Benefits of aggregation in woodlice: a factor in the terrestrialization process? von Broly, P., Deneubourg, J.-L., Devigne, C.

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A Proteome-Scale Map of the Human Interactome Network von Rolland, Thomas, Taşan, Murat, Charloteaux, Benoit, Pevzner, Samuel J., Zhong, Quan, Sahni, Nidhi, Yi, Song, Lemmens, Irma, Fontanillo, Celia, Mosca, Roberto, Kamburov, Atanas, Ghiassian, Susan D., Yang, Xinping, Ghamsari, Lila, Balcha, Dawit, Begg, Bridget E., Braun, Pascal, Brehme, Marc, Broly, Martin P., Carvunis, Anne-Ruxandra, Convery-Zupan, Dan, Corominas, Roser, Coulombe-Huntington, Jasmin, Dann, Elizabeth, Dreze, Matija, Dricot, Amélie, Fan, Changyu, Franzosa, Eric, Gebreab, Fana, Gutierrez, Bryan J., Hardy, Madeleine F., Jin, Mike, Kang, Shuli, Kiros, Ruth, Lin, Guan Ning, Luck, Katja, MacWilliams, Andrew, Menche, Jörg, Murray, Ryan R., Palagi, Alexandre, Poulin, Matthew M., Rambout, Xavier, Rasla, John, Reichert, Patrick, Romero, Viviana, Ruyssinck, Elien, Sahalie, Julie M., Scholz, Annemarie, Shah, Akash A., Sharma, Amitabh, Shen, Yun, Spirohn, Kerstin, Tam, Stanley, Tejeda, Alexander O., Wanamaker, Shelly A., Twizere, Jean-Claude, Vega, Kerwin, Walsh, Jennifer, Cusick, Michael E., Xia, Yu, Barabási, Albert-László, Iakoucheva, Lilia M., Aloy, Patrick, De Las Rivas, Javier, Tavernier, Jan, Calderwood, Michael A., Hill, David E., Hao, Tong, Roth, Frederick P., Vidal, Marc

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Propionibacterium/Cutibacterium species–related positive samples, identification, clinical and resistance features: a 10-year survey in a French hospital von Broly, M., Ruffier d’Epenoux, L., Guillouzouic, A, Le Gargasson, G., Juvin, M-E, Leroy, A.G., Bémer, P., Corvec, S.

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THUMPD1 bi-allelic variants cause loss of tRNA acetylation and a syndromic neurodevelopmental disorder von Broly, Martin, Polevoda, Bogdan V., Awayda, Kamel M., Tong, Ning, Lentini, Jenna, Besnard, Thomas, Deb, Wallid, O’Rourke, Declan, Baptista, Julia, Ellard, Sian, Almannai, Mohammed, Hashem, Mais, Abdulwahab, Ferdous, Shamseldin, Hanan, Al-Tala, Saeed, Alkuraya, Fowzan S., Leon, Alberta, van Loon, Rosa L.E., Ferlini, Alessandra, Sanchini, Mariabeatrice, Bigoni, Stefania, Ciorba, Andrea, van Bokhoven, Hans, Iqbal, Zafar, Al-Maawali, Almundher, Al-Murshedi, Fathiya, Ganesh, Anuradha, Al-Mamari, Watfa, Lim, Sze Chern, Pais, Lynn S., Brown, Natasha, Riazuddin, Saima, Bézieau, Stéphane, Fu, Dragony, Isidor, Bertrand, Cogné, Benjamin, O’Connell, Mitchell R.

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Protein interaction network of alternatively spliced isoforms from brain links genetic risk factors for autism von Corominas, Roser, Yang, Xinping, Lin, Guan Ning, Kang, Shuli, Shen, Yun, Ghamsari, Lila, Broly, Martin, Rodriguez, Maria, Tam, Stanley, Wanamaker, Shelly A., Fan, Changyu, Yi, Song, Tasan, Murat, Lemmens, Irma, Kuang, Xingyan, Zhao, Nan, Malhotra, Dheeraj, Michaelson, Jacob J., Vacic, Vladimir, Calderwood, Michael A., Roth, Frederick P., Tavernier, Jan, Horvath, Steve, Salehi-Ashtiani, Kourosh, Korkin, Dmitry, Sebat, Jonathan, Hill, David E., Hao, Tong, Vidal, Marc, Iakoucheva, Lilia M.

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Author Correction: Protein interaction network of alternatively spliced isoforms from brain links genetic risk factors for autism von Corominas, Roser, Yang, Xinping, Lin, Guan Ning, Kang, Shuli, Shen, Yun, Ghamsari, Lila, Broly, Martin, Rodriguez, Maria, Tam, Stanley, Wanamaker, Shelly A., Fan, Changyu, Yi, Song, Tasan, Murat, Lemmens, Irma, Kuang, Xingyan, Zhao, Nan, Malhotra, Dheeraj, Michaelson, Jacob J., Vacic, Vladimir, Calderwood, Michael A., Roth, Frederick P., Tavernier, Jan, Horvath, Steve, Salehi-Ashtiani, Kourosh, Korkin, Dmitry, Sebat, Jonathan, Hill, David E., Hao, Tong, Vidal, Marc, Iakoucheva, Lilia M.

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Genotypic analysis of thiopurine S-methyltransferase in patients with Crohn's disease and severe myelosuppression during azathioprine therapy von Colombel, Jean–frédéric, Ferrari, Nicolas, Debuysere, Hervé, Marteau, Philippe, Gendre, Jean–pierre, Bonaz, Bruno, Soulé, Jean-claude, Modigliani, Robert, Touze, Yvan, Catala, Pascale, Libersa, Christian, Broly, Franck

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Type 1 xanthinuria: Report on three cases von Diss, M, Ranchin, B, Broly, F, Pottier, N, Cochat, P

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Characterisation of novel defective thiopurine S-methyltransferase allelic variants von Garat, A., Cauffiez, C., Renault, N., Lo-Guidice, J.M., Allorge, D., Chevalier, D., Houdret, N., Chavatte, P., Loriot, M.A., Gala, J.L., Broly, F.

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Nonresponse to Clozapine and ultrarapid CYP1A2 activity: Clinical data and analysis of CYP1A2 gene von EAP, Chin B, BENDER, Stefan, JAQUENOUD SIROT, Eveline, CUCCHIA, Gianni, JONZIER-PEREY, Michèle, BAUMANN, Pierre, ALLORGE, Delphine, BROLY, Franck

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Cytochrome P450 2D6 genotype and methadone steady-state concentrations von EAP, Chin B, BROLY, Franck, KOSEL, Markus, PREISIG, Martin, BAUMANN, Pierre, MINO, Annie, HÄMMIG, Robert, DEGLON, Jean J, UEHLINGER, Claude, MEILI, Daniel, CHEVALLEY, Anne F, BERTSCHY, Gilles, ZULLINO, Daniele

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Identification of a novel splice‐site mutation in the CYP1A2 gene von Allorge, Delphine, Chevalier, Dany, Lo‐Guidice, Jean‐Marc, Cauffiez, Christelle, Suard, Françoise, Baumann, Pierre, Eap, Chin B., Broly, Franck

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Évaluation d’un questionnaire de qualité de vie spécifique de l’atteinte du visage dans la sclérodermie systémique : étude de 107 patients von Broly, M., Truchetet, M.-E., Lazaro, E., Constans, J., Viallard, J.-F., Mercie, P., Seneschal, J., Duffau, P., Doutre, M.-S.

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Protein interaction network of alternatively spliced isoforms from brain links genetic risk factors for autism von Corominas Castiñeira, Roser, Yang, Xinping, Lin, Guan Ning, Kang, Shuli, Shen, Yun, Ghamsari, Lila, Broly, Martin, Rodriguez, Maria, Tam, Stanley, Trigg, Shelly A, Fan, Changyu, Yi, Song, Tasan, Murat, Lemmens, Irma, Kuang, Xingyan, Zhao, Nan, Malhotra, Dheeraj, Michaelson, Jacob J, Vacic, Vladimir, Calderwood, Michael A, Roth, Frederick P, Tavernier, Jan, Horvath, Steve, Salehi-Ashtiani, Kourosh, Korkin, Dmitry, Sebat, Jonathan, Hill, David E, Hao, Tong, Vidal, Marc, Iakoucheva, Lilia M

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Effect of interferon α‐ribavirin bitherapy on cytochrome P450 1A2 and 2D6 and N‐acetyltransferase‐2 activities in patients with chronic active hepatitis C von Becquemont, Laurent, Chazouilleres, Olivier, Serfaty, Lawrence, Poirier, Jean Marie, Broly, Franck, Jaillon, Patrice, Poupon, Raoul, Funck‐Brentano, Christian

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Protein interaction network of alternatively spliced isoforms from brain links genetic risk factors for autism von Corominas, Roser, Yang, Xinping, Lin, Guan Ning, Kang, Shuli, Shen, Yun, Ghamsari, Lila, Broly, Martin, Rodriguez, Maria, Tam, Stanley, Trigg, Shelly A, Fan, Changyu, Yi, Song, Tasan, Murat, Lemmens, Irma, Kuang, Xingyan, Zhao, Nan, Malhotra, Dheeraj, Michaelson, Jacob J, Vacic, Vladimir, Calderwood, Michael A, Roth, Frederick P, Tavernier, Jan, Horvath, Steve, Salehi-Ashtiani, Kourosh, Korkin, Dmitry, Sebat, Jonathan, Hill, David E, Hao, Tong, Vidal, Marc, Iakoucheva, Lilia M

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Protein interaction network of alternatively spliced isoforms from brain links genetic risk factors for autism von Corominas, Roser, Yang, Xinping, Lin, Guan Ning, Kang, Shuli, Shen, Yun, Ghamsari, Lila, Broly, Martin, Rodriguez, Maria, Tam, Stanley, Trigg, Shelly A, Fan, Changyu, Yi, Song, Tasan, Murat, Lemmens, Irma, Kuang, Xingyan, Zhao, Nan, Malhotra, Dheeraj, Michaelson, Jacob J, Vacic, Vladimir, Calderwood, Michael A, Roth, Frederick P, Tavernier, Jan, Horvath, Steve, Salehi-Ashtiani, Kourosh, Korkin, Dmitry, Sebat, Jonathan, Hill, David E, Hao, Tong, Vidal, Marc, Iakoucheva, Lilia M

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Drug extrapyramidal side effects. CYP2D6 genotypes and phenotypes von VANDEL, P, HAFFEN, E, VANDEL, S, BONIN, B, NEZELOF, S, SECHTER, D, BROLY, F, BIZOUARD, P, DALERY, J

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Xanthinurie héréditaire de type 1 : à propos de trois cas von Diss, M., Ranchin, B., Broly, F., Pottier, N., Cochat, P.

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Clomipramine, fluoxetine and CYP2D6 metabolic capacity in depressed patients von Vandel, P., Haffen, E., Nezelof, S., Broly, F., Kantelip, J. P., Sechter, D.

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