Sökresultat - Seeleuthner, Yoann

Controlling for human population stratification in rare variant association studies av Bouaziz, Matthieu, Mullaert, Jimmy, Bigio, Benedetta, Seeleuthner, Yoann, Casanova, Jean-Laurent, Alcais, Alexandre, Abel, Laurent, Cobat, Aurélie

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Taking population stratification into account by local permutations in rare-variant association studies on small samples av Mullaert, Jimmy, Bouaziz, Matthieu, Seeleuthner, Yoann, Bigio, Benedetta, Casanova, Jean-Laurent, Alcaïs, Alexandre, Abel, Laurent, Cobat, Aurélie

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Accessing the genomic information of unculturable oceanic picoeukaryotes by combining multiple single cells av Mangot, Jean-François, Logares, Ramiro, Sánchez, Pablo, Latorre, Fran, Seeleuthner, Yoann, Mondy, Samuel, Sieracki, Michael E., Jaillon, Olivier, Wincker, Patrick, Vargas, Colomban de, Massana, Ramon

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Detection of homozygous and hemizygous complete or partial exon deletions by whole-exome sequencing av Bigio, Benedetta, Seeleuthner, Yoann, Kerner, Gaspard, Migaud, Mélanie, Rosain, Jérémie, Boisson, Bertrand, Nasca, Carla, Puel, Anne, Bustamante, Jacinta, Casanova, Jean-Laurent, Abel, Laurent, Cobat, Aurelie

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Survey of the green picoalga Bathycoccus genomes in the global ocean av Vannier, Thomas, Leconte, Jade, Seeleuthner, Yoann, Mondy, Samuel, Pelletier, Eric, Aury, Jean-Marc, de Vargas, Colomban, Sieracki, Michael, Iudicone, Daniele, Vaulot, Daniel, Wincker, Patrick, Jaillon, Olivier

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Homozygosity for TYK2 P1104A underlies tuberculosis in about 1% of patients in a cohort of European ancestry av Kerner, Gaspard, Ramirez-Alejo, Noe, Seeleuthner, Yoann, Yang, Rui, Ogishi, Masato, Cobat, Aurélie, Patin, Etienne, Quintana-Murci, Lluis, Boisson-Dupuis, Stéphanie, Casanova, Jean-Laurent, Abel, Laurent

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Common homozygosity for predicted loss-of-function variants reveals both redundant and advantageous effects of dispensable human genes av Rausell, Antonio, Luo, Yufei, Lopez, Marie, Seeleuthner, Yoann, Rapaport, Franck, Favier, Antoine, Stenson, Peter D., Cooper, David N., Patin, Etienne, Casanova, Jean-Laurent, Quintana-Murci, Lluis, Abel, Laurent

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Genome-wide association study of resistance to Mycobacterium tuberculosis infection identifies a locus at 10q26.2 in three distinct populations av Quistrebert, Jocelyn, Orlova, Marianna, Kerner, Gaspard, Ton, Le Thi, Luong, Nguyễn Trong, Danh, Nguyễn Thanh, Vincent, Quentin B., Jabot-Hanin, Fabienne, Seeleuthner, Yoann, Bustamante, Jacinta, Boisson-Dupuis, Stéphanie, Huong, Nguyen Thu, Ba, Nguyen Ngoc, Casanova, Jean-Laurent, Delacourt, Christophe, Hoal, Eileen G., Alcaïs, Alexandre, Thai, Vu Hong, Thành, Lai The, Abel, Laurent, Schurr, Erwin, Cobat, Aurélie

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Single-cell genomics of multiple uncultured stramenopiles reveals underestimated functional diversity across oceans av Seeleuthner, Yoann, Mondy, Samuel, Lombard, Vincent, Carradec, Quentin, Pelletier, Eric, Wessner, Marc, Leconte, Jade, Mangot, Jean-François, Poulain, Julie, Labadie, Karine, Logares, Ramiro, Sunagawa, Shinichi, de Berardinis, Véronique, Salanoubat, Marcel, Dimier, Céline, Kandels-Lewis, Stefanie, Picheral, Marc, Searson, Sarah, Pesant, Stephane, Poulton, Nicole, Stepanauskas, Ramunas, Bork, Peer, Bowler, Chris, Hingamp, Pascal, Sullivan, Matthew B., Iudicone, Daniele, Massana, Ramon, Aury, Jean-Marc, Henrissat, Bernard, Karsenti, Eric, Jaillon, Olivier, Sieracki, Mike, de Vargas, Colomban, Wincker, Patrick

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Inherited human IFN-γ deficiency underlies mycobacterial disease av Kerner, Gaspard, Rosain, Jérémie, Guérin, Antoine, Al-Khabaz, Ahmad, Oleaga-Quintas, Carmen, Rapaport, Franck, Massaad, Michel J., Ding, Jing-Ya, Khan, Taushif, Ali, Fatima Al, Rahman, Mahbuba, Deswarte, Caroline, Martinez-Barricarte, Rubén, Geha, Raif S., Jeanne-Julien, Valentine, Garcia, Diane, Chi, Chih-Yu, Yang, Rui, Roynard, Manon, Fleckenstein, Bernhard, Rozenberg, Flore, Boisson-Dupuis, Stéphanie, Ku, Cheng-Lung, Seeleuthner, Yoann, Béziat, Vivien, Marr, Nico, Abel, Laurent, Al-Herz, Waleed, Casanova, Jean-Laurent, Bustamante, Jacinta

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Herpes simplex encephalitis in a patient with a distinctive form of inherited IFNAR1 deficiency av Bastard, Paul, Manry, Jeremy, Chen, Jie, Rosain, Jérémie, Seeleuthner, Yoann, AbuZaitun, Omar, Lorenzo, Lazaro, Khan, Taushif, Hasek, Mary, Hernandez, Nicholas, Bigio, Benedetta, Zhang, Peng, Lévy, Romain, Shrot, Shai, Reino, Eduardo J. Garcia, Lee, Yoon-Seung, Boucherit, Soraya, Aubart, Mélodie, Gijsbers, Rik, Béziat, Vivien, Li, Zhi, Pellegrini, Sandra, Rozenberg, Flore, Marr, Nico, Meyts, Isabelle, Boisson, Bertrand, Cobat, Aurélie, Bustamante, Jacinta, Zhang, Qian, Jouangy, Emmanuelle, Abel, Laurent, Somech, Raz, Casanova, Jean-Laurent, Zhang, Shen-Ying

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A global ocean atlas of eukaryotic genes av Carradec, Quentin, Pelletier, Eric, Da Silva, Corinne, Alberti, Adriana, Seeleuthner, Yoann, Blanc-Mathieu, Romain, Lima-Mendez, Gipsi, Rocha, Fabio, Tirichine, Leila, Labadie, Karine, Kirilovsky, Amos, Bertrand, Alexis, Engelen, Stefan, Madoui, Mohammed-Amin, Méheust, Raphaël, Poulain, Julie, Romac, Sarah, Richter, Daniel J., Yoshikawa, Genki, Dimier, Céline, Kandels-Lewis, Stefanie, Picheral, Marc, Searson, Sarah, Jaillon, Olivier, Aury, Jean-Marc, Karsenti, Eric, Sullivan, Matthew B., Sunagawa, Shinichi, Bork, Peer, Not, Fabrice, Hingamp, Pascal, Raes, Jeroen, Guidi, Lionel, Ogata, Hiroyuki, de Vargas, Colomban, Iudicone, Daniele, Bowler, Chris, Wincker, Patrick

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Biochemically deleterious human NFKB1 variants underlie an autosomal dominant form of common variable immunodeficiency av Li, Juan, Lei, Wei-Te, Zhang, Peng, Rapaport, Franck, Seeleuthner, Yoann, Lyu, Bingnan, Asano, Takaki, Rosain, Jérémie, Hammadi, Boualem, Zhang, Yu, Pelham, Simon J., Spaan, András N., Migaud, Mélanie, Hum, David, Bigio, Benedetta, Chrabieh, Maya, Béziat, Vivien, Bustamante, Jacinta, Zhang, Shen-Ying, Jouanguy, Emmanuelle, Boisson-Dupuis, Stephanie, El Baghdadi, Jamila, Aimanianda, Vishukumar, Thoma, Katharina, Fliegauf, Manfred, Grimbacher, Bodo, Korganow, Anne-Sophie, Saunders, Carol, Rao, V. Koneti, Uzel, Gulbu, Freeman, Alexandra F., Holland, Steven M., Su, Helen C., Cunningham-Rundles, Charlotte, Fieschi, Claire, Abel, Laurent, Puel, Anne, Cobat, Aurélie, Casanova, Jean-Laurent, Zhang, Qian, Boisson, Bertrand

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Human T-bet governs innate and innate-like adaptive IFN-γ immunity against mycobacteria av Yang, Rui, Mele, Federico, Worley, Lisa, Langlais, David, Rosain, Jérémie, Benhsaien, Ibithal, Elarabi, Houda, Croft, Carys A., Doisne, Jean-Marc, Zhang, Peng, Weisshaar, Marc, Jarrossay, David, Latorre, Daniela, Shen, Yichao, Han, Jing, Ogishi, Masato, Gruber, Conor, Markle, Janet, Ali, Fatima Al, Rahman, Mahbuba, Khan, Taushif, Seeleuthner, Yoann, Kerner, Gaspard, Husquin, Lucas T., Maclsaac, Julia L., Jeljeli, Mohamed, Errami, Abderrahmane, Ailal, Fatima, Kobor, Michael S., Oleaga-Quintas, Carmen, Roynard, Manon, Bourgey, Mathieu, Baghdadi, Jamila El, Boisson-Dupuis, Stéphanie, Puel, Anne, Batteux, Fréderic, Rozenberg, Flore, Marr, Nico, Pan-Hammarström, Qiang, Bogunovic, Dusan, Quintana-Murci, Lluis, Carroll, Thomas, Ma, Cindy S, Abel, Laurent, Bousfiha, Aziz, Santo, James P. Di, Glimcher, Laurie H, Gros, Philippe, Tangye, Stuart G, Sallusto, Federica, Bustamante, Jacinta, Casanova, Jean-Laurent

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Auto-antibodies to type I IFNs can underlie adverse reactions to yellow fever live attenuated vaccine av Bastard, Paul, Michailidis, Eleftherios, Hoffmann, Hans-Heinrich, Chbihi, Marwa, Le Voyer, Tom, Rosain, Jérémie, Philippot, Quentin, Seeleuthner, Yoann, Gervais, Adrian, Materna, Marie, de Oliveira, Patricia Mouta Nunes, Maia, Maria de Lourdes S., Dinis Ano Bom, Ana Paula, Azamor, Tamiris, Araújo da Conceição, Deborah, Goudouris, Ekaterini, Homma, Akira, Slesak, Günther, Schäfer, Johannes, Pulendran, Bali, Miller, Joseph D., Huits, Ralph, Yang, Rui, Rosen, Lindsey B., Bizien, Lucy, Lorenzo, Lazaro, Chrabieh, Maya, Erazo, Lucia V., Rozenberg, Flore, Jeljeli, Mohamed Maxime, Béziat, Vivien, Holland, Steven M., Cobat, Aurélie, Notarangelo, Luigi D., Su, Helen C., Ahmed, Rafi, Puel, Anne, Zhang, Shen-Ying, Abel, Laurent, Seligman, Stephen J., Zhang, Qian, MacDonald, Margaret R., Jouanguy, Emmanuelle, Rice, Charles M., Casanova, Jean-Laurent

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Human IFN-γ immunity to mycobacteria is governed by both IL-12 and IL-23 av Markle, Janet G., Martĺnez-Barricarte, Rubén, Ma, Cindy S., Deenick, Elissa K., Ramírez-Alejo, Noé, Mele, Federico, Latorre, Daniela, Mahdaviani, Seyed Alireza, Aytekin, Caner, Mansouri, Davood, Bryant, Vanessa, Jabot-Hanin, Fabienne, Deswarte, Caroline, Nieto-Patlán, Alejandro, Surace, Laura, Kerner, Gaspard, Itan, Yuval, Jovic, Sandra, Avery, Danielle T., Wong, Natalie, Rao, Geetha, Patin, Etienne, Okada, Satoshi, Bigio, Benedetta, Boisson, Bertrand, Rapaport, Franck, Seeleuthner, Yoann, Schmidt, Monika, Ikinciogullari, Aydan, Dogu, Figen, Tanir, Gonul, Tabarsi, Payam, Bloursaz, Mohammed Reza, Joseph, Julia K., Heer, Avneet, Kong, Xiao-Fei, Migaud, Mélanie, Lazarov, Tomi, Geissmann, Frédéric, Fleckenstein, Bernhard, Arlehamn, Cecilia Lindestam, Sette, Alessandro, Puel, Anne, Emile, Jean-François, van de Vosse, Esther, Quintana-Murci, Lluis, Di Santo, James P., Abel, Laurent, Boisson-Dupuis, Stéphanie, Bustamante, Jacinta, Tangye, Stuart G., Sallusto, Federica, Casanova, Jean-Laurent

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Inherited IFNAR1 deficiency in otherwise healthy patients with adverse reaction to measles and yellow fever live vaccines av Hernandez, Nicholas, Bucciol, Giorgia, Moens, Leen, Le Pen, Jérémie, Shahrooei, Mohammad, Goudouris, Ekaterini, Shirkani, Afshin, Changi-Ashtiani, Majid, Rokni-Zadeh, Hassan, Sayar, Esra Hazar, Reisli, Ismail, Lefevre-Utile, Alain, Zijlmans, Dick, Jurado, Andrea, Pholien, Ruben, Drutman, Scott, Belkaya, Serkan, Cobat, Aurelie, Boudewijns, Robbert, Jochmans, Dirk, Neyts, Johan, Seeleuthner, Yoann, Lorenzo-Diaz, Lazaro, Enemchukwu, Chibuzo, Tietjen, Ian, Hoffmann, Hans-Heinrich, Momenilandi, Mana, Pöyhönen, Laura, Siqueira, Marilda M., de Lima, Sheila M. Barbosa, de Souza Matos, Denise C., Homma, Akira, Maia, Maria de Lourdes S., da Costa Barros, Tamiris Azamor, de Oliveira, Patricia Mouta Nunes, Mesquita, Emersom Ciclini, Gijsbers, Rik, Zhang, Shen-Ying, Seligman, Stephen J., Abel, Laurent, Hertzog, Paul, Marr, Nico, Martins, Reinaldo de Menezes, Meyts, Isabelle, Zhang, Qian, MacDonald, Margaret R., Rice, Charles M., Casanova, Jean-Laurent, Jouanguy, Emmanuelle, Bossuyt, Xavier

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Correction: Dominant-negative mutations in human IL6ST underlie hyper-IgE syndrome av Béziat, Vivien, Tavernier, Simon J., Chen, Yin-Huai, Ma, Cindy S., Materna, Marie, Laurence, Arian, Staal, Jens, Aschenbrenner, Dominik, Roels, Lisa, Worley, Lisa, Claes, Kathleen, Gartner, Lisa, Kohn, Lisa A., De Bruyne, Marieke, Schmitz-Abe, Klaus, Charbonnier, Louis-Marie, Keles, Sevgi, Nammour, Justine, Vladikine, Natasha, Luxman Maglorius Renkilaraj, Majistor Raj, Seeleuthner, Yoann, Migaud, Mélanie, Rosain, Jérémie, Jeljeli, Mohamed, Boisson, Bertrand, Van Braeckel, Eva, Rosenfeld, Jill A., Dai, Hongzheng, Burrage, Lindsay C., Murdock, David R., Lambrecht, Bart N., Avettand-Fenoel, Véronique, Vogel, Tiphanie P., Network, Undiagnosed Diseases, Esther, Charles R., Haskologlu, Sule, Dogu, Figen, Ciznar, Peter, Boutboul, David, Ouachée-Chardin, Marie, Amourette, Jean, Lebras, Marie-Noëlle, Gauvain, Clément, Tcherakian, Colas, Ikinciogullari, Aydan, Beyaert, Rudi, Abel, Laurent, Milner, Joshua D., Grimbacher, Bodo, Couderc, Louis-Jean, Butte, Manish J., Freeman, Alexandra F., Catherinot, Émilie, Fieschi, Claire, Chatila, Talal A., Tangye, Stuart G., Uhlig, Holm H., Haerynck, Filomeen, Casanova, Jean-Laurent, Puel, Anne

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Dominant-negative mutations in human IL6ST underlie hyper-IgE syndrome av Béziat, Vivien, Tavernier, Simon J., Chen, Yin-Huai, Ma, Cindy S., Materna, Marie, Laurence, Arian, Staal, Jens, Aschenbrenner, Dominik, Roels, Lisa, Worley, Lisa, Claes, Kathleen, Gartner, Lisa, Kohn, Lisa A., De Bruyne, Marieke, Schmitz-Abe, Klaus, Charbonnier, Louis-Marie, Keles, Sevgi, Nammour, Justine, Vladikine, Natasha, Maglorius Renkilaraj, Majistor Raj Luxman, Seeleuthner, Yoann, Migaud, Mélanie, Rosain, Jérémie, Jeljeli, Mohamed, Boisson, Bertrand, Van Braeckel, Eva, Rosenfeld, Jill A., Dai, Hongzheng, Burrage, Lindsay C., Murdock, David R., Lambrecht, Bart N., Avettand-Fenoel, Véronique, Vogel, Tiphanie P., Esther, Charles R., Haskologlu, Sule, Dogu, Figen, Ciznar, Peter, Boutboul, David, Ouachée-Chardin, Marie, Amourette, Jean, Lebras, Marie-Noëlle, Gauvain, Clément, Tcherakian, Colas, Ikinciogullari, Aydan, Beyaert, Rudi, Abel, Laurent, Milner, Joshua D., Grimbacher, Bodo, Couderc, Louis-Jean, Butte, Manish J., Freeman, Alexandra F., Catherinot, Émilie, Fieschi, Claire, Chatila, Talal A., Tangye, Stuart G., Uhlig, Holm H., Haerynck, Filomeen, Casanova, Jean-Laurent, Puel, Anne

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A loss-of-function IFNAR1 allele in Polynesia underlies severe viral diseases in homozygotes av Bastard, Paul, Hsiao, Kuang-Chih, Zhang, Qian, Choin, Jeremy, Best, Emma, Chen, Jie, Gervais, Adrian, Bizien, Lucy, Materna, Marie, Harmant, Christine, Roux, Maguelonne, Hawley, Nicola L., Weeks, Daniel E., McGarvey, Stephen T., Sandoval, Karla, Barberena-Jonas, Carmina, Quinto-Cortés, Consuelo D., Hagelberg, Erika, Mentzer, Alexander J., Robson, Kathryn, Coulibaly, Boubacar, Seeleuthner, Yoann, Bigio, Benedetta, Li, Zhi, Uzé, Gilles, Pellegrini, Sandra, Lorenzo, Lazaro, Sbihi, Zineb, Latour, Sylvain, Besnard, Marianne, Adam de Beaumais, Tiphaine, Jacqz Aigrain, Evelyne, Béziat, Vivien, Deka, Ranjan, Esera Tulifau, Litara, Viali, Satupa‘itea, Reupena, Muagututi‘a Sefuiva, Naseri, Take, McNaughton, Peter, Sarkozy, Vanessa, Peake, Jane, Blincoe, Annaliesse, Primhak, Sarah, Stables, Simon, Gibson, Kate, Woon, See-Tarn, Drake, Kylie Marie, Hill, Adrian V.S., Chan, Cheng-Yee, King, Richard, Ameratunga, Rohan, Teiti, Iotefa, Aubry, Maite, Cao-Lormeau, Van-Mai, Tangye, Stuart G., Zhang, Shen-Ying, Jouanguy, Emmanuelle, Gray, Paul, Abel, Laurent, Moreno-Estrada, Andrés, Minster, Ryan L., Quintana-Murci, Lluis, Wood, Andrew C., Casanova, Jean-Laurent

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