBPC3Δ25bp intronic deletion in hypertrophic cardiomyopathy patients and healthy Iranian population

2021 · Leila Emrahi, Shirin Shahbazi, et al. · Medical Journal of Tabriz University of Medical Sciences and Health Services

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P.276Childhood-onset spinal muscular atrophy or juvenile amyotrophic lateral sclerosis without pontocerebellar hypoplasia caused by a novel VRK1 splice variant

2019 · M. Sedghi, A. Moslemi, et al. · Neuromuscular Disorders

Works count: 15

Citation count: 174

H-index: 6

I10-index: 5