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226 results on '"Auton, Adam"'

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1. A phenome-wide association and Mendelian randomisation study of alcohol use variants in a diverse cohort comprising over 3 million individuals

2. MUSSEL: Enhanced Bayesian polygenic risk prediction leveraging information across multiple ancestry groups

3. Ancestry-independent risk of venous thromboembolism in individuals with sickle cell trait vs factor V Leiden

4. Discovery of 42 genome-wide significant loci associated with dyslexia

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

6. Multi-Trait Genetic Analysis Identifies Autoimmune Loci Associated with Cutaneous Melanoma

9. Prevalence of Alpha-1 Antitrypsin Deficiency, Self-Reported Behavior Change, and Health Care Engagement Among Direct-to-Consumer Recipients of a Personalized Genetic Risk Report

10. A genome-wide association study with 1,126,563 individuals identifies new risk loci for Alzheimer’s disease

11. Author Correction: Discovery of 42 genome-wide significant loci associated with dyslexia

12. Genetic analyses identify widespread sex-differential participation bias

14. Identification of novel risk loci, causal insights, and heritable risk for Parkinson's disease: a meta-analysis of genome-wide association studies

15. Association of Whole-Genome and NETRIN1 Signaling Pathway–Derived Polygenic Risk Scores for Major Depressive Disorder and White Matter Microstructure in the UK Biobank

16. Author Correction: A genome-wide association study with 1,126,563 individuals identifies new risk loci for Alzheimer’s disease

17. The estimation of recombination rates from population genetic data

18. Author Correction: A genome-wide association study with 1,126,563 individuals identifies new risk loci for Alzheimer’s disease

19. Replication and characterization of CADM2 and MSRA genes on human behavior

20. Analysis of rare Parkinson's disease variants in millions of people.

21. Multi-ancestry genome-wide meta-analysis identifies novel basal cell carcinoma loci and shared genetic effects with squamous cell carcinoma.

22. Correlations in sleeping patterns and circadian preference between spouses.

23. Using a polygenic score in a family design to understand genetic influences on musicality

24. Polygenic prediction of educational attainment within and between families from genome-wide association analyses in 3 million individuals

26. A Fine-Scale Chimpanzee Genetic Map from Population Sequencing

32. A multi-phenotype analysis reveals 19 susceptibility loci for basal cell carcinoma and 15 for squamous cell carcinoma.

33. Genome-wide association analyses of risk tolerance and risky behaviors in over 1 million individuals identify hundreds of loci and shared genetic influences

34. A global reference for human genetic variation

35. An integrated map of structural variation in 2,504 human genomes

36. Author Correction: Genome-wide association study of depression phenotypes in UK Biobank identifies variants in excitatory synaptic pathways

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

38. Genome-wide association study of musical beat synchronization demonstrates high polygenicity.

39. An integrated map of genetic variation from 1,092 human genomes

40. Genome-wide SNP and haplotype analyses reveal a rich history underlying dog domestication

41. Genes mirror geography within Europe

42. A genome-wide cross-phenotype meta-analysis of the association of blood pressure with migraine

43. Genetic analyses identify widespread sex-differential participation bias

44. Overlapping genetic architecture between Parkinson disease and melanoma

45. Meta-analysis of genome-wide association studies for neuroticism in 449,484 individuals identifies novel genetic loci and pathways

46. Characterizing mood disorders in the AFFECT study: a large, longitudinal, and phenotypically rich genetic cohort in the US.

47. Thyroid cancer susceptibility polymorphisms: confirmation of loci on chromosomes 9q22 and 14q13, validation of a recessive 8q24 locus and failure to replicate a locus on 5q24

48. The variant call format and VCFtools

49. A map of human genome variation from population-scale sequencing

50. Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls

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