Human Genome Epidemiology Literature Finder
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Records 1 - 7 (of 7 Records) |
| Query Trace: Amyotrophic Lateral Sclerosis and HLA-B[original query] |
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| Genome-wide copy number variation in sporadic amyotrophic lateral sclerosis in the Turkish population: deletion of EPHA3 is a possible protective factor. PloS one 2013 8 (8): e72381. Uyan Özgün, Ömür Özgür, A??m Zeynep Sena, Özo?uz Asl?han, Li Hong, Parman Ye?im, Deymeer Feza, Oflazer Piraye, Koç Filiz, Tan Ersin, Özçelik Hilmi, Ba?ak A Naz |
| Genetic variation associated with the occurrence and progression of neurological disorders. Neurotoxicology 2016 Oct . Little Julian, Barakat-Haddad Caroline, Martino Rosemary, Pringsheim Tamara, Tremlett Helen, McKay Kyla A, van Lieshout Pascal, Walsh Stephanie J, Gomes James, Krewski Dani |
| HLA-DRA/HLA-DRB5 polymorphism affects risk of sporadic ALS and survival in a southwest Chinese cohort. Journal of the neurological sciences 2017 Feb 373 124-128. Yang Xinglong, Zheng JinHua, Tian Sijia, Chen Yalan, An Ran, Zhao Quanzhen, Xu Yanmi |
| A C6orf10/LOC101929163 locus is associated with age of onset in C9orf72 carriers. Brain : a journal of neurology 2018 10 141 (10): 2895-2907. Zhang Ming, Ferrari Raffaele, Tartaglia Maria Carmela, Keith Julia, Surace Ezequiel I, Wolf Uri, Sato Christine, Grinberg Mark, Liang Yan, Xi Zhengrui, Dupont Kyle, McGoldrick Philip, Weichert Anna, McKeever Paul M, Schneider Raphael, McCorkindale Michael D, Manzoni Claudia, Rademakers Rosa, Graff-Radford Neill R, Dickson Dennis W, Parisi Joseph E, Boeve Bradley F, Petersen Ronald C, Miller Bruce L, Seeley William W, van Swieten John C, van Rooij Jeroen, Pijnenburg Yolande, van der Zee Julie, Van Broeckhoven Christine, Le Ber Isabelle, Van Deerlin Vivianna, Suh EunRan, Rohrer Jonathan D, Mead Simon, Graff Caroline, Öijerstedt Linn, Pickering-Brown Stuart, Rollinson Sara, Rossi Giacomina, Tagliavini Fabrizio, Brooks William S, Dobson-Stone Carol, Halliday Glenda M, Hodges John R, Piguet Olivier, Binetti Giuliano, Benussi Luisa, Ghidoni Roberta, Nacmias Benedetta, Sorbi Sandro, Bruni Amalia C, Galimberti Daniela, Scarpini Elio, Rainero Innocenzo, Rubino Elisa, Clarimon Jordi, Lleó Alberto, Ruiz Agustin, Hernández Isabel, Pastor Pau, Diez-Fairen Monica, Borroni Barbara, Pasquier Florence, Deramecourt Vincent, Lebouvier Thibaud, Perneczky Robert, Diehl-Schmid Janine, Grafman Jordan, Huey Edward D, Mayeux Richard, Nalls Michael A, Hernandez Dena, Singleton Andrew, Momeni Parastoo, Zeng Zhen, Hardy John, Robertson Janice, Zinman Lorne, Rogaeva Ekaterina, |
| Immune-related genetic enrichment in frontotemporal dementia: An analysis of genome-wide association studies. PLoS medicine 2018 1 15 (1): e1002487. Broce Iris, Karch Celeste M, Wen Natalie, Fan Chun C, Wang Yunpeng, Tan Chin Hong, Kouri Naomi, Ross Owen A, Höglinger Günter U, Muller Ulrich, Hardy John, , Momeni Parastoo, Hess Christopher P, Dillon William P, Miller Zachary A, Bonham Luke W, Rabinovici Gil D, Rosen Howard J, Schellenberg Gerard D, Franke Andre, Karlsen Tom H, Veldink Jan H, Ferrari Raffaele, Yokoyama Jennifer S, Miller Bruce L, Andreassen Ole A, Dale Anders M, Desikan Rahul S, Sugrue Leo |
| HLA and amyotrophic lateral sclerosis: a systematic review and meta-analysis. Amyotrophic lateral sclerosis & frontotemporal degeneration 2022 5 24 (1-2): 24-32. Nona R J, Greer J M, Henderson R D, McCombe P |
| Investigation of the causal relationship between ALS and autoimmune disorders: a Mendelian randomization study. BMC medicine 2022 11 20 (1): 382. Alipour Paria, Senkevich Konstantin, Ross Jay P, Spiegelman Dan, Manousaki Despoina, Dion Patrick A, Rouleau Guy |
- Page last reviewed:Feb 1, 2023
- Page last updated:Jun 02, 2023
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