Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 36 Records) |
Query Trace: Sclerosis and meta-analysis and HLA-A[original query] |
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No evidence of IL21 association with multiple sclerosis in a Swedish population. Tissue antigens 2011 Oct 78 (4): 271-4. Lindén M, Nohra R, Sundqvist E, Khademi M, Hillert J, Alfredsson L, Olsson T, Kockum |
The rs4774 CIITA missense variant is associated with risk of systemic lupus erythematosus. Genes and immunity 2011 Dec 12 (8): 667-71. Bronson P G, Goldstein B A, Ramsay P P, Beckman K B, Noble J A, Lane J A, Seldin M F, Kelly J A, Harley J B, Moser K L, Gaffney P M, Behrens T W, Criswell L A, Barcellos L |
Geographic differences in genetic susceptibility to IgA nephropathy: GWAS replication study and geospatial risk analysis. PLoS genetics 2012 8 (6): e1002765. Kiryluk Krzysztof, Li Yifu, Sanna-Cherchi Simone, Rohanizadegan Mersedeh, Suzuki Hitoshi, Eitner Frank, Snyder Holly J, Choi Murim, Hou Ping, Scolari Francesco, Izzi Claudia, Gigante Maddalena, Gesualdo Loreto, Savoldi Silvana, Amoroso Antonio, Cusi Daniele, Zamboli Pasquale, Julian Bruce A, Novak Jan, Wyatt Robert J, Mucha Krzysztof, Perola Markus, Kristiansson Kati, Viktorin Alexander, Magnusson Patrik K, Thorleifsson Gudmar, Thorsteinsdottir Unnur, Stefansson Kari, Boland Anne, Metzger Marie, Thibaudin Lise, Wanner Christoph, Jager Kitty J, Goto Shin, Maixnerova Dita, Karnib Hussein H, Nagy Judit, Panzer Ulf, Xie Jingyuan, Chen Nan, Tesar Vladimir, Narita Ichiei, Berthoux Francois, Floege Jürgen, Stengel Benedicte, Zhang Hong, Lifton Richard P, Gharavi Ali |
Genome-wide association study of multiple sclerosis confirms a novel locus at 5p13.1.
PloS one 2012 7 (5): e36140. Matesanz Fuencisla, González-Pérez Antonio, Lucas Miguel, Sanna Serena, Gayán Javier, Urcelay Elena, Zara Ilenia, Pitzalis Maristella, Cavanillas María L, Arroyo Rafael, Zoledziewska Magdalena, Marrosu Marisa, Fernández Oscar, Leyva Laura, Alcina Antonio, Fedetz Maria, Moreno-Rey Concha, Velasco Juan, Real Luis M, Ruiz-Peña Juan Luis, Cucca Francesco, Ruiz Agustín, Izquierdo Guiller |
A functional variant in ERAP1 predisposes to multiple sclerosis. PloS one 2012 7 (1): e29931. Guerini Franca Rosa, Cagliani Rachele, Forni Diego, Agliardi Cristina, Caputo Domenico, Cassinotti Andrea, Galimberti Daniela, Fenoglio Chiara, Biasin Mara, Asselta Rosanna, Scarpini Elio, Comi Giacomo P, Bresolin Nereo, Clerici Mario, Sironi Manue |
Network-based multiple sclerosis pathway analysis with GWAS data from 15,000 cases and 30,000 controls. American journal of human genetics 2013 Jun 92 (6): 854-65. Authors are not available |
Association of genetic markers with CSF oligoclonal bands in multiple sclerosis patients.
PloS one 2013 8 (6): e64408. Leone Maurizio A, Barizzone Nadia, Esposito Federica, Lucenti Ausiliatrice, Harbo Hanne F, Goris An, Kockum Ingrid, Oturai Annette Bang, Celius Elisabeth Gulowsen, Mero Inger L, Dubois Bénédicte, Olsson Tomas, Søndergaard Helle Bach, Cusi Daniele, Lupoli Sara, Andreassen Bettina Kulle, , , Myhr Kjell-Morten, Guerini Franca R, , , Comi Giancarlo, Martinelli-Boneschi Filippo, D'Alfonso Sand |
Role of the human endogenous retrovirus HERV-K18 in autoimmune disease susceptibility: study in the Spanish population and meta-analysis. PloS one 2013 8 (4): e62090. de la Hera Belén, Varadé Jezabel, García-Montojo Marta, Lamas José Ramón, de la Encarnación Ana, Arroyo Rafael, Fernández-Gutiérrez Benjamín, Alvarez-Lafuente Roberto, Urcelay Ele |
The systemic lupus erythematosus IRF5 risk haplotype is associated with systemic sclerosis. PloS one 2013 8 (1): 1. Carmona FD, Martin JE, Beretta L, Simeón CP, Carreira PE, Callejas JL, Fernández-Castro M, Sáez-Comet L, Beltrán E, Camps MT, Egurbide MV, Airó P, Scorza R, Lunardi C, Hunzelmann N, Riemekasten G, Witte T, Kreuter A, Distler JH, Madhok R, Shiels P, van Laar JM, Fonseca C, Denton C, Herrick A, Worthington J, Schuerwegh AJ, Vonk MC, Voskuyl AE, Radstake TR, Martín J |
A genome-wide association study follow-up suggests a possible role for PPARG in systemic sclerosis susceptibility. Arthritis research & therapy 2014 16 (1): R6. López-Isac Elena, Bossini-Castillo Lara, Simeon Carmen P, Egurbide María Victoria, Alegre-Sancho Juan José, Callejas Jose Luis, Roman-Ivorra José Andrés, Freire Mayka, Beretta Lorenzo, Santaniello Alessandro, Airó Paolo, Lunardi Claudio, Hunzelmann Nicolas, Riemekasten Gabriela, Witte Torsten, Kreuter Alexander, Distler Jörg H W, Schuerwegh Annemie J, Vonk Madelon C, Voskuyl Alexandre E, Shiels Paul G, van Laar Jacob M, Fonseca Carmen, Denton Christopher, Herrick Ariane, Worthington Jane, Assassi Shervin, Koeleman Bobby P, Mayes Maureen D, Radstake Timothy R D J, Martin Javier, |
IL2RA is associated with persistence of rheumatoid arthritis. Arthritis research & therapy 2015 17 (1): 244. van Steenbergen H W, van Nies J A B, Ruyssen-Witrand A, Huizinga T W J, Cantagrel Al, Berenbaum F, van der Helm-van Mil A H |
Influence of the LILRA3 Deletion on Multiple Sclerosis Risk: Original Data and Meta-Analysis. PloS one 2015 10 (8): e0134414. Ortiz Miguel A, Núñez Concepción, Ordóñez David, Alvarez-Cermeño José C, Martínez-Rodriguez José E, Sánchez Antonio J, Arroyo Rafael, Izquierdo Guillermo, Malhotra Sunny, Montalban Xavier, García-Merino Antonio, Munteis Elvira, Alcina Antonio, Comabella Manuel, Matesanz Fuencisla, Villar Luisa M, Urcelay Ele |
A rare P2X7 variant Arg307Gln with absent pore formation function protects against neuroinflammation in multiple sclerosis. Human molecular genetics 2015 Oct 24 (19): 5644-54. Gu Ben J, Field Judith, Dutertre Sébastien, Ou Amber, Kilpatrick Trevor J, Lechner-Scott Jeannette, Scott Rodney, Lea Rodney, Taylor Bruce V, Stankovich Jim, Butzkueven Helmut, Gresle Melissa, Laws Simon M, Petrou Steven, Hoffjan Sabine, Akkad Denis A, Graham Colin A, Hawkins Stanley, Glaser Anna, Bedri Sahl Khalid, Hillert Jan, Matute Carlos, Antiguedad Alfredo, , Wiley James |
Association between a Functional HLA-G 14-bp Insertion/deletion Polymorphism and Susceptibility to Autoimmune Diseases: A Meta-analysis. Cellular and molecular biology (Noisy-le-Grand, France) 2015 61 (8): 24-30. Lee Y H, Bae S |
Identification of Rare Variants in ATP8B4 as a Risk Factor for Systemic Sclerosis by Whole-Exome Sequencing. Arthritis & rheumatology (Hoboken, N.J.) 2015 Oct . Gao Li, Emond Mary J, Louie Tin, Cheadle Chris, Berger Alan E, Rafaels Nicholas, Vergara Candelaria, Kim Yoonhee, Taub Margaret A, Ruczinski Ingo, Mathai Stephen C, Rich Stephen S, Nickerson Deborah A, Hummers Laura K, Bamshad Michael J, Hassoun Paul M, Mathias Rasika A, , Barnes Kathleen |
Systems level analysis of systemic sclerosis shows a network of immune and profibrotic pathways connected with genetic polymorphisms. PLoS computational biology 2015 1 11 (1): e1004005. Mahoney J Matthew, Taroni Jaclyn, Martyanov Viktor, Wood Tammara A, Greene Casey S, Pioli Patricia A, Hinchcliff Monique E, Whitfield Michael |
Mendelian randomization shows a causal effect of low vitamin D on multiple sclerosis risk. Neurology. Genetics 2016 Oct 2 (5): e97. Rhead Brooke, Bäärnhielm Maria, Gianfrancesco Milena, Mok Amanda, Shao Xiaorong, Quach Hong, Shen Ling, Schaefer Catherine, Link Jenny, Gyllenberg Alexandra, Hedström Anna Karin, Olsson Tomas, Hillert Jan, Kockum Ingrid, Glymour M Maria, Alfredsson Lars, Barcellos Lisa |
Multiple sclerosis risk loci and disease severity in 7,125 individuals from 10 studies. Neurology. Genetics 2016 Aug 2 (4): e87. George Michaela F, Briggs Farren B S, Shao Xiaorong, Gianfrancesco Milena A, Kockum Ingrid, Harbo Hanne F, Celius Elisabeth G, Bos Steffan D, Hedström Anna, Shen Ling, Bernstein Allan, Alfredsson Lars, Hillert Jan, Olsson Tomas, Patsopoulos Nikolaos A, De Jager Philip L, Oturai Annette B, Søndergaard Helle B, Sellebjerg Finn, Sorensen Per S, Gomez Refujia, Caillier Stacy J, Cree Bruce A C, Oksenberg Jorge R, Hauser Stephen L, D'Alfonso Sandra, Leone Maurizio A, Martinelli Boneschi Filippo, Sorosina Melissa, van der Mei Ingrid, Taylor Bruce V, Zhou Yuan, Schaefer Catherine, Barcellos Lisa |
Genetic loci for Epstein-Barr virus nuclear antigen-1 are associated with risk of multiple sclerosis.
Multiple sclerosis (Houndmills, Basingstoke, England) 2016 Nov 22 (13): 1655-1664. Zhou Yuan, Zhu Gu, Charlesworth Jac C, Simpson Steve, Rubicz Rohina, Göring Harald Hh, Patsopoulos Nikolaos A, Laverty Caroline, Wu Feitong, Henders Anjali, Ellis Jonathan J, van der Mei Ingrid, Montgomery Grant W, Blangero John, Curran Joanne E, Johnson Matthew P, Martin Nicholas G, Nyholt Dale R, Taylor Bruce V, |
Evidence for a causal relationship between low vitamin D, high BMI, and pediatric-onset MS. Neurology 2017 Mar . Gianfrancesco Milena A, Stridh Pernilla, Rhead Brooke, Shao Xiaorong, Xu Edison, Graves Jennifer S, Chitnis Tanuja, Waldman Amy, Lotze Timothy, Schreiner Teri, Belman Anita, Greenberg Benjamin, Weinstock-Guttman Bianca, Aaen Gregory, Tillema Jan M, Hart Janace, Caillier Stacy, Ness Jayne, Harris Yolanda, Rubin Jennifer, Candee Meghan, Krupp Lauren, Gorman Mark, Benson Leslie, Rodriguez Moses, Mar Soe, Kahn Ilana, Rose John, Roalstad Shelly, Casper T Charles, Shen Ling, Quach Hong, Quach Diana, Hillert Jan, Bäärnhielm Maria, Hedstrom Anna, Olsson Tomas, Kockum Ingrid, Alfredsson Lars, Metayer Catherine, Schaefer Catherine, Barcellos Lisa F, Waubant Emmanuelle, |
Transethnic meta-analysis identifies GSDMA and PRDM1 as susceptibility genes to systemic sclerosis.
Annals of the rheumatic diseases 2017 Mar . Terao Chikashi, Kawaguchi Takahisa, Dieude Philippe, Varga John, Kuwana Masataka, Hudson Marie, Kawaguchi Yasushi, Matucci-Cerinic Marco, Ohmura Koichiro, Riemekasten Gabriela, Kawasaki Aya, Airo Paolo, Horita Tetsuya, Oka Akira, Hachulla Eric, Yoshifuji Hajime, Caramaschi Paola, Hunzelmann Nicolas, Baron Murray, Atsumi Tatsuya, Hassoun Paul, Torii Takeshi, Takahashi Meiko, Tabara Yasuharu, Shimizu Masakazu, Tochimoto Akiko, Ayuzawa Naho, Yanagida Hidetoshi, Furukawa Hiroshi, Tohma Shigeto, Hasegawa Minoru, Fujimoto Manabu, Ishikawa Osamu, Yamamoto Toshiyuki, Goto Daisuke, Asano Yoshihide, Jinnin Masatoshi, Endo Hirahito, Takahashi Hiroki, Takehara Kazuhiko, Sato Shinichi, Ihn Hironobu, Raychaudhuri Soumya, Liao Katherine, Gregersen Peter, Tsuchiya Naoyuki, Riccieri Valeria, Melchers Inga, Valentini Gabriele, Cauvet Anne, Martinez Maria, Mimori Tsuneyo, Matsuda Fumihiko, Allanore Yanni |
Genome-wide association study of classical Hodgkin lymphoma identifies key regulators of disease susceptibility.
Nature communications 2017 Dec 8 (1): 1892. Sud Amit, Thomsen Hauke, Law Philip J, Försti Asta, Filho Miguel Inacio da Silva, Holroyd Amy, Broderick Peter, Orlando Giulia, Lenive Oleg, Wright Lauren, Cooke Rosie, Easton Douglas, Pharoah Paul, Dunning Alison, Peto Julian, Canzian Federico, Eeles Rosalind, Kote-Jarai ZSofia, Muir Kenneth, Pashayan Nora, , Hoffmann Per, Nöthen Markus M, Jöckel Karl-Heinz, Strandmann Elke Pogge von, Lightfoot Tracy, Kane Eleanor, Roman Eve, Lake Annette, Montgomery Dorothy, Jarrett Ruth F, Swerdlow Anthony J, Engert Andreas, Orr Nick, Hemminki Kari, Houlston Richard |
Human leukocyte antigen (HLA)-DRB1 allele polymorphisms and systemic sclerosis. Modern rheumatology 2018 Sep 1-20. Xu Yanzhen, Mo Nanfang, Jiang Zhiwen, Lu Shaoming, Fu Shien, Wei Xinyan, Zhao Dong, Xie Zhibin, Jia Wenxian, Liu Jiayi, Wang Xiao, Shi Dongchen, Jiao Yang, Liu Chengwu, Yang Xiao |
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, |
HLA-DRB1 polymorphism and susceptibility to multiple sclerosis in the Middle East North Africa region: A systematic review and meta-analysis. Journal of neuroimmunology 2018 Aug 321 117-124. Mohajer Bahram, Abbasi Nooshin, Pishgar Farhad, Abdolalizadeh Amirhussein, Ebrahimi Hedyeh, Razaviyoun Taraneh, Mohebbi Farnam, Eskandarieh Sharareh, Sahraian Mohammad A |
DNA methylation as a mediator of HLA-DRB1*15:01 and a protective variant in multiple sclerosis. Nature communications 2018 6 9 (1): 2397. Kular Lara, Liu Yun, Ruhrmann Sabrina, Zheleznyakova Galina, Marabita Francesco, Gomez-Cabrero David, James Tojo, Ewing Ewoud, Lindén Magdalena, Górnikiewicz Bartosz, Aeinehband Shahin, Stridh Pernilla, Link Jenny, Andlauer Till F M, Gasperi Christiane, Wiendl Heinz, Zipp Frauke, Gold Ralf, Tackenberg Björn, Weber Frank, Hemmer Bernhard, Strauch Konstantin, Heilmann-Heimbach Stefanie, Rawal Rajesh, Schminke Ulf, Schmidt Carsten O, Kacprowski Tim, Franke Andre, Laudes Matthias, Dilthey Alexander T, Celius Elisabeth G, Søndergaard Helle B, Tegnér Jesper, Harbo Hanne F, Oturai Annette B, Olafsson Sigurgeir, Eggertsson Hannes P, Halldorsson Bjarni V, Hjaltason Haukur, Olafsson Elias, Jonsdottir Ingileif, Stefansson Kari, Olsson Tomas, Piehl Fredrik, Ekström Tomas J, Kockum Ingrid, Feinberg Andrew P, Jagodic Ma |
The Involvement of HLA Class II Alleles in Multiple Sclerosis: A Systematic Review with Meta-analysis. Disease markers 2019 11 2019 1409069. De Silvestri A, Capittini C, Mallucci G, Bergamaschi R, Rebuffi C, Pasi A, Martinetti M, Tinelli |
Treatment- and population-specific genetic risk factors for anti-drug antibodies against interferon-beta: a GWAS.
BMC medicine 2020 11 18 (1): 298. Andlauer Till F M, Link Jenny, Martin Dorothea, Ryner Malin, Hermanrud Christina, Grummel Verena, Auer Michael, Hegen Harald, Aly Lilian, Gasperi Christiane, Knier Benjamin, Müller-Myhsok Bertram, Jensen Poul Erik Hyldgaard, Sellebjerg Finn, Kockum Ingrid, Olsson Tomas, Pallardy Marc, Spindeldreher Sebastian, Deisenhammer Florian, Fogdell-Hahn Anna, Hemmer Bernhard, |
Neuromyelitis optica is an HLA associated disease different from Multiple Sclerosis: a systematic review with meta-analysis. Scientific reports 2021 Jan 11 (1): 152. Alvarenga Marcos Papais, do Carmo Luciana Ferreira, Vasconcelos Claudia Cristina Ferreira, Alvarenga Marina Papais, Alvarenga-Filho Helcio, de Melo Bento Cleonice Alves, Paiva Carmen Lucia Antão, Leyva-Fernández Laura, Fernández Óscar, Papais-Alvarenga Regina Mar |
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 |
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