Zeinab Fadaie

4PUBLICATIONS
21CO-AUTHORS
Genetic immunologyNeurogeneticsEpigenetics (incl. genome methylation and epigenomics)Neurology and neuromuscular diseases
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Publications (4)

|Nov 19, 2021
Whole genome sequencing and in vitro splice assays reveal genetic causes for inherited retinal diseases.

Zeinab Fadaie, Laura Whelan, Tamar Ben-Yosef

|Apr 29, 2021
BBS1 branchpoint variant is associated with non-syndromic retinitis pigmentosa.

Zeinab Fadaie, Laura Whelan, Adrian Dockery

|Apr 03, 2021
The Impact of Modern Technologies on Molecular Diagnostic Success Rates, with a Focus on Inherited Retinal Dystrophy and Hearing Loss.

Suzanne E de Bruijn, Zeinab Fadaie, Frans P M Cremers

|Aug 10, 2019
Identification of splice defects due to noncanonical splice site or deep-intronic variants in ABCA4.

Zeinab Fadaie, Mubeen Khan, Marta Del Pozo-Valero

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Frequent Collaborators

4 joint publications

Susanne Roosing

3 joint publications

Frans P M Cremers

2 joint publications

Laura Whelan

1 joint publications

Mubeen Khan