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75 results on '"Rhian Gwilliam"'

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1. Shared Genetic Risk Factors of Intracranial, Abdominal, and Thoracic Aneurysms

2. Novel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: a multi-ethnic meta-analysis of 45,891 individuals.

3. Powerful identification of cis-regulatory SNPs in human primary monocytes using allele-specific gene expression.

4. High prevalence of posterior polymorphous corneal dystrophy in the Czech Republic; linkage disequilibrium mapping and dating an ancestral mutation.

5. A genome-wide association search for type 2 diabetes genes in African Americans.

6. Correction: Genetic Evidence Implicates the Immune System and Cholesterol Metabolism in the Aetiology of Alzheimer's Disease.

7. Population genetic analysis of Plasmodium falciparum parasites using a customized Illumina GoldenGate genotyping assay.

8. Genetic evidence implicates the immune system and cholesterol metabolism in the aetiology of Alzheimer's disease.

9. Common genetic variation near the phospholamban gene is associated with cardiac repolarisation: meta-analysis of three genome-wide association studies.

10. Meta-analysis of genome-wide scans for human adult stature identifies novel Loci and associations with measures of skeletal frame size.

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

12. Sex-Dependent Shared and Nonshared Genetic Architecture Across Mood and Psychotic Disorders

14. The dopamine β-hydroxylase -1021C/T polymorphism is associated with the risk of Alzheimer's disease in the Epistasis Project

15. A Method to Exploit the Structure of Genetic Ancestry Space to Enhance Case-Control Studies

16. Cross-ancestry genome-wide association analysis of corneal thickness strengthens link between complex and Mendelian eye diseases

17. Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis

18. Common genetic variation near the phospholamban gene is associated with cardiac repolarisation: meta-analysis of three genome-wide association studies

19. Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease

20. A genome-wide association study in Europeans and South Asians identifies five new loci for coronary artery disease

21. Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls

22. Discovery and development of exome-based, co-dominant single nucleotide polymorphism markers in hexaploid wheat (Triticum aestivumL.)

23. Transferrin and HFE genes interact in Alzheimer's disease risk: the Epistasis Project

24. Transcript-specific, single-nucleotide polymorphism discovery and linkage analysis in hexaploid bread wheat (Triticum aestivum L.)

25. Common Variants at Abca7, Ms4A6A/Ms4A4E, Epha1, Cd33 and Cd2Ap Are Associated with Alzheimer'S Disease

26. Genetic Determinants of Major Blood Lipids in Pakistanis Compared With Europeans

27. Multiple common variants for celiac disease influencing immune gene expression

28. New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk

29. Genome-wide and fine-resolution association analysis of malaria in West Africa

30. Mosaic 22q13 deletions: evidence for concurrent mosaic segmental isodisomy and gene conversion

31. Newly identified genetic risk variants for celiac disease related to the immune response

32. Bone mineral density, osteoporosis, and osteoporotic fractures: a genome-wide association study

33. A haplotype map of the human genome

34. The DNA sequence of the human X chromosome

35. Genomic Organization of Human CDS2 and Evaluation as a Candidate Gene for Corneal Hereditary Endothelial Dystrophy 2 on Chromosome 20p13

36. Analysis of 41 kb of the DNA sequence from the right arm of chromosome II ofSchizosaccharomyces pombe

37. Subtelomeric sequence from the right arm ofSchizosaccharomyces pombe chromosome I contains seven permease genes

38. Analysis of 114 kb of DNA sequence from fission yeast chromosome 2 immediately centromere-distal tohis5

39. High-Resolution Landmark Framework for the Sequence-Ready Mapping of Xq23–q26.1

40. A Detailed Physical and Transcriptional Map of the Region of Chromosome 20 That Is Deleted in Myeloproliferative Disorders and Refinement of the Common Deleted Region

41. From Long Range Mapping to Sequence-Ready Contigs on Human Chromosome 6

42. A variant in LDLR is associated with abdominal aortic aneurysm

43. High prevalence of posterior polymorphous corneal dystrophy in the czech republic; linkage disequilibrium mapping and dating an ancestral mutation

44. Powerful Identification of Cis-regulatory SNPs in Human Primary Monocytes Using Allele-Specific Gene Expression

45. The Role of Variation at A beta PP, PSEN1, PSEN2, and MAPT in Late Onset Alzheimer's Disease

46. Abdominal Aortic Aneurysm Is Associated with a Variant in Low-Density Lipoprotein Receptor-Related Protein 1

47. Population genetic analysis of Plasmodium falciparum parasites using a customized Illumina GoldenGate genotyping assay

48. A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium

49. Replication by the Epistasis Project of the interaction between the genes for IL-6 and IL-10 in the risk of Alzheimer's disease

50. P4‐133: Genome‐wide association study of age at onset of Alzheimer's disease

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