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

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6. A Hypothesis-Driven Association Study of 28 Nuclear-Encoded Mitochondrial Genes with Antipsychotic-Induced Weight Gain in Schizophrenia
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18. Examining the role of common and rare mitochondrial variants in schizophrenia
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19. A Phenome-Wide Mendelian Randomization Study of Pancreatic Cancer Using Summary Genetic Data
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20. Pathogen-specific innate immune response patterns are distinctly affected by genetic diversity
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21. Retrospective Binary-Trait Association Test Elucidates Genetic Architecture of Crohn Disease
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22. eMERGE Phenome-Wide Association Study (PheWAS) identifies clinical associations and pleiotropy for stop-gain variants
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23. Pathway-Based Analysis of Genome-Wide Association Data Identified SNPs in HMMR as Biomarker for Chemotherapy- Induced Neutropenia in Breast Cancer Patients
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24. Whole Exome Sequencing of Patients from Multicase Families with Systemic Lupus Erythematosus Identifies Multiple Rare Variants
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25. OpenMendel: a cooperative programming project for statistical genetics
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26. The protective variant rs7173049 at LOXL1 locus impacts on retinoic acid signaling pathway in pseudoexfoliation syndrome
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27. GWAS on Imputed Whole-Genome Resequencing From Genotyping-by-Sequencing Data for Farrowing Interval of Different Parities in Pigs
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28. Machine learning on genome-wide association studies to predict the risk of radiation-associated contralateral breast cancer in the WECARE Study
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29. The MUC6/AP2A2 Locus and Its Relevance to Alzheimer’s Disease: A Review
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30. European genetic ancestry associated with risk of childhood ependymoma
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31. HLA-DQB1 6672G>C (rs113332494) is associated with clozapine-induced neutropenia and agranulocytosis in individuals of European ancestry
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32. Collection of genetic data at scale for a nationally representative population: the UK Millennium Cohort Study
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34. Common variants on 9p21.3 are associated with brain arteriovenous malformations with accompanying arterial aneurysms
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35. Genome-wide association and admixture analysis of glaucoma in the Women's Health Initiative
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36. NLRC4 Inflammasome Is an Important Regulator of Interleukin-18 Levels in Patients With Acute Coronary Syndromes
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37. Genome-Wide Association Study of Heavy Smoking and Daily/Nondaily Smoking in the Hispanic Community Health Study/Study of Latinos (HCHS/SOL)
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38. Genome‐wide association study of facial emotion recognition in children and association with polygenic risk for mental health disorders
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39. Polygenic signal for symptom dimensions and cognitive performance in patients with chronic schizophrenia
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40. Genome-wide association analysis of hippocampal volume identifies enrichment of neurogenesis-related pathways
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41. Tissue-specific microRNA expression alters cancer susceptibility conferred by a TP53 noncoding variant
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42. In search of rare variants: Preliminary results from whole genome sequencing of 1,325 individuals with psychophysiological endophenotypes
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47. Neurobiological substrates underlying the effect of genomic risk for depression on the conversion of amnestic mild cognitive impairment
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49. Comprehensive Multiple eQTL Detection and Its Application to GWAS Interpretation
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50. Multi-omics analysis to identify susceptibility genes for colorectal cancer
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57. A Common Variant at the 14q32 Endometrial Cancer Risk Locus Activates AKT1 through YY1 Binding
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58. Susceptibility to Childhood Pneumonia: A Genome-Wide Analysis
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59. Genetic variation in the geneLRP2increases relapse risk in multiple sclerosis
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61. Common genetic variation and novel loci associated with volumetric mammographic density
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65. Comparison among three variant callers and assessment of the accuracy of imputation from SNP array data to whole-genome sequence level in chicken
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67. Coding Variants at Hexa-allelic Amino Acid 13 of HLA-DRB1 Explain Independent SNP Associations with Follicular Lymphoma Risk
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68. Susceptibility Loci for Clinical Coronary Artery Disease and Subclinical Coronary Atherosclerosis Throughout the Life-Course
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70. Evaluation of associations between genetically predicted circulating protein biomarkers and breast cancer risk
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71. Rare Variants Imputation in Admixed Populations: Comparison Across Reference Panels and Bioinformatics Tools
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74. Sex-Specific Genetic Associations for Barrett’s Esophagus and Esophageal Adenocarcinoma
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75. Genetic variations of DNA bindings of FOXA1 and co-factors in breast cancer susceptibility
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76. The construction of a haplotype reference panel using extremely low coverage whole genome sequences and its application in genome-wide association studies and genomic prediction in Duroc pigs
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77. Imputation accuracy across global human populations
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78. Identification of two novel mammographic density loci at 6Q25.1
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79. Association of orexin receptor polymorphisms with antipsychotic-induced weight gain
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80. Systematic assessment of imputation performance using the 1000 Genomes reference panels
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81. Relationships of Measured and Genetically Determined Height With the Cardiac Conduction System in Healthy Adults
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82. Improving power of association tests using multiple sets of imputed genotypes from distributed reference panels
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83. Constraints on eQTL Fine Mapping in the Presence of Multisite Local Regulation of Gene Expression
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84. Identification of an emphysema-associated genetic variant near TGFB2 with regulatory effects in lung fibroblasts
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85. Replication of FTO gene associated with lean mass in a meta-analysis of genome-wide association studies
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86. Genetic, individual, and familial risk correlates of brain network controllability in major depressive disorder
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87. A General Efficient and Flexible Approach for Genome-Wide Association Analyses of Imputed Genotypes in Family-Based Designs
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88. Genetic variants in the receptor for advanced glycation end products ( RAGE ) gene were associated with circulating soluble RAGE level but not with renal function among Asians with type 2 diabetes: a genome-wide association study
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89. HIV peptidome-wide association study reveals patient-specific epitope repertoires associated with HIV control
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90. Haplotype-based genome-wide association increases the predictability of leaf rust (Puccinia triticina) resistance in wheat
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91. Immunity and amyloid beta, total tau and neurofilament light chain: Findings from a community‐based cohort study
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92. Africa-specific human genetic variation near CHD1L associates with HIV-1 load
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