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1. Inherited polygenic effects on common hematological traits influence clonal selection on JAK2V617F and the development of myeloproliferative neoplasms

2. A genome-wide association study of blood cell morphology identifies cellular proteins implicated in disease aetiology

3. Federated analysis of the contribution of recessive coding variants to 29,745 developmental disorder patients from diverse populations

5. GWAS of genetic factors affecting white blood cell morphological parameters in Sardinians uncovers influence of chromosome 11 innate immunity gene cluster on eosinophil morphology

6. Whole-exome sequencing identifies rare genetic variants associated with human plasma metabolites

7. Genetic associations at regulatory phenotypes improve fine-mapping of causal variants for 12 immune-mediated diseases

8. Whole-genome sequencing in diverse subjects identifies genetic correlates of leukocyte traits: The NHLBI TOPMed program

10. Effects of adiposity on the human plasma proteome: observational and Mendelian randomisation estimates

11. Genetic perturbation of PU.1 binding and chromatin looping at neutrophil enhancers associates with autoimmune disease

12. The Polygenic and Monogenic Basis of Blood Traits and Diseases

13. Effects of adiposity on the human plasma proteome: Observational and Mendelian randomization estimates

14. Genetic Analyses of Blood Cell Structure for Biological and Pharmacological Inference

15. Genetic associations at regulatory phenotypes improve fine-mapping of causal variants for twelve immune-mediated diseases

16. Cover Image

18. Variation in PU.1 binding and chromatin looping at neutrophil enhancers influences autoimmune disease susceptibility

20. Author Correction: Cohort-wide deep whole genome sequencing and the allelic architecture of complex traits

21. The influence of rare variants in circulating metabolic biomarkers

22. Cohort-wide deep whole genome sequencing and the allelic architecture of complex traits

23. Automated typing of red blood cell and platelet antigens: a whole-genome sequencing study

24. Cohort-wide deep whole genome sequencing and the allelic architecture of complex traits

25. Whole-Genome Sequencing Coupled to Imputation Discovers Genetic Signals for Anthropometric Traits

27. An Organismal CNV Mutator Phenotype Restricted to Early Human Development

28. Genetic Drivers of Epigenetic and Transcriptional Variation in Human Immune Cells

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

30. Whole-Exome Sequencing Identifies Loci Associated with Blood Cell Traits and Reveals a Role for Alternative GFI1B Splice Variants in Human Hematopoiesis

31. Whole-Exome Sequencing Identifies Loci Associated with Blood Cell Traits and Reveals a Role for Alternative GFI1B Splice Variants in Human Hematopoiesis

32. A reference panel of 64,976 haplotypes for genotype imputation

33. Monoallelic and Biallelic Mutations in MAB21L2 Cause a Spectrum of Major Eye Malformations

34. Multiple de novo copy number variations in two subjects with developmental problems and multiple congenital anomalies

35. Deep short-read sequencing of chromosome 17 from the mouse strains A/J and CAST/Ei identifies significant germline variation and candidate genes that regulate liver triglyceride levels

36. Accurate whole human genome sequencing using reversible terminator chemistry

37. Increased Human IgE Induced by Killing Schistosoma mansoni In Vivo Is Associated with Pretreatment Th2 Cytokine Responsiveness to Worm Antigens

38. Factors Affecting Human IgE and IgG Responses to Allergen-Like Schistosoma mansoni Antigens: Molecular Structure and Patterns of in vivo Exposure

39. Characterisation of conserved non-coding sequences in vertebrate genomes using bioinformatics, statistics and functional studies

42. Highly Conserved Non-Coding Sequences Are Associated with Vertebrate Development

43. Increases in Human T Helper 2 Cytokine Responses toSchistosoma mansoniWorm and Worm‐Tegument Antigens Are Induced by Treatment with Praziquantel

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