Mubeen Khan

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

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

Publications

Tabea V Riepe, Mubeen Khan, Susanne Roosing, Frans P M Cremers, Peter A C 't Hoen
Benchmarking deep learning splice prediction tools using functional splice assays. Human mutation 42 (7) (2021)
Manon H C A Peeters, Mubeen Khan, Anoek A M B Rooijakkers, Timo Mulders, Lonneke Haer-Wigman, Camiel J F Boon, Caroline C W Klaver, L Ingeborgh van den Born, Carel B Hoyng, Frans P M Cremers, Anneke I den Hollander, Claire-Marie Dhaenens, Rob W J Collin
PRPH2 mutation update: In silico assessment of 245 reported and 7 novel variants in patients with retinal disease. Human mutation 42 (12) (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)
Mubeen Khan, Stéphanie S Cornelis, Muhammad Imran Khan, Duaa Elmelik, Eline Manders, Sem Bakker, Ronny Derks, Kornelia Neveling, Maartje van de Vorst, Christian Gilissen, Isabelle Meunier, Sabine Defoort, Bernard Puech, Aurore Devos, Heidi L Schulz, Heidi Stöhr, Felix Grassmann, Bernhard H F Weber, Claire-Marie Dhaenens, Frans P M Cremers
Cost-effective molecular inversion probe-based ABCA4 sequencing reveals deep-intronic variants in Stargardt disease. Human mutation 40 (10) (2019)

Mubeen Khan.css-eqlu8i{font-size:small;padding-left:4px;}