Guideline for Care of Patients With the Diagnoses of Craniosynostosis: Working Group on Craniosynostosis

by Mathijssen, Irene M.J.
Published in J Craniofac Surg (2015)

Introduction to Updated Guideline on Treatment and Management of Craniosynostosis

by Mathijssen, Irene M.J.
Published in J Craniofac Surg (2021)

Updated Guideline on Treatment and Management of Craniosynostosis

by Mathijssen, Irene M.J.
Published in J Craniofac Surg (2021)

Genetic Causes of Craniosynostosis: An Update

by Goos, Jacqueline A.C., Mathijssen, Irene M.J.
Published in Mol Syndromol (2019)

Is Cortical Complexity Development Affected By Syndromic Craniosynostosis?

by Wilson, Alexander T., Vrooman, Henri A., Mathijssen, Irene M. J.
Published in Plast Reconstr Surg Glob Open (2020)

Health-related problems and quality of life in patients with syndromic and complex craniosynostosis

by de Jong, Tim, Maliepaard, Marianne, Bannink, Natalja, Raat, Hein, Mathijssen, Irene M. J.
Published 2012

Assessing Nonacceptance of the Facial Appearance in Adult Patients After Complete Treatment of Their Rare Facial Cleft

by van den Elzen, Marijke E. P., Versnel, Sarah L., Duivenvoorden, Hugo J., Mathijssen, Irene M. J.
Published 2012

Testing for Implicit Gender Bias among Plastic Surgeons

by Bucknor, Alexandra, Ngaage, Ledibabari M., Taylor, Kirsten J., Kamali, Parisa, Rakhorst, Hinne A., Mathijssen, Irene M. J., Furnas, Heather
Published in Plast Reconstr Surg Glob Open (2021)

Intracranial Hypertension and Cortical Thickness in Syndromic Craniosynostosis

by Wilson, Alexander T., den Ottelander, Bianca K., de Goederen, Robbin G., Dremmen, Marjolein H. G., Vrooman, Henri A., Mathijssen, Irene M. J.
Published in Plast Reconstr Surg Glob Open (2019)

Using Perfusion Contrast for Spatial Normalization of ASL MRI Images in a Pediatric Craniosynostosis Population

by de Planque, Catherine A., Mutsaerts, Henk J. M. M., Keil, Vera C., Erler, Nicole S., Dremmen, Marjolein H. G., Mathijssen, Irene M. J., Petr, Jan
Published in Front Neurosci (2021)

Management and outcomes of obstructive sleep apnea in children with Robin sequence, a cross-sectional study

by van Lieshout, Manouk J.S., Joosten, Koen F.M., Koudstaal, Maarten J., van der Schroeff, Marc P., Dulfer, Karolijn, Mathijssen, Irene M.J., Wolvius, Eppo B.
Published in Clin Oral Investig (2016)

Cortical Thickness in Crouzon–Pfeiffer Syndrome: Findings in Relation to Primary Cranial Vault Expansion

by Wilson, Alexander T., de Planque, Catherine A., Yang, Sumin S., Tasker, Robert C., van Veelen, Marie-Lise C., Dremmen, Marjolein H.G., Vrooman, Henri A., Mathijssen, Irene M.J.
Published in Plast Reconstr Surg Glob Open (2020)

Improvement in Sleep Architecture is associated with the Indication of Surgery in Syndromic Craniosynostosis

by de Goederen, Robbin, Joosten, Koen F.M., den Ottelander, Bianca K., van der Oest, Mark J.W., Bröker-Schenk, Els M.M., van Veelen, Marie-Lise C., Wolvius, Eppo B., Versnel, Sarah L., Tasker, Robert C., Mathijssen, Irene M.J.
Published in Plast Reconstr Surg Glob Open (2019)

Craniosynostosis affects the majority of mucopolysaccharidosis patients and can contribute to increased intracranial pressure

by Oussoren, Esmee, Mathijssen, Irene M. J., Wagenmakers, Margreet, Verdijk, Rob M., Bredero-Boelhouwer, Hansje H., van Veelen-Vincent, Marie-Lise C., van der Meijden, Jan C., van den Hout, Johanna M. P., Ruijter, George J. G., van der Ploeg, Ans T., Langeveld, Mirjam
Published in J Inherit Metab Dis (2018)

Frontorhiny, a Distinctive Presentation of Frontonasal Dysplasia Caused by Recessive Mutations in the ALX3 Homeobox Gene

by Twigg, Stephen R.F., Versnel, Sarah L., Nürnberg, Gudrun, Lees, Melissa M., Bhat, Meenakshi, Hammond, Peter, Hennekam, Raoul C.M., Hoogeboom, A. Jeannette M., Hurst, Jane A., Johnson, David, Robinson, Alexis A., Scambler, Peter J., Gerrelli, Dianne, Nürnberg, Peter, Mathijssen, Irene M.J., Wilkie, Andrew O.M.
Published 2009

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

by Nieminen, Pekka, Morgan, Neil V., Fenwick, Aimée L., Parmanen, Satu, Veistinen, Lotta, Mikkola, Marja L., van der Spek, Peter J., Giraud, Andrew, Judd, Louise, Arte, Sirpa, Brueton, Louise A., Wall, Steven A., Mathijssen, Irene M.J., Maher, Eamonn R., Wilkie, Andrew O.M., Kreiborg, Sven, Thesleff, Irma
Published 2011

RAB23 Mutations in Carpenter Syndrome Imply an Unexpected Role for Hedgehog Signaling in Cranial-Suture Development and Obesity

by Jenkins, Dagan , Seelow, Dominik , Jehee, Fernanda S. , Perlyn, Chad A. , Alonso, Luís G. , Bueno, Daniela F. , Donnai, Dian , Josifiova, Dragana , Mathijssen, Irene M. J. , Morton, Jenny E. V. , Ørstavik, Karen Helene , Sweeney, Elizabeth , Wall, Steven A. , Marsh, Jeffrey L. , Nürnberg, Peter , Passos-Bueno, Maria Rita , Wilkie, Andrew O. M. 
Published 2007

The Origin of EFNB1 Mutations in Craniofrontonasal Syndrome: Frequent Somatic Mosaicism and Explanation of the Paucity of Carrier Males

by Twigg, Stephen R. F., Matsumoto, Kazuya, Kidd, Alexa M. J., Goriely, Anne, Taylor, Indira B., Fisher, Richard B., Hoogeboom, A. Jeannette M., Mathijssen, Irene M. J., Lourenço, M. Teresa, Morton, Jenny E. V., Sweeney, Elizabeth, Wilson, Louise C., Brunner, Han G., Mulliken, John B., Wall, Steven A., Wilkie, Andrew O. M.
Published 2006

A de novo substitution in BCL11B leads to loss of interaction with transcriptional complexes and craniosynostosis

by Goos, Jacqueline A C, Vogel, Walter K, Mlcochova, Hana, Millard, Christopher J, Esfandiari, Elahe, Selman, Wisam H, Calpena, Eduardo, Koelling, Nils, Carpenter, Evan L, Swagemakers, Sigrid M A, van der Spek, Peter J, Filtz, Theresa M, Schwabe, John W R, Iwaniec, Urszula T, Mathijssen, Irene M J, Leid, Mark, Twigg, Stephen R F
Published in Hum Mol Genet (2019)

Identification of Intragenic Exon Deletions and Duplication of TCF12 by Whole Genome or Targeted Sequencing as a Cause of TCF12‐Related Craniosynostosis

by Goos, Jacqueline A.C., Fenwick, Aimee L., Swagemakers, Sigrid M.A., McGowan, Simon J., Knight, Samantha J.L., Twigg, Stephen R.F., Hoogeboom, A. Jeannette M., van Dooren, Marieke F., Magielsen, Frank J., Wall, Steven A., Mathijssen, Irene M.J., Wilkie, Andrew O.M., van der Spek, Peter J., van den Ouweland, Ans M.W.
Published in Hum Mutat (2016)