Not logged in Human SNORA31 variations impair cortical neuron-intrinsic immunity to HSV-1 and underlie herpes simplex encephalitis Lafaille, Fabien G.; Harschnitz, Oliver; Lee, Yoon Seung; Zhang, Peng; Hasek, Mary L.; Kerner, Gaspard; Itan, Yuval; Ewaleifoh, Osefame; Rapaport, Franck; Carlile, Thomas M.; Carter-Timofte, Madalina E.; Paquet, Dominik; Dobbs, Kerry; Zimmer, Bastian; Gao, Daxing; Rojas-Duran, Maria F.; Kwart, Dylan; Rattina, Vimel; Ciancanelli, Michael J.; McAlpine, Jessica L.; Lorenzo, Lazaro; Boucherit, Soraya; Rozenberg, Flore; Halwani, Rabih; Henry, Benoit; Amenzoui, Naima; Alsum, Zobaida; Marques, Laura; Church, Joseph A.; Al-Muhsen, Saleh; Tardieu, Marc; Bousfiha, Ahmed Aziz; Paludan, Soren R.; Mogensen, Trine Hyrup; Quintana-Murci, Lluis; Tessier-Lavigne, Marc; Smith, Gregory A.; Notarangelo, Luigi D.; Studer, Lorenz; Gilbert, Wendy; Abel, Laurent; Casanova, Jean-Laurent; Zhang, Shen-Ying Share Save
Development and evaluation of a genome-wide Coffee 8.5K SNP array and its application for high-density genetic mapping and for investigating the origin of Coffea arabica L. Merot-L'anthoene, Virginie; Tournebize, Remi; Darracq, Olivier; Rattina, Vimel; Lepelley, Maud; Bellanger, Laurence; Tranchant-Dubreuil, Christine; Coulee, Manon; Pegard, Marie; Metairon, Sylviane; Fournier, Coralie; Stoffelen, Piet; Janssens, Steven B.; Kiwuka, Catherine; Musoli, Pascal; Sumirat, Ucu; Legnate, Hyacinthe; Kambale, Jean-Leon; da Costa Neto, Joao Ferreira; Revel, Clara; de Kochko, Alexandre; Descombes, Patrick; Crouzillat, Dominique; Poncet, Valerie Share Save
Life-threatening influenza pneumonitis in a child with inherited IRF9 deficiency Hernandez, Nicholas; Melki, Isabelle; Jing, Huie; Habib, Tanwir; Huang, Susie S. Y.; Danielson, Jeffrey; Kula, Tomasz; Drutman, Scott; Belkaya, Serkan; Rattina, Vimel; Lorenzo-Diaz, Lazaro; Boulai, Anais; Rose, Yoann; Kitabayashi, Naoki; Rodero, Mathieu P.; Dumaine, Cecile; Blanche, Stephane; Lebras, Marie-Noelle; Leung, Man Chun; Mathew, Lisa Sara; Boisson, Bertrand; Zhang, Shen-Ying; Boisson-Dupuis, Stephanie; Giliani, Silvia; Chaussabel, Damien; Notarangelo, Luigi D.; Elledge, Stephen J.; Ciancanelli, Michael J.; Abel, Laurent; Zhang, Qian; Marr, Nico; Crow, Yanick J.; Su, Helen C.; Casanova, Jean-Laurent Share Save
Inherited p40phox deficiency differs from classic chronic granulomatous disease van de Geer, Annemarie; Nieto-Patlan, Alejandro; Kuhns, Douglas B.; Tool, Anton T. J.; Arias, Andres A.; Bouaziz, Matthieu; de Boer, Martin; Luis Franco, Jose; Gazendam, Roel P.; van Hamme, John L.; van Houdt, Michel; van Leeuwen, Karin; Verkuijlen, Paul J. H.; van den Berg, Timo K.; Alzate, Juan F.; Arango-Franco, Carlos A.; Batura, Vritika; Bernasconi, Andrea R.; Boardman, Barbara; Booth, Claire; Burns, Siobhan O.; Cabarcas, Felipe; Bensussan, Nadine Cerf; Charbit-Henrion, Fabienne; Corveleyn, Anniek; Deswarte, Caroline; Esnaola Azcoiti, Maria; Foell, Dirk; Gallin, John I.; Garces, Carlos; Guedes, Margarida; Hinze, Claas H.; Holland, Steven M.; Hughes, Stephen M.; Ibanez, Patricio; Malech, Harry L.; Meyts, Isabelle; Moncada-Velez, Marcela; Moriya, Kunihiko; Neves, Esmeralda; Oleastro, Matias; Perez, Laura; Rattina, Vimel; Oleaga-Quintas, Carmen; Warner, Neil; Muise, Aleixo M.; Serafin Lopez, Jeanet; Trindade, Eunice; Vasconcelos, Julia; Vermeire, Severine; Wittkowski, Helmut; Worth, Austen; Abel, Laurent; Dinauer, Mary C.; Arkwright, Peter D.; Roos, Dirk; Casanova, Jean-Laurent; Kuijpers, Taco W.; Bustamante, Jacinta Share Save
A recessive form of hyper-IgE syndrome by disruption of ZNF341-dependent STAT3 transcription and activity Beziat, Vivien; Li, Juan; Lin, Jian-Xin; Ma, Cindy S.; Li, Peng; Bousfiha, Aziz; Pellier, Isabelle; Zoghi, Samaneh; Baris, Safa; Keles, Sevgi; Gray, Paul; Du, Ning; Wang, Yi; Zerbib, Yoann; Levy, Romain; Leclercq, Thibaut; About, Fredegonde; Lim, Ai Ing; Rao, Geetha; Payne, Kathryn; Pelham, Simon J.; Avery, Danielle T.; Deenick, Elissa K.; Pillay, Bethany; Chou, Janet; Guery, Romain; Belkadi, Aziz; Guerin, Antoine; Migaud, Melanie; Rattina, Vimel; Ailal, Fatima; Benhsaien, Ibtihal; Bouaziz, Matthieu; Habib, Tanwir; Chaussabel, Damien; Marr, Nico; El-Benna, Jamel; Grimbacher, Bodo; Wargon, Orli; Bustamante, Jacinta; Boisson, Bertrand; Mueller-Fleckenstein, Ingrid; Fleckenstein, Bernhard; Chandesris, Marie-Olivia; Titeux, Matthias; Fraitag, Sylvie; Alyanakian, Marie-Alexandra; Leruez-Ville, Marianne; Picard, Capucine; Meyts, Isabelle; Di Santo, James P.; Hovnanian, Alain; Somer, Ayper; Ozen, Ahmet; Rezaei, Nima; Chatila, Talal A.; Abel, Laurent; Leonard, Warren J.; Tangye, Stuart G.; Puel, Anne; Casanova, Jean-Laurent Share Save
Mendelian Susceptibility to Mycobacterial Disease Caused by a Novel Founder IL12B Mutation in Saudi Arabia Alodayani, Abdulrahman N.; Al-Otaibi, Abdulnasir M.; Deswarte, Caroline; Frayha, Husn Habib; Bouaziz, Matthieu; AlHelale, Maryam; Le Voyer, Tom; Nieto-Patlan, Alejandro; Rattina, Vimel; AlZahrani, Mofareh; Halwani, Rabih; Al Sohime, Fahad; Al-Mousa, Hamoud; Al-Muhsen, Saleh; Alhajjar, Sami H.; Dhayhi, Nabil S.; Abel, Laurent; Casanova, Jean-Laurent; Bin-Hussain, Ibrahim; AlBarrak, May S.; Al-Jumaah, Suliman A.; Bustamante, Jacinta Share Save
IRF4 haploinsufficiency in a family with Whipple's disease Guerin, Antoine; Kerner, Gaspard; Marr, Nico; Markle, Janet G.; Fenollar, Florence; Wong, Natalie; Boughorbel, Sabri; Avery, Danielle T.; Ma, Cindy S.; Bougarn, Salim; Bouaziz, Matthieu; Beziat, Vivien; Della Mina, Erika; Oleaga-Quintas, Carmen; Lazarov, Tomi; Worley, Lisa; Tina Nguyen; Patin, Etienne; Deswarte, Caroline; Martinez-Barricarte, Ruben; Boucherit, Soraya; Ayral, Xavier; Edouard, Sophie; Boisson-Dupuis, Stephanie; Rattina, Vimel; Bigio, Benedetta; Vogt, Guillaume; Geissmann, Frederic; Quintana-Murci, Lluis; Chaussabel, Damien; Tangye, Stuart G.; Raoult, Didier; Abel, Laurent; Bustamante, Jacinta; Casanova, Jean-Laurent Share Save
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