Hanka Venselaar

The NewProt Self-Service Portal for Protein Engineering

Gert Vriend, Peter Haase, Andreas Schwarte, 2014, SWAT4LS.

NewProt – a protein engineering portal

Jaroslav Bendl, Jan Stourac, Gert Vriend, 2017, Protein engineering, design & selection : PEDS.

Status quo of annotation of human disease variants

Gert Vriend, Hanka Venselaar, Franscesca Camilli, 2013, BMC Bioinformatics.

Protein structure analysis of mutations causing inheritable diseases. An e-Science approach with life scientist friendly interfaces

Gert Vriend, Hanka Venselaar, Maarten L. Hekkelman, 2010, BMC Bioinformatics.

Homology modelling and spectroscopy, a never-ending love story

Bas Vroling, Gert Vriend, Hanka Venselaar, 2009, European Biophysics Journal.

Whole exome sequencing identifies a heterozygous missense variant in the PRDM5 gene in a family with Axenfeld–Rieger syndrome

Hanka Venselaar, Raheel Qamar, Saemah Nuzhat Zafar, 2015, neurogenetics.

Mutations in DDX3X Are a Common Cause of Unexplained Intellectual Disability with Gender-Specific Effects on Wnt Signaling.

Michael J Parker, Katrina Tatton-Brown, Christian Gilissen, 2015, American journal of human genetics.

Functional Analysis of the Kv1.1 N255D Mutation Associated with Autosomal Dominant Hypomagnesemia*

Hanka Venselaar, H. Venselaar, J. Hoenderop, 2009, The Journal of Biological Chemistry.