Rare and common variants: twenty arguments

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4. Genome-wide association studies: assessing trait characteristics in model and crop plants
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5. Genetic Modifiers and Oligogenic Inheritance
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8. The continuum of causality in human genetic disorders
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9. Whole-Exome Sequencing of 2,000 Danish Individuals and the Role of Rare Coding Variants in Type 2 Diabetes
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10. Towards precision medicine: advances in computational approaches for the analysis of human variants
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11. Performance and Robustness of Penalized and Unpenalized Methods for Genetic Prediction of Complex Human Disease
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12. Genetic diversity and genome-wide association analysis of cooking time in dry bean (Phaseolus vulgaris L.)
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13. Beyond large-effect loci: large-scale GWAS reveals a mixed large-effect and polygenic architecture for age at maturity of Atlantic salmon
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14. A Conservative Assessment of the Major Genetic Causes of Idiopathic Chronic Pancreatitis: Data from a Comprehensive Analysis of PRSS1, SPINK1, CTRC and CFTR Genes in 253 Young French Patients
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15. Constitutively active SARM1 variants that induce neuropathy are enriched in ALS patients
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16. Integrating Genetics and Social Science: Genetic Risk Scores
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17. Mapping of Immune-Mediated Disease Genes
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18. GWAS Analysis and QTL Identification of Fiber Quality Traits and Yield Components in Upland Cotton Using Enriched High-Density SNP Markers
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19. Radiogenomics: Radiobiology Enters the Era of Big Data and Team Science
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20. Genomics of elite sporting performance: what little we know and necessary advances
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21. The genomics of local adaptation in trees: are we out of the woods yet?
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22. Genomic risk prediction of complex human disease and its clinical application
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23. The Pattern and Distribution of Deleterious Mutations in Maize
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24. MECOM-associated syndrome: a heterogeneous inherited bone marrow failure syndrome with amegakaryocytic thrombocytopenia
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25. A Neurosurgical Functional Dissection of the Middle Precentral Gyrus during Speech Production
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26. Genome-wide association study implicates NDST3 in schizophrenia and bipolar disorder
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27. The overdue promise of short tandem repeat variation for heritability
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28. The genetics of depression: successful genome-wide association studies introduce new challenges
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29. Genetic Interaction Networks: Toward an Understanding of Heritability
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30. Systematic identification of interaction effects between genome- and environment-wide associations in type 2 diabetes mellitus
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31. Drug discovery for autism spectrum disorder: challenges and opportunities
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32. Genetics of Gestational Diabetes Mellitus and Maternal Metabolism
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33. Experience-Dependent Modulation of Feedback Integration during Singing: Role of the Right Anterior Insula
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34. Next generation sequencing: implications in personalized medicine and pharmacogenomics
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35. Avatars of information: towards an inclusive evolutionary synthesis
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36. Cortical Activity Predicts Which Older Adults Recognize Speech in Noise and When
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37. Molecular genetics and subjective well-being
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38. Genome-Wide Association Mapping of Flowering and Ripening Periods in Apple
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39. Revealing the role of the human blood plasma proteome in obesity using genetic drivers
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40. It’s not magic – Hsp90 and its effects on genetic and epigenetic variation
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41. Common genetic risk variants identified in the SPARK cohort support DDHD2 as a candidate risk gene for autism
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42. Exploring and Harnessing Haplotype Diversity to Improve Yield Stability in Crops
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43. Protein-coding variants implicate novel genes related to lipid homeostasis contributing to body-fat distribution
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44. Periodontal inflammation: Integrating genes and dysbiosis
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45. Understanding rare and common diseases in the context of human evolution
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46. Network-assisted analysis to prioritize GWAS results: principles, methods and perspectives
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47. New mutations in non-syndromic primary ovarian insufficiency patients identified via whole-exome sequencing
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48. Phenotypic and genome-wide association with the local environment of Arabidopsis
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49. Genome‐wide association study reveals putative regulators of bioenergy traits in Populus deltoides
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50. Polygenic Risk for Externalizing Disorders
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51. Natural Genetic Variation for Acclimation of Photosynthetic Light Use Efficiency to Growth Irradiance in Arabidopsis
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52. Genetic Landscape of Common Epilepsies: Advancing towards Precision in Treatment
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53. Statistical methods for mediation analysis in the era of high-throughput genomics: Current successes and future challenges
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54. Differential Representation of Articulatory Gestures and Phonemes in Precentral and Inferior Frontal Gyri
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55. Musical Expertise and Second Language Learning
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56. Germline Genetic Contributions to Risk for Esophageal Adenocarcinoma, Barrett's Esophagus, and Gastroesophageal Reflux
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57. GWAS for BMI: a treasure trove of fundamental insights into the genetic basis of obesity
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58. Primers on nutrigenetics and nutri(epi)genomics: Origins and development of precision nutrition
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59. Statistical methods for SNP heritability estimation and partition: A review
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60. Rare variants contribute disproportionately to quantitative trait variation in yeast
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61. Genetic factors related to gastric cancer susceptibility identified using a genome‐wide association study
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62. Radiogenomics – current status, challenges and future directions
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63. Genomics to systems biology in animal and veterinary sciences: Progress, lessons and opportunities
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64. Genomic insights into ayurvedic and western approaches to personalized medicine
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65. Predicting Functional Effects of Synonymous Variants: A Systematic Review and Perspectives
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66. Maternal substance use during pregnancy and offspring conduct problems: A meta-analysis
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67. Genome sequencing in the clinic: the past, present, and future of genomic medicine
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68. Evaluation of linkage disequilibrium, population structure, and genetic diversity in the U.S. peanut mini core collection
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69. Polygenic risk and the development and course of asthma: an analysis of data from a four-decade longitudinal study
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70. Eleven Candidate Susceptibility Genes for Common Familial Colorectal Cancer
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71. Genome-wide association mapping revealed a diverse genetic basis of seed dormancy across subpopulations in rice (Oryza sativa L.)
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72. Impact of genetic variation on three dimensional structure and function of proteins
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73. Application of Whole Exome Sequencing to Identify Disease-Causing Variants in Inherited Human Diseases
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74. The interface between genetics and psychology: lessons from developmental dyslexia
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76. Triangulation of the neurocomputational architecture underpinning reading aloud
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77. The association of attempted suicide with genetic variants in the SLC6A4 and TPH genes depends on the definition of suicidal behavior: a systematic review and meta-analysis
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78. Genetic architecture of nonadditive inheritance in Arabidopsis thaliana hybrids
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79. Are minor alleles more likely to be risk alleles?
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80. Rare genetic variants in CX3CR1 and their contribution to the increased risk of schizophrenia and autism spectrum disorders
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81. Genomic approaches for understanding the genetics of complex disease
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82. Using the tools of genetic epidemiology to understand sex differences in neuropsychiatric disorders
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83. Polygenic Scores Predict Alcohol Problems in an Independent Sample and Show Moderation by the Environment
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84. Identification of QTL with large effect on seed weight in a selective population of soybean with genome-wide association and fixation index analyses
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85. Meta-analysis of genome-wide association studies of aggressive and chronic periodontitis identifies two novel risk loci
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86. Transcriptome-Wide Association Supplements Genome-Wide Association in Zea mays
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87. MicroRNA dysregulation in neuropsychiatric disorders and cognitive dysfunction
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88. Usefulness of a Multiparent Advanced Generation Intercross Population With a Greatly Reduced Mating Design for Genetic Studies in Winter Wheat
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89. The genetic underpinnings of callous-unemotional traits: A systematic research review
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90. The complete and fully-phased diploid genome of a male Han Chinese
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91. Combining Multiple Hypothesis Testing with Machine Learning Increases the Statistical Power of Genome-wide Association Studies
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92. Genetics of Callous-Unemotional Behavior in Children
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93. Ultrafast homomorphic encryption models enable secure outsourcing of genotype imputation
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94. Missing compared to what? Revisiting heritability, genes and culture
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95. Linkage and regional association analysis reveal two new tightly-linked major-QTLs for pod number and seed number per pod in rapeseed (Brassica napus L.)
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96. Cross-Tissue and Tissue-Specific eQTLs: Partitioning the Heritability of a Complex Trait
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97. Update on the Role of the Non-Canonical Wnt/Planar Cell Polarity Pathway in Neural Tube Defects
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98. Genetic architecture of body size in mammals
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99. Personalized medicine: Genetic risk prediction of drug response
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100. Genomic and molecular characterization of preterm birth
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