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180 results on '"Masahiro, Kanai"'

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1. Causal relevance of different blood pressure traits on risk of cardiovascular diseases: GWAS and Mendelian randomisation in 100,000 Chinese adults

2. A unified framework for estimating country-specific cumulative incidence for 18 diseases stratified by polygenic risk

3. X-chromosome and kidney function: evidence from a multi-trait genetic analysis of 908,697 individuals reveals sex-specific and sex-differential findings in genes regulated by androgen response elements

4. TWINGEN: protocol for an observational clinical biobank recall and biomarker cohort study to identify Finnish individuals with high risk of Alzheimer’s disease

5. Polygenic prediction across populations is influenced by ancestry, genetic architecture, and methodology

6. Genome-wide screen of otosclerosis in population biobanks: 27 loci and shared associations with skeletal structure

7. A case of primary renal oncocytic tumor: Chromophobe renal cell carcinoma or oncocytoma?

8. Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis

9. Dramatic response to pembrolizumab after pseudoprogression in a patient with advanced metastatic castration‐resistant prostate cancer

10. eQTL Catalogue 2023: New datasets, X chromosome QTLs, and improved detection and visualisation of transcript-level QTLs.

11. Coordinated linear and rotational movements of endothelial cells compartmentalized by VE-cadherin drive angiogenic sprouting

12. Inframe insertion and splice site variants in MFGE8 associate with protection against coronary atherosclerosis

13. The whole blood transcriptional regulation landscape in 465 COVID-19 infected samples from Japan COVID-19 Task Force

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

15. Global Biobank analyses provide lessons for developing polygenic risk scores across diverse cohorts

16. Recontacting biobank participants to collect lifestyle, behavioural and cognitive information via online questionnaires: lessons from a pilot study within FinnGen

17. Leveraging supervised learning for functionally informed fine-mapping of cis-eQTLs identifies an additional 20,913 putative causal eQTLs

18. Population-specific causal disease effect sizes in functionally important regions impacted by selection

19. Genome-wide risk prediction of common diseases across ancestries in one million people

20. Dimensionality reduction reveals fine-scale structure in the Japanese population with consequences for polygenic risk prediction

21. Prioritizing disease and trait causal variants at the TNFAIP3 locus using functional and genomic features

22. Associations of autozygosity with a broad range of human phenotypes

23. Characterizing rare and low-frequency height-associated variants in the Japanese population

24. Analysis of genetic dominance in the UK Biobank

25. Elucidating the genetic architecture of reproductive ageing in the Japanese population

26. Deep whole-genome sequencing reveals recent selection signatures linked to evolution and disease risk of Japanese

29. A second update on mapping the human genetic architecture of COVID-19

30. A second update on mapping the human genetic architecture of COVID-19

31. Successfully Treated Lung and Renal Metastases from Primary Chondrosarcoma of the Scapula with Radiofrequency Ablation and Surgical Resection

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

33. Systematic visualisation of molecular QTLs reveals variant mechanisms at GWAS loci

34. New insights into the genetic etiology of Alzheimer's disease and related dementias

36. Global Biobank analyses provide lessons for developing polygenic risk scores across diverse cohorts

38. Causal relevance of different blood pressure traits on risk of cardiovascular diseases: GWAS and Mendelian randomisation in 100,000 Chinese adults

39. Nuclear genetic control of mtDNA copy number and heteroplasmy in humans

40. Genome-wide screen of otosclerosis in population biobanks: 27 loci and shared associations with skeletal structure

41. Author Correction: Characterizing rare and low-frequency height-associated variants in the Japanese population

42. Responsible use of polygenic risk scores in the clinic: potential benefits, risks and gaps

43. Polygenic prediction across populations is influenced by ancestry, genetic architecture, and methodology

44. Meta-analysis fine-mapping is often miscalibrated at single-variant resolution

45. Tissue-specific enhancer-gene maps from multimodal single-cell data identify causal disease alleles

46. Improving fine-mapping by modeling infinitesimal effects

48. A cross-population atlas of genetic associations for 220 human phenotypes

49. Direct characterization of cis-regulatory elements and functional dissection of complex genetic associations using HCR–FlowFISH

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