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dr. M.J.H. van den Boogaard

dr. M.J.H. van den Boogaard

Assistant Professor - medical

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Research Output (94)

The association between WNT10A variants and dental development in patients with isolated oligodontia

Dhamo Brunilda, Fennis Willem, Creton MA, Vucic Strahinja, Cune Marco, Ploos van Amstel Hans Kristian, Wolvius Eppo B, van den Boogaard MJH, Ongkosuwito Edwin M Jan 2017, In: European Journal of Human Genetics. 25 , p. 59–65 7 p.

Postoperatief delirium herkennen bij ouderen

Numan Tianne, Van Den Boogaard Mark, Kamper Adriaan M., Rood Paul J T, Peelen Linda M., Slooter Arjen J.C. 2017, In: Nederlands Tijdschrift voor Geneeskunde. 161

Best Practices for the Diagnosis and Evaluation of Infants With Robin Sequence:A Clinical Consensus Report

Breugem Corstiaan C, Evans Kelly N, Poets Christian F, Suri Sunjay, Picard Arnaud, Filip Charles, Paes Emma C, Mehendale Felicity V, Saal Howard M, Basart Hanneke, Murthy Jyotsna, Joosten Koen F M, Speleman Lucienne, Collares Marcus V M, van den Boogaard Marie-José H, Muradin Marvick, Andersson Maud Els-Marie, Kogo Mikihiko, Farlie Peter G, Don Griot Peter, Mossey Peter A, Slator Rona, Abadie Veronique, Hong Paul 1 Sep 2016, In: JAMA Pediatrics. 170 , p. 894-902

Compound heterozygous NEK1 variants in two siblings with oral-facial-digital syndrome type II (Mohr syndrome)

Monroe Glen R, Kappen Isabelle Fpm, Stokman Marijn F, Terhal Paulien A, van den Boogaard Marie-José H, Savelberg Sanne Mc, van der Veken Lars T, van Es Robert J J, Lens Susanne M, Hengeveld Rutger C, Creton Marijn A, Janssen Nard G, Mink van der Molen Aebele B, Ebbeling Michelle B, Giles Rachel H, Knoers Nine V, van Haaften Gijs 17 Aug 2016, In: European Journal of Human Genetics. 24 , p. 1752–1760

Shift in DNA diagnostics; Shift in Clinical Practise

van den Boogaard MJH 2016,

MSX1 and hypodontia, orofacial clefting and the Witkop syndrome

van den Boogaard MJH, Ploos van Amstel JK 2016, p. 703-706

genetica in de tandheelkunde, presentatie nascholingsavond tandartsen

van den Boogaard MJH 27 Oct 2015,

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

Massink Maarten P G, Creton Marijn A. , Spanevello Francesca, Fennis Willem M M, Cune Marco S., Savelberg Sanne M C, Nijman Isaäc J., Maurice Madelon M., vandenBoogaard Marie José H, van Haaften Gijs 1 Oct 2015, In: American Journal of Human Genetics. 97 , p. 621–626

Etiology and pathogenesis of robin sequence in a large Dutch cohort

Basart Hanneke, Paes Emma C., Maas Saskia M., van den Boogaard Marie Jose H, van Hagen Johanna M., Breugem Corstiaan C., Cobben Jan Maarten, Griot J. Peter W Don, Lachmeijer Augusta M A, Lichtenbelt Klaske D., van Nunen DPF, van der Horst Chantal M., Hennekam Raoul C. 1 Jan 2015, In: American Journal of Medical Genetics. Part A. 167 , p. 1983-1992 10 p.

Birth prevalence of Robin sequence in the Netherlands from 2000-2010:A retrospective population-based study in a large Dutch cohort and review of the literature

Paes Emma C., van Nunen Daan P F, Basart Hanneke, Don Griot J. Peter W, van Hagen Johanna M., van der Horst Chantal M A M, van den Boogaard Marie José H, Breugem Corstiaan C. 1 Jan 2015, In: American Journal of Medical Genetics. Part A. 167 , p. 1972-1982 11 p.

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