Sascha Vermeer

Reviewing the genetic causes of spastic-ataxias

H. Kremer, S. Vermeer, M. Willemsen, 2012, Neurology.

Massively parallel sequencing of ataxia genes after array‐based enrichment

Christian Gilissen, Alexander Hoischen, Nienke Wieskamp, 2010, Human mutation.

A Post‐Hoc Comparison of the Utility of Sanger Sequencing and Exome Sequencing for the Diagnosis of Heterogeneous Diseases

Christian Gilissen, Ilse Feenstra, Nienke Wieskamp, 2013, Human mutation.

Clinical and genetic characterisation of autosomal recessive cerebellar ataxias.

S. Vermeer, Sascha Vermeer, 2012 .

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.