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236 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. 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)

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

43. Schizophrenia genetic variants are not associated with intelligence

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

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

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

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

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