Marieke J.H. Baars

Amsterdam University Medical Centers — Netherlands

Biochemistry, Genetics and Molecular Biology · Life Sciences

21h-index1.7kcitations59works7.02yr avg
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Research Topics

Congenital heart defects research(16), Connective tissue disorders research(14), BRCA gene mutations in cancer(9), Congenital Heart Disease Studies(8), Aortic Disease and Treatment Approaches(8)

Publications59 total

Author Reply
BJOG An International Journal of Obstetrics & Gynaecology·2025
Pregnancy and Delivery Outcomes in Vascular Ehlers–Danlos Syndrome: A Retrospective Multicentre Cohort Study
BJOG An International Journal of Obstetrics & Gynaecology·2025· 5 citedOpen Access
Large‐ and medium‐sized arterial aneurysms in two patients with <scp><i>SMAD4</i></scp>‐related juvenile polyposis syndrome
American Journal of Medical Genetics Part A·2024· 2 citedOpen Access
Vascular Ehlers-Danlos Syndrome: A Comprehensive Natural History Study in a Dutch National Cohort of 142 Patients
Circulation Genomic and Precision Medicine·2024· 21 citedOpen Access
Expanding the genetic and phenotypic spectrum of ACTA2-related vasculopathies in a Dutch cohort
Genetics in Medicine·2023Open Access
HTAD patient pathway: Strategy for diagnostic work-up of patients and families with (suspected) heritable thoracic aortic diseases (HTAD). A statement from the HTAD working group of VASCERN
European Journal of Medical Genetics·2022· 17 citedOpen Access
Growth charts for Marfan syndrome in the Netherlands and analysis of genotype–phenotype relationships
American Journal of Medical Genetics Part A·2022· 6 citedOpen Access
No prominent role for complement C1-esterase inhibitor in Marfan syndrome mice
Vascular Biology·2022· 2 citedOpen Access
Poster No. 132 HTAD PATIENT PATHWAY: Strategy for diagnostic work-up of patients and families with (suspected) Heritable Thoracic Aortic Diseases (HTAD). A statement from the HTAD Working Group of VASCERN
Cardiovascular Research·2022Open Access
Expanding the genetic and phenotypic spectrum of ACTA2-related vasculopathies in a Dutch cohort
Genetics in Medicine·2022· 4 citedOpen Access
A tailored approach to informing relatives at risk of inherited cardiac conditions: results of a randomised controlled trial
European Journal of Human Genetics·2021· 21 citedOpen Access
A tailored approach towards informing relatives at risk of inherited cardiac diseases : preliminary results of a randomized controlled trial
Data Archiving and Networked Services (DANS)·2020
Nederlands Netwerk Marfan : Netwerken in de zorg voor zeldzaam
Data Archiving and Networked Services (DANS)·2020
Phenotypic spectrum of <i>TGFB3</i> disease‐causing variants in a Dutch‐French cohort and first report of a homozygous patient
Clinical Genetics·2020· 23 citedOpen Access
Author response for "Phenotypic spectrum of &lt;i&gt;TGFB3&lt;/i&gt; disease‐causing variants in a Dutch‐French cohort and first report of a homozygous patient"
2019
P6497Loeys-Dietz syndrome-5: phenotypic spectrum of TGFB3 mutations in an international cohort and first report of a homozygous patient
European Heart Journal·2019
Hereditary thoracic aortic disease associated with cysteine substitution c.937T &gt; G p.(Cys313Gly) in FBN1
Netherlands Heart Journal·2019· 3 citedOpen Access
Results of next-generation sequencing gene panel diagnostics including copy-number variation analysis in 810 patients suspected of heritable thoracic aortic disorders
Human Mutation·2018· 57 citedOpen Access
Clinical and Genetic Aspects of Bicuspid Aortic Valve: A Proposed Model for Family Screening Based on a Review of Literature
Cardiogenetics·2015· 1 citedOpen Access
Spontaneous Intracranial Hypotension as First Symptom of Aneurysms‐Osteoarthritis Syndrome: A Case Report
Headache The Journal of Head and Face Pain·2015· 1 citedOpen Access
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Frequent Co-authors

Barbara J.M. Mulder(14), Alex V. Postma(13), Klaartje van Engelen(13), Arjan C. Houweling(12), Yvonne Hilhorst‐Hofstee(10), Alessandra Maugeri(10), Leo P. ten Kate(9), Marlies Kempers(9), Eline Overwater(9), J. Peter van Tintelen(8), Eelco Dulfer(8), Ingrid M.B.H. van de Laar(7), Maarten Groenink(6), Imke Christiaans(5), Annette F. Baas(5), Bart Loeys(5), Caroline Benjamin(5), Kirsty Challen(5), R Harris(5), Antoon F.M. Moorman(4)