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129 results on '"Lili Milani"'

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1. Genetic Risk Score for Intracranial Aneurysms: Prediction of Subarachnoid Hemorrhage and Role in Clinical Heterogeneity

2. Genomic Insights into Myasthenia Gravis Identify Distinct Immunological Mechanisms in Early and Late Onset Disease

3. Rare coding variants in ten genes confer substantial risk for schizophrenia

4. Genome-wide association meta-analysis identifies 48 risk variants and highlights the role of the stria vascularis in hearing loss

5. Sex-Dependent Shared and Nonshared Genetic Architecture Across Mood and Psychotic Disorders

6. Dissecting the Shared Genetic Architecture of Suicide Attempt, Psychiatric Disorders, and Known Risk Factors

7. Response to comment on 'Evaluating the cardiovascular safety of sclerostin inhibition using evidence from meta-analysis of clinical trials and human genetics'

8. Cohort Profile:COVIDMENT: COVID-19 cohorts on mental health across six nations

9. The individual and global impact of copy-number variants on complex human traits

10. Assessment of the genetic and clinical determinants of hip fracture risk: Genome-wide association and Mendelian randomization study

11. Large-scale cis- and trans-eQTL analyses identify thousands of genetic loci and polygenic scores that regulate blood gene expression

12. Genetic insights into biological mechanisms governing human ovarian ageing

13. Stratification of Type 2 Diabetes by Age of Diagnosis in the UK Biobank Reveals Subgroup-Specific Genetic Associations and Causal Risk Profiles

14. Genetic regulation of spermine oxidase activity and cancer risk: a Mendelian randomization study

15. Genome-wide association studies identify 137 genetic loci for DNA methylation biomarkers of aging

16. Translating pharmacogenomics into clinical decisions: do not let the perfect be the enemy of the good

17. Interferon signature in patients with STAT1 gain‐of‐function mutation is epigenetically determined

18. Multiancestry Genome-Wide Association Study of Lipid Levels Incorporating Gene-Alcohol Interactions

19. SARS-CoV-2 susceptibility and COVID-19 disease severity are associated with genetic variants affecting gene expression in a variety of tissues

20. Evidence for increased genetic risk load for major depression in patients assigned to electroconvulsive therapy

21. A Comparison of Ten Polygenic Score Methods for Psychiatric Disorders Applied Across Multiple Cohorts

22. Genome-wide association study identifies 48 common genetic variants associated with handedness

23. Genome-wide association study of more than 40,000 bipolar disorder cases provides new insights into the underlying biology

24. Hybrid Modelling for Stroke Care: Review and suggestions of new approaches for risk assessment and simulation of scenarios

25. Clinical Characteristics and Risk Factors for COVID-19 Infection and Disease Severity: A Nationwide Observational Study in Estonia

26. A cross-disorder dosage sensitivity map of the human genome

27. Longitudinal proteomic profiling reveals increased early inflammation and sustained apoptosis proteins in severe COVID-19

28. Genomic and phenotypic insights from an atlas of genetic effects on DNA methylation

29. A data-driven medication score predicts 10-year mortality among aging adults

30. Refining Attention-Deficit/Hyperactivity Disorder and Autism Spectrum Disorder Genetic Loci by Integrating Summary Data From Genome-wide Association, Gene Expression, and DNA Methylation Studies

31. Genome-wide association study of more than 40,000 bipolar disorder cases provides new insights into the underlying biology

32. Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine

33. Multi-ancestry genome-wide gene-sleep interactions identify novel loci for blood pressure

34. The effect of LRRK2 loss-of-function variants in humans

35. Gene-educational attainment interactions in a multi-ancestry genome-wide meta-analysis identify novel blood pressure loci

36. Genome-wide Study Identifies Association between HLA-B

37. The effect of LRRK2 loss-of-function variants in humans

38. Global Frequencies of Clinically Important HLA Alleles and Their Implications For the Cost‐Effectiveness of Preemptive Pharmacogenetic Testing

39. An epigenome-wide association study of metabolic syndrome and its components

40. Genetic predisposition to coronary artery disease in type 2 diabetes mellitus

41. Differences in local population history at the finest level: the case of the Estonian population

42. Does Childhood Trauma Moderate Polygenic Risk for Depression?

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

44. Variation near <scp>MTNR</scp> 1A associates with early development and interacts with seasons

45. Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression

46. Resource profile and user guide of the Polygenic Index Repository

47. Genetic risk scores and family history as predictors of schizophrenia in Nordic registers

48. Genotype–covariate interaction effects and the heritability of adult body mass index

49. Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects

50. Evidence of causal effect of major depression on alcohol dependence: Findings from the psychiatric genomics consortium

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