Human Genome Epidemiology Literature Finder
Records 1 - 7 (of 7 Records) |
Query Trace: SEMA6D[original query] |
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Novel genetic susceptibility loci for diabetic end-stage renal disease identified through robust naive Bayes classification. Diabetologia 2014 Aug 57 (8): 1611-22. Sambo Francesco, Malovini Alberto, Sandholm Niina, Stavarachi Monica, Forsblom Carol, Mäkinen Ville-Petteri, Harjutsalo Valma, Lithovius Raija, Gordin Daniel, Parkkonen Maija, Saraheimo Markku, Thorn Lena M, Tolonen Nina, Wadén Johan, He Bing, Osterholm Anne-May, Tuomilehto Jaako, Lajer Maria, Salem Rany M, McKnight Amy Jayne, , Tarnow Lise, Panduru Nicolae M, Barbarini Nicola, Di Camillo Barbara, Toffolo Gianna M, Tryggvason Karl, Bellazzi Riccardo, Cobelli Claudio, , Groop Per-Henr |
Identification of novel risk loci for restless legs syndrome in genome-wide association studies in individuals of European ancestry: a meta-analysis.
The Lancet. Neurology 2017 Nov 16 (11): 898-907. Schormair Barbara, Zhao Chen, Bell Steven, Tilch Erik, Salminen Aaro V, Pütz Benno, Dauvilliers Yves, Stefani Ambra, Högl Birgit, Poewe Werner, Kemlink David, Sonka Karel, Bachmann Cornelius G, Paulus Walter, Trenkwalder Claudia, Oertel Wolfgang H, Hornyak Magdolna, Teder-Laving Maris, Metspalu Andres, Hadjigeorgiou Georgios M, Polo Olli, Fietze Ingo, Ross Owen A, Wszolek Zbigniew, Butterworth Adam S, Soranzo Nicole, Ouwehand Willem H, Roberts David J, Danesh John, Allen Richard P, Earley Christopher J, Ondo William G, Xiong Lan, Montplaisir Jacques, Gan-Or Ziv, Perola Markus, Vodicka Pavel, Dina Christian, Franke Andre, Tittmann Lukas, Stewart Alexandre F R, Shah Svati H, Gieger Christian, Peters Annette, Rouleau Guy A, Berger Klaus, Oexle Konrad, Di Angelantonio Emanuele, Hinds David A, Müller-Myhsok Bertram, Winkelmann Juliane, , |
Somatic mutations in early onset luminal breast cancer. Oncotarget 2018 Apr 9 (32): 22460-22479. Encinas Giselly, Sabelnykova Veronica Y, de Lyra Eduardo Carneiro, Hirata Katayama Maria Lucia, Maistro Simone, de Vasconcellos Valle Pedro Wilson Mompean, de Lima Pereira Gláucia Fernanda, Rodrigues Lívia Munhoz, de Menezes Pacheco Serio Pedro Adolpho, de Gouvêa Ana Carolina Ribeiro Chaves, Geyer Felipe Correa, Basso Ricardo Alves, Pasini Fátima Solange, Del Pilar Esteves Diz Maria, Brentani Maria Mitzi, Guedes Sampaio Góes João Carlos, Chammas Roger, Boutros Paul C, Koike Folgueira Maria Aparecida Azeve |
Identification of an Immune-Related Risk Signature Correlates With Immunophenotype and Predicts Anti-PD-L1 Efficacy of Urothelial Cancer. Frontiers in cell and developmental biology 2021 4 9 646982. Li Pengju, Hao Shihui, Ye Yongkang, Wei Jinhuan, Tang Yiming, Tan Lei, Liao Zhuangyao, Zhang Mingxiao, Li Jiaying, Gui Chengpeng, Xiao Jiefei, Huang Yong, Chen Xu, Cao Jiazheng, Luo Junhang, Chen W |
COVID-19 in pediatrics: Genetic susceptibility.
Frontiers in genetics 2022 9 13 928466. Glessner Joseph T, Chang Xiao, Mentch Frank, Qu Huiqi, Abrams Debra J, Thomas Alexandria, Sleiman Patrick M A, Hakonarson Hak |
Genetic insights into smoking behaviours in 10,558 men of African ancestry from continental Africa and the UK.
Scientific reports 2022 11 12 (1): 18828. Piga Noemi-Nicole, Boua Palwende Romuald, Soremekun Chisom, Shrine Nick, Coley Kayesha, Brandenburg Jean-Tristan, Tobin Martin D, Ramsay Michèle, Fatumo Segun, Choudhury Ananyo, Batini Chia |
Genome-wide association analysis reveals the associations of NPHP4, TYW1-AUTS2 and SEMA6D for Behçet's disease and HLA-B*46:01 for its intestinal involvement. Digestive and liver disease : official journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver 2023 11 . Eun Suk Jung, David Ellinghaus, Frauke Degenhardt, Akira Meguro, Seik-Soon Khor, Sören Mucha, Mareike Wendorff, Simonas Juzenas, Nobuhisa Mizuki, Katsushi Tokunaga, Seung Won Kim, Min Goo Lee, Stefan Schreiber, Won Ho Kim, Andre Franke, Jae Hee Che |
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