Fast and accurate genotype imputation in genome-wide association studies through pre-phasing

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18. Imputation of canine genotype array data using 365 whole-genome sequences improves power of genome-wide association studies
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19. Systems Genetics in Human Endothelial Cells Identifies Non-coding Variants Modifying Enhancers, Expression, and Complex Disease Traits
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20. Imputation accuracy to whole-genome sequence in Nellore cattle
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21. Impact of pre-imputation SNP-filtering on genotype imputation results
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22. Imputation-Based Genomic Coverage Assessments of Current Human Genotyping Arrays
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24. Genome-wide approach identifies a novel gene-maternal pre-pregnancy BMI interaction on preterm birth
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25. Genotype effects contribute to variation in longitudinal methylome patterns in older people
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26. Single-Cell RNA Sequencing in Parkinson’s Disease
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28. Polymorphisms in sweet taste genes (TAS1R2 and GLUT2), sweet liking, and dental caries prevalence in an adult Italian population
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29. Genotype imputation in the domestic dog
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31. Sparse Convolutional Denoising Autoencoders for Genotype Imputation
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32. A multiethnic genome-wide analysis of 44,039 individuals identifies 41 new loci associated with central corneal thickness
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33. A Mendelian randomization of γ′ and total fibrinogen levels in relation to venous thromboembolism and ischemic stroke
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35. Family-GWAS reveals effects of environment and mating on genetic associations
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37. The future for genetic studies in reproduction
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38. Genome-wide association analysis on normal hearing function identifiesPCDH20andSLC28A3as candidates for hearing function and loss
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39. Genome-wide association study identified SNP on 15q24 associated with bladder cancer risk in Japanese population
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40. Genotype imputation performance of three reference panels using African ancestry individuals
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41. Genotype Imputation in Genome‐Wide Association Studies
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42. The Duffy-null genotype and risk of infection
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43. A comparative analysis of current phasing and imputation software
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44. Contemporary Considerations for Constructing a Genetic Risk Score: An Empirical Approach
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45. Expression and Replication Studies to Identify New Candidate Genes Involved in Normal Hearing Function
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47. A combined reference panel from the 1000 Genomes and UK10K projects improved rare variant imputation in European and Chinese samples
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48. Human genetic variation in VAC14 regulates Salmonella invasion and typhoid fever through modulation of cholesterol
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51. Privacy-preserving genotype imputation with fully homomorphic encryption
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52. Phenotypic and genetic heterogeneity among subjects with mild airflow obstruction in COPDGene
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54. Imputation of the Rare HOXB13 G84E Mutation and Cancer Risk in a Large Population-Based Cohort
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58. Genome-wide association study of paliperidone efficacy
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59. Genetic variant predictors of gene expression provide new insight into risk of colorectal cancer
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60. Lowering of Circulating Sclerostin May Increase Risk of Atherosclerosis and Its Risk Factors: Evidence From a <scp>Genome‐Wide</scp> Association <scp>Meta‐Analysis</scp> Followed by Mendelian Randomization
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61. Meta-analysis of genome-wide association studies in multiethnic Asians identifies two loci for age-related nuclear cataract
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62. Improving accuracy of rare variant imputation with a two-step imputation approach
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63. A Quantitative Proteomics Tool To Identify DNA–Protein Interactions in Primary Cells or Blood
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65. Comparing performance of modern genotype imputation methods in different ethnicities
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66. EFhd2/Swiprosin-1 is a common genetic determinator for sensation-seeking/low anxiety and alcohol addiction
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71. Systemic and specific effects of antihypertensive and lipid-lowering medication on plasma protein biomarkers for cardiovascular diseases
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72. Clinical and genetic differences between bipolar disorder type 1 and 2 in multiplex families
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73. Fast and Scalable Private Genotype Imputation Using Machine Learning and Partially Homomorphic Encryption
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74. Measurement and genetics of human subcortical and hippocampal asymmetries in large datasets
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77. Multi-Ancestry Genome-Wide Association Study of Spontaneous Clearance of Hepatitis C Virus
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78. Genome‐wide survey of copy number variants finds MAPT duplications in progressive supranuclear palsy
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79. Bipolar multiplex families have an increased burden of common risk variants for psychiatric disorders
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80. The α3β4* nicotinic ACh receptor subtype mediates physical dependence to morphine: mouse and human studies
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82. Genome-Wide Association Study of Warfarin Maintenance Dose in a Brazilian Sample
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83. Predictors of Optimal Cognitive Aging in 80+ Women: The Women’s Health Initiative Memory Study
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85. Genome-Wide Polygenic Scores Predict Reading Performance Throughout the School Years
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86. Imputation-Aware Tag SNP Selection To Improve Power for Large-Scale, Multi-ethnic Association Studies
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87. Multitrait genome association analysis identifies new susceptibility genes for human anthropometric variation in the GCAT cohort
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88. Differential associations of allergic disease genetic variants with developmental profiles of eczema, wheeze and rhinitis
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89. A conditional multi-trait sequence GWAS discovers pleiotropic candidate genes and variants for sheep wool, skin wrinkle and breech cover traits
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90. Variations in the FRA10AC1 Fragile Site and 15q21 Are Associated with Cerebrospinal Fluid Aβ1-42 Level
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91. Genotype Imputation Methods and Their Effects on Genomic Predictions in Cattle
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92. Genome-wide study of resistant hypertension identified from electronic health records
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93. Genome-wide association study in a Korean population identifies six novel susceptibility loci for rheumatoid arthritis
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