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4. Multi-ancestry genome-wide study identifies effector genes and druggable pathways for coronary artery calcification

8. Identification of a regulatory pathway governing TRAF1 via an arthritis-associated non-coding variant

11. DNA methylation of the TPMT gene and azathioprine pharmacokinetics in children with very early onset inflammatory bowel disease

14. Multi‐phenotype analyses of hemostatic traits with cardiovascular events reveal novel genetic associations

16. Differential and shared genetic effects on kidney function between diabetic and non-diabetic individuals

19. Curating Genetic Associations With Rheumatologic Autoimmune Diseases to Improve Patient Outcomes.

28. Further evidence supporting a potential role for ADH1B in obesity

31. SMIM1 absence is associated with reduced energy expenditure and excess weight

33. Genome-Wide Association Study Meta-Analysis of Stroke in 22 000 Individuals of African Descent Identifies Novel Associations With Stroke

36. Deep Resequencing of the 1q22 Locus in Non‐Lobar Intracerebral Hemorrhage.

37. Identification of a regulatory pathway governing TRAF1 via an arthritis-associated non-coding variant

38. A Novel Metastatic Estrogen Receptor-Expressing Breast Cancer Model with Antiestrogen Responsiveness.

39. Combining Imaging and Genetics to Predict Recurrence of Anticoagulation-Associated Intracerebral Hemorrhage

41. Type 2 Diabetes: Evidence for Linkage on Chromosome 20 in 716 Finnish Affected Sib Pairs

42. Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes

45. HLA-DRB1*11 and variants of the MHC class II locus are strong risk factors for systemic juvenile idiopathic arthritis

46. Genetic associations of leptin-related polymorphisms with systemic lupus erythematosus

47. Hypertension and intracerebral hemorrhage recurrence among white, black, and Hispanic individuals

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