Shadab Salehpour

Publication Activity (10 Years)

Years Active: 2022-2024
Publications (10 Years): 6

Top Topics

Urinary Tract Infection

Intellectual Disability

Top Venues

BMC medical genomics

Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology

Biochemical genetics

This page only lists publications with an associated author ORCID identifier.

Publications

Sahand Tehrani Fateh, Nadia Mohammad Zadeh, Shadab Salehpour, Feyzollah Hashemi-Gorji, Ashkan Omidi, Hossein Sadeghi, Reza Mirfakhraie, Parinaz Moghimi, Sepideh Keyvanfar, Sepideh Mohammadi Sarvaleh, Mohammad Miryounesi, Mohammad Reza Ghasemi
Comprehensive review and expanding the genetic landscape of Cornelia-de-Lange spectrum: insights from novel mutations and skin biopsy in exome-negative cases. BMC medical genomics 17 (1) (2024)
Sahand Tehrani Fateh, Nadia Mohammad Zadeh, Shadab Salehpour, Feyzollah Hashemi-Gorji, Ashkan Omidi, Hossein Sadeghi, Reza Mirfakhraie, Parinaz Moghimi, Sepideh Keyvanfar, Sepideh Mohammadi Sarvaleh, Mohammad Miryounesi, Mohammad Reza Ghasemi
Comprehensive review and expanding the genetic landscape of Cornelia-de-Lange spectrum: insights from novel mutations and skin biopsy in exome-negative cases. BMC medical genomics 17 (1) (2024)
Sahand Tehrani Fateh, Nadia Mohammad Zadeh, Shadab Salehpour, Feyzollah Hashemi-Gorji, Ashkan Omidi, Hossein Sadeghi, Reza Mirfakhraie, Parinaz Moghimi, Sepideh Keyvanfar, Sepideh Mohammadi Sarvaleh, Mohammad Miryounesi, Mohammad Reza Ghasemi
Comprehensive review and expanding the genetic landscape of Cornelia-de-Lange spectrum: insights from novel mutations and skin biopsy in exome-negative cases. BMC medical genomics 17 (1) (2024)
Parinaz Moghimi, Feyzollah Hashemi-Gorji, Sanaz Jamshidi, Sahand Tehrani Fateh, Shadab Salehpour, Hossein Sadeghi, Fatemeh Norouzi Rostami, Reza Mirfakhraie, Mohammad Miryounesi, Mohammad Reza Ghasemi
Broadening the Phenotype and Genotype Spectrum of Glycogen Storage Disease by Unraveling Novel Variants in an Iranian Patient Cohort. Biochemical genetics (2024)
Sahand Tehrani Fateh, Saman Bagheri, Hossein Sadeghi, Shadab Salehpour, Fatemehsadat Fazeli Bavandpour, Behnia Sadeghi, Sanaz Jamshidi, Seyed Hassan Tonekaboni, Reza Mirfakhraie, Mohammad Miryounesi, Mohammad Reza Ghasemi
Extending and outlining the genotypic and phenotypic spectrum of novel mutations of NALCN gene in IHPRF1 syndrome: identifying recurrent urinary tract infection. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology (2023)
Sepide Dashti, Shadab Salehpour, Mohammad Reza Ghasemi, Hossein Sadeghi, Masoumeh Rostami, Feyzollah Hashemi-Gorji, Reza Mirfakhraie, Vahid Reza Yassaee, Mohammad Miryounesi
Identification of a novel de novo mutation in the CTNNB1 gene in an Iranian patient with intellectual disability. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 43 (4) (2022)