Identification of novel risk loci and causal insights for sporadic Creutzfeldt-Jakob disease: a genome-wide association study
散发性克雅氏病新风险位点的鉴定及致病机制的阐明：一项全基因组关联研究
期刊:Lancet Neurology
影响因子:45.5
doi:10.1016/S1474-4422(20)30273-8
Jones, Emma; Hummerich, Holger; Viré, Emmanuelle; Uphill, James; Dimitriadis, Athanasios; Speedy, Helen; Campbell, Tracy; Norsworthy, Penny; Quinn, Liam; Whitfield, Jerome; Linehan, Jacqueline; Jaunmuktane, Zane; Brandner, Sebastian; Jat, Parmjit; Nihat, Akin; How Mok, Tze; Ahmed, Parvin; Collins, Steven; Stehmann, Christiane; Sarros, Shannon; Kovacs, Gabor G; Geschwind, Michael D; Golubjatnikov, Aili; Frontzek, Karl; Budka, Herbert; Aguzzi, Adriano; Karamujić-Čomić, Hata; van der Lee, Sven J; Ibrahim-Verbaas, Carla A; van Duijn, Cornelia M; Sikorska, Beata; Golanska, Ewa; Liberski, Pawel P; Calero, Miguel; Calero, Olga; Sanchez-Juan, Pascual; Salas, Antonio; Martinón-Torres, Federico; Bouaziz-Amar, Elodie; Haïk, Stéphane; Laplanche, Jean-Louis; Brandel, Jean-Phillipe; Amouyel, Phillipe; Lambert, Jean-Charles; Parchi, Piero; Bartoletti-Stella, Anna; Capellari, Sabina; Poleggi, Anna; Ladogana, Anna; Pocchiari, Maurizio; Aneli, Serena; Matullo, Giuseppe; Knight, Richard; Zafar, Saima; Zerr, Inga; Booth, Stephanie; Coulthart, Michael B; Jansen, Gerard H; Glisic, Katie; Blevins, Janis; Gambetti, Pierluigi; Safar, Jiri; Appleby, Brian; Collinge, John; Mead, Simon
