Human Genome Epidemiology Literature Finder
Rare Diseases
Records 1 - 4 (of 4 Records) |
Query Trace: Myasthenia Gravis[original query] |
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Risk for myasthenia gravis maps to a (151) Pro?Ala change in TNIP1 and to human leukocyte antigen-B*08.
Annals of neurology 2012 Dec 72 (6): 927-35. Gregersen Peter K, Kosoy Roman, Lee Annette T, Lamb Janine, Sussman Jon, McKee David, Simpfendorfer Kim R, Pirskanen-Matell Ritva, Piehl Frederik, Pan-Hammarstrom Qiang, Verschuuren Jan J G M, Titulaer Maarten J, Niks Erik H, Marx Alexander, Ströbel Philipp, Tackenberg Björn, Pütz Michael, Maniaol Angelina, Elsais Ahmed, Tallaksen Chantal, Harbo Hanne F, Lie Benedicte A, Raychaudhuri Soumya, de Bakker Paul I W, Melms Arthur, Garchon Henri-Jean, Willcox Nicholas, Hammarstrom Lennart, Seldin Michael |
A genome-wide association study of myasthenia gravis.
JAMA neurology 2015 Apr 72 (4): 396-404. Renton Alan E, Pliner Hannah A, Provenzano Carlo, Evoli Amelia, Ricciardi Roberta, Nalls Michael A, Marangi Giuseppe, Abramzon Yevgeniya, Arepalli Sampath, Chong Sean, Hernandez Dena G, Johnson Janel O, Bartoccioni Emanuela, Scuderi Flavia, Maestri Michelangelo, Gibbs J Raphael, Errichiello Edoardo, Chiò Adriano, Restagno Gabriella, Sabatelli Mario, Macek Mark, Scholz Sonja W, Corse Andrea, Chaudhry Vinay, Benatar Michael, Barohn Richard J, McVey April, Pasnoor Mamatha, Dimachkie Mazen M, Rowin Julie, Kissel John, Freimer Miriam, Kaminski Henry J, Sanders Donald B, Lipscomb Bernadette, Massey Janice M, Chopra Manisha, Howard James F, Koopman Wilma J, Nicolle Michael W, Pascuzzi Robert M, Pestronk Alan, Wulf Charlie, Florence Julaine, Blackmore Derrick, Soloway Aimee, Siddiqi Zaeem, Muppidi Srikanth, Wolfe Gil, Richman David, Mezei Michelle M, Jiwa Theresa, Oger Joel, Drachman Daniel B, Traynor Bryan |
Genome-Wide Association Study of Late-Onset Myasthenia Gravis: Confirmation of TNFRSF11A and Identification of ZBTB10 and Three Distinct HLA Associations.
Molecular medicine (Cambridge, Mass.) 2015 Oct . Seldin Michael F, Alkhairy Omar K, Lee Annette T, Lamb Janine A, Sussman Jon, Pirskanen-Matell Ritva, Piehl Fredrik, Verschuuren J J G M, Kostera-Pruszczyk Anna, Szczudlik Piotr, Mckee David, Maniaol Angelina H, Harbo Hanne F, Lie Benedicte A, Melms Arthur, Garchon Henri-Jean, Willcox Nicholas, Gregersen Peter K, Hammarstrom Lenna |
Identification of genetic risk loci and prioritization of genes and pathways for myasthenia gravis: a genome-wide association study.
Proceedings of the National Academy of Sciences of the United States of America 2022 02 119 (5): . Chia Ruth, Saez-Atienzar Sara, Murphy Natalie, Chiò Adriano, Blauwendraat Cornelis, , Roda Ricardo H, Tienari Pentti J, Kaminski Henry J, Ricciardi Roberta, Guida Melania, De Rosa Anna, Petrucci Loredana, Evoli Amelia, Provenzano Carlo, Drachman Daniel B, Traynor Bryan |
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