Hossein Jafari Khamirani

Publication Activity (10 Years)

Years Active: 2021-2024
Publications (10 Years): 13

Top Topics

Duchenne Muscular Dystrophy

Top Venues

Human genome variation

Molecular genetics & genomic medicine

Immunological investigations

Archives of Iranian medicine

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

Publications

Maryam Fazelzadeh Haghighi, Hossein Jafari Khamirani, Jafar Fallahi, Ali Arabi Monfared, Korosh Ashrafi Dehkordi, Seyed Mohammad Bagher Tabei
Novel insight into FCSK-congenital disorder of glycosylation through a CRISPR-generated cell model. Molecular genetics & genomic medicine 12 (5) (2024)
Maryam Fazelzadeh Haghighi, Hossein Jafari Khamirani, Jafar Fallahi, Ali Arabi Monfared, Korosh Ashrafi Dehkordi, Seyed Mohammad Bagher Tabei
Novel insight into FCSK-congenital disorder of glycosylation through a CRISPR-generated cell model. Molecular genetics & genomic medicine 12 (5) (2024)
Maryam Fazelzadeh Haghighi, Hossein Jafari Khamirani, Jafar Fallahi, Ali Arabi Monfared, Korosh Ashrafi Dehkordi, Seyed Mohammad Bagher Tabei
Novel insight into FCSK-congenital disorder of glycosylation through a CRISPR-generated cell model. Molecular genetics & genomic medicine 12 (5) (2024)
Negin Fazelzadeh Haghighi, Neda Kamal, Hossein Jafari Khamirani, Maryam Fazelzadeh Haghighi, Seyed Alireza Dastgheib, Mehdi Dianatpour, Seyed Mohammad Bagher Tabei
Novel insight into the ectodermal dysplasia 11A: Splicing variant of the EDARADD gene in a family with clinical variability and literature review. The Journal of dermatology (2023)
Zahra Abbasi, Hossein Jafari Khamirani, Seyed Mohammad Bagher Tabei, Jamal Manoochehri, Mehdi Dianatpour, Seyed Alireza Dastgheib
EPS8 variant causes deafness, autosomal recessive 102 (DFNB102) and literature review. Human genome variation 10 (1) (2023)
Sanaz Mohammadi, Hossein Jafari Khamirani, Maryam Baneshi, Neda Kamal, Jamal Manoocheri, Mahsa Saffar, Mehdi Dianatpour, Seyed Mohammad Bagher Tabei, Seyed Alireza Dastgheib
A novel nonsense variant in the ATL3 gene is associated with disturbed pain sensitivity, numbness of distal limbs and muscle weakness. Annals of human genetics (2023)
Zahra Abbasi, Hossein Jafari Khamirani, Seyed Mohammad Bagher Tabei, Jamal Manoochehri, Mehdi Dianatpour, Seyed Alireza Dastgheib
EPS8 variant causes deafness, autosomal recessive 102 (DFNB102) and literature review. Human genome variation 10 (1) (2023)
Amir Anushiravani, Hossein Jafari Khamirani, Ashraf Mohamadkhani, Arya Mani, Mehdi Dianatpour, Reza Malekzadeh
A Form of Metabolic-Associated Fatty Liver Disease Associated with a Novel LIPA Variant. Archives of Iranian medicine 26 (2) (2023)
Hossein Jafari Khamirani, Mehdi Dianatpour, Sina Zoghi, Sanaz Mohammadi, Ashkan Habib, Seyed Alireza Dastgheib, Seyed Mohammad Bagher Tabei, Mohadeseh Molayemat, Babak Shiraziyeganeh
Recurrent Infections and Immunodeficiency Caused by Severe Pancytopenia Associated with a Novel Life-Threatening Mutation in Hypoxia-Upregulated Protein 1. Immunological investigations 51 (6) (2022)
Jamal Manoochehri, Seyed Alireza Dastgheib, Hossein Jafari Khamirani, Maryam Mollaie, Zahra Sharifi, Sina Zoghi, Seyed Mohammad Bagher Tabei, Sanaz Mohammadi, Fatemeh Dehghanian, Zahra Farbod, Mehdi Dianatpour
A novel frameshift pathogenic variant in ST3GAL5 causing salt and pepper developmental regression syndrome (SPDRS): A case report. Human genome variation 8 (1) (2021)
Ashkan Habib, Alireza Shojazadeh, Mohadeseh Molayemat, Hossein Jafari Khamirani, Sina Zoghi, Seyed Alireza Dastgheib, Asadollah Habib
A single-amino-acid in-frame deletion in CYP17A1 results in combined 17-hydroxylase and 17,20-lyase deficiency in an Iranian family despite the protein mutation site. Human genome variation 8 (1) (2021)
Omid Alavi, Hossein Jafari Khamirani, Sina Zoghi, Afrooz Feili, Seyed Alireza Dastgheib, Seyed Mohammad Bagher Tabei, Jamal Manoochehri, Seyed Mehdi Panahandeh, Majid Kamali, Mehdi Dianatpour
Two novel Warburg micro syndrome 1 cases caused by pathogenic variants in RAB3GAP1. Human genome variation 8 (1) (2021)
Jamal Manoochehri, Seyed Alireza Dastgheib, Hossein Jafari Khamirani, Maryam Mollaie, Zahra Sharifi, Sina Zoghi, Seyed Mohammad Bagher Tabei, Sanaz Mohammadi, Fatemeh Dehghanian, Zahra Farbod, Mehdi Dianatpour
Correction: A novel frameshift pathogenic variant in ST3GAL5 causing salt and pepper developmental regression syndrome (SPDRS): a case report. Human genome variation 8 (1) (2021)