Patrick J. Van Der Vliet-Van Der List

Leiden, ZH, Netherlands

Last Updated: 09/26/2026

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Found 34 publications

Fibro-adipogenic progenitors enhance functional and structural properties of human 3D tissue engineered skeletal muscles.

Fibro-adipogenic progenitors enhance functional and structural properties of human 3D tissue engineered skeletal muscles.

Journal: Journal of tissue engineering

Published: January 13, 2026

KLF18 is a necessary component of the DUX4-initiated transcriptional network and a candidate locus for phenotypic diversity.

KLF18 is a necessary component of the DUX4-initiated transcriptional network and a candidate locus for phenotypic diversity.

Journal: Genes & development

Published: August 10, 2025

Three-dimensional tissue engineered skeletal muscle modelling facioscapulohumeral muscular dystrophy.

Three-dimensional tissue engineered skeletal muscle modelling facioscapulohumeral muscular dystrophy.

Journal: Brain : a journal of neurology

Published: July 18, 2024

Double trouble: a comprehensive study into unrelated genetic comorbidities in adult patients with Facioscapulohumeral Muscular Dystrophy Type I.

Double trouble: a comprehensive study into unrelated genetic comorbidities in adult patients with Facioscapulohumeral Muscular Dystrophy Type I.

Journal: European journal of human genetics : EJHG

Published: July 17, 2024

Best practice guidelines on genetic diagnostics of facioscapulohumeral muscular dystrophy: Update of the 2012 guidelines.

Best practice guidelines on genetic diagnostics of facioscapulohumeral muscular dystrophy: Update of the 2012 guidelines.

Journal: Clinical genetics

Published: December 07, 2023

Less Pain, but no changes in maximal inclination angles during an overhead reach task following local anesthetic in patients with ongoing shoulder pain.

Less Pain, but no changes in maximal inclination angles during an overhead reach task following local anesthetic in patients with ongoing shoulder pain.

Journal: Journal of electromyography and kinesiology : official journal of the International Society of Electrophysiological Kinesiology

Published: October 04, 2023

Optical Genome Mapping for the Molecular Diagnosis of Facioscapulohumeral Muscular Dystrophy: Advancement and Challenges.

Optical Genome Mapping for the Molecular Diagnosis of Facioscapulohumeral Muscular Dystrophy: Advancement and Challenges.

Journal: Biomolecules

Published: August 18, 2023

The first genetically confirmed cohort of Facioscapulohumeral Muscular Dystrophy from Northern India.

The first genetically confirmed cohort of Facioscapulohumeral Muscular Dystrophy from Northern India.

Journal: European journal of human genetics : EJHG

Published: July 09, 2023

Neuromuscular disease genetics in under-represented populations: increasing data diversity.

Neuromuscular disease genetics in under-represented populations: increasing data diversity.

Journal: Brain : a journal of neurology

Published: May 22, 2023

Autosomal dominant in cis D4Z4 repeat array duplication alleles in facioscapulohumeral dystrophy.

Autosomal dominant in cis D4Z4 repeat array duplication alleles in facioscapulohumeral dystrophy.

Journal: Brain : a journal of neurology

Published: May 17, 2023

DUX4 expression in cancer induces a metastable early embryonic totipotent program.

DUX4 expression in cancer induces a metastable early embryonic totipotent program.

Journal: Cell reports

Published: March 01, 2023

High-resolution breakpoint junction mapping of proximally extended D4Z4 deletions in FSHD1 reveals evidence for a founder effect.

High-resolution breakpoint junction mapping of proximally extended D4Z4 deletions in FSHD1 reveals evidence for a founder effect.

Journal: Human molecular genetics

Published: April 27, 2021

Showing 1-12 of 34

Last Updated: 09/26/2026