Publications by authors named "Mostafa Neissi"

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PIGC-related encephalopathy: Lessons learned from 18 new probands.
Allan Bayat, Maria Carla Borroto, Smrithi Salian, Maha S Zaki, Hind Benkerroum, Mostafa Neissi

Eur J Hum Genet· December 2025

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Genetic Diagnosis of Oculocutaneous Albinism Type 1A: A Novel Variant.
Raghad N Shihab, Rusul Thabit Hamid, Mostafa Neissi, Javad Mohammadi-Asl, Motahareh Sheikh-Hosseini

Clin Case Rep· September 2025

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Gene variant analysis in pediatrics with early-onset epilepsy: Identification of novel variants.
Pooyan Alizadeh, Armin Jahangiri Babadi, Nemat Ghadiri, Mostafa Neissi, Masoud Zeinali

Pract Lab Med· July 2025

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Oculocutaneous albinism in a patient with an variant: molecular and clinical insights.
Mostafa Neissi, Sahar Kareem Al-Mozani, Ayoob Radhi Al-Zaalan, Samaneh Sanavi Shiri, Motahareh Sheikh-Hosseini

Asian Biomed (Res Rev News)· June 2025

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Identification and characterization of gene mutations in an Iranian patient with Leber congenital amaurosis 9.
Mostafa Neissi, Motahareh Sheikh-Hosseini, Misagh Mohammadi-Asl, Adnan Issa Al-Badran, Mojdeh Roghani

Clin Case Rep· October 2024

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Usher Syndrome Type 2 in An Iranian Family: A Novel Founder Variation in The Gene.
Mostafa Neissi, Javad Mohammadi-Asl, Misagh Mohammadi-Asl, Mojdeh Roghani, Motahareh Sheikh-Hosseini

Cell J· August 2024

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Retinitis pigmentosa-1 due to an mutation in a consanguineous Iranian family: Report of a novel mutation.
Mostafa Neissi, Motahareh Sheikh-Hosseini, Javad Mohammadi-Asl

Clin Case Rep· March 2024

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A Novel Deleterious MYO15A Gene Mutation Causes Nonsyndromic Hearing Loss.
Mostafa Neissi, Adnan Issa Al-Badran, Javad Mohammadi-Asl

Iran J Otorhinolaryngol· January 2024

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AHI1 gene mutation in a consanguineous Iranian family affected by Joubert syndrome: A case report.
Mostafa Neissi, Hadideh Mabudi, Javad Mohammadi-Asl

Clin Case Rep· October 2021

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Identification of a Novel WFS1 Mutation Using the Whole Exome Sequencing in an Iranian Pedigree with Autosomal Dominant Hearing Loss.
Javad Mohammadi-Asl, Nader Saki, Masoud Dehdashtiyan, Mostafa Neissi, Farideh Ghanbari Mardasi

Iran J Otorhinolaryngol· May 2021

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