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1. Doping induced site-selective Mott insulating phase in LaFeO$_3$

7. Predictors for a dementia gene mutation based on gene-panel next-generation sequencing of a large dementia referral series

8. Author Correction: Common variants in Alzheimer’s disease and risk stratification by polygenic risk scores (Nature Communications, (2021), 12, 1, (3417), 10.1038/s41467-021-22491-8)

9. Population-specific and cross-ancestry genome-wide association study identifies shared genetic architecture and 6 new risk loci including CAMK2D associated for Brugada syndrome

10. Modeling familial sinus node dysfunction with a large intergenic deletion between PITX2 and ANK2 using iPS cell-derived sinoatrial nodal-like cardiomyocytes

11. New insights into the genetic etiology of Alzheimer's disease and related dementias

12. Associations between ASL-derived cerebrovascular health and cognitive performance: results from the Insight 46 study

13. Cardiovascular and cerebrovascular health in 70-year-olds: a population-based ASL study

15. Non-coding deletion induces 3D chromatin remodelling and PITX2 expression dysregulation associated with a syndromic cardiac disorder

17. Emulating randomized clinical trials in relapsing-remitting multiple sclerosis with nonrandomized real-world evidence: an application using data from the MSBase registry

20. Syndromic cardiac disorder is associated with a non-coding deletion that induces a 3D chromatin remodeling and PITX2 expression dysregulation

23. Cadherin 2-Related Arrhythmogenic Cardiomyopathy: Prevalence and Clinical Features

24. Enhancing rare variant interpretation in inherited arrhythmias through quantitative analysis of consortium disease cohorts and population controls

28. SCN5A mutation type and a genetic risk score associate variably with brugada syndrome phenotype in SCN5A families

29. 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)

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

38. Functional, structural and molecular characterization of a new mitral valve prolapse animal model : The FLNA-P637Q KI rat

46. Functional, structural and molecular characterization of a new mitral valve prolapse animal model: the FLNA-P637Q KI rat

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