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Your search keyword '"Van Eijk K.R."' showing total 24 results

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24 results on '"Van Eijk K.R."'

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1. Associations between polygenic risk score loading, psychosis liability, and clozapine use among individuals with schizophrenia

2. Genome-wide study of DNA methylation shows alterations in metabolic, inflammatory, and cholesterol pathways in ALS

3. Author Correction: Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology

4. Cross-reactive probes on Illumina DNA methylation arrays: a large study on ALS shows that a cautionary approach is warranted in interpreting epigenome-wide association studies

5. Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology

6. Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology

7. NEK1 variants confer susceptibility to amyotrophic lateral sclerosis

8. Reconsidering the causality of TIA1 mutations in ALS

9. Project MinE: study design and pilot analyses of a large-scale whole-genome sequencing study in amyotrophic lateral sclerosis

10. Genetic architecture of subcortical brain structures in 38,851 individuals

11. Human genetics and neuropathology suggest a link between miR-218 and amyotrophic lateral sclerosis pathophysiology

12. Associations of autozygosity with a broad range of human phenotypes

13. Novel genetic loci associated with hippocampal volume

14. Characterization of genome-methylome interactions in 22 nuclear pedigrees

15. Quantitative studies of DNA methylation and gene expression in neuropsychiatric traits

16. Novel genetic loci underlying human intracranial volume identified through genome-wide association

17. Common genetic variants influence human subcortical brain structures

19. Characterization of genome-methylome interactions in 22 nuclear pedigrees

21. Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology

22. The role of rare compound heterozygous events in autism spectrum disorder

23. Human genetics and neuropathology suggest a link between miR-218 and amyotrophic lateral sclerosis pathophysiology

24. Genome-wide Analyses Identify KIF5A as a Novel ALS Gene

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