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1. Understanding the genetic complexity of puberty timing across the allele frequency spectrum.

4. Genetic variants for head size share genes and pathways with cancer

7. 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.

8. Characterizing prostate cancer risk through multi-ancestry genome-wide discovery of 187 novel risk variants.

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

11. The genetic basis of endometriosis and comorbidity with other pain and inflammatory conditions

12. Publisher Correction: Understanding the genetic complexity of puberty timing across the allele frequency spectrum

14. Genome-wide association study of lung adenocarcinoma in East Asia and comparison with a European population

15. Genetic diversity fuels gene discovery for tobacco and alcohol use

16. Genetic Risk Stratification of Primary Open-Angle Glaucoma in Japanese Individuals

18. Quantification of escape from X chromosome inactivation with single-cell omics data reveals heterogeneity across cell types and tissues

19. Androgen receptor binding sites enabling genetic prediction of mortality due to prostate cancer in cancer-free subjects

20. Hyperfructosemia in sleep disordered breathing: metabolome analysis of Nagahama study

24. Mobile element variation contributes to population-specific genome diversification, gene regulation and disease risk

25. Genome-Wide Meta-analysis Identifies Genetic Variants Associated With Glycemic Response to Sulfonylureas

27. Genome-wide analysis identifies novel susceptibility loci for myocardial infarction

28. Genome-wide meta-analysis identifies 127 open-angle glaucoma loci with consistent effect across ancestries.

29. Whole genome sequence analyses of eGFR in 23,732 people representing multiple ancestries in the NHLBI trans-omics for precision medicine (TOPMed) consortium

30. Cross-ancestry genome-wide analysis of atrial fibrillation unveils disease biology and enables cardioembolic risk prediction

32. Cerebral small vessel disease genomics and its implications across the lifespan.

33. Genome-wide association study of intracranial aneurysms identifies 17 risk loci and genetic overlap with clinical risk factors

34. Discovery and systematic characterization of risk variants and genes for coronary artery disease in over a million participants

36. Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations

37. Identification of type 2 diabetes loci in 433,540 East Asian individuals

38. Comparative genetic architectures of schizophrenia in East Asian and European populations

39. Stroke genetics informs drug discovery and risk prediction across ancestries

40. Multi-ancestry genome-wide association analyses identify novel genetic mechanisms in rheumatoid arthritis

41. A saturated map of common genetic variants associated with human height

43. Large-scale genome-wide association study of coronary artery disease in genetically diverse populations

44. Genetic analysis of right heart structure and function in 40,000 people

45. Polygenic burden in focal and generalized epilepsies

46. Genome‐Wide Association and Functional Studies Reveal Novel Pharmacological Mechanisms for Allopurinol

47. Association studies of up to 1.2 million individuals yield new insights into the genetic etiology of tobacco and alcohol use

48. Trans-ethnic kidney function association study reveals putative causal genes and effects on kidney-specific disease aetiologies.

50. A multi-layer functional genomic analysis to understand noncoding genetic variation in lipids

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