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Publications by Orange, Jordan S.

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Number of items: 3.

Journal article

Hagl, Beate; Spielberger, Benedikt D.; Thoene, Silvia; Bonnal, Sophie; Mertes, Christian; Winter, Christof; Nijman, Isaac J.; Verduin, Shira; Eberherr, Andreas C.; Puel, Anne; Schindler, Detlev; Ruland, Jürgen; Meitinger, Thomas; Gagneur, Julien; Orange, Jordan S.; Gijn, Marielle E. van; Renner, Ellen D. (2018): Somatic alterations compromised molecular diagnosis of DOCK8 hyper-IgE syndrome caused by a novel intronic splice site mutation. In: Scientific Reports, Vol. 8, 16719 [PDF, 3MB]

Netter, Petra; Chan, Sanny K.; Banerjee, Pinaki P.; Monaco-Shawver, Linda; Noroski, Lenora M.; Hanson, Imelda C.; Forbes, Lisa R.; Mace, Emily M.; Chinen, Javier; Gaspar, H. Bobby; Sleiman, Patrick; Hakonarson, Hakon; Klein, Christoph; Ehlayel, Mohammad S.; Orange, Jordan S. (2016): A novel Rab27a mutation binds melanophilin, but not Munc13-4, causing immunodeficiency without albinism. In: Journal of Allergy and Clinical Immunology, Vol. 138, No. 2: pp. 599-601

Li, Jin; Jørgensen, Silje F.; Maggadottir, S. Melkorka; Bakay, Marina; Warnatz, Klaus; Glessner, Joseph; Pandey, Rahul; Salzer, Ulrich; Schmidt, Reinhold E.; Perez, Elena; Resnick, Elena; Goldacker, Sigune; Buchta, Mary; Witte, Torsten; Padyukov, Leonid; Videm, Vibeke; Folseraas, Trine; Atschekzei, Faranaz; Elder, James T.; Nair, Rajan P.; Winkelmann, Juliane; Gieger, Christian; Nöthen, Markus M.; Büning, Carsten; Brand, Stephan; Sullivan, Kathleen E.; Orange, Jordan S.; Fevang, Børre; Schreiber, Stefan; Lieb, Wolfgang; Aukrust, Pål; Chapel, Helen; Cunningham-Rundles, Charlotte; Franke, Andre; Karlsen, Tom H.; Grimbacher, Bodo; Hakonarson, Hakon; Hammarström, Lennart; Ellinghaus, Eva (2015): Association of CLEC16A with human common variable immunodeficiency disorder and role in murine B cells. In: Nature Communications, Vol. 6, 6804 [PDF, 807kB]

This list was generated on Tue Oct 26 02:44:51 2021 CEST.