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1. Insights into the genetic architecture of osteoarthritis from stage 1 of the arcOGEN study

2. Multiple sclerosis genomic map implicates peripheral immune cells and microglia in susceptibility

3. Author Correction: Cross-ancestry genome-wide association analysis of corneal thickness strengthens link between complex and Mendelian eye diseases

4. Quality control and conduct of genome-wide association meta-analyses

5. Association scan of 14,500 nonsynonymous SNPs in four diseases identifies autoimmunity variants

6. Large-scale gene-centric analysis identifies novel variants for coronary artery disease

7. Serum iron levels and the risk of Parkinson Disease: a Mendelian randomization study

8. Genetically Determined Height and Coronary Artery Disease

9. Hypothesis-based analysis of gene-gene interactions and risk of myocardial infarction

10. Identification of ADAMTS7 as a novel locus for coronary atherosclerosis and association of ABO with myocardial infarction in the presence of coronary atherosclerosis: two genome-wide association studies

11. Multiple common variants for celiac disease influencing immnune gene expression

12. The DNA sequence of the human X chromosome

13. A 'Candidate-Interactome' Aggregate Analysis of Genome-Wide Association Data in Multiple Sclerosis

14. Genome-wide association analysis identifies 13 new risk loci for schizophrenia

15. Interaction between ERAP1 and HLA-B27 in ankylosing spondylitis implicates peptide handling in the mechanism for HLA-B27 in disease susceptibility

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

17. Meta-analysis of genome-wide association studies confirms a susceptibility locus for knee osteoarthritis on chromosome 7q22

18. Genome-wide association study of ulcerative colitis identifies three new susceptibility loci, including the HNF4A region

19. Genetic Loci for Retinal Arteriolar Microcirculation

20. Thigh muscle strength in senior athletes and healthy controls.

21. Getting it straight: Web resources on scoliosis.

22. Parkinson's disease resources on the Web.

23. Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis

24. Genome-wide association study identifies eight loci associated with blood pressure

25. Genetic studies of body mass index yield new insights for obesity biology

26. New genetic loci link adipose and insulin biology to body fat distribution

27. A genome-wide association study of anorexia nervosa

28. Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture

29. Mapping MAVE data for use in human genomics applications.

30. Ensembl 2024.

31. Olympic Class Sailing Injuries and Illness: A 15-Year Study of a World Cup Regatta Venue.

32. The complete sequence of a human Y chromosome.

33. DECIPHER: Improving Genetic Diagnosis Through Dynamic Integration of Genomic and Clinical Data.

34. EyeG2P: an automated variant filtering approach improves efficiency of diagnostic genomic testing for inherited ophthalmic disorders.

35. SUsPECT: a pipeline for variant effect prediction based on custom long-read transcriptomes for improved clinical variant annotation.

36. Ensembl 2023.

37. Online Patient Reviews of Breast Reconstruction: RealSelf Analysis.

38. Annotating and prioritizing genomic variants using the Ensembl Variant Effect Predictor-A tutorial.

39. DECIPHER: Supporting the interpretation and sharing of rare disease phenotype-linked variant data to advance diagnosis and research.

40. Ensembl 2022.

41. The European Variation Archive: a FAIR resource of genomic variation for all species.

42. The Ensembl COVID-19 resource: ongoing integration of public SARS-CoV-2 data.

43. Scripting Analyses of Genomes in Ensembl Plants.

44. GA4GH: International policies and standards for data sharing across genomic research and healthcare.

45. The GA4GH Variation Representation Specification: A computational framework for variation representation and federated identification.

46. Ensembl 2021.

47. Red Blood Cell Folate Likely Overestimated in Australian National Survey: Implications for Neural Tube Defect Risk.

48. Ensembl 2020.

49. Ensembl Genomes 2020-enabling non-vertebrate genomic research.

50. Suboptimal Biochemical Riboflavin Status Is Associated with Lower Hemoglobin and Higher Rates of Anemia in a Sample of Canadian and Malaysian Women of Reproductive Age.

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