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1. Systemic inflammation in relation to exceptional memory in the Long Life Family Study (LLFS)

2. MEF2C Common Genetic Variation Is Associated With Different Aspects of Cognition in Non-Hispanic White and Caribbean Hispanic Non-demented Older Adults

3. Novel genetic loci associated with hippocampal volume

4. Episodic memory performance in a multi-ethnic longitudinal study of 13,037 elderly.

5. Data from a cross-sectional study on Apolipoprotein E (APOE-ε4) and snoring/sleep apnea in non-demented older adults

6. Candidate sequence variants and fetal hemoglobin in children with sickle cell disease treated with hydroxyurea.

7. Data from CpG Island Methylator Phenotype Associates with Low-Degree Chromosomal Abnormalities in Colorectal Cancer

8. CCR Translation on this Article from CpG Island Methylator Phenotype Associates with Low-Degree Chromosomal Abnormalities in Colorectal Cancer

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

10. Estudio comparativo del sindrome de burnout en una muestra multiocupacional ecuatoriana

11. Repercusiones del temor al contagio por covid-19 en la salud mental de mujeres trabajadoras embarazadas en ecuador

12. Integration of GWAS and brain transcriptomic analyses in a multiethnic sample of 35,245 older adults identifies DCDC2 gene as predictor of episodic memory maintenance

13. Midlife Vascular Factors and Prevalence of Mild Cognitive Impairment in Late-Life in Mexico

14. Association between late maternal age and age-related endophenotypes in the Long Life Family Study

15. Genome-Wide Meta-Analysis of Late-Onset Alzheimer’s Disease Using Rare Variant Imputation in 65,602 Subjects Identifies Novel Rare Variant Locus NCK2: The International Genomics of Alzheimer’s Project (IGAP)

16. Analysis of individual families implicates noncoding DNA variation and multiple biological pathways in Alzheimer’s disease risk

17. The role of Native American ancestry in Alzheimer’s disease and related dementias

18. Illiteracy and risk of mild cognitive impairment among Mexican older adults: Data from the Mexican Health and Aging Study (MHAS)

19. Collection of genetic data in population‐based studies across urban and rural areas: The challenges of the Mexican Health and Aging Study

20. Genome‐wide gene‐based analysis of episodic memory trajectories in the Mexican Health and Aging Study (MHAS)

21. APOE ‐stratified, genome‐wide, gene‐based analysis of episodic memory trajectories in a multi‐ethnic sample of 24,769 elderly

22. Prevalence of Mild Cognitive Impairment in Mexican Older Adults: Data from the Mexican Health and Aging Study (MHAS)

23. Polygenic score for sleep duration. Association with cognition

24. A dopamine receptor genetic variant enhances perceptual speed in cognitive healthy subjects

25. Age-Related Biomarkers in LLFS Families With Exceptional Cognitive Abilities

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

27. MEF2C Common Genetic Variation Is Associated With Different Aspects of Cognition in Non-Hispanic White and Caribbean Hispanic Non-demented Older Adults.

28. A comparison of genetic imputation methods using Long Life Family Study genotypes and sequence data with the 1000 Genome reference panel

29. Episodic memory performance in a multi-ethnic longitudinal study of 13,037 elderly

30. P1‐156: GENE‐BASED ANALYSES IN WHOLE GENOME SEQUENCING OF FAMILIAL LATE‐ONSET ALZHEIMER'S DISEASE

31. P2‐140: GENOME‐WIDE ASSOCIATION STUDY FOR ALZHEIMER'S DISEASE IN A LARGE SAMPLE OF CARIBBEAN HISPANICS

32. P2‐108: WHOLE‐GENOME SEQUENCING IN NON‐HISPANIC WHITE FAMILIES IMPLICATES RARE VARIATION IN LATE‐ONSET ALZHEIMER'S DISEASE RISK

33. Analysis of Pedigree Data in Populations with Multiple Ancestries: Strategies for Dealing with Admixture in Caribbean Hispanic Families from the ADSP

34. Genetic Variation in Genes Underlying Diverse Dementias May Explain a Small Proportion of Cases in the Alzheimer's Disease Sequencing Project

35. Linkage analyses in Caribbean Hispanic families identify novel loci associated with familial late‐onset Alzheimer's disease

36. Rare coding mutations identified by sequencing of <scp>A</scp> lzheimer disease genome‐wide association studies loci

37. Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease

38. [O2–08–03]: WHOLE‐GENOME SEQUENCING IN FAMILIAL LATE‐ONSET ALZHEIMER's DISEASE IDENTIFIES RARE VARIATION IN AD CANDIDATE GENES

39. [P4–083]: A DOPAMINE RECEPTOR GENETIC VARIANT ENHANCES PERCEPTUAL SPEED IN COGNITIVELY HEALTHY SUBJECTS

40. Ultra-rare mutations in

41. Novel genetic loci associated with hippocampal volume

42. Novel genetic loci underlying human intracranial volume identified through genome-wide association

43. P4-097: RARE VARIANTS IN FAMILIAL LATE-ONSET ALZHEIMER'S DISEASE IDENTIFIED FROM LARGE SCALE WHOLE GENOME SEQUENCING

44. Emerging science of hydroxyurea therapy for pediatric sickle cell disease

45. O1‐09‐03: Whole Genome Sequencing in Familial Late‐Onset Alzheimer’s Disease Identifies Variations in TTC3 and FSIP2

47. Targeted re-sequencing of linkage region on 2q21 identifies a novel functional variant for hip and knee osteoarthritis

48. Heritability of Different Forms of Memory in the Late Onset Alzheimer's Disease Family Study

49. Rare genetic variation implicated in non-Hispanic white families with Alzheimer disease

50. Genetic modifiers of HbF and response to hydroxyurea in sickle cell disease

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