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810 results on '"Sambrook, J."'

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1. Altered TMPRSS2 usage by SARS-CoV-2 Omicron impacts infectivity and fusogenicity

2. Author Correction: Somatic mosaicism and common genetic variation contribute to the risk of very-early-onset inflammatory bowel disease (Nature Communications, (2020), 11, 1, (995), 10.1038/s41467-019-14275-y)

6. Comparative performances of machine learning methods for classifying Crohn Disease patients using genome-wide genotyping data

8. Thrombocytopenia with Absent Radii (TAR) syndrome is cause by compound inheritance of low-frequency regulatory SNPs and a rare null mutation in exon-junction complex subunit RBM8A: 18

9. NOX1 loss-of-function genetic variants in patients with inflammatory bowel disease

10. The FANCM:p.Arg658* truncating variant is associated with risk of triple-negative breast cancer

13. The FANCM:p.Arg658* truncating variant is associated with risk of triple-negative breast cancer.

14. The FANCM:p.Arg658* truncating variant is associated with risk of triple-negative breast cancer

15. Evidence for three genetic loci involved in both anorexia nervosa risk and variation of body mass index

16. NOX1 loss-of-function genetic variants in patients with inflammatory bowel disease

17. Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure

18. NOX1 loss-of-function genetic variants in patients with inflammatory bowel disease

19. NOX1 loss-of-function genetic variants in patients with inflammatory bowel disease

28. RAD51B in familial breast cancer.

29. Evidence for three genetic loci involved in both anorexia nervosa risk and variation of body mass index

30. Genome-wide association study of primary sclerosing cholangitis identifies new risk loci and quantifies the genetic relationship with inflammatory bowel disease

33. Trans-ethnic meta-analysis of white blood cell phenotypes

34. Novel Approach Identifies SNPs in SLC2A10 and KCNK9 with Evidence for Parent-of-Origin Effect on Body Mass Index

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

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

38. A GWAS sequence variant for platelet volume marks an alternative DNM3 promoter in megakaryocytes near a MEIS1 binding site

39. The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease

40. blood pressure loci identified with a gene-centricarray

41. A genome-wide association study of anorexia nervosa

42. Using ancestry-informative markers to identify fine structure across 15 populations of European origin

43. Thrombocytopenia with Absent Radii (TAR) syndrome is cause by compound inheritance of low-frequency regulatory SNPs and a rare null mutation in exon-junction complex subunit RBM8A

44. Rare and functional SIAE variants are not associated with autoimmune disease risk in up to 66,924 individuals of European ancestry

46. Novel loci affecting iron homeostasis and their effects in individuals at risk for hemochromatosis

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

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

49. The Saccharomyces cerevisiae DPM1 Gene Encoding Dolichol-Phosphate-Mannose Synthase Is Able To Complement a Glycosylation-Defective Mammalian Cell Line

50. Persistent Infections

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