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Publications

HspB1 phosphorylation regulates its intramolecular dynamics and mechanosensitive molecular chaperone interaction with filamin C.

Collier MP. et al, (2019), Science advances, 5, eaav8421 - eaav8421

A Novel Familial Cardiac Arrhythmia Syndrome with Widespread ST-Segment Depression.

Bundgaard H. et al, (2018), The New England journal of medicine, 379, 1780 - 1781

Placental protein-13 (PP13) in combination with PAPP-A and free leptin index (fLI) in first trimester maternal serum screening for severe and early preeclampsia.

De Villiers CP. et al, (2017), Clin Chem Lab Med, 56, 65 - 74

Combination of Whole Genome Sequencing, Linkage and Functional Studies Implicates a Missense Mutation in Titin as a Cause of Autosomal Dominant Cardiomyopathy with Features of Left Ventricular Non-Compaction.

Gehmlich K., (2016), Circulation: Cardiovascular Genetics

Filamin C: a novel component of the KCNE2 interactome during hypoxia

Neethling A. et al, (2016), Cardiovascular Journal Of Africa, 27, 4 - 11

AKAP9 is a genetic modifier of congenital long-QT syndrome type 1.

de Villiers CP. et al, (2014), Circ Cardiovasc Genet, 7, 599 - 606

PLACENTAL PROTEIN-13 (PP13) IN COMBINATION WITH PAPP-A AND FREE LEPTIN INDEX (FLI) IN FIRST TRIMESTER MATERNAL SERUM SCREENING FOR SEVERE AND EARLY PREECLAMPSIA

De Villiers CP. et al, (2010), PLACENTA, 31, A122 - A122

Long QT syndrome - a genetic cardiac channelopathy.

Szeliga MA. et al, (2010), Kardiol Pol, 68, 575 - 583

Include forthcoming?