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1. Implementing Individually Tailored Prescription of Physical Activity in Routine Clinical Care: Protocol of the Physicians Implement Exercise = Medicine (PIE=M) Development and Implementation Project

2. Stress and anxiety during pregnancy and length of gestation: a federated study using data from five Canadian and European birth cohorts

3. Social inequalities in child mental health trajectories: a longitudinal study using birth cohort data 12 countries

6. Prioritization of Kidney Cell Types Highlights Myofibroblast Cells in Regulating Human Blood Pressure

10. Urban environment in pregnancy and postpartum depression: An individual participant data meta-analysis of 12 European birth cohorts

11. Comprehensive evaluation of smoking exposures and their interactions on DNA methylation

12. Genome-wide analysis identifies genetic effects on reproductive success and ongoing natural selection at the FADS locus

13. A Solve-RD ClinVar-based reanalysis of 1522 index cases from ERN-ITHACA reveals common pitfalls and misinterpretations in exome sequencing

14. Altered and allele-specific open chromatin landscape reveals epigenetic and genetic regulators of innate immunity in COVID-19

15. Multi-ancestry sleep-by-SNP interaction analysis in 126,926 individuals reveals lipid loci stratified by sleep duration.

16. Semantic modelling of common data elements for rare disease registries, and a prototype workflow for their deployment over registry data

17. FAIR Genomes metadata schema promoting Next Generation Sequencing data reuse in Dutch healthcare and research

19. Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project

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

21. DNA Methylation Analysis Identifies Loci for Blood Pressure Regulation

22. MOLGENIS VIP: an open-source and modular pipeline for high-throughput and integrated DNA variant analysis

23. Prioritization of Kidney Cell Types Highlights Myofibroblast Cells in Regulating Human Blood Pressure

24. The Data Use Ontology to streamline responsible access to human biomedical datasets

25. The LifeCycle Project-EU Child Cohort Network : a federated analysis infrastructure and harmonized data of more than 250,000 children and parents

26. Meta-analysis uncovers genome-wide significant variants for rapid kidney function decline

27. Urban environment in pregnancy and postpartum depression:An individual participant data meta-analysis of 12 European birth cohorts

28. Position paper on management of personal data in environment and health research in Europe

29. LongITools: Dynamic longitudinal exposome trajectories in cardiovascular and metabolic noncommunicable diseases

30. Metadata for Data dIscoverability aNd Study rEplicability in obseRVAtional Studies (MINERVA): Lessons Learnt From the MINERVA Project in Europe.

31. Metadata for Data dIscoverability aNd Study rEplicability in obseRVAtional Studies (MINERVA): Development and Pilot of a Metadata List and Catalogue in Europe.

32. Comprehensive evaluation of smoking exposures and their interactions on DNA methylation

34. A high-quality human reference panel reveals the complexity and distribution of genomic structural variants.

35. Meta-analysis of 49 549 individuals imputed with the 1000 Genomes Project reveals an exonic damaging variant in ANGPTL4 determining fasting TG levels

36. The FAIR Guiding Principles for scientific data management and stewardship.

39. Author Correction: Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project

40. A Resource for Guiding Data Stewards to Make European Rare Disease Patient Registries FAIR

41. Surveyed common data access policies preferences amongst European Reference Networks

42. Characteristics of de novo structural changes in the human genome

43. Genome of The Netherlands population-specific imputations identify an ABCA6 variant associated with cholesterol levels.

44. Fine mapping the CETP region reveals a common intronic insertion associated to HDL-C

45. Lessons learned from whole exome sequencing in multiplex families affected by a complex genetic disorder, intracranial aneurysm.

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

47. Comparing Sequence-Based and Literature Based Pathogenicity Scoring Methods for Human Variants.

48. Advancing tools for human early lifecourse exposome research and translation (ATHLETE): Project overview

49. Ten quick tips for building FAIR workflows

50. Curation and expansion of the Human Phenotype Ontology for systemic autoinflammatory diseases improves phenotype-driven disease-matching

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