Deep phenotyping for precision medicine von Robinson, Peter N.

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Phenolyzer: phenotype-based prioritization of candidate genes for human diseases von Yang, Hui, Robinson, Peter N, Wang, Kai

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Task-Based Language Learning: A Review of Issues von Robinson, Peter

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Classification, Ontology, and Precision Medicine von Haendel, Melissa A, Chute, Christopher G, Robinson, Peter N

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How Gay Men Prepare for Death: The Dying Business von Robinson, Peter

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FABIAN-variant: predicting the effects of DNA variants on transcription factor binding von Steinhaus, Robin, Robinson, Peter N, Seelow, Dominik

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clinker & clustermap.js: automatic generation of gene cluster comparison figures von Gilchrist, Cameron L M, Chooi, Yit-Heng

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The dynamic brain: from spiking neurons to neural masses and cortical fields von Deco, Gustavo, Jirsa, Viktor K, Robinson, Peter A, Breakspear, Michael, Friston, Karl

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Phenotype ontologies and cross-species analysis for translational research von Robinson, Peter N, Webber, Caleb

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Pervasive and CpG-dependent promoter-like characteristics of transcribed enhancers von Steinhaus, Robin, Gonzalez, Tonatiuh, Seelow, Dominik, Robinson, Peter N

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CAFE 5 models variation in evolutionary rates among gene families von Mendes, Fábio K, Vanderpool, Dan, Fulton, Ben, Hahn, Matthew W

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Annotation of biologically relevant ligands in UniProtKB using ChEBI von Coudert, Elisabeth, Gehant, Sebastien, de Castro, Edouard, Pozzato, Monica, Baratin, Delphine, Neto, Teresa, Sigrist, Christian J A, Redaschi, Nicole, Bridge, Alan

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pyGenomeTracks: reproducible plots for multivariate genomic datasets von Lopez-Delisle, Lucille, Rabbani, Leily, Wolff, Joachim, Bhardwaj, Vivek, Backofen, Rolf, Grüning, Björn, Ramírez, Fidel, Manke, Thomas

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Long-Range Dependent Curve Time Series von Li, Degui, Robinson, Peter M., Shang, Han Lin

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Biometric and structural ocular manifestations of Marfan syndrome von Gehle, Petra, Goergen, Barbara, Pilger, Daniel, Ruokonen, Peter, Robinson, Peter N, Salchow, Daniel J

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Geometric constraints on human brain function von Pang, James C., Aquino, Kevin M., Oldehinkel, Marianne, Robinson, Peter A., Fulcher, Ben D., Breakspear, Michael, Fornito, Alex

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A Whole-Genome Analysis Framework for Effective Identification of Pathogenic Regulatory Variants in Mendelian Disease von Smedley, Damian, Schubach, Max, Jacobsen, Julius O.B., Köhler, Sebastian, Zemojtel, Tomasz, Spielmann, Malte, Jäger, Marten, Hochheiser, Harry, Washington, Nicole L., McMurry, Julie A., Haendel, Melissa A., Mungall, Christopher J., Lewis, Suzanna E., Groza, Tudor, Valentini, Giorgio, Robinson, Peter N.

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The Human Phenotype Ontology in 2021 von Köhler, Sebastian, Gargano, Michael, Matentzoglu, Nicolas, Carmody, Leigh C, Lewis-Smith, David, Vasilevsky, Nicole A, Danis, Daniel, Balagura, Ganna, Baynam, Gareth, Brower, Amy M, Callahan, Tiffany J, Chute, Christopher G, Est, Johanna L, Galer, Peter D, Ganesan, Shiva, Griese, Matthias, Haimel, Matthias, Pazmandi, Julia, Hanauer, Marc, Harris, Nomi L, Hartnett, Michael J, Hastreiter, Maximilian, Hauck, Fabian, He, Yongqun, Jeske, Tim, Kearney, Hugh, Kindle, Gerhard, Klein, Christoph, Knoflach, Katrin, Krause, Roland, Lagorce, David, McMurry, Julie A, Miller, Jillian A, Munoz-Torres, Monica C, Peters, Rebecca L, Rapp, Christina K, Rath, Ana M, Rind, Shahmir A, Rosenberg, Avi Z, Segal, Michael M, Seidel, Markus G, Smedley, Damian, Talmy, Tomer, Thomas, Yarlalu, Wiafe, Samuel A, Xian, Julie, Yüksel, Zafer, Helbig, Ingo, Mungall, Christopher J, Haendel, Melissa A, Robinson, Peter N

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Deep phenotyping: symptom annotation made simple with SAMS von Steinhaus, Robin, Proft, Sebastian, Seelow, Evelyn, Schalau, Tobias, Robinson, Peter N, Seelow, Dominik

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plotsr: visualizing structural similarities and rearrangements between multiple genomes von Goel, Manish, Schneeberger, Korbinian

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