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109 results on '"Veldink, J."'

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1. Author Correction: Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology (Nature Genetics, (2021), 53, 12, (1636-1648), 10.1038/s41588-021-00973-1)

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

3. Correction for both common and rare cell types in blood is important to identify genes that correlate with age

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

5. Effect modification of the association between total cigarette smoking and ALS risk by intensity, duration and time-since-quitting: Euro-MOTOR

6. Author Correction: Genome-wide association analyses identify new Brugada syndrome risk loci and highlight a new mechanism of sodium channel regulation in disease susceptibility (Nature Genetics, (2022), 54, 3, (232-239), 10.1038/s41588-021-01007-6)

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

9. Common variant at 16p11.2 conferring risk of psychosis

10. Effect modification of the association between total cigarette smoking and ALS risk by intensity, duration and time-since-quitting: Euro-MOTOR

11. Large-scale cis- and trans-eQTL analyses identify thousands of genetic loci and polygenic scores that regulate blood gene expression

12. Publisher Correction : Altered perivascular fibroblast activity precedes ALS disease onset (Nature Medicine, (2021), 27, 4, (640-646), 10.1038/s41591-021-01295-9)

13. Association of Variants in the SPTLC1 Gene With Juvenile Amyotrophic Lateral Sclerosis

14. Multicentre, cross-cultural, population-based, case-control study of physical activity as risk factor for amyotrophic lateral sclerosis

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

16. Transethnic genome-wide association study provides insights in the genetic architecture and heritability of long QT syndrome

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

20. Using the structure of genome data in the design of deep neural networks for predicting amyotrophic lateral sclerosis from genotype

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

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

23. Multicentre, population-based, case-control study of particulates, combustion products and amyotrophic lateral sclerosis risk

24. Association between alcohol exposure and the risk of amyotrophic lateral sclerosis in the Euro-MOTOR study

25. Prediction of personalised prognosis in patients with amyotrophic lateral sclerosis: development and validation of a prediction model

26. A SNP panel for identification of DNA and RNA specimens

27. Exome sequencing in amyotrophic lateral sclerosis identifies risk genes and pathways

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

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

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

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

32. Variability in Working Memory Performance Explained by Epistasis vs Polygenic Scores in the ZNF804A Pathway

33. Schizophrenia genetic variants are not associated with intelligence

35. Susceptible genes and disease mechanisms identified in frontotemporal dementia and frontotemporal dementia with Amyotrophic Lateral Sclerosis by DNA-methylation and GWAS

36. No association between Borrelia burgdorferi antibodies and amyotrophic lateral sclerosis in a case-control study

37. Genome-wide association study identifies five new schizophrenia loci

38. Evaluation of genetic risk loci for intracranial aneurysms in sporadic arteriovenous malformations of the brain

39. Evaluation of genetic risk loci for intracranial aneurysms in sporadic arteriovenous malformations of the brain

40. All SNPs are not created equal: genome-wide association studies reveal a consistent pattern of enrichment among functionally annotated SNPs

41. Genetic schizophrenia risk variants jointly modulate total brain and white matter volume

42. Genome-wide association study identifies five new schizophrenia loci

43. Common variants at VRK2 and TCF4 conferring risk of schizophrenia

44. The verbal fluency index: Dutch normative data for cognitive testing in ALS

45. Common variant at 16p11.2 conferring risk of psychosis

46. Association study of common genetic variants and HIV-1 acquisition in 6,300 infected cases and 7,200 controls

47. European genome-wide association study identifies SLC14A1 as a new urinary bladder cancer susceptibility gene.

48. The epidemiology and treatment of ALS: focus on the heterogeneity of the disease and critical appraisal of therapeutic trials

49. Multiple common variants for celiac disease influencing immune gene expression

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