VarI-COSI 2018: a forum for research advances in variant interpretation and diagnostics by Yana Bromberg, Emidio Capriotti, Hannah Carter

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ThermoScan: Semi-automatic Identification of Protein Stability Data From PubMed by Paola Turina, Piero Fariselli, Emidio Capriotti

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Challenges in predicting stabilizing variations: An exploration by Silvia Benevenuta, Giovanni Birolo, Tiziana Sanavia, Emidio Capriotti, Piero Fariselli

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DDGun: an untrained method for the prediction of protein stability changes upon single and multiple point variations by Ludovica Montanucci, Emidio Capriotti, Yotam Frank, Nir Ben-Tal, Piero Fariselli

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Protein Stability Perturbation Contributes to the Loss of Function in Haploinsufficient Genes by Giovanni Birolo, Silvia Benevenuta, Piero Fariselli, Emidio Capriotti, Elisa Giorgio, Tiziana Sanavia

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Limitations and challenges in protein stability prediction upon genome variations: towards future applications in precision medicine by Tiziana Sanavia, Giovanni Birolo, Ludovica Montanucci, Paola Turina, Emidio Capriotti, Piero Fariselli

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Analysis and Interpretation of the Impact of Missense Variants in Cancer by Maria Petrosino, Leonore Novak, Alessandra Pasquo, Roberta Chiaraluce, Paola Turina, Emidio Capriotti, Valerio Consalvi

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A Deep-Learning Sequence-Based Method to Predict Protein Stability Changes Upon Genetic Variations by Corrado Pancotti, Silvia Benevenuta, Valeria Repetto, Giovanni Birolo, Emidio Capriotti, Tiziana Sanavia, Piero Fariselli

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The complex impact of cancer-related missense mutations on the stability and on the biophysical and biochemical properties of MAPK1 and MAPK3 somatic variants by Maria Petrosino, Leonore Novak, Alessandra Pasquo, Paola Turina, Emidio Capriotti, Velia Minicozzi, Valerio Consalvi, Roberta Chiaraluce

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Identification of Driver Epistatic Gene Pairs Combining Germline and Somatic Mutations in Cancer by Jairo Rocha, Jaume Sastre, Emilia Amengual-Cladera, Jessica Hernandez-Rodriguez, Victor Asensio-Landa, Damià Heine-Suñer, Emidio Capriotti

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Resources and tools for rare disease variant interpretation by Luana Licata, Allegra Via, Paola Turina, Giulia Babbi, Silvia Benevenuta, Claudio Carta, Rita Casadio, Andrea Cicconardi, Andrea Cicconardi, Angelo Facchiano, Piero Fariselli, Deborah Giordano, Federica Isidori, Anna Marabotti, Pier Luigi Martelli, Stefano Pascarella, Michele Pinelli, Tommaso Pippucci, Roberta Russo, Roberta Russo, Castrense Savojardo, Bernardina Scafuri, Lucrezia Valeriani, Emidio Capriotti

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Phased whole-genome genetic risk in a family quartet using a major allele reference sequence. by Frederick E Dewey, Rong Chen, Sergio P Cordero, Kelly E Ormond, Colleen Caleshu, Konrad J Karczewski, Michelle Whirl-Carrillo, Matthew T Wheeler, Joel T Dudley, Jake K Byrnes, Omar E Cornejo, Joshua W Knowles, Mark Woon, Katrin Sangkuhl, Li Gong, Caroline F Thorn, Joan M Hebert, Emidio Capriotti, Sean P David, Aleksandra Pavlovic, Anne West, Joseph V Thakuria, Madeleine P Ball, Alexander W Zaranek, Heidi L Rehm, George M Church, John S West, Carlos D Bustamante, Michael Snyder, Russ B Altman, Teri E Klein, Atul J Butte, Euan A Ashley

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