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Avery, Danielle T., Deenick, Elissa K., Ma, Cindy S., Suryani, Santi, Simpson, Nicholas, Chew, Gary Y., Chan, Tyani D., Palendira, Umamainthan, Bustamante, Jacinta, Boisson-Dupuis, Stephanie, Choo, Sharon, Bleasel, Karl E., Peake, Jane, King, Cecile, French, Martyn A., Engelhard, Dan, Al-Hajjar, Sami, Al-Muhsen, Saleh, Magdorf, Klaus, Roesler, Joachim, Arkwright, Peter D., Hissaria, Pravin, Riminton, D. Sean, Wong, Melanie, Brink, Robert, Fulcher, David A., Casanova, Jean Laurent, Cook, Mathew C. and Tangye, Stuart G. (2010) B cell-intrinsic signaling through IL-21 receptor and STAT3 is required for establishing long-lived antibody responses in humans. Journal of Experimental Medicine, 207 1: 155-171. doi:10.1084/jem.20091706 92   113 Cited 119 times in Scopus119 1
Ma, Cindy S., Avery, Danielle T., Chan, Anna, Batten, Marcel, Bustamante, Jacinta, Boisson-Dupuis, Stephanie, Arkwright, Peter D., Kreins, Alexandra Y., Averbuch, Diana, Engelhard, Dan, Magdorf, Klaus, Kilic, Sara S., Minegishi, Yoshiyuki, Nonoyama, Shigeaki, French, Martyn A., Choo, Sharon, Smart, Joanne M., Peake, Jane, Wong, Melanie, Gray, Paul, Cook, Matthew C., Fulcher, David A., Casanova, Jean-Laurent, Deenick, Elissa K. and Tangye, Stuart G. (2012) Functional STAT3 deficiency compromises the generation of human T follicular helper cells. Blood, 119 17: 3997-4008. doi:10.1182/blood-2011-11-392985 67   66 Cited 63 times in Scopus63 0
Bolze, Alexandre, Byun, Minji, McDonald, David, Morgan, Neil V., Abhyankar, Avinash, Premkumar, Lakshmanane, Puel, Anne, Bacon, Chris M., Rieuz-Laucat, Frédéric, Pang, Ki, Britland, Alison, Abel, Laurent, Cant, Andrew, Maher, Eamonn R., Riedl. Stefan J., Hambleton, Sophie and Casanova, Jean-Laurent (2010) Whole-exome-sequencing-based discovery of human FADD deficiency. American Journal of Human Genetics, 87 6: 873-881. doi:10.1016/j.ajhg.2010.10.028 64   69 Cited 75 times in Scopus75 2
Wildin, Robert S., Ramsdell, Fred, Peake, Jane, Faravelli, Francesca, Casanova, Jean-Laurent, Buist, Neil, Levy-Lahad, Ephrat, Mazzella, Massimo, Goulet, Olivier, Perroni, Lucia, Bricarelli, Franca Dagna, Byrne, Geoffrey, McEuen, Mark, Proll, Sean, Appleby, Mark and Brunkow, Mary E. (2001) X-linked neonatal diabetes mellitus, enteropathy and endocrinopathy syndrome is the human equivalent of mouse scurfy. Nature Genetics, 27 1: 18-20. doi:10.1038/83707 150   874 Cited 956 times in Scopus956 3