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2. UNITY: A low-field magnetic resonance neuroimaging initiative to characterize neurodevelopment in low and middle-income settings

5. UNITY: A low-field magnetic resonance neuroimaging initiative to characterize neurodevelopment in low and middle-income settings.

6. Self-reported knee pain and disability among healthy individuals: reference data and factors associated with the Knee injury and Osteoarthritis Outcome Score (KOOS) and KOOS-Child

7. Whole-genome sequencing reveals host factors underlying critical COVID-19

8. A first update on mapping the human genetic architecture of COVID-19

10. Interleukin 1 Receptor-Like 1 Protein (ST2) is a Potential Biomarker for Cardiomyopathy in Duchenne Muscular Dystrophy

12. Generalization and fine mapping of European ancestry-based central adiposity variants in African ancestry populations

13. Whole genome sequencing reveals host factors underlying critical Covid-19

14. Phenotype Harmonization in the GLIDE2 Oral Health Genomics Consortium.

15. Phenotype harmonization in the GLIDE2 oral health genomics consortium

16. Genome-wide meta-analysis identifies six novel loci associated with habitual coffee consumption

17. AS3MT, Locus 10q24 and arsenic metabolism biomarkers in American Indians: The Strong Heart Family Study

25. Development of clinical practice guidelines for allied health and nursing assessment and management of Duchenne muscular dystrophy.

29. Chromosome Xq23 is associated with lower atherogenic lipid concentrations and favorable cardiometabolic indices

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

33. The power of genetic diversity in genome-wide association studies of lipids

34. The trans-ancestral genomic architecture of glycemic traits

35. The trans-ancestral genomic architecture of glycemic traits

38. Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity (Nature Genetics, (2018), 50, 1, (26-41), 10.1038/s41588-017-0011-x)

39. Large trans-ethnic meta-analysis identifies AKR1C4 as a novel gene associated with age at menarche

41. Meta-analysis of up to 622,409 individuals identifies 40 novel smoking behaviour associated genetic loci

42. TCTEX1D1 is a genetic modifier of disease progression in Duchenne muscular dystrophy

44. Visual spatial learning outcomes for clinical trials in neurofibromatosis type 1

45. TCTEX1D1 is a genetic modifier of disease progression in Duchenne muscular dystrophy

46. The relationship between deficit in digit span and genotype in nonsense mutation Duchenne muscular dystrophy

49. Lipoprotein receptor-related protein 1 variants and dietary fatty acids: meta-analysis of European origin and African American studies

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