Marie‐José H. van den Boogaard

Author

Also Known As

Marie-Jose H. Van Den Boogaard, Marie-Jose H. van den Boogaard, Marie-Jose´ H van den Boogaard, Marie-José H van den Boogaard, Marie-José H. Van Den Boogaard, Marie-José H. van den Boogaard, Marie-José H. van den Boogaard, Marie-José van den Boogaard, Marie‐Jose H. van den Boogaard, Marie‐José H. van den Boogaard

Publications

1.6K

Citations

H-Index

Concepts

All Affiliations

University Medical Center Utrecht Wilhelmina Children's Hospital University of Amsterdam Radboud University Medical Center Radboud University Nijmegen

About

Marie‐José H. van den Boogaard is an author at University Medical Center Utrecht specializing in medicine, genetics, and pediatrics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	10	10	1.1K
2	Public Health	2	2	93
3	Health Sciences	1	1	58
4	Natural Sciences	1	1	20
5	Social Sciences	1	1	19

Marie‐José H. van den Boogaard

Publications

1.3K

Citations

H-Index

Page 1

	Year	Citations
MSX1 mutation is associated with orofacial clefting and tooth agenesis in humans Marie‐José H. van den Boogaard, M. Dorland, Frits A. Beemer, Nature Genetics Developmental AnomalyOrofacial CleftingDevelopmental BiologyGenetic DisorderMedicine	2000	584
Loss-of-Function Mutations in the WNT Co-receptor LRP6 Cause Autosomal-Dominant Oligodontia Maarten P.G. Massink, Marijn Créton, Francesca Spanevello, The American Journal of Human Genetics Signal TransductionDevelopmental BiologyGenetic DisorderGeneticsReceptor (Biochemistry)	2015	115
Genotype‐phenotype correlation in adult‐onset acid maltase deficiency John H. J. Wokke, Margreet G.E.M. Ausems, Marie‐José H. van den Boogaard, Annals of Neurology Serum Creatine KinaseElectrolyte DisorderAdult FormMedicineGenetics	1995	82
Variants in members of the cadherin–catenin complex, CDH1 and CTNND1, cause blepharocheilodontic syndrome Anneke J.A. Kievit, Federico Tessadori, Hannie Douben, European Journal of Human Genetics Signal TransductionCadherin–catenin ComplexPathologyDegenerative DiseaseNeuropathology	2018	69
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, Journal of Clinical Medicine Cleft TeamsOral MedicineSurgeryClinical Practice GuidelinesCpg Development	2021	58
Mortality in Robin sequence: identification of risk factors Robrecht J. H. Logjes, Maartje Haasnoot, Petra Lemmers, European Journal of Pediatrics	2018	51
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 Emma C. Paes, Daan P. F. van Nunen, Hanneke Basart, American Journal of Medical Genetics Part A Birth PrevalenceCleft LipGlobal HealthClinical EpidemiologyPediatrics	2015	48
Etiology and pathogenesis of robin sequence in a large Dutch cohort Hanneke Basart, Emma C. Paes, Saskia M. Maas, American Journal of Medical Genetics Part A Cleft LipMendelian DisorderGenetic DisorderGeneticsPathogenesis	2015	45
<scp> <i>HNRNPH1</i> </scp> ‐related syndromic intellectual disability: Seven additional cases suggestive of a distinct syndromic neurodevelopmental syndrome Sara L. Reichert, Rachel Li, Scott A. Turner, Clinical Genetics	2020	43
The MSX1 allele 4 homozygous child exposed to smoking at periconception is most sensitive in developing nonsyndromic orofacial clefts Marie‐José H. van den Boogaard, Dominique de Costa, Ingrid P.C. Krapels, Human Genetics	2008	37

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