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59 results on '"RISK LOCI"'

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1. Sharing lessons learnt across European cardiovascular research consortia

2. Parkinson's disease age at onset genome‐wide association study: Defining heritability, genetic loci, and α‐synuclein mechanisms

3. High-density genetic mapping identifies new susceptibility loci for rheumatoid arthritis

4. The genetic architecture of the human thalamus and its overlap with ten common brain disorders

5. MicroRNA analysis of childhood atopic dermatitis reveals a role for miR-451a

6. Association of a CARD9 Gene Haplotype with Behcet's Disease in a Chinese Han Population

7. Type 2 Diabetes Is Associated With The Mtnr1B Gene, A Genetic Bridge Between Circadian Rhythm And Glucose Metabolism, In A Turkish Population

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

9. A missense variant in mitochondrial amidoxime reducing component 1 gene and protection against liver disease

10. Evaluation of three polygenic risk score models for the prediction of breast cancer risk in Singapore Chinese

11. Genetic association analysis identifies variants associated with disease progression in primary sclerosing cholangitis

12. Genetic association study of exfoliation syndrome identifies a protective rare variant at LOXL1 and five new susceptibility loci

13. A cross-ethnic survey of CFB and SLC44A4, Indian ulcerative colitis GWAS hits, underscores their potential role in disease susceptibility

14. Multi-ancestry genome-wide gene-smoking interaction study of 387,272 individuals identifies new loci associated with serum lipids

15. Genetic landscape of chronic obstructive pulmonary disease identifies heterogeneous cell-type and phenotype associations

16. Analysis of the genetic component of systemic sclerosis in Iranian and Turkish populations through a genome-wide association study

17. HSPA6 is an ulcerative colitis susceptibility factor that is induced by cigarette smoke and protects intestinal epithelial cells by stabilizing anti-apoptotic Bcl-XL

18. Rapporteur summaries of plenary, symposia, and oral sessions from the XXIIIrd World Congress of Psychiatric Genetics Meeting in Toronto, Canada, 16-20 October 2015

19. Genetic identification of cell types underlying brain complex traits yields insights into the etiology of Parkinson's disease

20. A Perception on Genome-Wide Genetic Analysis of Metabolic Traits in Arab Populations

21. Variants associating with uterine leiomyoma highlight genetic background shared by various cancers and hormone-related traits

22. Identification of 64 Novel Genetic Loci Provides an Expanded View on the Genetic Architecture of Coronary Artery Disease

23. Intracranial Aneurysm-Associated Single-Nucleotide Polymorphisms Alter Regulatory DNA in the Human Circle of Willis

24. Rare gene deletions in genetic generalized and Rolandic epilepsies

25. Identification of nine new susceptibility loci for endometrial cancer

26. Genome-wide association study of classical Hodgkin lymphoma identifies key regulators of disease susceptibility

27. The Zinc Transporter Slc30a8/ZnT8 Is Required in a Subpopulation of Pancreatic α-Cells for Hypoglycemia-induced Glucagon Secretion

28. Phenome-wide association studies across large population cohorts support drug target validation

29. From SNPs to pathways: Biological interpretation of type 2 diabetes (T2DM) genome wide association study (GWAS) results

30. Association analyses based on false discovery rate implicate new loci for coronary artery disease

31. Fine-mapping and functional studies highlight potential causal variants for rheumatoid arthritis and type 1 diabetes

32. Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24.32 and a significant overlap with schizophrenia

33. BACH2 immunodeficiency illustrates an association between super-enhancers and haploinsufficiency

34. Additional Candidate Genes for Human Atherosclerotic Disease Identified Through Annotation Based on Chromatin Organization

35. Unmet Needs in Dystonia

36. Epigenome-wide association study of cognitive functioning in middle-aged monozygotic twins

37. Pancreatic alpha cell-selective deletion of Tcf7l2 impairs glucagon secretion and counter-regulatory responses to hypoglycaemia in mice

38. HLA and non-HLA genes and familial predisposition to autoimmune diseases in families with a child affected by type 1 diabetes

39. Genetic architecture of subcortical brain structures in 38,851 individuals

40. Association study reveals novel risk loci for sporadic inclusion body myositis

41. Shared genetic variants suggest common pathways in allergy and autoimmune diseases

42. Heritability enrichment of specifically expressed genes identifies disease-relevant tissues and cell types

43. Genome-wide assessment of Parkinson's disease in a Southern Spanish population

44. Integrating epigenomic data and 3D genomic structure with a new measure of chromatin assortativity

45. Enrichment of putative PAX8 target genes at serous epithelial ovarian cancer susceptibility loci

46. Investigating the Causal Relationship of C-Reactive Protein with 32 Complex Somatic and Psychiatric Outcomes : A Large-Scale Cross-Consortium Mendelian Randomization Study

47. Immunochip analysis identifies novel susceptibility loci in the human leukocyte antigen region for acquired thrombotic thrombocytopenic purpura

48. Cross-cancer genome-wide analysis of lung, ovary, breast, prostate and colorectal cancer reveals novel pleiotropic associations

49. Analysis of five chronic inflammatory diseases identifies 27 new associations and highlights disease-specific patterns at shared loci

50. Three new pancreatic cancer susceptibility signals identified on chromosomes 1q32.1, 5p15.33 and 8q24.21

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