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Medrxiv : the Preprint Server for Health Sciences|February 13, 2023
Large scale genome-wide association analyses identify novel genetic loci and mechanisms in hypertrophic cardiomyopathyRafik Tadros, Sean L Zheng, Christopher Grace, et al.
Nature Genetics|February 18, 2025
Large-scale genome-wide association analyses identify novel genetic loci and mechanisms in hypertrophic cardiomyopathyRafik Tadros, Sean L Zheng, Christopher Grace, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|October 7, 2015
Cutaneous Lymphoma International Consortium Study of Outcome in Advanced Stages of Mycosis Fungoides and Sézary Syndrome: Effect of Specific Prognostic Markers on Survival and Development of a Prognostic ModelJulia J Scarisbrick, H Miles Prince, Maarten H Vermeer, et al.
Nature|August 20, 2025
Cancer-induced nerve injury promotes resistance to anti-PD-1 therapyErez N Baruch, Frederico O Gleber-Netto, Priyadharsini Nagarajan, et al.
Medrxiv : the Preprint Server for Health Sciences|July 15, 2024
Biallelic variants in POPDC2 cause a novel autosomal recessive syndrome presenting with cardiac conduction defects and variable hypertrophic cardiomyopathyMichele Nicastro, Alexa M C Vermeer, Pieter G Postema, et al.
The Lancet. Neurology|May 19, 2024
Safety and efficacy of active blood-pressure reduction to the recommended thresholds for intravenous thrombolysis in patients with acute ischaemic stroke in the Netherlands (TRUTH): a prospective, observational, cluster-based, parallel-group studyThomas P Zonneveld, Sarah E Vermeer, Erik W van Zwet, et al.
Nature Genetics|January 26, 2021
Shared genetic pathways contribute to risk of hypertrophic and dilated cardiomyopathies with opposite directions of effectRafik Tadros, Catherine Francis, Xiao Xu, et al.
American Journal of Human Genetics|May 23, 2025
Bi-allelic variants in POPDC2 cause an autosomal recessive syndrome presenting with cardiac conduction defects and hypertrophic cardiomyopathyMichele Nicastro, Alexa M C Vermeer, Pieter G Postema, et al.
American Journal of Human Genetics|August 4, 2015
Mutations in DDX3X Are a Common Cause of Unexplained Intellectual Disability with Gender-Specific Effects on Wnt SignalingLot Snijders Blok, Erik Madsen, Jane Juusola, et al.
The British Journal of Dermatology|September 30, 2018
The PROCLIPI international registry of early-stage mycosis fungoides identifies substantial diagnostic delay in most patientsJ J Scarisbrick, P Quaglino, H M Prince, et al.
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