Marie‐José H. van den Boogaard

MSX1 mutation is associated with orofacial clefting and tooth agenesis in humans

Marie‐José H. van den Boogaard, M. Dorland, Frits A. Beemer et al. · Nature Genetics · 2000 · 584 citations

Developmental Anomaly, Orofacial Clefting, Developmental Biology +10

Loss-of-Function Mutations in the WNT Co-receptor LRP6 Cause Autosomal-Dominant Oligodontia

Maarten P.G. Massink, Marijn Créton, Francesca Spanevello et al. · The American Journal of Human Genetics · 2015 · 115 citations · Full text

Signal Transduction, Developmental Biology, Genetic Disorder +5

Genotype‐phenotype correlation in adult‐onset acid maltase deficiency

John H. J. Wokke, Margreet G.E.M. Ausems, Marie‐José H. van den Boogaard et al. · Annals of Neurology · 1995 · 82 citations · Full text

Serum Creatine Kinase, Electrolyte Disorder, Adult Form +12

Variants in members of the cadherin–catenin complex, CDH1 and CTNND1, cause blepharocheilodontic syndrome

Anneke J.A. Kievit, Federico Tessadori, Hannie Douben et al. · European Journal of Human Genetics · 2018 · 69 citations · Full text

Signal Transduction, Cadherin–catenin Complex, Pathology +7

Clinical Practice Guidelines on the Treatment of Patients with Cleft Lip, Alveolus, and Palate: An Executive Summary

Aebele B. Mink van der Molen, Johanna M. M. van Breugel, Nard G. Janssen et al. · Journal of Clinical Medicine · 2021 · 58 citations · Full text

Cleft Teams, Oral Medicine, Surgery +21