Hedwig M Velde (H M Velde)

Publication Activity (10 Years)

Years Active: 2021-2023
Publications (10 Years): 3

Top Topics

Combination Therapy

Gene Expression

Diabetic Retinopathy

Top Venues

Journal of medical genetics

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

Publications

Hedwig M Velde, Nienke C Homans, André Goedegebure, Cornelis P Lanting, Ronald J E Pennings, Hannie Kremer
Analysis of Rotterdam Study cohorts confirms a previously identified RIPOR2 in-frame deletion as a prevalent genetic factor in phenotypically variable adult-onset hearing loss (DFNA21) in the Netherlands. Journal of medical genetics (2023)
Hedwig M Velde, Janine Reurink, Sebastian Held, Catherina H Z Li, Suzanne Yzer, Jaap Oostrik, Jack Weeda, Lonneke Haer-Wigman, Helger G Yntema, Susanne Roosing, Laurenz J B Pauleikhoff, Clemens A Lange, Laura Whelan, Adrian Dockery, Julia Zhu, David J Keegan, Gwyneth Jane Farrar, Hannie Kremer, Cornelis P Lanting, Markus Damme, Ronald J E Pennings
Usher syndrome type IV: clinically and molecularly confirmed by novel ARSG variants. Human genetics 141 (11) (2022)
Inge Stegeman, Hedwig M Velde, Pierre A J T Robe, R J Stokroos, A L Smit
Tinnitus treatment by vagus nerve stimulation: A systematic review. PloS one 16 (3) (2021)