Irene MJ Mathijssen

Mutations of 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. · The Lancet · 2013 · 34 citations · Full text

Dentistry, Molecular Biology, Molecular Genetics +16

Apparently synonymous substitutions in FGFR2affect splicing and result in mild Crouzon syndrome

Aimée L Fenwick, Jacqueline A.C. Goos, Julia Rankin et al. · BMC Medical Genetics · 2014 · 19 citations · Full text

Dentistry, Genetics, Molecular Genetics +16

Is There an Effect of Obstructive Sleep Apnea Syndrome on Oxidative Stress and Inflammatory Parameters in Patients With Craniofacial Anomalies?

Caroline Driessen, Raul G. Plomp, Peter J. van der Spek et al. · Journal of Craniofacial Surgery · 2013 · 10 citations

Medicine, Craniofacial Biology, Craniofacial Genetics +14