Author

Haleh Mokabber

Observed name: Haleh Mokaber

Institution: Islamic Azad University Ardabil

Observed institutions: Ardabil University of Medical Sciences, Islamic Azad University Ardabil, Islamic Azad University of Shiraz

ORCID: 0000-0002-8536-9952

Observed ORCID: 0000-0002-8536-9952

OpenAlex ID: A5007615391

miR‐124 promotes neural differentiation in mouse bulge stem cells by repressing Ptbp1 and Sox9

2018 · Haleh Mokabber, Nowruz Najafzadeh, et al. · Journal of Cellular Physiology · 40

GJB2 mutations in Iranian Azeri population with autosomal recessive nonsyndromic hearing loss (ARNSHL): First report of c.238 C>A mutation in Iran

2021 · Ehsan Abbaspour Rodbaneh, Mohammad Panahi, et al. · Journal of Clinical Laboratory Analysis · 10

The regulatory role of microRNAs in the development, cyclic changes, and cell differentiation of the hair follicle

2022 · Haleh Mokabber, Mohammad Amin Vatankhah, et al. · Process Biochemistry · 7

Genetic investigation of patients with autosomal recessive ataxia and identification of two novel variants in the SQSTM1 and SYNE1 genes

2024 · Diana Mokhtari, Mohammad Jahanpanah, et al. · Human Genome Variation · 5

A novel variant in ASNS gene responsible for syndromic intellectual disability and microcephaly: Case report and literature review

2024 · Mohammad Jahanpanah, Diana Mokhtari, et al. · Molecular Genetics & Genomic Medicine · 4

Unraveling the Genetic Landscape of Hearing Loss: A Comprehensive Study of Azeri Families in Ardabil, Iran

2025 · Marzieh Mohseni, Farzane Zare Ashrafi, et al. · Molecular Genetics & Genomic Medicine · 3

The Role of a Novel TRIP12 Mutation in Intellectual Disability: A Molecular and Clinical Investigation in Multiplex Family

2025 · Ramiz Nobakht, Sara Arish, et al. · Journal of Molecular Neuroscience · 2

Molecular Analysis of the HGD Gene in 9 Families With Alkaptonuric Ochronosis in Iran and Identification of Two Novel Variants

2025 · Ahad Azami, Mohammad Jahanpanah, et al. · Molecular Genetics & Genomic Medicine · 1

Identification of a Novel TBCK Variation in an A zari Consanguineous Family With Psychomotor Developmental Disorder

2026 · Sara Arish, Ramiz Nobakht, et al. · American Journal of Medical Genetics Part A

A novel compound heterozygous of β-thalassemia with HbG-Coushatta: case report of Iran

2023 · Narges Soozangar, Ehsan Abbaspour, et al. · Human Genome Variation

Works count: 11

Citation count: 72

H-index: 4

I10-index: 2