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282 results on '"Veldink, J.H."'

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

2. Genetic characterization of primary lateral sclerosis.

3. Functional genomics analysis identifies T and NK cell activation as a driver of epigenetic clock progression

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

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

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

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

9. Genome-wide identification of the genetic basis of amyotrophic lateral sclerosis

10. Mendelian randomization integrating GWAS and eQTL data reveals genetic determinants of complex and clinical traits

11. Occupational exposure to gases/fumes and mineral dust affect DNA methylation levels of genes regulating expression

12. Genotype-phenotype correlations of KIF5A stalk domain variants

13. Incidence, Prevalence, and Geographical Clustering of Motor Neuron Disease in the Netherlands

14. Meta-analysis of genome-wide DNA methylation identifies shared associations across neurodegenerative disorders

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

16. 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

17. A characterization of cis- and trans-heritability of RNA-Seq-based gene expression

18. Intake of polyunsaturated fatty acids and vitamin E reduces the risk of developing amyotrophic lateral sclerosis

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

20. Transethnic Genome-Wide Association Study Provides Insights in the Genetic Architecture and Heritability of Long QT Syndrome .

21. Distinctive pattern of temporal atrophy in patients with frontotemporal dementia and the I383V variant in TARDBP

22. Genome-wide identification of genes regulating DNA methylation using genetic anchors for causal inference

23. The genetic architecture of the human cerebral cortex

24. Significant out-of-sample classification from methylation profile scoring for amyotrophic lateral sclerosis

25. Reconsidering the causality of TIA1 mutations in ALS

26. WGS-based telomere length analysis in Dutch family trios implicates stronger maternal inheritance and a role for RRM1 gene

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

28. Joint sequencing of human and pathogen genomes reveals the genetics of pneumococcal meningitis

29. The expanded clinical spectrum of anti-GABABR encephalitis and added value of KCTD16 autoantibodies

30. Mendelian randomization integrating GWAS and eQTL data reveals genetic determinants of complex and clinical traits

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

32. NEK1 variants confer susceptibility to amyotrophic lateral sclerosis

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

34. Association of NIPA1 repeat expansions with amyotrophic lateral sclerosis in a large international cohort

35. Genome-wide identification of directed gene networks using large-scale population genomics data

36. CHCHD10 variants in amyotrophic lateral sclerosis: where Is the evidence?

37. Association of maternal prenatal smoking GFI1-locus and cardio-metabolic phenotypes in 18,212 adults

38. Autosomal genetic variation is associated with DNA methylation in regions variably escaping X-chromosome inactivation

39. Skewed X-inactivation is common in the general female population

40. Genome-wide identification of directed gene networks using large-scale population genomics data

42. No association between gluten sensitivity and amyotrophic lateral sclerosis

43. Exploring the fitness hypothesis in ALS: a population-based case-control study of parental cause of death and lifespan

44. A replication study of genetic risk loci for ischemic stroke in a Dutch population: A case-control study

45. Blood lipids influence DNA methylation in circulating cells

46. Rare genetic variation in UNC13A may modify survival in amyotrophic lateral sclerosis

47. Age-related accrual of methylomic variability is linked to fundamental ageing mechanisms

48. Genome-wide patterns and properties of de novo mutations in humans

49. Susceptibility loci for sporadic brain arteriovenous malformation; a replication study and meta-analysis

50. Large-scale screening in sporadic amyotrophic lateral sclerosis identifies genetic modifiers in C9orf72 repeat carriers

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