Irene M. J. Mathijssen

Mutations in TCF12, encoding a basic helix-loop-helix partner of TWIST1, are a frequent cause of coronal craniosynostosis

Vikram Sharma, Aimée L Fenwick, Mia Brockop et al. · Nature Genetics · 2013 · 218 citations · Full text

Frequent Cause, Molecular Biology, Craniofacial Development +6

Increase of prevalence of craniosynostosis

Martijn J. Cornelissen, B. den Ottelander, Dimitris Rizopoulos et al. · Journal of Cranio-Maxillofacial Surgery · 2016 · 204 citations

Craniofacial Disorder, Craniofacial Anomalies, Spine Deformity +4

Inactivation of IL11 Signaling Causes Craniosynostosis, Delayed Tooth Eruption, and Supernumerary Teeth

Pekka Nieminen, Neil V. Morgan, Aimée L Fenwick et al. · The American Journal of Human Genetics · 2011 · 192 citations · Full text

The Increase of Metopic Synostosis

Jacques van der Meulen, René R. W. J. van der Hulst, Leon van Adrichem et al. · Journal of Craniofacial Surgery · 2009 · 146 citations

Rheumatology, Scleroderma, Neurological Disorder +15

Diagnostic value of exome and whole genome sequencing in craniosynostosis

Kerry A. Miller, Stephen R.F. Twigg, Simon J. McGowan et al. · Journal of Medical Genetics · 2016 · 120 citations · Full text