Zeinab Fadaie

Publication Activity (10 Years)

Years Active: 2019-2021
Publications (10 Years): 4

Top Topics

Circulating Tumor

Top Venues

NPJ genomic medicine

Journal of medical genetics

International journal of molecular sciences

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

Publications

Zeinab Fadaie, Laura Whelan, Tamar Ben-Yosef, Adrian Dockery, Zelia Corradi, Christian Gilissen, Lonneke Haer-Wigman, Jordi Corominas, Galuh D N Astuti, Laura de Rooij, L Ingeborgh van den Born, Caroline C W Klaver, Carel B Hoyng, Niamh Wynne, Emma S Duignan, Paul F Kenna, Frans P M Cremers, G Jane Farrar, Susanne Roosing
Whole genome sequencing and in vitro splice assays reveal genetic causes for inherited retinal diseases. NPJ genomic medicine 6 (1) (2021)
Suzanne E de Bruijn, Zeinab Fadaie, Frans P M Cremers, Hannie Kremer, Susanne Roosing
The Impact of Modern Technologies on Molecular Diagnostic Success Rates, with a Focus on Inherited Retinal Dystrophy and Hearing Loss. International journal of molecular sciences 22 (6) (2021)
Zeinab Fadaie, Laura Whelan, Adrian Dockery, Catherina H Z Li, L Ingeborgh van den Born, Carel B Hoyng, Christian Gilissen, Christian Gilissen, Charlie F Rowlands, Roly Megaw, Anne K Lampe, Frans P M Cremers, Gwyneth Jane Farrar, Jamie M Ellingford, Paul F Kenna, Susanne Roosing
BBS1 branchpoint variant is associated with non-syndromic retinitis pigmentosa. Journal of medical genetics (2021)
Zeinab Fadaie, Mubeen Khan, Marta Del Pozo-Valero, Stéphanie S Cornelis, Carmen Ayuso, Frans P M Cremers, Susanne Roosing, null The Abca Study Group
Identification of splice defects due to noncanonical splice site or deep-intronic variants in ABCA4. Human mutation 40 (12) (2019)