Marieke H. Baars

Amsterdam, NH, Netherlands

Last Updated: 09/26/2026

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Found 16 publications

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Journal: BJOG : an international journal of obstetrics and gynaecology

Published: May 13, 2025

Pregnancy and Delivery Outcomes in Vascular Ehlers-Danlos Syndrome: A Retrospective Multicentre Cohort Study.

Pregnancy and Delivery Outcomes in Vascular Ehlers-Danlos Syndrome: A Retrospective Multicentre Cohort Study.

Journal: BJOG : an international journal of obstetrics and gynaecology

Published: December 05, 2024

Vascular Ehlers-Danlos Syndrome: A Comprehensive Natural History Study in a Dutch National Cohort of 142 Patients.

Vascular Ehlers-Danlos Syndrome: A Comprehensive Natural History Study in a Dutch National Cohort of 142 Patients.

Journal: Circulation. Genomic and precision medicine

Published: April 16, 2024

Expanding the genetic and phenotypic spectrum of ACTA2-related vasculopathies in a Dutch cohort.

Expanding the genetic and phenotypic spectrum of ACTA2-related vasculopathies in a Dutch cohort.

Journal: Genetics in medicine : official journal of the American College of Medical Genetics

Published: December 12, 2023

Growth charts for Marfan syndrome in the Netherlands and analysis of genotype-phenotype relationships.

Growth charts for Marfan syndrome in the Netherlands and analysis of genotype-phenotype relationships.

Journal: American journal of medical genetics. Part A

Published: July 11, 2022

Expanding the genetic and phenotypic spectrum of ACTA2-related vasculopathies in a Dutch cohort.

Expanding the genetic and phenotypic spectrum of ACTA2-related vasculopathies in a Dutch cohort.

Journal: Genetics in medicine : official journal of the American College of Medical Genetics

Published: December 15, 2021

A tailored approach to informing relatives at risk of inherited cardiac conditions: results of a randomised controlled trial.

A tailored approach to informing relatives at risk of inherited cardiac conditions: results of a randomised controlled trial.

Journal: European journal of human genetics : EJHG

Published: March 03, 2021

Phenotypic spectrum of TGFB3 disease-causing variants in a Dutch-French cohort and first report of a homozygous patient.

Phenotypic spectrum of TGFB3 disease-causing variants in a Dutch-French cohort and first report of a homozygous patient.

Journal: Clinical genetics

Published: October 12, 2019

Results of next-generation sequencing gene panel diagnostics including copy-number variation analysis in 810 patients suspected of heritable thoracic aortic disorders.

Results of next-generation sequencing gene panel diagnostics including copy-number variation analysis in 810 patients suspected of heritable thoracic aortic disorders.

Journal: Human mutation

Published: December 12, 2017

Spontaneous intracranial hypotension as first symptom of aneurysms-osteoarthritis syndrome: a case report.

Spontaneous intracranial hypotension as first symptom of aneurysms-osteoarthritis syndrome: a case report.

Journal: Headache

Published: February 20, 2015

HCN4 mutations in multiple families with bradycardia and left ventricular noncompaction cardiomyopathy.

HCN4 mutations in multiple families with bradycardia and left ventricular noncompaction cardiomyopathy.

Journal: Journal of the American College of Cardiology

Published: May 12, 2014

A mutation in the Kozak sequence of GATA4 hampers translation in a family with atrial septal defects.

A mutation in the Kozak sequence of GATA4 hampers translation in a family with atrial septal defects.

Journal: American journal of medical genetics. Part A

Published: October 07, 2013

Showing 1-12 of 16

Last Updated: 09/26/2026