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95 results on '"Farrell, John"'

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1. MAPT subhaplotypes and chronic traumatic encephalopathy

2. Blood‐derived mitochondrial DNA copy number is associated with Alzheimer’s Disease through the regulation of plasma lipid and amino acid metabolism

3. Association Between HSV‐1 and Risk of Alzheimer’s Disease Detected by a Propensity‐Score Matched Case Design

4. Identification of rare coding variants associated with Alzheimer’s disease.

5. DNA from multiple viral species is associated with Alzheimer's disease risk

7. Novel loci for Alzheimer's disease identified by a genome‐wide association study in Ashkenazi Jews

9. Identification of Genetic Variants and Serum Metabolites Associated with Blood‐derived Mitochondrial DNA Copy Number

10. Novel Loci for Alzheimer Disease Identified by Genome Wide Association Study in Ashkenazi Jews

11. Spatial Distribution of Rare Missense Variants Within Protein Structures is Associated with AD Risk

12. Multiple Viruses Detected in Human DNA are Associated with Alzheimer Disease Risk

16. Management of anaphylaxis due to COVID‐19 vaccines in the elderly

20. ARIA digital anamorphosis: Digital transformation of health and care in airway diseases from research to practice

24. Spatiotemporal ecology of juvenile Muskellunge ( Esox masquinongy ) and Northern Pike ( Esox lucius ) in upper St. Lawrence River nursery bays during their inaugural fall and winter

25. Combining population genomics and forward simulations to investigate stocking impacts: A case study of Muskellunge ( Esox masquinongy ) from the St. Lawrence River basin

26. Modification of the cyclopropyl moiety of abacavir provides insight into the structure activity relationship between HLA‐B*57:01 binding and T‐cell activation

27. O3-13-01: HIGHLY PENETRANT LATE-ONSET ALZHEIMER DISEASE VARIANTS IN NOTCH3 IN ASHKENAZI JEWS

40. SEX-SPECIFIC ANALYSIS OF THE ADSP CASE-CONTROL WHOLE-EXOME SEQUENCING DATASET

41. [P3-090]: THE ALZHEIMER's DISEASE SEQUENCING PROJECT (ADSP) DATA UPDATE 2017

42. ALZHEIMER'S DISEASE SEQUENCING PROJECT: CASE-CONTROL ANALYSES

43. NOVEL GENETIC VARIANTS ASSOCIATED WITH FAMILIAL LATE-ONSET ALZHEIMER DISEASE IN THE ALZHEIMER’S DISEASE SEQUENCING PROJECT

45. A variant Sp1 (R218Q) transcription factor might enhance HbF expression in β0-thalassaemia homozygotes

46. A candidate transacting modulator of fetal hemoglobin gene expression in the Arab-Indian haplotype of sickle cell anemia

47. 7th Drug hypersensitivity meeting: part two

48. P1-129: Structural Variation (SV) in Heterogenous Whole-Genome Sequencing Data from 111 Families at Risk For Alzheimer's Disease: Alzheimer's Disease Sequencing Project SV Study

49. Homozygosity for a haplotype in theHBG2-OR51B4region is exclusive to Arab-Indian haplotype sickle cell anemia

50. The genetic basis of asymptomatic codon 8 frame‐shift (HBB:c25_26delAA) β0‐thalassaemia homozygotes

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