Computing Floating-Point Square Roots via Bivariate Polynomial Evaluation von Jeannerod, Claude-Pierre, Knochel, Hervé, Monat, C, Revy, G

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Automatic Generation of Fast and Certified Code for Polynomial Evaluation von Mouilleron, C., Revy, G.

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How to Square Floats Accurately and Efficiently on the ST231 Integer Processor von Jeannerod, Claude-Pierre, Jourdan-Lu, Jingyan, Monat, C., Revy, G.

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A New Binary Floating-Point Division Algorithm and Its Software Implementation on the ST231 Processor von Jeannerod, C.-P., Knochel, H., Monat, C., Revy, G., Villard, G.

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Multiplicative Square Root Algorithms for FPGAs von de Dinechin, F, Joldes, M, Pasca, B, Revy, G

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Design of fixed-point embedded systems (DEFIS) French ANR project von Menard, D., Rocher, R., Sentieys, O., Simon, N., Didier, L., Hilaire, T., Lopez, B., Goubault, E., Putot, S., Vedrine, F., Najahi, A., Revy, G., Fangain, L., Samoyeau, C., Lemonnier, F., Clienti, C.

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Faster floating-point square root for integer processors von Jeannerod, C.-P., Knochel, H., Monat, C., Revy, G.

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Unraveling Ewing Sarcoma Tumorigenesis Originating from Patient-Derived Mesenchymal Stem Cells von Sole, Anna, Grossetete, Sandrine, Heintze, Maxime, Babin, Loelia, Zaidi, Sakina, Revy, Patrick, Renouf, Benjamin, De Cian, Anne, Giovannangeli, Carine, Pierre-Eugene, Cecile, Janoueix-Lerosey, Isabelle, Couronne, Lucile, Kaltenbach, Sophie, Tomishima, Mark, Jasin, Maria, Gruenewald, Thomas G. P., Delattre, Olivier, Surdez, Didier, Brunet, Erika

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Activation-Induced Cytidine Deaminase (AID) Deficiency Causes the Autosomal Recessive Form of the Hyper-IgM Syndrome (HIGM2) von Revy, Patrick, Muto, Taro, Levy, Yves, Geissmann, Frédéric, Plebani, Alessandro, Sanal, Ozden, Catalan, Nadia, Forveille, Monique, Dufourcq-Lagelouse, Rémi, Gennery, Andrew, Tezcan, Ilhan, Ersoy, Fugen, Kayserili, Hulya, Ugazio, Alberto G, Brousse, Nicole, Muramatsu, Masamichi, Notarangelo, Luigi D, Kinoshita, Kazuo, Honjo, Tasuku, Fischer, Alain, Durandy, Anne

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V(D)J and immunoglobulin class switch recombinations: a paradigm to study the regulation of DNA end-joining von Soulas-Sprauel, P, Rivera-Munoz, P, Malivert, L, Le Guyader, G, Abramowski, V, Revy, P, de Villartay, J-P

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Mutations in SNORD118 cause the cerebral microangiopathy leukoencephalopathy with calcifications and cysts von Jenkinson, Emma M, Rodero, Mathieu P, Kasher, Paul R, Uggenti, Carolina, Oojageer, Anthony, Goosey, Laurence C, Rose, Yoann, Kershaw, Christopher J, Urquhart, Jill E, Williams, Simon G, Bhaskar, Sanjeev S, O'Sullivan, James, Baerlocher, Gabriela M, Haubitz, Monika, Aubert, Geraldine, Barañano, Kristin W, Barnicoat, Angela J, Battini, Roberta, Berger, Andrea, Blair, Edward M, Brunstrom-Hernandez, Janice E, Buckard, Johannes A, Cassiman, David M, Caumes, Rosaline, Cordelli, Duccio M, De Waele, Liesbeth M, Fay, Alexander J, Ferreira, Patrick, Fletcher, Nicholas A, Fryer, Alan E, Goel, Himanshu, Hemingway, Cheryl A, Henneke, Marco, Hughes, Imelda, Jefferson, Rosalind J, Kumar, Ram, Lagae, Lieven, Landrieu, Pierre G, Lourenço, Charles M, Malpas, Timothy J, Mehta, Sarju G, Metz, Imke, Naidu, Sakkubai, Õunap, Katrin, Panzer, Axel, Prabhakar, Prab, Quaghebeur, Gerardine, Schiffmann, Raphael, Sherr, Elliott H, Sinnathuray, Kanaga R, Soh, Calvin, Stewart, Helen S, Stone, John, Van Esch, Hilde, Van Mol, Christine E G, Vanderver, Adeline, Wakeling, Emma L, Whitney, Andrea, Pavitt, Graham D, Griffiths-Jones, Sam, Rice, Gillian I, Revy, Patrick, van der Knaap, Marjo S, Livingston, John H, O'Keefe, Raymond T, Crow, Yanick J

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Human uracil-DNA glycosylase deficiency associated with profoundly impaired immunoglobulin class-switch recombination von Forveille, Monique, Imai, Kohsuke, Krokan, Hans E, Kavli, Bodil, Fischer, Alain, Durandy, Anne, Nonoyama, Shigeaki, Catalan, Nadia, Ochs, Hans D, Lee, Wen-I, Revy, Patrick, Slupphaug, Geir, Yel, Leman

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Gain-of-function mutations in RPA1 cause a syndrome with short telomeres and somatic genetic rescue von Sharma, Richa, Sahoo, Sushree S., Honda, Masayoshi, Granger, Sophie L., Goodings, Charnise, Sanchez, Louis, Künstner, Axel, Busch, Hauke, Beier, Fabian, Pruett-Miller, Shondra M., Valentine, Marcus B., Fernandez, Alfonso G., Chang, Ti-Cheng, Géli, Vincent, Churikov, Dmitri, Hirschi, Sandrine, Pastor, Victor B., Boerries, Melanie, Lauten, Melchior, Kelaidi, Charikleia, Cooper, Megan A., Nicholas, Sarah, Rosenfeld, Jill A., Polychronopoulou, Sophia, Kannengiesser, Caroline, Saintomé, Carole, Niemeyer, Charlotte M., Revy, Patrick, Wold, Marc S., Spies, Maria, Erlacher, Miriam, Coulon, Stéphane, Wlodarski, Marcin W.

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Genotoxic Signature in Cord Blood Cells of Newborns Exposed In Utero to a Zidovudine-Based Antiretroviral Combination von André-Schmutz, Isabelle, Dal-Cortivo, Liliane, Six, Emmanuelle, Kaltenbach, Sophie, Cocchiarella, Fabienne, Le Chenadec, Jerome, Cagnard, Nicolas, Cordier, Anne-Gael, Benachi, Alexandra, Mandelbrot, Laurent, Azria, Elie, Bouallag, Naima, Luce, Sonia, Ternaux, Brigitte, Reimann, Christian, Revy, Patrick, Radford-Weiss, Isabelle, Leschi, Cristina, Recchia, Alessandra, Mavilio, Fulvio, Cavazzana, Marina, Blanche, Stéphane

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Cernunnos influences human immunoglobulin class switch recombination and may be associated with B cell lymphomagenesis von Du, Likun, Peng, Roujun, Björkman, Andrea, Filipe de Miranda, Noel, Rosner, Cornelia, Kotnis, Ashwin, Berglund, Mattias, Liu, Chonghai, Rosenquist, Richard, Enblad, Gunilla, Sundström, Christer, Hojjat-Farsangi, Mohammad, Rabbani, Hodjattallah, Teixeira, Manuel R, Revy, Patrick, Durandy, Anne, Zeng, Yixin, Gennery, Andrew R, de Villartay, Jean-Pierre, Pan-Hammarström, Qiang

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Mutations in XLF/NHEJ1/Cernunnos gene results in downregulation of telomerase genes expression and telomere shortening von Carrillo, Jaime, Calvete, Oriol, Pintado-Berninches, Laura, Manguan-García, Cristina, Sevilla Navarro, Julian, Arias-Salgado, Elena G, Sastre, Leandro, Guenechea, Guillermo, López Granados, Eduardo, de Villartay, Jean-Pierre, Revy, Patrick, Benitez, Javier, Perona, Rosario

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Corrigendum: Mutations in SNORD118 cause the cerebral microangiopathy leukoencephalopathy with calcifications and cysts von Jenkinson, Emma M, Rodero, Mathieu P, Kasher, Paul R, Uggenti, Carolina, Oojageer, Anthony, Goosey, Laurence C, Rose, Yoann, Kershaw, Christopher J, Urquhart, Jill E, Williams, Simon G, Bhaskar, Sanjeev S, O'Sullivan, James, Baerlocher, Gabriela M, Haubitz, Monika, Aubert, Geraldine, Barañano, Kristin W, Barnicoat, Angela J, Battini, Roberta, Berger, Andrea, Blair, Edward M, Brunstrom-Hernandez, Janice E, Buckard, Johannes A, Cassiman, David M, Caumes, Rosaline, Cordelli, Duccio M, De Waele, Liesbeth M, Fay, Alexander J, Ferreira, Patrick, Fletcher, Nicholas A, Fryer, Alan E, Goel, Himanshu, Hemingway, Cheryl A, Henneke, Marco, Hughes, Imelda, Jefferson, Rosalind J, Kumar, Ram, Lagae, Lieven, Landrieu, Pierre G, Lourenço, Charles M, Malpas, Timothy J, Mehta, Sarju G, Metz, Imke, Naidu, Sakkubai, Õunap, Katrin, Panzer, Axel, Prabhakar, Prab, Quaghebeur, Gerardine, Schiffmann, Raphael, Sherr, Elliott H, Sinnathuray, Kanaga R, Soh, Calvin, Stewart, Helen S, Stone, John, Van Esch, Hilde, Van Mol, Christine E G, Vanderver, Adeline, Wakeling, Emma L, Whitney, Andrea, Pavitt, Graham D, Griffiths-Jones, Sam, Rice, Gillian I, Revy, Patrick, van der Knaap, Marjo S, Livingston, John H, O'Keefe, Raymond T, Crow, Yanick J

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T cell adhesion lowers the threshold for antigen detection von Randriamampita, Clotilde, Boulla, Geneviève, Revy, Patrick, Lemaitre, Fabrice, Trautmann, Alain

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Correction: Corrigendum: Mutations in SNORD118 cause the cerebral microangiopathy leukoencephalopathy with calcifications and cysts von Jenkinson, Emma M, Rodero, Mathieu P, Kasher, Paul R, Uggenti, Carolina, Oojageer, Anthony, Goosey, Laurence C, Rose, Yoann, Kershaw, Christopher J, Urquhart, Jill E, Williams, Simon G, Bhaskar, Sanjeev S, O'Sullivan, James, Baerlocher, Gabriela M, Haubitz, Monika, Aubert, Geraldine, Barañano, Kristin W, Barnicoat, Angela J, Battini, Roberta, Berger, Andrea, Blair, Edward M, Brunstrom-Hernandez, Janice E, Buckard, Johannes A, Cassiman, David M, Caumes, Rosaline, Cordelli, Duccio M, De Waele, Liesbeth M, Fay, Alexander J, Ferreira, Patrick, Fletcher, Nicholas A, Fryer, Alan E, Goel, Himanshu, Hemingway, Cheryl A, Henneke, Marco, Hughes, Imelda, Jefferson, Rosalind J, Kumar, Ram, Lagae, Lieven, Landrieu, Pierre G, Lourenço, Charles M, Malpas, Timothy J, Mehta, Sarju G, Metz, Imke, Naidu, Sakkubai, Õunap, Katrin, Panzer, Axel, Prabhakar, Prab, Quaghebeur, Gerardine, Schiffmann, Raphael, Sherr, Elliott H, Sinnathuray, Kanaga R, Soh, Calvin, Stewart, Helen S, Stone, John, Van Esch, Hilde, Van Mol, Christine E G, Vanderver, Adeline, Wakeling, Emma L, Whitney, Andrea, Pavitt, Graham D, Griffiths-Jones, Sam, Rice, Gillian I, Revy, Patrick, van der Knaap, Marjo S, Livingston, John H, O'Keefe, Raymond T, Crow, Yanick J

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Corrigendum: Mutations in SNORD118 cause the cerebral microangiopathy leukoencephalopathy with calcifications and cysts von Jenkinson, Emma M, Rodero, Mathieu P, Kasher, Paul R, Uggenti, Carolina, Oojageer, Anthony, Goosey, Laurence C, Rose, Yoann, Kershaw, Christopher J, Urquhart, Jill E, Williams, Simon G, Bhaskar, Sanjeev S, O'Sullivan, James, Baerlocher, Gabriela M, Haubitz, Monika, Aubert, Geraldine, Barañano, Kristin W, Barnicoat, Angela J, Battini, Roberta, Berger, Andrea, Blair, Edward M, Brunstrom-Hernandez, Janice E, Buckard, Johannes A, Cassiman, David M, Caumes, Rosaline, Cordelli, Duccio M, De Waele, Liesbeth M, Fay, Alexander J, Ferreira, Patrick, Fletcher, Nicholas A, Fryer, Alan E, Goel, Himanshu, Hemingway, Cheryl A, Henneke, Marco, Hughes, Imelda, Jefferson, Rosalind J, Kumar, Ram, Lagae, Lieven, Landrieu, Pierre G, Lourenço, Charles M, Malpas, Timothy J, Mehta, Sarju G, Metz, Imke, Naidu, Sakkubai, Õunap, Katrin, Panzer, Axel, Prabhakar, Prab, Quaghebeur, Gerardine, Schiffmann, Raphael, Sherr, Elliott H, Sinnathuray, Kanaga R, Soh, Calvin, Stewart, Helen S, Stone, John, Van Esch, Hilde, Van Mol, Christine E.G, Vanderver, Adeline, Wakeling, Emma L, Whitney, Andrea, Pavitt, Graham D, Griffiths-Jones, Sam, Rice, Gillian I, Revy, Patrick, van der Knaap, Marjo S, Livingston, John H, O'Keefe, Raymond T, Crow, Yanick J

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