Systematic Localization of Common Disease-Associated Variation in Regulatory DNA

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    Guia Guffanti, Simona Gaudi, James H. Fallon, Janet L. Sobell, Steven G. Potkin, Carlos N. Pato, Fabio M. Macciardi · 2014 · American Journal of Medical Genetics Part B Neuropsychiatric Genetics
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    Chen, Wenan, McDonnell, Shannon K, Thibodeau, Stephen N, Tillmans, Lori S, Schaid, Daniel J · 2016 · Genetics
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    Sarah Rennie, Maria Dalby, Lucas van Duin, Robin Andersson · 2018 · Nature Communications
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    Katie Marie Sullivan, Katalin Suszták · 2020 · Nature Reviews Nephrology
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    Carla Márquez‐Luna, Steven Gazal, Po‐Ru Loh, Samuel Sungil Kim, Nicholas A. Furlotte, Adam Auton, Alkes L. Price · 2018 · bioRxiv (Cold Spring Harbor Laboratory)
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    Gusev, Alexander, Shi, Huwenbo, Kichaev, Gleb, Pomerantz, Mark, Li, Fugen, Long, Henry W., Ingles, Sue A., Kittles, Rick A., Strom, Sara S., Rybicki, Benjamin A. et al. · 2016 · Nature Communications
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  60. BET-ting on chromatin-based therapeutics for heart failure
    Saptarsi M. Haldar, Timothy A. McKinsey · 2014 · Journal of Molecular and Cellular Cardiology
  61. Determining causality and consequence of expression quantitative trait loci
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    Zheng Quan Xu, Guosheng Zhang, Fulai Jin, Mengjie Chen, Terrence S. Furey, Patrick F. Sullivan, Zhaohui Steve Qin, Ming Hu, Yun Li · 2015 · Bioinformatics
  63. Context-specific effects of genetic variants associated with autoimmune disease
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  66. A novel k -mer set memory (KSM) motif representation improves regulatory variant prediction
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  68. A Prox1 enhancer represses haematopoiesis in the lymphatic vasculature
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  69. Non-coding RNA in control of gene regulatory programs in cardiac development and disease
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  70. Eukaryotic enhancers: common features, regulation, and participation in diseases
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  71. Genetic Basis of Common Human Disease: Insight into the Role of Missense SNPs from Genome-Wide Association Studies
    Lipika R. Pal, John Moult · 2015 · Journal of Molecular Biology
  72. Inferring causality and functional significance of human coding DNA variants
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  73. Multi-scale chromatin state annotation using a hierarchical hidden Markov model
    Eugenio Marco, Wouter R. A. Meuleman, Jialiang Huang, Kimberly Glass, Luca Pinello, Jianrong Wang, M Kellis, Guo‐Cheng Yuan · 2017 · Nature Communications
  74. Using the structure of genome data in the design of deep neural networks for predicting amyotrophic lateral sclerosis from genotype
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  75. Spatial chromatin architecture alteration by structural variations in human genomes at the population scale
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  76. Gene-set association and epistatic analyses reveal complex gene interaction networks affecting flowering time in a worldwide barley collection
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  77. Simultaneous quantification of mRNA and protein in single cells reveals post-transcriptional effects of genetic variation
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  78. Functional evaluation of genetic variants associated with endometriosis near GREB1
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  79. Integration of genomics and transcriptomics predicts diabetic retinopathy susceptibility genes
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  80. Rewriting regulatory DNA to dissect and reprogram gene expression
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  81. Synthesis of 53 tissue and cell line expression QTL datasets reveals master eQTLs
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  82. Distal enhancers: new insights into heart development and disease
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  83. Decoding a Signature-Based Model of Transcription Cofactor Recruitment Dictated by Cardinal Cis-Regulatory Elements in Proximal Promoter Regions
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  84. Enhancer alterations in cancer: a source for a cell identity crisis
    Ken J. Kron, Swneke Donovan Bailey, Mathieu Lupien · 2014 · Genome Medicine
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  89. A review of CRISPR associated genome engineering: application, advances and future prospects of genome targeting tool for crop improvement
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  90. Population genetics of rare variants and complex diseases
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  91. A human brain vascular atlas reveals diverse cell mediators of Alzheimer’s disease risk
    Yang, Andrew C., Vest, Ryan T., Kern, Fabian, Lee, Davis P., Maat, Christina A., Losada, Patricia M., Chen, Michelle B., Agam, Maayan, Schaum, Nicholas, Khoury, Nathalie et al. · 2021
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  94. Genome-wide association studies of late-onset cardiovascular disease
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