Marieke J.H. Baars - Concepedia

Author

Marieke J.H. Baars

Amsterdam UMC Location University of Amsterdam ORCID

Also Known As

M J H Baars, M. J. H. Baars, Marieke Baars, Marieke J Baars, Marieke J H Baars, Marieke J. Baars, Marieke J. H. Baars, Marieke J.H. Baars, Marieke JH Baars, Marieke J.H. Baars

Publications

1.7K

Citations

H-Index

Concepts

All Affiliations

Amsterdam UMC Location University of Amsterdam Amsterdam UMC Location Vrije Universiteit Amsterdam Radboud University Nijmegen Netherlands Heart Institute Leiden University Medical Center

About

Marieke J.H. Baars is an author at Amsterdam UMC Location University of Amsterdam specializing in medicine, public health, and genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	14	15	919
2	Public Health	9	9	534
3	Natural Sciences	1	1	79
4	Nursing	1	1	11
5	Biochemistry	1	1	79

Marieke J.H. Baars

Publications

1.4K

Citations

H-Index

Page 1

	Year	Citations
Deficiency of knowledge of genetics and genetic tests among general practitioners, gynecologists, and pediatricians: A global problem Marieke J.H. Baars, Lidewij Henneman, Leo P. ten Kate Genetics in Medicine InfertilityGenetic TestingGenetic TestsGeneral PractitionersPrenatal Genetic Testing	2005	232
HCN4 Mutations in Multiple Families With Bradycardia and Left Ventricular Noncompaction Cardiomyopathy Annalisa Milano, Alexa M.C. Vermeer, Elisabeth M. Lodder, Journal of the American College of Cardiology Cardiac MuscleCardiomyopathyHeart FailureHcn4 MutationsGenetics	2014	195
Mutations in the Sarcomere Gene <i>MYH7</i> in Ebstein Anomaly Alex V. Postma, Klaartje van Engelen, Judith van de Meerakker, Circulation Cardiovascular Genetics	2010	186
A Mutation in C2orf64 Causes Impaired Cytochrome c Oxidase Assembly and Mitochondrial Cardiomyopathy Merei Huigsloot, Leo Nijtmans, Radek Szklarczyk, The American Journal of Human Genetics Mitochondrial BiogenesisBiochemistryMitochondrial FunctionNatural SciencesGenetics	2011	79
Inflammation Aggravates Disease Severity in Marfan Syndrome Patients Teodora Radonic, Piet de Witte, Maarten Groenink, PLoS ONE	2012	77
Mild phenotypes in a series of patients with Opitz GBBB syndrome with <i>MID1</i> mutations Joyce So, Vanessa Suckow, Zofia Kijas, American Journal of Medical Genetics Part A GeneticsGenetic EpidemiologyPathologyMolecular GeneticsDisease Gene Identification	2004	72
Deficient knowledge of genetics relevant for daily practice among medical students nearing graduation Marieke J.H. Baars, Albert Scherpbier, Lambert Schuwirth, Genetics in Medicine Genetic TestingDeficient KnowledgeDaily PracticeGenetic FactorPublic Health Genetics	2005	69
22q11.2 Deletion Syndrome is under-recognised in adult patients with tetralogy of Fallot and pulmonary atresia: Table 1 Klaartje van Engelen, Ana Töpf, Bernard Keavney, Heart	2010	58
Results of next-generation sequencing gene panel diagnostics including copy-number variation analysis in 810 patients suspected of heritable thoracic aortic disorders Eline Overwater, Luisa Marsili, Marieke J.H. Baars, Human Mutation Cnv AnalysisGeneticsPathologyDisease Gene IdentificationGenomics	2018	57
The Ambiguous Role of NKX2-5 Mutations in Thyroid Dysgenesis Klaartje van Engelen, Mathilda T.M. Mommersteeg, Marieke J.H. Baars, PLoS ONE Transcriptional RegulationDevelopmental BiologyGenetic DisorderLymphocyte DevelopmentGenetics	2012	43

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