Marja W. Wessels
Erasmus MC(NL)Erasmus University Rotterdam(NL)
Publications by Year
Research Areas
Connective tissue disorders research, Congenital heart defects research, Cardiomyopathy and Myosin Studies, Congenital Heart Disease Studies, Genetics and Neurodevelopmental Disorders
Most-Cited Works
- → Mutations in SMAD3 cause a syndromic form of aortic aneurysms and dissections with early-onset osteoarthritis(2011)663 cited
- → Mutations in the facilitative glucose transporter GLUT10 alter angiogenesis and cause arterial tortuosity syndrome(2006)396 cited
- → Mutations in SWI/SNF chromatin remodeling complex gene ARID1B cause Coffin-Siris syndrome(2012)349 cited
- → Mutations in XPR1 cause primary familial brain calcification associated with altered phosphate export(2015)309 cited
- → Mutations in a TGF-β Ligand, TGFB3, Cause Syndromic Aortic Aneurysms and Dissections(2015)291 cited
- → Deciphering the Glycosylome of Dystroglycanopathies Using Haploid Screens for Lassa Virus Entry(2013)279 cited
- → MCIDAS mutations result in a mucociliary clearance disorder with reduced generation of multiple motile cilia