Alihossein Saberi

ORCID

Publication Activity (10 Years)

Years Active: 2018-2024
Publications (10 Years): 10

Top Venues

Molecular genetics & genomic medicine

Movement disorders : official journal of the Movement Disorder Society

Clinical case reports

Andrologia

Ahvaz Jondishapour University of Medical Sciences Faculty of Medicine

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

Affiliation History

Ahvaz Jondishapour University of Medical Sciences Faculty of Medicine

Iran

associate professor, group leader :: medical genetic

Publications

Roya Sinaei, Maryam Eslami, Mohammadreza Dadfar, Alihossein Saberi
Identification of a new mutation in the ACTL9 gene in men with unexplained infertility. Molecular genetics & genomic medicine 12 (5) (2024)
Roya Sinaei, Maryam Eslami, Mohammadreza Dadfar, Alihossein Saberi
Identification of a new mutation in the ACTL9 gene in men with unexplained infertility. Molecular genetics & genomic medicine 12 (5) (2024)
Juan Dario Ortigoza-Escobar, Mina Zamani, Nathalie Dorison, Saeid Sadeghian, Reza Azizimalamiri, Javeria Raza Alvi, Tipu Sultan, Hamid Galehdari, Gholamreza Shariati, Alihossein Saberi, Lisette Leeuwen, Giovanni Zifarelli, Peter Bauer, Vincent d'Hardemare, Diane Doummar, Emmanuel Roze, Lorena Travaglini, Francesco Nicita, Núria Ojea Ponce, Seyed Mohammadsaleh Zahraei, Lama Alabdi, Abdullah Tamim, Mais O Hashem, Faroug Ababneh, Michelle M Morrow, Cynthia Curry, Allison Tam, Jessica Ruedy, Vikas Bhambhani, Regan Veith, Petter Strømme, Stephanie Efthymiou, Fowzan S Alkuraya, Andrés Moreno De Luca, Lydie Burglen, Henry Houlden, Reza Maroofian
Biallelic ZBTB11 Variants: A Neurodevelopmental Condition with Progressive Complex Movement Disorders. Movement disorders : official journal of the Movement Disorder Society (2024)
Juan Dario Ortigoza-Escobar, Mina Zamani, Nathalie Dorison, Saeid Sadeghian, Reza Azizimalamiri, Javeria Raza Alvi, Tipu Sultan, Hamid Galehdari, Gholamreza Shariati, Alihossein Saberi, Lisette Leeuwen, Giovanni Zifarelli, Peter Bauer, Vincent d'Hardemare, Diane Doummar, Emmanuel Roze, Lorena Travaglini, Francesco Nicita, Núria Ojea Ponce, Seyed Mohammadsaleh Zahraei, Lama Alabdi, Abdullah Tamim, Mais O Hashem, Faroug Ababneh, Michelle M Morrow, Cynthia Curry, Allison Tam, Jessica Ruedy, Vikas Bhambhani, Regan Veith, Petter Strømme, Stephanie Efthymiou, Fowzan S Alkuraya, Andrés Moreno De Luca, Lydie Burglen, Henry Houlden, Reza Maroofian
Biallelic ZBTB11 Variants: A Neurodevelopmental Condition with Progressive Complex Movement Disorders. Movement disorders : official journal of the Movement Disorder Society (2024)
Roya Sinaei, Maryam Eslami, Mohammadreza Dadfar, Alihossein Saberi
Identification of a new mutation in the ACTL9 gene in men with unexplained infertility. Molecular genetics & genomic medicine 12 (5) (2024)
Seyed Reza Kazemi Nezhad, Pegah Namdar Aligoodarzi, Golale Rostami, Gholamreza Shariati, Hamid Galehdari, Alihossein Saberi, Alireza Sedaghat, Mohammad Hamid
Genotypic variants of the tetrahydrobiopterin (BH4) biosynthesis genes in patients with hyperphenylalaninemia from different regions of Iran. Molecular genetics & genomic medicine (2023)
Siavash Shakerian, Homeira Rashidi, Maryam Tahmasebi Birgani, Alihossein Saberi
KCNQ1 rs2237895 polymorphism is associated with the therapeutic response to sulfonylureas in Iranian type 2 diabetes mellitus patients. Journal of diabetes and metabolic disorders 21 (1) (2022)
Mahzad Nasirshalal, Maryam Tahmasebi Birgani, Mohammadreza Dadfar, Roshan Nikbakht, Alihossein Saberi, Pegah Ghandil
Identification of the PRM1 gene mutations in oligoasthenoteratozoospermic men. Andrologia 52 (11) (2020)
Mohammad Hamid, Ebtesam Zargan Nezhad, Hamid Galehdari, Alihossein Saberi, Gholamreza Shariati, Alireza Sedaghat
A First Report of Hb Alesha [β67(E11)Val>Met, GTG>ATG] in an Iranian Patient Iranian biomedical journal 23 (6) (2018)
Gholamreza Shariati, Alihossein Saberi, Mohammad Hamid, Hamid Galehdari, Alireza Sedaghat, Nehzat Abdorasuli
Prenatal diagnosis of a rare de novo 1q22-q25.1 chromosomal deletion syndrome using oligo array CGH. Clinical case reports 6 (8) (2018)

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Publication Activity (10 Years)

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Alihossein Saberi