V. Wouters

PTHR1 mutations associated with Ollier disease result in receptor loss of function.

M. Vikkula, B. Gérard, B. Grandchamp, 2008, Human molecular genetics.

Somatic Mutations in the Angiopoietin-Receptor TIE2 Can Cause Both Solitary and Multiple Sporadic Venous Malformations

J. Mulliken, M. Vikkula, L. Eklund, 2008, Nature Genetics.

Common Somatic Alterations Identified in Maffucci Syndrome by Molecular Karyotyping

I. Kaitila, J. Mulliken, M. Vikkula, 2014, Molecular Syndromology.

Hereditary cutaneomucosal venous malformations are caused by TIE2 mutations with widely variable hyper-phosphorylating effects

A. Irrthum, J. Mulliken, M. Vikkula, 2010, European Journal of Human Genetics.

TIE2 and cutaneomucosal venous malformation

J. Mulliken, M. Vikkula, L. Boon, 2008 .