Shadab Salehpour
5PUBLICATIONS
16CO-AUTHORS
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Publications (5)
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|Apr 19, 2025
Exome Sequencing in 9 Iranian Patients Expands the Mutational and Clinical Spectrum of Bardet-Biedl Syndrome.Mohammad Reza Seyedtaghia, Mohsen Habibi, Farzad Hashemi-Gorji
|Apr 15, 2024
Broadening the Phenotype and Genotype Spectrum of Glycogen Storage Disease by Unraveling Novel Variants in an Iranian Patient Cohort.Parinaz Moghimi, Farzad Hashemi-Gorji, Sanaz Jamshidi
|Jan 12, 2024
Comprehensive review and expanding the genetic landscape of Cornelia-de-Lange spectrum: insights from novel mutations and skin biopsy in exome-negative cases.Sahand Tehrani Fateh, Nadia Mohammad Zadeh, Shadab Salehpour
|Jul 15, 2023
Extending and outlining the genotypic and phenotypic spectrum of novel mutations of NALCN gene in IHPRF1 syndrome: identifying recurrent urinary tract infection.Sahand Tehrani Fateh, Saman Bagheri, Hossein Sadeghi
|Jan 31, 2022
Identification of a novel de novo mutation in the CTNNB1 gene in an Iranian patient with intellectual disability.Sepide Dashti, Shadab Salehpour, Mohammad-Reza Ghasemi
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Frequent Collaborators
5 joint publications
Mohammad-Reza Ghasemi
5 joint publications
Hossein Sadeghi
5 joint publications
Reza Mirfakhraie
5 joint publications
Mohammad Miryounesi
4 joint publications
Farzad Hashemi-Gorji
4 joint publications
Sahand Tehrani-Fateh
3 joint publications
Parinaz Moghimi
1 joint publications
Vahid Reza Yassaee
1 joint publications
Saman Bagheri
1 joint publications
Seyed Hassan Tonekaboni
