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2. Regulatory sites for splicing in human basal ganglia are enriched for disease-relevant information.

4. Polygenic risk score adds to a clinical risk score in the prediction of cardiovascular disease in a clinical setting

5. A systematic evaluation of the performance and properties of the UK Biobank Polygenic Risk Score (PRS) Release.

6. Validation of an Integrated Risk Tool, Including Polygenic Risk Score, for Atherosclerotic Cardiovascular Disease in Multiple Ethnicities and Ancestries

7. A polygenic risk score added to a QRISK®2 cardiovascular disease risk calculator demonstrated robust clinical acceptance and clinical utility in the primary care setting

8. The impact of donor and recipient common clinical and genetic variation on estimated glomerular filtration rate in a European renal transplant population

9. Long- and short-term outcomes in renal allografts with deceased donors: A large recipient and donor genome-wide association study

10. Genetic Signatures Reveal High-Altitude Adaptation in a Set of Ethiopian Populations

12. Little genetic differentiation as assessed by uniparental markers in the presence of substantial language variation in peoples of the Cross River region of Nigeria

16. Dense sampling of ethnic groups within African countries reveals fine-scale genetic structure and extensive historical admixture

17. Dense sampling of ethnic groups within African countries reveals fine-scale genetic structure and extensive historical admixture

19. Gene Variants at Loci Related to Blood Pressure Account for Variation in Response to Antihypertensive Drugs Between Black and White Individuals: Genomic Precision Medicine May Dispense With Ethnicity

21. Analysis of subcellular RNA fractions demonstrates significant genetic regulation of gene expression in human brain post-transcriptionally.

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

24. Analysis of nucleus and cytoplasm-specific RNA fractions demonstrates that a significant proportion of the genetic regulation of gene expression across the human brain occurs post-transcriptionally

25. Natural selection on EPAS1 (HIF2α) associated with low hemoglobin concentration in Tibetan highlanders

28. A survey of genetic simulation software for population and epidemiological studies

29. The ENIGMA Consortium: large-scale collaborative analyses of neuroimaging and genetic data

31. Chromosome 9p21 in sporadic amyotrophic lateral sclerosis in the UK and seven other countries: a genome-wide association study

32. A survey of current software for haplotype phase inference

33. Abstract 11316: Analytical Validation for an Integrated Risk Tool for Cardiovascular Disease Combining Conventional Risk Factors and Polygenic Risk Inferred from Snp Array and Low-Pass Whole Genome Sequencing

34. Abstract 12101: Clinical Implications of Integrating Polygenic Risk Into Established Cardiovascular Disease Risk Scores

35. Recursive splicing in long vertebrate genes

36. Common genetic variants influence human subcortical brain structures

37. Genomics software: The view from 10,000 feet

39. A genome-wide association meta-analysis identifies a novel locus at 17q11.2 associated with sporadic amyotrophic lateral sclerosis

40. Rare coding variants in the phospholipase D3 gene confer risk for Alzheimer’s disease

41. Integrated Polygenic Tool Substantially Enhances Coronary Artery Disease Prediction

43. Multicentre search for genetic susceptibility loci in sporadic epilepsy syndrome and seizure types: a case-control study

44. Evolution of a length polymorphism in the human PER3 gene, a component of the circadian system

46. Epilepsy, hippocampal sclerosis and febrile seizures linked by common genetic variation around SCN1A

47. The Val158Met COMT polymorphism is a modifier of the age at onset in Parkinsonʼs disease with a sexual dimorphism

49. Initial Assessment of the Pathogenic Mechanisms of the Recently Identified Alzheimer Risk Loci

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