Kristel R. Van Eijk

Utrecht, UT 3584CG, Netherlands

Last Updated: 09/26/2026

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Found 70 publications

Correction: A rare missense variant impacting NEK1 kinase function is associated with ALS.

Correction: A rare missense variant impacting NEK1 kinase function is associated with ALS.

Journal: Acta neuropathologica communications

Published: July 21, 2026

A rare missense variant impacting NEK1 kinase function is associated with ALS.

A rare missense variant impacting NEK1 kinase function is associated with ALS.

Journal: Acta neuropathologica communications

Published: February 25, 2026

Large-scale exome analyses reveal new rare variant contributions in amyotrophic lateral sclerosis.

Large-scale exome analyses reveal new rare variant contributions in amyotrophic lateral sclerosis.

Journal: Nature genetics

Published: August 15, 2025

Sex-specific DNA methylation differences in Amyotrophic lateral sclerosis.

Sex-specific DNA methylation differences in Amyotrophic lateral sclerosis.

Journal: bioRxiv : the preprint server for biology

Published: December 09, 2024

Author Correction: Integrative genetic analysis illuminates ALS heritability and identifies risk genes.

Author Correction: Integrative genetic analysis illuminates ALS heritability and identifies risk genes.

Journal: Nature communications

Published: December 04, 2023

Association of Risk Variants in the CFH Gene With Elevated Levels of Coagulation and Complement Factors in Idiopathic Multifocal Choroiditis.

Association of Risk Variants in the CFH Gene With Elevated Levels of Coagulation and Complement Factors in Idiopathic Multifocal Choroiditis.

Journal: JAMA ophthalmology

Published: July 06, 2023

Rare and common genetic determinants of mitochondrial function determine severity but not risk of amyotrophic lateral sclerosis.

Rare and common genetic determinants of mitochondrial function determine severity but not risk of amyotrophic lateral sclerosis.

Journal: Heliyon

Published: June 19, 2023

Heritable defects in telomere and mitotic function selectively predispose to sarcomas.

Heritable defects in telomere and mitotic function selectively predispose to sarcomas.

Journal: Science (New York, N.Y.)

Published: January 19, 2023

Associations Between Polygenic Risk Score Loading, Psychosis Liability, and Clozapine Use Among Individuals With Schizophrenia.

Associations Between Polygenic Risk Score Loading, Psychosis Liability, and Clozapine Use Among Individuals With Schizophrenia.

Journal: JAMA psychiatry

Published: December 21, 2022

Associations between genetic liabilities to smoking behavior and schizophrenia symptoms in patients with a psychotic disorder, their siblings and healthy controls.

Associations between genetic liabilities to smoking behavior and schizophrenia symptoms in patients with a psychotic disorder, their siblings and healthy controls.

Journal: Psychiatry research

Published: December 15, 2022

Genetic variability in sporadic amyotrophic lateral sclerosis.

Genetic variability in sporadic amyotrophic lateral sclerosis.

Journal: Brain : a journal of neurology

Published: November 16, 2022

Telomere length analysis in amyotrophic lateral sclerosis using large-scale whole genome sequence data.

Telomere length analysis in amyotrophic lateral sclerosis using large-scale whole genome sequence data.

Journal: Frontiers in cellular neuroscience

Published: September 21, 2022

Showing 1-12 of 70

Last Updated: 09/26/2026