Genetic and Clinical Characteristics of Patients in the Middle East With Multisystem Inflammatory Syndrome in Children.
Jama Network Open
Abuhammour, Walid W; Yavuz, Lemis L; Jain, Ruchi R; Abu Hammour, Khawla K; Al-Hammouri, Ghalia F GF; El Naofal, Maha M; Halabi, Nour N; Yaslam, Sawsan S; Ramaswamy, Sathishkumar S; Taylor, Alan A; Wafadari, Deena D; Alsarhan, Ali A; Khansaheb, Hamda H; Deesi, Zulfa Omar ZO; Varghese, Rupa Murthy RM; Uddin, Mohammed M; Al Suwaidi, Hanan H; Al-Hammadi, Suleiman S; Alkhaja, Abdulmajeed A; AlDabal, Laila Mohamed LM; Loney, Tom T; Nowotny, Norbert N; Al Khayat, Abdulla A; Alsheikh-Ali, Alawi A; Abou Tayoun, Ahmad A
Publication Date: 2022-05-02
Variant appearance in text: IFNL2: 562C>T; Arg188Ter
Genomic and Transcriptomic Characterization Links Cell Lines with Aggressive Head and Neck Cancers.
Cell Reports
Cheng, Hui H; Yang, Xinping X; Si, Han H; Saleh, Anthony D AD; Xiao, Wenming W; Coupar, Jamie J; Gollin, Susanne M SM; Ferris, Robert L RL; Issaeva, Natalia N; Yarbrough, Wendell G WG; Prince, Mark E ME; Carey, Thomas E TE; Van Waes, Carter C; Chen, Zhong Z
Publication Date: 2018-10-30
Variant appearance in text: IFNL2: R188X; rs200581777
A Landscape of Pharmacogenomic Interactions in Cancer.
Cell
Iorio, Francesco F; Knijnenburg, Theo A TA; Vis, Daniel J DJ; Bignell, Graham R GR; Menden, Michael P MP; Schubert, Michael M; Aben, Nanne N; Gonçalves, Emanuel E; Barthorpe, Syd S; Lightfoot, Howard H; Cokelaer, Thomas T; Greninger, Patricia P; van Dyk, Ewald E; Chang, Han H; de Silva, Heshani H; Heyn, Holger H; Deng, Xianming X; Egan, Regina K RK; Liu, Qingsong Q; Mironenko, Tatiana T; Mitropoulos, Xeni X; Richardson, Laura L; Wang, Jinhua J; Zhang, Tinghu T; Moran, Sebastian S; Sayols, Sergi S; Soleimani, Maryam M; Tamborero, David D; Lopez-Bigas, Nuria N; Ross-Macdonald, Petra P; Esteller, Manel M; Gray, Nathanael S NS; Haber, Daniel A DA; Stratton, Michael R MR; Benes, Cyril H CH; Wessels, Lodewyk F A LFA; Saez-Rodriguez, Julio J; McDermott, Ultan U; Garnett, Mathew J MJ
Using exome sequencing to reveal mutations in TREM2 presenting as a frontotemporal dementia-like syndrome without bone involvement.
Jama Neurology
Guerreiro, Rita João RJ; Lohmann, Ebba E; Brás, José Miguel JM; Gibbs, Jesse Raphael JR; Rohrer, Jonathan D JD; Gurunlian, Nicole N; Dursun, Burcu B; Bilgic, Basar B; Hanagasi, Hasmet H; Gurvit, Hakan H; Emre, Murat M; Singleton, Andrew A; Hardy, John J