Sjoerd G. Van Duinen

Rotterdam, ZH, Netherlands

Last Updated: 09/26/2026

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Found 80 publications

Metastatic conjunctival melanoma: a multicentre international study.

Metastatic conjunctival melanoma: a multicentre international study.

Journal: The British journal of ophthalmology

Published: June 20, 2024

Bi-allelic NIT1 variants cause a brain small vessel disease characterized by movement disorders, massively dilated perivascular spaces, and intracerebral hemorrhage.

Bi-allelic NIT1 variants cause a brain small vessel disease characterized by movement disorders, massively dilated perivascular spaces, and intracerebral hemorrhage.

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

Published: October 18, 2023

De novo heterozygous missense variants in CELSR1 as cause of fetal pleural effusions and progressive fetal hydrops.

De novo heterozygous missense variants in CELSR1 as cause of fetal pleural effusions and progressive fetal hydrops.

Journal: Journal of medical genetics

Published: October 17, 2023

RNA-sequencing to discover genes and signaling pathways associated with venous thromboembolism in glioblastoma patients: A case-control study.

RNA-sequencing to discover genes and signaling pathways associated with venous thromboembolism in glioblastoma patients: A case-control study.

Journal: Thrombosis research

Published: July 27, 2023

Increased Histological Tumor Pigmentation in Uveal Melanoma Is Related to Eye Color and Loss of Chromosome 3/BAP1.

Increased Histological Tumor Pigmentation in Uveal Melanoma Is Related to Eye Color and Loss of Chromosome 3/BAP1.

Journal: Ophthalmology science

Published: October 29, 2022

Diffusion-tensor magnetic resonance imaging captures increased skeletal muscle fibre diameters in Becker muscular dystrophy.

Diffusion-tensor magnetic resonance imaging captures increased skeletal muscle fibre diameters in Becker muscular dystrophy.

Journal: Journal of cachexia, sarcopenia and muscle

Published: September 13, 2022

Targeted DNA sequencing to identify genetic aberrations in glioblastoma that underlie venous thromboembolism; a cohort study.

Targeted DNA sequencing to identify genetic aberrations in glioblastoma that underlie venous thromboembolism; a cohort study.

Journal: Thrombosis research

Published: August 18, 2022

IDH1/2 wildtype gliomas grade 2 and 3 with molecular glioblastoma-like profile have a distinct course of epilepsy compared to IDH1/2 wildtype glioblastomas.

IDH1/2 wildtype gliomas grade 2 and 3 with molecular glioblastoma-like profile have a distinct course of epilepsy compared to IDH1/2 wildtype glioblastomas.

Journal: Neuro-oncology

Published: August 16, 2022

Biallelic loss of LDB3 leads to a lethal pediatric dilated cardiomyopathy.

Biallelic loss of LDB3 leads to a lethal pediatric dilated cardiomyopathy.

Journal: European journal of human genetics : EJHG

Published: May 27, 2022

Post-mortem 7T MR imaging and neuropathology in middle stage juvenile-onset Huntington disease: A case report.

Post-mortem 7T MR imaging and neuropathology in middle stage juvenile-onset Huntington disease: A case report.

Journal: Neuropathology and applied neurobiology

Published: May 19, 2022

Exploring macrophage differentiation and its relation to Modic changes in human herniated disc tissue.

Exploring macrophage differentiation and its relation to Modic changes in human herniated disc tissue.

Journal: Brain & spine

Published: March 01, 2022

Incidence and determinants of thrombotic and bleeding complications in patients with glioblastoma.

Incidence and determinants of thrombotic and bleeding complications in patients with glioblastoma.

Journal: Journal of thrombosis and haemostasis : JTH

Published: December 13, 2021

Showing 1-12 of 80

Last Updated: 09/26/2026