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1. Systematic rare variant analyses identify RAB32 as a susceptibility gene for familial Parkinson’s disease

2. Molecular pathology, developmental changes and synaptic dysfunction in (pre-) symptomatic human C9ORF72-ALS/FTD cerebral organoids

4. ATAXIN-2 intermediate-length polyglutamine expansions elicit ALS-associated metabolic and immune phenotypes

5. Author Correction: The SOD1-mediated ALS phenotype shows a decoupling between age of symptom onset and disease duration

6. Functional characterisation of the amyotrophic lateral sclerosis risk locus GPX3/TNIP1

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

9. Integrative genetic analysis illuminates ALS heritability and identifies risk genes

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

12. Genome-wide association study of intracranial aneurysms identifies 17 risk loci and genetic overlap with clinical risk factors

14. The contribution of Neanderthal introgression and natural selection to neurodegenerative diseases

15. Analysis of shared common genetic risk between amyotrophic lateral sclerosis and epilepsy

16. Whole genome sequencing analysis reveals post-zygotic mutation variability in monozygotic twins discordant for amyotrophic lateral sclerosis

18. Whole-genome sequencing reveals that variants in the Interleukin 18 Receptor Accessory Protein 3′UTR protect against ALS

19. Genetic variants associated with longitudinal changes in brain structure across the lifespan

20. Genome-wide association analyses identify new Brugada syndrome risk loci and highlight a new mechanism of sodium channel regulation in disease susceptibility

21. Structural variation analysis of 6,500 whole genome sequences in amyotrophic lateral sclerosis

22. The SOD1-mediated ALS phenotype shows a decoupling between age of symptom onset and disease duration

23. Letter to the editor on a paper by Kaivola et al. (2020): carriership of two copies of C9orf72 hexanucleotide repeat intermediate-length alleles is not associated with amyotrophic lateral sclerosis or frontotemporal dementia

26. Genetic Risk Score for Intracranial Aneurysms: Prediction of Subarachnoid Hemorrhage and Role in Clinical Heterogeneity

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

28. Correction: Immune-related genetic enrichment in frontotemporal dementia: An analysis of genome-wide association studies.

29. Immune-related genetic enrichment in frontotemporal dementia: An analysis of genome-wide association studies

30. DNA Methylation Analysis Identifies Loci for Blood Pressure Regulation

31. Contribution of Common Genetic Variants to Risk of Early Onset Ischemic Stroke

33. Genetic correlation between amyotrophic lateral sclerosis and schizophrenia.

34. Analysis of aneurysmal subarachnoid hemorrhage as a multistep process

35. Familial motor neuron disease: co-occurrence of PLS and ALS (-FTD)

36. Mutations in the tail and rod domains of the neurofilament heavy-chain gene increase the risk of ALS

38. Shared genetic pathways contribute to risk of hypertrophic and dilated cardiomyopathies with opposite directions of effect

40. Computing linkage disequilibrium aware genome embeddings using autoencoders.

43. Epigenome-wide Association Study of Attention-Deficit/Hyperactivity Disorder Symptoms in Adults

44. Common Genetic Variants Contribute to Risk of Transposition of the Great Arteries

46. OTTERS:a powerful TWAS framework leveraging summary-level reference data

47. Author Correction: Genome-wide association analyses identify new Brugada syndrome risk loci and highlight a new mechanism of sodium channel regulation in disease susceptibility

48. No evidence for shared genetic basis of common variants in multiple sclerosis and amyotrophic lateral sclerosis

49. Assessment of risk of ALS conferred by the GGGGCC hexanucleotide repeat expansion in C9orf72 among first-degree relatives of patients with ALS carrying the repeat expansion.

50. Familial motor neuron disease: co-occurrence of PLS and ALS (-FTD).

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