Human Genome Epidemiology Literature Finder
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Records 1 - 14 (of 14 Records) |
| Query Trace: Multiple Sclerosis and TYK2[original query] |
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Genome-wide association study identifies new multiple sclerosis susceptibility loci on chromosomes 12 and 20.
Nature genetics 2009 Jul 41 (7): 824-8. Authors are not available |
| Replication analysis identifies TYK2 as a multiple sclerosis susceptibility factor. European journal of human genetics : EJHG 2009 Oct 17 (10): 1309-13. Ban Maria, Goris An, Lorentzen Aslaug R, Baker Amie, Mihalova Tania, Ingram Gillian, Booth David R, Heard Robert N, Stewart Graeme J, Bogaert Elke, Dubois Bénédicte, Harbo Hanne F, Celius Elisabeth G, Spurkland Anne, Strange Richard, Hawkins Clive, Robertson Neil P, Dudbridge Frank, Wason James, De Jager Philip L, Hafler David, Rioux John D, Ivinson Adrian J, McCauley Jacob L, Pericak-Vance Margaret, Oksenberg Jorge R, Hauser Stephen L, Sexton David, Haines Jonathan, Sawcer Stephen, , Compston Alasta |
| The imprinted DLK1-MEG3 gene region on chromosome 14q32.2 alters susceptibility to type 1 diabetes.
Nature genetics 2010 Jan 42 (1): 68-71. Wallace Chris, Smyth Deborah J, Maisuria-Armer Meeta, Walker Neil M, Todd John A, Clayton David |
| A rare variant of the TYK2 gene is confirmed to be associated with multiple sclerosis. European journal of human genetics : EJHG 2010 Apr 18 (4): 502-4. Mero Inger-Lise, Lorentzen Aslaug R, Ban Maria, Smestad Cathrine, Celius Elisabeth G, Aarseth Jan H, Myhr Kjell-Morten, Link Jenny, Hillert Jan, Olsson Tomas, Kockum Ingrid, Masterman Thomas, Oturai Annette Bang, Søndergaard Helle Bach, Sellebjerg Finn, Saarela Janna, Kemppinen Anu, Elovaara Irina, Spurkland Anne, Dudbridge Frank, Lie Benedicte A, Harbo Hanne |
| Multiple sclerosis susceptibility alleles in African Americans. Genes and immunity 2010 Jun 11 (4): 343-50. Johnson B A, Wang J, Taylor E M, Caillier S J, Herbert J, Khan O A, Cross A H, De Jager P L, Gourraud P-A F, Cree B C A, Hauser S L, Oksenberg J |
| Tyrosine kinase 2 variant influences T lymphocyte polarization and multiple sclerosis susceptibility. Brain : a journal of neurology 2011 Mar 134 (Pt 3): 693-703. Couturier Nicolas, Bucciarelli Florence, Nurtdinov Ramil N, Debouverie Marc, Lebrun-Frenay Christine, Defer Gilles, Moreau Thibault, Confavreux Christian, Vukusic Sandra, Cournu-Rebeix Isabelle, Goertsches Robert H, Zettl Uwe K, Comabella Manuel, Montalban Xavier, Rieckmann Peter, Weber Frank, Müller-Myhsok Bertram, Edan Gilles, Fontaine Bertrand, Mars Lennart T, Saoudi Abdelhadi, Oksenberg Jorge R, Clanet Michel, Liblau Roland S, Brassat Dav |
| Exome sequencing identifies a novel multiple sclerosis susceptibility variant in the TYK2 gene. Neurology 2012 Jul 79 (5): 406-11. Dyment David A, Cader M Zameel, Chao Michael J, Lincoln Matthew R, Morrison Katie M, Disanto Giulio, Morahan Julia M, De Luca Gabriele C, Sadovnick A Dessa, Lepage Pierre, Montpetit Alexandre, Ebers George C, Ramagopalan Sreeram |
| The influence of non-HLA gene polymorphisms and interactions on disease risk in a Western Australian multiple sclerosis cohort. Journal of neuroimmunology 2013 Aug 261 (1-2): 92-7. Qiu Wei, Pham Kym, James Ian, Nolan David, Castley Allison, Christiansen Frank T, Czarniak Petra, Luo Yuebei, Wu Jingshan, Garlepp Michael, Wilton Steve, Carroll William M, Mastaglia Frank L, Kermode Allan |
| Multiple sclerosis risk loci correlate with cervical cord atrophy and may explain the course of disability. Neurogenetics 2015 Jul 16 (3): 161-8. Akkad Denis A, Bellenberg Barbara, Esser Sarika, Weiler Florian, Epplen Jörg T, Gold Ralf, Lukas Carsten, Haghikia Aid |
| A survey of endogenous retrovirus (ERV) sequences in the vicinity of multiple sclerosis (MS)-associated single nucleotide polymorphisms (SNPs). Molecular biology reports 2016 May . Brütting Christine, Emmer Alexander, Kornhuber Malte, Staege Martin |
| Fourteen sequence variants that associate with multiple sclerosis discovered by meta-analysis informed by genetic correlations. NPJ genomic medicine 2017 2 24. Olafsson Sigurgeir, Stridh Pernilla, Bos Steffan Daniël, Ingason Andres, Euesden Jack, Sulem Patrick, Thorleifsson Gudmar, Gustafsson Omar, Johannesson Ari, Geirsson Arni J, Thorsson Arni V, Sigurgeirsson Bardur, Ludviksson Bjorn Runar, Olafsson Elias, Kristjansdottir Helga, Jonasson Jon G, Olafsson Jon Hjaltalin, Orvar Kjartan B, Benediktsson Rafn, Bjarnason Ragnar, Kristjansdottir Sjofn, Gislason Thorarinn, Valdimarsson Trausti, Mikaelsdottir Evgenia, Sigurdsson Snaevar, Jonsson Stefan, Rafnar Thorunn, Aarsland Dag, Djurovic Srdjan, Fladby Tormod, Knudsen Gun Peggy, Celius Elisabeth G, Myhr Kjell-Morten, Grondal Gerdur, Steinsson Kristjan, Valdimarsson Helgi, Bjornsson Sigurdur, Bjornsdottir Unnur S, Bjornsson Einar S, Nilsson Bjorn, Andreassen Ole A, Alfredsson Lars, Hillert Jan, Kockum Ingrid Skelton, Masson Gisli, Thorsteinsdottir Unnur, Gudbjartsson Daniel F, Stefansson Hreinn, Hjaltason Haukur, Harbo Hanne F, Olsson Tomas, Jonsdottir Ingileif, Stefansson Ka |
| Pharmacogenetics of glatiramer acetate therapy for multiple sclerosis: the impact of genome-wide association studies identified disease risk loci. Pharmacogenomics 2017 Nov . Kulakova Olga, Bashinskaya Vitalina, Kiselev Ivan, Baulina Natalia, Tsareva Ekaterina, Nikolaev Ruslan, Kozin Maxim, Shchur Sergey, Favorov Alexander, Boyko Alexey, Favorova Ol |
| Multiple Sclerosis patients carry an increased burden of exceedingly rare genetic variants in the inflammasome regulatory genes. Scientific reports 2019 Jun 9 (1): 9171. Vidmar Lovro, Maver Ales, Drulovi? Jelena, Sep?i? Juraj, Novakovi? Ivana, Risti? Smiljana, Šega Saša, Peterlin Bor |
| Association of TYK2 polymorphisms with autoimmune diseases: A comprehensive and updated systematic review with meta-analysis. Genetics and molecular biology 2021 5 44 (2): e20200425. Pellenz Felipe Mateus, Dieter Cristine, Lemos Natália Emerim, Bauer Andrea Carla, Souza Bianca Marmontel de, Crispim Dai |
- Page last reviewed:Oct 1, 2023
- Page last updated:Dec 01, 2023
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