Mojgan Babanejad (M Babanejad)

Publication Activity (10 Years)

Years Active: 2018-2023
Publications (10 Years): 2

Top Topics

Transcription Factor

Autism Spectrum Disorder

Intellectual Disability

Top Venues

Molecular genetics & genomic medicine

Clinical genetics

University of Social Welfare and Rehabilitation Science (PHD)

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

Education History

University of Social Welfare and Rehabilitation Science Jan 01 2011

Iran

PHD :: Genetic Research Center

Publications

Fereshteh Jamshidi, Ebrahim Shokouhian, Marzieh Mohseni, Kimia Kahrizi, Hossein Najmabadi, Mojgan Babanejad
Identification of a homozygous frameshift mutation in the FGF3 gene in a consanguineous Iranian family: First report of labyrinthine aplasia, microtia, and microdontia syndrome in Iran and literature review. Molecular genetics & genomic medicine (2023)
Kevin T A Booth, Kimia Kahrizi, Mojgan Babanejad, H Daghagh, Güney Bademci, S Arzhangi, D Zareabdollahi, Duygu Duman, Aziz El-Amraoui, Mustafa Tekin, Hossein Najmabadi, Hela Azaiez, Richard J H Smith
Variants in CIB2 cause DFNB48 and not USH1J. Clinical genetics 93 (4) (2018)