Elisabeth M. Lodder

Amsterdam, NH 1105AZ, Netherlands

Last Updated: 09/26/2026

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Found 61 publications

Additional genetic variants in cardiomyopathy patients with the pathogenic PLN p.(Arg14del) founder variant.

Additional genetic variants in cardiomyopathy patients with the pathogenic PLN p.(Arg14del) founder variant.

Journal: International journal of cardiology

Published: January 31, 2025

HCN4 in the atrioventricular node.

HCN4 in the atrioventricular node.

Journal: Heart rhythm

Published: September 10, 2024

Bi-allelic variants in POPDC2 cause an autosomal recessive syndrome presenting with cardiac conduction defects and hypertrophic cardiomyopathy.

Bi-allelic variants in POPDC2 cause an autosomal recessive syndrome presenting with cardiac conduction defects and hypertrophic cardiomyopathy.

Journal: American journal of human genetics

Published: August 18, 2024

Biallelic variants in POPDC2 cause a novel autosomal recessive syndrome presenting with cardiac conduction defects and variable hypertrophic cardiomyopathy.

Biallelic variants in POPDC2 cause a novel autosomal recessive syndrome presenting with cardiac conduction defects and variable hypertrophic cardiomyopathy.

Journal: medRxiv : the preprint server for health sciences

Published: July 15, 2024

Reduced kinase function in two ultra-rare TNNI3K variants in families with congenital junctional ectopic tachycardia.

Reduced kinase function in two ultra-rare TNNI3K variants in families with congenital junctional ectopic tachycardia.

Journal: Clinical genetics

Published: December 04, 2023

Genetic Burden of TNNI3K in Diagnostic Testing of Patients With Dilated Cardiomyopathy and Supraventricular Arrhythmias.

Genetic Burden of TNNI3K in Diagnostic Testing of Patients With Dilated Cardiomyopathy and Supraventricular Arrhythmias.

Journal: Circulation. Genomic and precision medicine

Published: May 18, 2023

Risk of Sudden Infant Death Syndrome Among Siblings of Children Who Died of Sudden Infant Death Syndrome in Denmark.

Risk of Sudden Infant Death Syndrome Among Siblings of Children Who Died of Sudden Infant Death Syndrome in Denmark.

Journal: JAMA network open

Published: January 25, 2023

Reclassification of a likely pathogenic Dutch founder variant in KCNH2; implications of reduced penetrance.

Reclassification of a likely pathogenic Dutch founder variant in KCNH2; implications of reduced penetrance.

Journal: Human molecular genetics

Published: August 23, 2022

Common Genetic Variants Contribute to Risk of Transposition of the Great Arteries.

Common Genetic Variants Contribute to Risk of Transposition of the Great Arteries.

Journal: Circulation research

Published: December 10, 2021

Correction to: Rare variants in KDR, encoding VEGF Receptor 2, are associated with tetralogy of Fallot.

Correction to: Rare variants in KDR, encoding VEGF Receptor 2, are associated with tetralogy of Fallot.

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

Published: September 15, 2021

The earliest events in BRAF-mutant colorectal cancer: exome sequencing of sessile serrated lesions with a tiny focus dysplasia or cancer reveals recurring mutations in two distinct progression pathways.

The earliest events in BRAF-mutant colorectal cancer: exome sequencing of sessile serrated lesions with a tiny focus dysplasia or cancer reveals recurring mutations in two distinct progression pathways.

Journal: The Journal of pathology

Published: August 02, 2021

Targeting the Microtubule EB1-CLASP2 Complex Modulates NaV1.5 at Intercalated Discs.

Targeting the Microtubule EB1-CLASP2 Complex Modulates NaV1.5 at Intercalated Discs.

Journal: Circulation research

Published: June 07, 2021

Showing 1-12 of 61

Last Updated: 09/26/2026