Richard Jlf Lemmers

11PUBLICATIONS
71CO-AUTHORS
Epigenetics (incl. genome methylation and epigenomics)Cell and nuclear divisionMicroelectromechanical systems (MEMS)Gene expression (incl. microarray and other genome-wide approaches)Gene and molecular therapy
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Publications (11)

|Jun 05, 2026
The emergence and diversification of the DUX gene family across placental mammals.

|Jan 08, 2025
Double trouble: a comprehensive study into unrelated genetic comorbidities in adult patients with Facioscapulohumeral Muscular Dystrophy Type I.

Angela Puma, Giulia Tammam, Andra Ezaru

|Nov 18, 2024
Three-dimensional tissue engineered skeletal muscle modelling facioscapulohumeral muscular dystrophy.

Marnix Franken, Erik van der Wal, Dongxu Zheng

|Apr 29, 2024
Best practice guidelines on genetic diagnostics of facioscapulohumeral muscular dystrophy: Update of the 2012 guidelines.

Emiliano Giardina, Pilar Camaño, Sarah Burton-Jones

|Jan 25, 2024
Regional and bilateral MRI and gene signatures in facioscapulohumeral dystrophy: implications for clinical trial design and mechanisms of disease progression.

Chao-Jen Wong, Seth D Friedman, Lauren Snider

|Sep 13, 2023
Autosomal dominant in cis D4Z4 repeat array duplication alleles in facioscapulohumeral dystrophy.

Richard J L F Lemmers, Russell Butterfield, Patrick J van der Vliet

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Frequent Collaborators

6 joint publications

Silvère M van der Maarel

3 joint publications

Stephen J Tapscott

2 joint publications

Franclo Henning

2 joint publications

Venugopalan Y Vishnu