Search

Your search keyword '"Johnsen, Jill"' showing total 49 results

Search Constraints

Start Over You searched for: Author "Johnsen, Jill" Remove constraint Author: "Johnsen, Jill" Search Limiters Peer Reviewed Remove constraint Search Limiters: Peer Reviewed
49 results on '"Johnsen, Jill"'

Search Results

1. Validation of human telomere length multi-ancestry meta-analysis association signals identifies POP5 and KBTBD6 as human telomere length regulation genes

2. Genetics of Latin American Diversity Project: Insights into population genetics and association studies in admixed groups in the Americas

3. A genetic association study of circulating coagulation factor VIII and von Willebrand factor levels

4. Aberrant activation of TCL1A promotes stem cell expansion in clonal haematopoiesis

6. Epigenome-wide DNA methylation association study of circulating IgE levels identifies novel targets for asthma

7. Heterogeneity in the half-life of factor VIII concentrate in patients with hemophilia A is due to variability in the clearance of endogenous von Willebrand factor

9. Extent to which array genotyping and imputation with large reference panels approximate deep whole-genome sequencing

11. Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program

12. Whole Genome Sequencing Identifies CRISPLD2 as a Lung Function Gene in Children With Asthma

13. Illustrated State‐of‐the‐Art Capsules of the ISTH 2019 Congress in Melbourne, Australia

14. Validated Reference Panel from Renewable Source of Genomic DNA Available for Standardization of Blood Group Genotyping

19. Loss-of-function genomic variants highlight potential therapeutic targets for cardiovascular disease

20. Women and girls with inherited bleeding disorders: Focus on haemophilia carriers and heavy menstrual bleeding.

22. Whole-Exome Sequencing Identifies Rare and Low-Frequency Coding Variants Associated with LDL Cholesterol

24. Common and rare von Willebrand factor (VWF) coding variants, VWF levels, and factor VIII levels in African Americans: the NHLBI Exome Sequencing Project

25. Imputation of Exome Sequence Variants into Population- Based Samples and Blood-Cell-Trait-Associated Loci in African Americans: NHLBI GO Exome Sequencing Project

27. Building the foundation for a community-generated national research blueprint for inherited bleeding disorders: research priorities to transform the care of people with hemophilia.

31. Whole-exome sequencing of 14 389 individuals from the ESP and CHARGE consortia identifies novel rare variation associated with hemostatic factors.

32. Sixth Åland Island Conference on von Willebrand disease.

35. von Willebrand disease: Diagnosis and treatment, treatment of women, and genomic approach to diagnosis.

36. Diversity of variant alleles encoding Kidd, Duffy, and Kell antigens in individuals with sickle cell disease using whole genome sequencing data from the NHLBI TOPMed Program.

37. Biological mechanisms underlying inter‐individual variation in factor VIII clearance in haemophilia.

38. The national blueprint for pregnancy/birth longitudinal cohorts to study factor VIII immunogenicity: NHLBI State of the Science (SOS) Workshop on factor VIII inhibitors.

41. Analysis of exome sequencing data sets reveals structural variation in the coding region of ABO in individuals of African ancestry.

42. Red blood cell antigen genotype analysis for 9087 Asian, Asian American, and Native American blood donors.

43. Expression of the Blood-Group-Related Gene B4galnt2 Alters Susceptibility to Salmonella Infection.

44. Nanopatterns - using network archetypes as an approach to understanding emergence of properties at scale.

45. Complex Changes in von Willebrand Factor-Associated Parameters Are Acquired during Uncomplicated Pregnancy.

46. A Variational Bayes Discrete Mixture Test for Rare Variant Association.

47. Expression of the blood-group-related glycosyltransferase B4galnt2 influences the intestinal microbiota in mice.

48. MUCIN 1 (MUC1) LEVELS AND GLYCOSYLATION PATTERNS IN SALIVA OF PATIENTS WITH BURNING MOUTH SYNDROME (BMS): A CASE-CONTROL STUDY.

49. Genetic control of mRNA splicing as a potential mechanism for incomplete penetrance of rare coding variants.

Catalog

Books, media, physical & digital resources