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1. Genetic and multi-omic resources for Alzheimer disease and related dementia from the Knight Alzheimer Disease Research Center

2. Advanced structural brain aging in preclinical autosomal dominant Alzheimer disease

3. Proteome wide association studies of LRRK2 variants identify novel causal and druggable proteins for Parkinson’s disease

4. Cell-free RNA signatures predict Alzheimer’s disease

6. Circular RNA detection identifies circPSEN1 alterations in brain specific to autosomal dominant Alzheimer's disease

8. Functional genomic analyses uncover APOE-mediated regulation of brain and cerebrospinal fluid beta-amyloid levels in Parkinson disease

9. A single-nuclei RNA sequencing study of Mendelian and sporadic AD in the human brain

10. TREM2 brain transcript-specific studies in AD and TREM2 mutation carriers

11. Parkinson disease polygenic risk score is associated with Parkinson disease status and age at onset but not with alpha-synuclein cerebrospinal fluid levels

12. Abstract WMP6: Genetic Variation In KLF5 Is Associated With Initial Stress Glucose Ratio In Acute Ischemic Stroke

13. Genome-wide Association Study Points to Novel Locus for Gilles de la Tourette Syndrome

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

15. Investigation of gene-environment interactions in relation to tic severity

16. Pleiotropic Effects of Variants in Dementia Genes in Parkinson Disease

17. Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders

18. Multi-Ancestry GWAS reveals excitotoxicity associated with outcome after ischaemic stroke

19. Multi-phenotype analyses of hemostatic traits with cardiovascular events reveal novel genetic associations

20. Inhibition of the enzyme autotaxin reduces cortical excitability and ameliorates the outcome in stroke

21. Examination of the Effect of Rare Variants in TREM2, ABI3, and PLCG2 in LOAD Through Multiple Phenotypes

22. CCL23: A Chemokine Associated with Progression from Mild Cognitive Impairment to Alzheimer’s Disease

23. Duration of US Residence And Resource Needs In Immigrant Families With Young Children

24. Prediction of Alzheimer disease using plasma RNA sequences from dementia genes

25. Circular RNA detection identifies circPSEN1 alterations in brain specific to Autosomal Dominant Alzheimer Disease

26. Editorial for the Genetics of Alzheimer's Disease Special Issue: October 2021

27. Advances in Genetic and Molecular Understanding of Alzheimer’s Disease

29. Investigation of gene-environment interactions in relation to tic severity

30. TREM2 brain transcript-specific studies in AD and TREM2 mutation carriers

31. Polygenic Risk Scores in Neurodegenerative Diseases: a Review

32. PATJ Low Frequency Variants Are Associated With Worse Ischemic Stroke Functional Outcome

33. Causal Effect of MMP-1 (Matrix Metalloproteinase-1), MMP-8, and MMP-12 Levels on Ischemic Stroke: A Mendelian Randomization Study

34. Early Neurological Change After Ischemic Stroke Is Associated With 90-Day Outcome

35. A comprehensive analysis of dementia cerebrospinal fluid biomarkers using GWAs, polygenic risk scores and Mendelian randomization in Parkinson’s disease

36. Prediction of Alzheimer’s disease using plasma RNA sequences

37. A Mendelian randomization approach to characterize overlap in the pathophysiology of neurological disorders

38. MULTI-ANCESTRY GENETIC STUDY IN 5,876 PATIENTS IDENTIFIES AN ASSOCIATION BETWEEN EXCITOTOXIC GENES AND EARLY OUTCOMES AFTER ACUTE ISCHEMIC STROKE

39. Genome-wide association, Mendelian Randomization and polygenic risk score studies converge on a role of β−amyloid and APOE locus in Parkinson disease

40. Genomic and multi-tissue proteomic integration for understanding the biology of disease and other complex traits

41. The influence of CYP enzymes and ABCB1 on treatment outcomes in schizophrenia: association of CYP1A2 activity with adverse effects

42. Investigation of previously implicated genetic variants in chronic tic disorders

43. Genetic susceptibility to invasive pneumococcal disease

44. Polygenic risk score of sporadic late‐onset Alzheimer's disease reveals a shared architecture with the familial and early‐onset forms

45. A common haplotype lowers PU.1 expression in myeloid cells and delays onset of Alzheimer's disease

46. Genome-Wide Association Study of White Blood Cell Counts in Patients With Ischemic Stroke

47. Overlapping Genetic Architecture between Parkinson Disease and Melanoma

48. The TMEM106B FTLD-protective variant, rs1990621, is also associated with increased neuronal proportion

49. A single-nuclei RNA sequencing study of Mendelian and sporadic AD in the human brain

50. The TMEM106B rs1990621 protective variant is also associated with increased neuronal proportion

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