Rob Zwart
Amsterdam, NH, Netherlands
Last Updated: 09/26/2026
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Found 23 publications
Tracing the pathogenic PLN p.(Arg14del) variant across the globe; more than just a local curiosity.
Journal: Journal of cardiovascular translational research
Published: January 23, 2026
Integrative epigenetic and transcriptomic profiling of whole blood and fibroblasts in Hao-Fountain syndrome.
Journal: Frontiers in cell and developmental biology
Published: January 07, 2026
Generation of two human induced pluripotent stem cell lines (iPSC) from patients with Hao-Fountain Syndrome.
Journal: Stem cell research
Published: September 15, 2025
Generation of a human induced pluripotent stem cell line (iPSC) from a patient with Clark-Baraitser Syndrome.
Journal: Stem cell research
Published: September 03, 2025
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.
Journal: medRxiv : the preprint server for health sciences
Published: July 15, 2024
Germline variants in HEY2 functional domains lead to congenital heart defects and thoracic aortic aneurysms.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: April 08, 2022
PRDM10 directs FLCN expression in a novel disorder overlapping with Birt-Hogg-Dubé syndrome and familial lipomatosis.
Journal: Human molecular genetics
Published: February 22, 2022
Tissue tropism and pathology of highly pathogenic avian influenza H5N6 virus in chickens and Pekin ducks.
Journal: Research in veterinary science
Published: July 27, 2021
Clinical and Pathological Findings in SARS-CoV-2 Disease Outbreaks in Farmed Mink (Neovison vison).
Journal: Veterinary pathology
Published: July 15, 2020
Germline variants in HEY2 functional domains lead to congenital heart defects and thoracic aortic aneurysms.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: May 08, 2020
Arrhythmogenic Right Ventricular Cardiomyopathy-Associated Desmosomal Variants Are Rarely De Novo.
Journal: Circulation. Genomic and precision medicine
Published: August 07, 2019
Last Updated: 09/26/2026