Genetic variability in the regulation of gene expression in ten regions of the human brain

UK Brain Expression Consortium, Ramasamy, Adaikalavan, North American Brain Expression Consortium, Trabzuni, Daniah, Guelfi, Sebastian, Varghese, Vibin, Smith, Colin, Walker, Robert +8 more·2014·Nature Neuroscience

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    Aliza P. Wingo, Lynn M. Almli, Jennifer Strafford Stevens, Tanja Jovanović, Thomas S. Wingo, Gregory K. Tharp, Yun Li, Adriana Lori, Maria A. Briscione, P Jin et al. · 2016 · Molecular Psychiatry
  96. Allele-specific NKX2-5 binding underlies multiple genetic associations with human electrocardiographic traits
    Paola Benaglio, Agnieszka D’Antonio‐Chronowska, Wubin Ma, Feng Yang, William W. Young Greenwald, Margaret K. R. Donovan, Christopher DeBoever, He Li, Frauke Drees, Sanghamitra Singhal et al. · 2019 · Nature Genetics
  97. Genetic variant rs763361 regulates multiple sclerosis CD226 gene expression
    Guiyou Liu, Yang Hu, Shuilin Jin, Qinghua Jiang · 2017 · Proceedings of the National Academy of Sciences
  98. cindr, the Drosophila Homolog of the CD2AP Alzheimer’s Disease Risk Gene, Is Required for Synaptic Transmission and Proteostasis
    Ojelade, Shamsideen A., Lee, Tom V., Giagtzoglou, Nikolaos, Yu, Lei, Ugur, Berrak, Li, Yarong, Duraine, Lita, Zuo, Zhongyuan, Petyuk, Vlad, De Jager, Philip L. et al. · 2019 · Cell Reports
  99. Multi-omic insights into Parkinson's Disease: From genetic associations to functional mechanisms
    Brian M. Schilder, Elisa Navarro, Towfique Raj · 2021 · Neurobiology of Disease
  100. Weighted Protein Interaction Network Analysis of Frontotemporal Dementia
    Raffaele Ferrari, Ruth C. Lovering, John Hardy, Patrick Alfryn Lewis, Claudia Manzoni · 2016 · Journal of Proteome Research