Sirous Zeinali

ORCID

Publication Activity (10 Years)

Years Active: 2018-2023
Publications (10 Years): 8

Top Venues

Molecular genetics & genomic medicine

Journal of arrhythmia

Journal of inherited metabolic disease

Hereditas

Pasteur Institute of Iran (PHD)

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

Education History

Pasteur Institute of Iran

Iran

PHD :: biotechnology

Publications

Fereshteh Maryami, Elham Davoudi-Dehaghani, Nasrin Khalesi, Elham Rismani, Hamzeh Rahimi, Saeed Talebi, Sirous Zeinali
Identification and characterization of the largest deletion in the PCCA gene causing severe acute early-onset form of propionic acidemia. Molecular genetics and genomics : MGG (2023)
Fereshteh Maryami, Elham Rismani, Elham Davoudi-Dehaghani, Nasrin Khalesi, Fatemeh Zafarghandi Motlagh, Alireza Kordafshari, Saeed Talebi, Hamzeh Rahimi, Sirous Zeinali
Identifying and predicting the pathogenic effects of a novel variant inducing severe early onset MMA: a bioinformatics approach. Hereditas 160 (1) (2023)
Sarah Azadmehr, Faezeh Rahiminejad, Fatemeh Zafarghandi Motlagh, Mojdeh Jamali, Pardis Ghazizadeh Tehrani, Tina Shirzadeh, Hamideh Bagherian, Morteza Karimipoor, Elham Davoudi-Dehaghani, Sirous Zeinali
The Spectrum of Pathogenic Variants in Iranian Families with Hemophilia A. Archives of Iranian medicine 24 (12) (2021)
Marzieh Mojbafan, Reza Bahmani, Samira Dabbagh Bagheri, Zohreh Sharifi, Sirous Zeinali
Mutational spectrum of autosomal recessive limb-girdle muscular dystrophies in a cohort of 112 Iranian patients and reporting of a possible founder effect. Orphanet journal of rare diseases 15 (1) (2020)
Marzieh Mojbafan, Shirzadeh Tina, Fatemeh Zafarghandi Motlagh, Andrei Surguchov, Yalda Nilipour, Sirous Zeinali
Genetic variability in Iranian limb-girdle muscular dystrophy type 2B patients: An evidence of a founder effect. Molecular genetics & genomic medicine 7 (12) (2019)
Azam Amirian, Zahra Zafari, Zohreh Sharifi, Alireza Kordafshari, Morteza Karimipoor, Sirous Zeinali
Characterization and haplotype study of 6 novel STR markers related to the KCNQ1 gene in heterogeneous cardiovascular disorders in the Iranian population Turkish journal of medical sciences 49 (2) (2019)
Tina Shirzadeh, Amir Hossein Saeidian, Hamideh Bagherian, Shadab Salehpour, Aria Setoodeh, Mohammad Reza Alaei, Leila Youssefian, Ashraf Samavat, Andrew Touati, Mohammad-Sadegh Fallah, Hassan Vahidnezhad, Morteza Karimipoor, Sarah Azadmehr, Marzieh Raeisi, Ameneh Bandehi Sarhadi, Fatemeh Zafarghandi Motlagh, Mojdeh Jamali, Zahra Zeinali, Maryam Abiri, Sirous Zeinali, null null
Molecular genetics of a cohort of 635 cases of phenylketonuria in a consanguineous population. Journal of inherited metabolic disease 41 (6) (2018)
Azam Amirian, Zahra Zafari, Mohammad Dalili, Siamak Saber, Morteza Karimipoor, Samira Dabbagh Bagheri, Amir Farjam Fazelifar, Sirous Zeinali
Detection of a new KCNQ1 frameshift mutation associated with Jervell and Lange-Nielsen syndrome in 2 Iranian families. Journal of arrhythmia 34 (3) (2018)

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Publication Activity (10 Years)

Top Topics

Top Venues

Sirous Zeinali