Ahoura Nozari

A Pathogenic Homozygous Mutation in The Pleckstrin Homology Domain of RASA1 Is Responsible for Familial Tricuspid Atresia in An Iranian Consanguineous Family

F. Behjati, Ahoura Nozari, Ehsan Aghaei-Moghadam, 2018, Cell journal.

Whole-Exome Sequencing Identifies Three Candidate Homozygous Variants in a Consanguineous Iranian Family with Autism Spectrum Disorder and Skeletal Problems

F. Hadipour, Z. Hadipour, F. Behjati, 2020, Molecular Syndromology.

Investigation of Chromosomal Abnormalities and Microdeletion/ Microduplication(s) in Fifty Iranian Patients with Multiple Congenital Anomalies.

A. Kariminejad, H. Najmabadi, Z. Chavoshzadeh, 2019, Cell journal.

A novel splicing variant in FLNC gene responsible for a highly penetrant familial dilated cardiomyopathy in an extended Iranian family.

H. Najmabadi, F. Behjati, R. Mollazadeh, 2018, Gene.

Bi-allelic Mutations in ALDH5A1 is associated with succinic semialdehyde dehydrogenase deficiency and severe intellectual disability.

F. Behjati, Vahid Asghariazar, Ahoura Nozari, 2020, Gene.

A Novel Missense Mutation in the TGF-β-binding Protein-Like Domain 3 of FBN1 Causes Weill–Marchesani Syndrome with Intellectual Disability

A. Sadeghi, Ahoura Nozari, S. Taghizadeh, 2023, Advanced biomedical research.