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1. Risk of Midlife Stroke After Adverse Pregnancy Outcomes: The FinnGen Study

3. Shared genetic origin of asthma, hay fever and eczema elucidates allergic disease biology

4. Rare variant analysis in eczema identifies exonic variants in DUSP1, NOTCH4 and SLC9A4

7. Mapping the functional impact of non-coding regulatory elements in primary T cells through single-cell CRISPR screens

8. DNA methylation within melatonin receptor 1A (MTNR1A) mediates paternally transmitted genetic variant effect on asthma plus rhinitis

10. A genome-wide association study reveals 2 new susceptibility loci for atopic dermatitis

11. Mapping the human genetic architecture of COVID-19

12. Age-of-onset information helps identify 76 genetic variants associated with allergic disease

15. A functional IL-6 receptor (IL6R) variant is a risk factor for persistent atopic dermatitis

21. De Novo Gene Conversion in the RCA Gene Cluster (1q32) Causes Mutations in Complement Factor H Associated With Atypical Hemolytic Uremic Syndrome

25. The ANO3/MUC15 locus is associated with eczema in families ascertained through asthma

26. Multi-locus stepwise regression: a haplotype-based algorithm for finding genetic associations applied to atopic dermatitis

28. Single-cell transcriptomics identifies an effectorness gradient shaping the response of CD4+ T cells to cytokines

29. Chromatin activity at GWAS loci identifies T cell states driving complex immune diseases

30. Immune disease risk variants regulate gene expression dynamics during CD4+T cell activation

31. Identification of new therapeutic targets for osteoarthritis through genome-wide analyses of UK Biobank

32. Trans-ancestry analysis reveals genetic and nongenetic associations with COVID-19 susceptibility and severity

33. Abstracts from the Food Allergy and Anaphylaxis Meeting 2016

34. Shared genetic origin of asthma, hay fever and eczema elucidates allergic disease biology.

35. Meta-analysis identifies seven susceptibility loci involved in the atopic march

36. The Molecular Basis of 3-Methylcrotonylglycinuria, a Disorder of Leucine Catabolism

37. Multi-ancestry genome-wide association study of 21,000 cases and 95,000 controls identifies new risk loci for atopic dermatitis

38. Identification of new therapeutic targets for osteoarthritis through genome-wide analyses of UK Biobank data

39. Genome-wide Comparative Analysis of Atopic Dermatitis and Psoriasis Gives Insight into Opposing Genetic Mechanisms

41. Maternal Filaggrin Mutations Increase the Risk of Atopic Dermatitis in Children: An Effect Independent of Mutation Inheritance

42. A Large-Scale, Consortium-Based Genomewide Association Study of Asthma

44. The molecular basis of 3-methylcrotonylglycinuria, a disorder of the leucine catabolism

46. High-density genotyping study identifies four new susceptibility loci for atopic dermatitis

47. Gain-of-function mutations in complement factor B are associated with atypical hemolytic uremic syndrome

48. De novo gene conversion in the RCA gene cluster (1q32) causes mutations in complement factor H associated with atypical hemolytic uremic syndrome

49. The human complement factor H: Functional roles, genetic variations and disease associations

50. Association Screening in the Epidermal Differentiation Complex (EDC) Identifies an SPRR3 Repeat Number Variant as a Risk Factor for Eczema

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