Color Tuning by Oxide Addition in PEDOT:PSS-Based Electrochromic Devices von Levasseur, Delphin, Mjejri, Issam, Rolland, Thomas, Rougier, Aline

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A Chaperome Subnetwork Safeguards Proteostasis in Aging and Neurodegenerative Disease von Brehme, Marc, Voisine, Cindy, Rolland, Thomas, Wachi, Shinichiro, Soper, James H., Zhu, Yitan, Orton, Kai, Villella, Adriana, Garza, Dan, Vidal, Marc, Ge, Hui, Morimoto, Richard I.

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Protein domain-level landscape of cancer-type-specific somatic mutations von Yang, Fan, Petsalaki, Evangelia, Rolland, Thomas, Hill, David E, Vidal, Marc, Roth, Frederick P

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Exploration of Binary Virus–Host Interactions Using an Infectious Protein Complementation Assay von Munier, Sandie, Rolland, Thomas, Diot, Cédric, Jacob, Yves, Naffakh, Nadia

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Systematic screening reveals a role for BRCA1 in the response to transcription-associated DNA damage von Hill, Sarah J, Rolland, Thomas, Adelmant, Guillaume, Xia, Xianfang, Owen, Matthew S, Dricot, Amélie, Zack, Travis I, Sahni, Nidhi, Jacob, Yves, Hao, Tong, McKinney, Kristine M, Clark, Allison P, Reyon, Deepak, Tsai, Shengdar Q, Joung, J Keith, Beroukhim, Rameen, Marto, Jarrod A, Vidal, Marc, Gaudet, Suzanne, Hill, David E, Livingston, David M

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Insertion of Horizontally Transferred Genes within Conserved Syntenic Regions of Yeast Genomes von Rolland, Thomas, Neuveglise, Cecile, Sacerdot, Christine, Dujon, Bernard

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An inter‐species protein–protein interaction network across vast evolutionary distance von Zhong, Quan, Pevzner, Samuel J, Hao, Tong, Wang, Yang, Mosca, Roberto, Menche, Jörg, Taipale, Mikko, Taşan, Murat, Fan, Changyu, Yang, Xinping, Haley, Patrick, Murray, Ryan R, Mer, Flora, Gebreab, Fana, Tam, Stanley, MacWilliams, Andrew, Dricot, Amélie, Reichert, Patrick, Santhanam, Balaji, Ghamsari, Lila, Calderwood, Michael A, Rolland, Thomas, Charloteaux, Benoit, Lindquist, Susan, Barabási, Albert‐László, Hill, David E, Aloy, Patrick, Cusick, Michael E, Xia, Yu, Roth, Frederick P, Vidal, Marc

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Operative list of genes associated with autism and neurodevelopmental disorders based on database review von Leblond, Claire S., Le, Thuy-Linh, Malesys, Simon, Cliquet, Freddy, Tabet, Anne-Claude, Delorme, Richard, Rolland, Thomas, Bourgeron, Thomas

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A reference map of the human binary protein interactome von Luck, Katja, Kim, Dae-Kyum, Lambourne, Luke, Spirohn, Kerstin, Begg, Bridget E., Bian, Wenting, Brignall, Ruth, Cafarelli, Tiziana, Campos-Laborie, Francisco J., Charloteaux, Benoit, Choi, Dongsic, Coté, Atina G., Daley, Meaghan, Deimling, Steven, Desbuleux, Alice, Dricot, Amélie, Gebbia, Marinella, Hardy, Madeleine F., Kishore, Nishka, Knapp, Jennifer J., Kovács, István A., Lemmens, Irma, Mee, Miles W., Mellor, Joseph C., Pollis, Carl, Pons, Carles, Richardson, Aaron D., Schlabach, Sadie, Teeking, Bridget, Yadav, Anupama, Babor, Mariana, Balcha, Dawit, Basha, Omer, Bowman-Colin, Christian, Chin, Suet-Feung, Choi, Soon Gang, Colabella, Claudia, Coppin, Georges, D’Amata, Cassandra, De Ridder, David, De Rouck, Steffi, Duran-Frigola, Miquel, Ennajdaoui, Hanane, Goebels, Florian, Goehring, Liana, Gopal, Anjali, Haddad, Ghazal, Hatchi, Elodie, Helmy, Mohamed, Jacob, Yves, Kassa, Yoseph, Landini, Serena, Li, Roujia, van Lieshout, Natascha, MacWilliams, Andrew, Markey, Dylan, Paulson, Joseph N., Rangarajan, Sudharshan, Rasla, John, Rayhan, Ashyad, Rolland, Thomas, San-Miguel, Adriana, Shen, Yun, Sheykhkarimli, Dayag, Sheynkman, Gloria M., Simonovsky, Eyal, Taşan, Murat, Tejeda, Alexander, Tropepe, Vincent, Twizere, Jean-Claude, Wang, Yang, Weatheritt, Robert J., Weile, Jochen, Xia, Yu, Yang, Xinping, Yeger-Lotem, Esti, Zhong, Quan, Aloy, Patrick, Bader, Gary D., De Las Rivas, Javier, Gaudet, Suzanne, Hao, Tong, Rak, Janusz, Tavernier, Jan, Hill, David E., Vidal, Marc, Roth, Frederick P., Calderwood, Michael A.

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Proto-genes and de novo gene birth von Carvunis, Anne-Ruxandra, Rolland, Thomas, Wapinski, Ilan, Calderwood, Michael A., Yildirim, Muhammed A., Simonis, Nicolas, Charloteaux, Benoit, Hidalgo, César A., Barbette, Justin, Santhanam, Balaji, Brar, Gloria A., Weissman, Jonathan S., Regev, Aviv, Thierry-Mieg, Nicolas, Cusick, Michael E., Vidal, Marc

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Phenotypic effects of genetic variants associated with autism von Rolland, Thomas, Cliquet, Freddy, Anney, Richard J. L., Moreau, Clara, Traut, Nicolas, Mathieu, Alexandre, Huguet, Guillaume, Duan, Jinjie, Warrier, Varun, Portalier, Swan, Dry, Louise, Leblond, Claire S., Douard, Elise, Amsellem, Frédérique, Malesys, Simon, Maruani, Anna, Toro, Roberto, Børglum, Anders D., Grove, Jakob, Baron-Cohen, Simon, Packer, Alan, Chung, Wendy K., Jacquemont, Sébastien, Delorme, Richard, Bourgeron, Thomas

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A Genetic Bridge Between Medicine and Neurodiversity for Autism von Leblond, Claire S, Rolland, Thomas, Barthome, Eli, Mougin, Zakaria, Fleury, Mathis, Ecker, Christine, Bonnot-Briey, Stéf, Cliquet, Freddy, Tabet, Anne-Claude, Maruani, Anna, Chaumette, Boris, Green, Jonathan, Delorme, Richard, Bourgeron, Thomas

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Yeasty clocks: Dating genomic changes in yeasts von Rolland, Thomas, Dujon, Bernard

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Safety and efficacy of flecainide associated with beta-blockers in arrhythmogenic right ventricular cardiomyopathy von Rolland, Thomas, Badenco, Nicolas, Maupain, Carole, Duthoit, Guillaume, Waintraub, Xavier, Laredo, Mikael, Himbert, Caroline, Frank, Robert, Hidden-Lucet, Francoise, Gandjbakhch, Estelle

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Evidence for Network Evolution in an "Arabidopsis" Interactome Map von CONSORTIUM, Mapping

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GENETIC CORRELATES AND CONSEQUENCES OF PHENOTYPIC HETEROGENEITY IN AUTISM von Warrier, Varun, Cliquet, Freddy, Grove, Jakob, Martin, Hilary, Leblond, Claire, Rolland, Thomas, Børglum, Anders, Robinson, Elise, Bourgeron, Thomas, Baron-Cohen, Simon

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Heritability of the melatonin synthesis variability in autism spectrum disorders von Benabou, Marion, Rolland, Thomas, Leblond, Claire S., Millot, Gaël A., Huguet, Guillaume, Delorme, Richard, Leboyer, Marion, Pagan, Cécile, Callebert, Jacques, Maronde, Erik, Bourgeron, Thomas

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SUB-DIAGNOSTIC EFFECTS OF GENETIC VARIANTS ASSOCIATED WITH AUTISM von Rolland, Thomas, Cliquet, Freddy, Anney, Richard, Moreau, Clara, Huguet, Guillaume, Duan, Jinjie, Warrier, Varun, Børglum, Anders, Grove, Jakob, Baron-Cohen, Simon, Packer, Alan, Chung, Wendy, Jacquemont, Sébastien, Delorme, Richard, Bourgeron, Thomas

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Dissecting the 22q13 region to explore the genetic and phenotypic diversity of patients with Phelan-McDermid syndrome von Vitrac, Aline, Leblond, Claire S., Rolland, Thomas, Cliquet, Freddy, Mathieu, Alexandre, Maruani, Anna, Delorme, Richard, Schön, Michael, Grabrucker, Andreas M., van Ravenswaaij-Arts, Conny, Phelan, Katy, Tabet, Anne-Claude, Bourgeron, Thomas

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Genetic Heterogeneity Shapes Brain Connectivity in Psychiatry von Moreau, Clara A., Harvey, Annabelle, Kumar, Kuldeep, Huguet, Guillaume, Urchs, Sebastian G.W., Douard, Elise A., Schultz, Laura M., Sharmarke, Hanad, Jizi, Khadije, Martin, Charles-Olivier, Younis, Nadine, Tamer, Petra, Rolland, Thomas, Martineau, Jean-Louis, Orban, Pierre, Silva, Ana Isabel, Hall, Jeremy, van den Bree, Marianne B.M., Owen, Michael J., Linden, David E.J., Labbe, Aurelie, Lippé, Sarah, Bearden, Carrie E., Almasy, Laura, Glahn, David C., Thompson, Paul M., Bourgeron, Thomas, Bellec, Pierre, Jacquemont, Sebastien

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