Mojgan Babanejad

3PUBLICATIONS
10CO-AUTHORS
Peripheral nervous systemEpigenetics (incl. genome methylation and epigenomics)Gene expression (incl. microarray and other genome-wide approaches)
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Publications (3)

|Jan 23, 2025
Genetic etiology of Perrault syndrome in Iranian families: first report from Iran and literature review.

Ebrahim Shokouhian, Kimia Kahrizi, Hossein Najmabadi

|Mar 19, 2023
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.

Fereshteh Jamshidi, Ebrahim Shokouhian, Marzieh Mohseni

|Nov 08, 2017
Variants in CIB2 cause DFNB48 and not USH1J.

K T Booth, K Kahrizi, M Babanejad

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Frequent Collaborators

2 joint publications

Kimia Kahrizi

2 joint publications

Hossein Najmabadi

1 joint publications

K T Booth

1 joint publications

G Bademci