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182 results on '"Andrew D Paterson"'

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1. Statistical power in COVID-19 case-control host genomic study design

2. Linkage analysis identifies an isolated strabismus locus at 14q12 overlapping with FOXG1 syndrome region

3. 1501 Genetics of age at systemic lupus erythematosus diagnosis

4. Major sex differences in allele frequencies for X chromosome variants in the 1000 Genomes Project data

5. Association of Coding Variants in Hydroxysteroid 17-beta Dehydrogenase 14 (HSD17B14) with Reduced Progression to End Stage Kidney Disease in Type 1 Diabetes

6. Fish and chips: the origin of human gene families is a predictor of the location of GWAS signals

7. Rare Genetic Variants of Large Effect Influence Risk of Type 1 Diabetes

8. Characterization of direct and/or indirect genetic associations for multiple traits in longitudinal studies of disease progression

9. Type IV Collagen Variants in CKD: Performance of Computational Predictions for Identifying Pathogenic Variants

10. Nuclear genome-wide associations with mitochondrial heteroplasmy

11. Large-scale association analyses identify host factors influencing human gut microbiome composition

12. Associations of NOD2 polymorphisms with Erysipelotrichaceae in stool of in healthy first degree relatives of Crohn’s disease subjects

13. Genome-Wide Association for HbA1c in Malay Identified Deletion on SLC4A1 that Influences HbA1c Independent of Glycemia

14. Large-scale association analyses identify host factors influencing human gut microbiome composition

15. Enhancer-gene rewiring in the pathogenesis of Quebec platelet disorder

16. Evidence of batch effects masking treatment effect in GAW20 methylation data

17. FUT2 genotype and secretory status are not associated with fecal microbial composition and inferred function in healthy subjects

18. Meta-genome-wide association studies identify a locus on chromosome 1 and multiple variants in the MHC region for serum C-peptide in type 1 diabetes

19. Genetic Variants Associated with Circulating Parathyroid Hormone

20. Genome-wide Association Study of Pediatric Obsessive-Compulsive Traits: Shared Genetic Risk between Traits and Disorder

21. Analysis of Genetic Association of Intestinal Permeability in Healthy First-degree Relatives of Patients with Crohn's Disease

22. Segregating patterns of copy number variations in extended autism spectrum disorder (ASD) pedigrees

23. Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24.32 and a significant overlap with schizophrenia

24. Genome-Wide DNA Methylation Analysis Reveals Epigenetic Dysregulation of MicroRNA-34A in TP53-Associated Cancer Susceptibility

25. Association of host genome with intestinal microbial composition in a large healthy cohort

26. Genome-Wide Association Study of Diabetic Kidney Disease Highlights Biology Involved in Glomerular Basement Membrane Collagen

27. Genome-wide association study of diabetic kidney disease highlights biology involved in renal basement membrane collagen

28. A genome-wide linkage study of autism spectrum disorder and the broad autism phenotype in extended pedigrees

29. Prevalence Estimates of Polycystic Kidney and Liver Disease by Population Sequencing

30. Variation in SLC19A3 and Protection From Microvascular Damage in Type 1 Diabetes

31. Resampling to Address the Winner's Curse in Genetic Association Analysis of Time to Event

32. A135 MICROBIOME IN CROHN’S DISEASE PATIENTS: A COMPILATION OF PUBLICLY AVAILABLE DATASETS

33. A Functional Polymorphism of Ptpn22 Is Associated with Type 1 Diabetes in the BioBreeding Rat

34. The origins of breast cancer associated with mammographic density: a testable biological hypothesis

35. Novel 25 kb Deletion of MERTK Causes Retinitis Pigmentosa With Severe Progression

36. The duplication mutation of Quebec platelet disorder dysregulates PLAU, but not C10orf55, selectively increasing production of normal PLAU transcripts by megakaryocytes but not granulocytes

37. COPY NUMBER VARIANTS IN BRAIN-RELATED GENES ARE ASSOCIATED WITH NEUROPSYCHIATRIC TRAITS IN CHILDHOOD

38. Using extended pedigrees to identify novel autism spectrum disorder (ASD) candidate genes

39. Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization

40. Convergence of Genes and Cellular Pathways Dysregulated in Autism Spectrum Disorders

41. Letter to the editor: expression of concern, reaffirmed

42. The C-type lectin receptor CLEC4M binds, internalizes, and clears von Willebrand factor and contributes to the variation in plasma von Willebrand factor levels

43. An enzyme linked immunosorbent assay (ELISA) for the determination of the human haptoglobin phenotype

44. The Genetic Landscape of Renal Complications in Type 1 Diabetes

45. Metaphyseal Dysplasia with Maxillary Hypoplasia and Brachydactyly Is Caused by a Duplication in RUNX2

46. Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia

47. Quality control analysis of the 1000 Genomes Project Omni2.5 genotypes

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

49. Thymectomy and radiation-induced type 1 diabetes in nonlymphopenic BB rats

50. Epigenomic profiling reveals an association between persistence of DNA methylation and metabolic memory in the DCCT/EDIC type 1 diabetes cohort

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