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1. Lack of association between classical HLA genes and asymptomatic SARS-CoV-2 infection

2. Epigenome-wide association study of COVID-19 severity with respiratory failure

3. PSP/DEGESCO: A Progressive Supranuclear Palsy Genome‐Wide Association Study in the Spanish Population

5. Genetic Associations Between Modifiable Risk Factors and Alzheimer Disease

6. A second update on mapping the human genetic architecture of COVID-19

8. Decoding the Human Genetic and Immunological Basis of COVID-19 mRNA Vaccine-Induced Myocarditis

9. Identification of a sex-specific genetic signature in dementia with Lewy bodies: a meta-analysis of genome-wide association studies

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

11. The risk of COVID-19 death is much greater and age-dependent with type I IFN autoantibodies

13. Genetic screening of Alzheimer's disease genes in Iberian and African samples yields novel mutations in presenilins and APP

14. Assessing the role of TUBA4A gene in frontotemporal degeneration

15. Common variants in Alzheimer's disease and risk stratification by polygenic risk scores

16. Epigenome-wide association study of COVID-19 severity with respiratory failure

18. The novel EPTP repeat defines a superfamily of proteins implicated in epileptic disorders

20. Assessing the role of the TREM2 p.R47H variant as a risk factor for Alzheimer's disease and frontotemporal dementia

21. Rare copy number variation in the GR@ACE/DEGESCO dementia dataset of spanish population.

23. Susceptibility Locus for Alzheimer's Disease on Chromosome 10

24. Genome-Wide Analysis of the Parkinsonism-Dementia Complex of Guam

25. Autosomal Dominant Lateral Temporal Epilepsy: Clinical Spectrum, New Epitempin Mutations, and Genetic Heterogeneity in Seven European Families

29. Genetic Studies on Chromosome 12 in Late-Onset Alzheimer Disease

33. Atypical parkinsonism in the French West Indies

35. Rare Variants in Calcium Homeostasis Modulator 1 (CALHM1) Found in Early Onset Alzheimer's Disease Patients Alter Calcium Homeostasis

36. PM20D1is a quantitative trait locus associated with Alzheimer’s disease

37. LRRK2 haplotype‐sharing analysis in Parkinson's disease reveals a novel p.S1761R mutation

38. LGI1 Is a Nogo Receptor 1 Ligand that Antagonizes Myelin-Based Growth Inhibition

39. Genetic linkage of autosomal dominant progressive supranuclear palsy to 1q31.1

40. ApoE ?3-haplotype modulates Alzheimer beta-amyloid deposition in the brain

46. No association between TAU haplotype and Alzheimer's disease in population or clinic based series or in familial disease

47. Alzheimer disease PS-1 exon 9 deletion defined

49. Apolipoprotein E genotype does not affect the age of onset of dementia in families with defined tau mutations

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