Najim Lahrouchi

Amsterdam, NH, Netherlands

Last Updated: 09/26/2026

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Found 41 publications

An Updated Evidence Assessment of the Genetic Causes of Dilated Cardiomyopathy.

An Updated Evidence Assessment of the Genetic Causes of Dilated Cardiomyopathy.

Journal: Circulation

Published: September 08, 2026

Genetic analyses across cardiovascular traits: leveraging genetic correlations to empower locus discovery and prediction in common cardiovascular diseases.

Genetic analyses across cardiovascular traits: leveraging genetic correlations to empower locus discovery and prediction in common cardiovascular diseases.

Journal: NPJ genomic medicine

Published: September 13, 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

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

Genetic analyses of the electrocardiographic QT interval and its components identify additional loci and pathways.

Genetic analyses of the electrocardiographic QT interval and its components identify additional loci and pathways.

Journal: Nature communications

Published: November 19, 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

Evidence-Based Assessment of Genes in Dilated Cardiomyopathy.

Evidence-Based Assessment of Genes in Dilated Cardiomyopathy.

Journal: Circulation

Published: May 05, 2021

Publisher Correction: Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals.

Publisher Correction: Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals.

Journal: Nature genetics

Published: March 17, 2021

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

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: December 27, 2020

Biallelic loss-of-function variants in PLD1 cause congenital right-sided cardiac valve defects and neonatal cardiomyopathy.

Biallelic loss-of-function variants in PLD1 cause congenital right-sided cardiac valve defects and neonatal cardiomyopathy.

Journal: The Journal of clinical investigation

Published: July 09, 2020

Enhancing rare variant interpretation in inherited arrhythmias through quantitative analysis of consortium disease cohorts and population controls.

Enhancing rare variant interpretation in inherited arrhythmias through quantitative analysis of consortium disease cohorts and population controls.

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

Published: June 01, 2020

Showing 1-12 of 41

Last Updated: 09/26/2026