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1. Exome sequencing identifies rare damaging variants in ATP8B4 and ABCA1 as risk factors for Alzheimer’s disease

2. Meta-analysis of genome-wide association studies identifies ancestry-specific associations underlying circulating total tau levels

3. Author Correction: Common variants in Alzheimer’s disease and risk stratification by polygenic risk scores

5. Genetic and lifestyle risk factors for MRI-defined brain infarcts in a population-based setting

6. Multi‐phenotype analyses of hemostatic traits with cardiovascular events reveal novel genetic associations

8. The plasma miRNAome in ADNI: Signatures to aid the detection of at‐risk individuals.

9. Exome Chip Analysis Identifies Low-Frequency and Rare Variants in MRPL38 for White Matter Hyperintensities on Brain Magnetic Resonance Imaging

10. Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes

11. Whole genome sequence analyses of brain imaging measures in the Framingham Study

12. Genetically elevated high-density lipoprotein cholesterol through the cholesteryl ester transfer protein gene does not associate with risk of Alzheimer's disease.

13. Bone mineral density and the risk of incident dementia:A meta-analysis

14. Key variants via the Alzheimer's Disease Sequencing Project whole genome sequence data

15. Rare Functional Variant in TM2D3 is Associated with Late-Onset Alzheimer's Disease.

16. Polygenic Overlap Between C-Reactive Protein, Plasma Lipids, and Alzheimer Disease

17. NeuroX, a fast and efficient genotyping platform for investigation of neurodegenerative diseases

18. Common variants in Alzheimer’s disease and risk stratification by polygenic risk scores

19. Quality control and integration of genotypes from two calling pipelines for whole genome sequence data in the Alzheimer's disease sequencing project

20. Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease

21. Predicting stroke through genetic risk functions: the CHARGE Risk Score Project.

23. Bone mineral density and the risk of incident dementia: A meta‐analysis

24. Genetic architecture of subcortical brain structures in 38,851 individuals

25. Identifying rare variants from exome scans: the GAW17 experience

26. Association of Common and Rare Variants with Alzheimer's Disease in over 13,000 Diverse Individuals with Whole-Genome Sequencing from the Alzheimer's Disease Sequencing Project

27. The Gly2019Ser mutation in LRRK2is not fully penetrant in familial Parkinson's disease: the GenePD study

28. The Gly2019Ser mutation in LRRK2 is not fully penetrant in familial Parkinson's disease: the GenePD study.

29. Bone mineral density and the risk of incident dementia: A meta‐analysis.

31. Identification of additional risk loci for stroke and small vessel disease: a meta-analysis of genome-wide association studies

32. Genome-wide linkage analyses of non-Hispanic white families identify novel loci for familial late-onset Alzheimer's disease

33. Serum magnesium and calcium levels in relation to ischemic stroke: Mendelian randomization study

34. Genome-wide Studies of Verbal Declarative Memory in Nondemented Older People: The Cohorts for Heart and Aging Research in Genomic Epidemiology Consortium

36. Functional Annotations‐Informed Whole Genome Sequence Analysis Identifies Novel Rare Variants for AD in the Alzheimer’s Disease Sequencing Project

37. Whole-Exome Sequencing Identifies Rare and Low-Frequency Coding Variants Associated with LDL Cholesterol

38. Author Correction: Genetic meta-analysis of diagnosed Alzheimer’s disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing

39. Publisher Correction: Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes

42. Stroke genetics informs drug discovery and risk prediction across ancestries

43. Genetic risk factors for ischaemic stroke and its subtypes (the METASTROKE Collaboration): a meta-analysis of genome-wide association studies

44. Association of Common and Rare Variants with Alzheimer's Disease in 16,905 individuals with Whole‐Genome Sequence Data from the Alzheimer's Disease Sequencing Project.

45. RNA-sequencing of human post-mortem hypothalamus and nucleus accumbens identifies expression profiles associated with obesity.

46. Mutation of FOXC1 and PITX2 induces cerebral small-vessel disease

49. Rare and Coding Region Genetic Variants Associated With Risk of Ischemic Stroke: The NHLBI Exome Sequence Project

50. PLD3 variants in population studies

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