La construction de l’étruscologie au début du xxe siècle von Benelli, Enrico, Delpino, Filippo, Haack, Marie-Laurence, Harari, Maurizio, Krämer, Robinson Peter, Michetti, Laura M, Miller, Martin, Pesditschek, Martina, Prost, Célia, Rey, Sarah

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Les Étrusques au temps du fascisme et du nazisme von Belfiore, Valentina, Bellelli, Vincenzo, Benelli, Enrico, Da Vela, Raffaella, Delpino, Filippo, Haack, Marie-Laurence, Harari, Maurizio, Krämer, Robinson Peter, Legendre, Jean-Pierre, Miller, Martin, Pucci, Giuseppe, Rey, Sarah, Thuillier, Jean-Paul

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

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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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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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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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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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Walking the Interactome for Prioritization of Candidate Disease Genes von Köhler, Sebastian, Bauer, Sebastian, Horn, Denise, Robinson, Peter N.

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The Monarch Initiative in 2019: an integrative data and analytic platform connecting phenotypes to genotypes across species von Shefchek, Kent A, Harris, Nomi L, Gargano, Michael, Matentzoglu, Nicolas, Unni, Deepak, Brush, Matthew, Keith, Daniel, Conlin, Tom, Vasilevsky, Nicole, Zhang, Xingmin Aaron, Balhoff, James P, Babb, Larry, Bello, Susan M, Blau, Hannah, Bradford, Yvonne, Carbon, Seth, Carmody, Leigh, Chan, Lauren E, Cipriani, Valentina, Cuzick, Alayne, Della Rocca, Maria, Dunn, Nathan, Essaid, Shahim, Fey, Petra, Grove, Chris, Gourdine, Jean-Phillipe, Hamosh, Ada, Harris, Midori, Helbig, Ingo, Hoatlin, Maureen, Joachimiak, Marcin, Jupp, Simon, Lett, Kenneth B, Lewis, Suzanna E, McNamara, Craig, Pendlington, Zoë M, Pilgrim, Clare, Putman, Tim, Ravanmehr, Vida, Reese, Justin, Riggs, Erin, Robb, Sofia, Roncaglia, Paola, Seager, James, Segerdell, Erik, Similuk, Morgan, Storm, Andrea L, Thaxon, Courtney, Thessen, Anne, Jacobsen, Julius O B, McMurry, Julie A, Groza, Tudor, Köhler, Sebastian, Smedley, Damian, Robinson, Peter N, Mungall, Christopher J, Haendel, Melissa A, Munoz-Torres, Monica C, Osumi-Sutherland, David

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Imbalance-Aware Machine Learning for Predicting Rare and Common Disease-Associated Non-Coding Variants von Schubach, Max, Re, Matteo, Robinson, Peter N., Valentini, Giorgio

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Ontologizer 2.0—a multifunctional tool for GO term enrichment analysis and data exploration von Bauer, Sebastian, Grossmann, Steffen, Vingron, Martin, Robinson, Peter N.

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

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The Human Phenotype Ontology: A Tool for Annotating and Analyzing Human Hereditary Disease von Robinson, Peter N., Köhler, Sebastian, Bauer, Sebastian, Seelow, Dominik, Horn, Denise, Mundlos, Stefan

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The Monarch Initiative: an integrative data and analytic platform connecting phenotypes to genotypes across species von Mungall, Christopher J, McMurry, Julie A, Köhler, Sebastian, Balhoff, James P, Borromeo, Charles, Brush, Matthew, Carbon, Seth, Conlin, Tom, Dunn, Nathan, Engelstad, Mark, Foster, Erin, Gourdine, J P, Jacobsen, Julius O B, Keith, Dan, Laraway, Bryan, Lewis, Suzanna E, NguyenXuan, Jeremy, Shefchek, Kent, Vasilevsky, Nicole, Yuan, Zhou, Washington, Nicole, Hochheiser, Harry, Groza, Tudor, Smedley, Damian, Robinson, Peter N, Haendel, Melissa A

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Improved exome prioritization of disease genes through cross-species phenotype comparison von Robinson, Peter N, Köhler, Sebastian, Oellrich, Anika, Wang, Kai, Mungall, Christopher J, Lewis, Suzanna E, Washington, Nicole, Bauer, Sebastian, Seelow, Dominik, Krawitz, Peter, Gilissen, Christian, Haendel, Melissa, Smedley, Damian

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Deep phenotyping for precision medicine von Robinson, Peter N.

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

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Interpretable prioritization of splice variants in diagnostic next-generation sequencing von Danis, Daniel, Jacobsen, Julius O.B., Carmody, Leigh C., Gargano, Michael A., McMurry, Julie A., Hegde, Ayushi, Haendel, Melissa A., Valentini, Giorgio, Smedley, Damian, Robinson, Peter N.

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The Human Phenotype Ontology: Semantic Unification of Common and Rare Disease von Groza, Tudor, Köhler, Sebastian, Moldenhauer, Dawid, Vasilevsky, Nicole, Baynam, Gareth, Zemojtel, Tomasz, Schriml, Lynn Marie, Kibbe, Warren Alden, Schofield, Paul N., Beck, Tim, Vasant, Drashtti, Brookes, Anthony J., Zankl, Andreas, Washington, Nicole L., Mungall, Christopher J., Lewis, Suzanna E., Haendel, Melissa A., Parkinson, Helen, Robinson, Peter N.

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