Human Genome Epidemiology Literature Finder
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Records 1 - 11 (of 11 Records) |
| Query Trace: Disease and DPP6[original query] |
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A genome-wide association study of sporadic ALS in a homogenous Irish population.
Human molecular genetics 2008 Mar 17 (5): 768-74. Cronin Simon, Berger Stephen, Ding Jinhui, Schymick Jennifer C, Washecka Nicole, Hernandez Dena G, Greenway Matthew J, Bradley Daniel G, Traynor Bryan J, Hardiman Or |
| A two-stage genome-wide association study of sporadic amyotrophic lateral sclerosis. Human molecular genetics 2009 Apr 18 (8): 1524-32. Chiò Adriano, Schymick Jennifer C, Restagno Gabriella, Scholz Sonja W, Lombardo Federica, Lai Shiao-Lin, Mora Gabriele, Fung Hon-Chung, Britton Angela, Arepalli Sampath, Gibbs J Raphael, Nalls Michael, Berger Stephen, Kwee Lydia Coulter, Oddone Eugene Z, Ding Jinhui, Crews Cynthia, Rafferty Ian, Washecka Nicole, Hernandez Dena, Ferrucci Luigi, Bandinelli Stefania, Guralnik Jack, Macciardi Fabio, Torri Federica, Lupoli Sara, Chanock Stephen J, Thomas Gilles, Hunter David J, Gieger Christian, Wichmann H Erich, Calvo Andrea, Mutani Roberto, Battistini Stefania, Giannini Fabio, Caponnetto Claudia, Mancardi Giovanni Luigi, La Bella Vincenzo, Valentino Francesca, Monsurrò Maria Rosaria, Tedeschi Gioacchino, Marinou Kalliopi, Sabatelli Mario, Conte Amelia, Mandrioli Jessica, Sola Patrizia, Salvi Fabrizio, Bartolomei Ilaria, Siciliano Gabriele, Carlesi Cecilia, Orrell Richard W, Talbot Kevin, Simmons Zachary, Connor James, Pioro Erik P, Dunkley Travis, Stephan Dietrich A, Kasperaviciute Dalia, Fisher Elizabeth M, Jabonka Sibylle, Sendtner Michael, Beck Marcus, Bruijn Lucie, Rothstein Jeffrey, Schmidt Silke, Singleton Andrew, Hardy John, Traynor Bryan |
| A large genome scan for rare CNVs in amyotrophic lateral sclerosis. Human molecular genetics 2010 Oct 19 (20): 4091-9. Blauw Hylke M, Al-Chalabi Ammar, Andersen Peter M, van Vught Paul W J, Diekstra Frank P, van Es Michael A, Saris Christiaan G J, Groen Ewout J N, van Rheenen Wouter, Koppers Max, Van't Slot Ruben, Strengman Eric, Estrada Karol, Rivadeneira Fernando, Hofman Albert, Uitterlinden Andre G, Kiemeney Lambertus A, Vermeulen Sita H M, Birve Anna, Waibel Stefan, Meyer Thomas, Cronin Simon, McLaughlin Russell L, Hardiman Orla, Sapp Peter C, Tobin Martin D, Wain Louise V, Tomik Barbara, Slowik Agnieszka, Lemmens Robin, Rujescu Dan, Schulte Claudia, Gasser Thomas, Brown Robert H, Landers John E, Robberecht Wim, Ludolph Albert C, Ophoff Roel A, Veldink Jan H, van den Berg Leonard |
| Association between DPP6 polymorphism and the risk of sporadic amyotrophic lateral sclerosis in Chinese patients. Chinese medical journal 2009 Dec 122 (24): 2989-92. Li Xiao-Guang, Zhang Jiang-Hu, Xie Man-Qing, Liu Ming-Sheng, Li Ben-Hong, Zhao Yan-Huan, Ren Hai-Tao, Cui Li-Yi |
| Association between DPP6 polymorphism and the risk of progressive multiple sclerosis in Northern and Southern Europeans. Neuroscience letters 2012 Nov 530 (2): 155-60. Brambilla Paola, Esposito Federica, Lindstrom Eva, Sorosina Melissa, Giacalone Giacomo, Clarelli Ferdinando, Rodegher Mariaemma, Colombo Bruno, Moiola Lucia, Ghezzi Angelo, Capra Ruggero, Collimedaglia Laura, Coniglio Gabriella, Celius Elisabeth G, Galimberti Daniela, Sørensen Per Soelberg, Martinelli Vittorio, Oturai Annette B, Harbo Hanne F, Hillert Jan, Comi Giancarlo, Martinelli-Boneschi Filip |
| Genomic Study of Cardiovascular Continuum Comorbidity. Acta naturae 0 7 (3): 89-99. Makeeva O A, Sleptsov A A, Kulish E V, Barbarash O L, Mazur A M, Prokhorchuk E B, Chekanov N N, Stepanov V A, Puzyrev V |
| Effect of Ascertainment Bias on Estimates of Patient Mortality in Inherited Cardiac Diseases. Circulation. Genomic and precision medicine 2018 10 11 (10): e001797. Nannenberg Eline A, van Rijsingen Ingrid A W, van der Zwaag Paul A, van den Berg Maarten P, van Tintelen J Peter, Tanck Michael W T, Ackerman Michael J, Wilde Arthur A M, Christiaans Im |
| Hypertensive APOL1 risk allele carriers demonstrate greater blood pressure reduction with angiotensin receptor blockade compared to low risk carriers. PloS one 2019 14 (9): e0221957. Cunningham Patrick N, Wang Zhiying, Grove Megan L, Cooper-DeHoff Rhonda M, Beitelshees Amber L, Gong Yan, Gums John G, Johnson Julie A, Turner Stephen T, Boerwinkle Eric, Chapman Arlene |
| Genome-wide analyses as part of the international FTLD-TDP whole-genome sequencing consortium reveals novel disease risk factors and increases support for immune dysfunction in FTLD. Acta neuropathologica 2019 Feb . Pottier Cyril, Ren Yingxue, Perkerson Ralph B, Baker Matt, Jenkins Gregory D, van Blitterswijk Marka, DeJesus-Hernandez Mariely, van Rooij Jeroen G J, Murray Melissa E, Christopher Elizabeth, McDonnell Shannon K, Fogarty Zachary, Batzler Anthony, Tian Shulan, Vicente Cristina T, Matchett Billie, Karydas Anna M, Hsiung Ging-Yuek Robin, Seelaar Harro, Mol Merel O, Finger Elizabeth C, Graff Caroline, Öijerstedt Linn, Neumann Manuela, Heutink Peter, Synofzik Matthis, Wilke Carlo, Prudlo Johannes, Rizzu Patrizia, Simon-Sanchez Javier, Edbauer Dieter, Roeber Sigrun, Diehl-Schmid Janine, Evers Bret M, King Andrew, Mesulam M Marsel, Weintraub Sandra, Geula Changiz, Bieniek Kevin F, Petrucelli Leonard, Ahern Geoffrey L, Reiman Eric M, Woodruff Bryan K, Caselli Richard J, Huey Edward D, Farlow Martin R, Grafman Jordan, Mead Simon, Grinberg Lea T, Spina Salvatore, Grossman Murray, Irwin David J, Lee Edward B, Suh EunRan, Snowden Julie, Mann David, Ertekin-Taner Nilufer, Uitti Ryan J, Wszolek Zbigniew K, Josephs Keith A, Parisi Joseph E, Knopman David S, Petersen Ronald C, Hodges John R, Piguet Olivier, Geier Ethan G, Yokoyama Jennifer S, Rissman Robert A, Rogaeva Ekaterina, Keith Julia, Zinman Lorne, Tartaglia Maria Carmela, Cairns Nigel J, Cruchaga Carlos, Ghetti Bernardino, Kofler Julia, Lopez Oscar L, Beach Thomas G, Arzberger Thomas, Herms Jochen, Honig Lawrence S, Vonsattel Jean Paul, Halliday Glenda M, Kwok John B, White Charles L, Gearing Marla, Glass Jonathan, Rollinson Sara, Pickering-Brown Stuart, Rohrer Jonathan D, Trojanowski John Q, Van Deerlin Vivianna, Bigio Eileen H, Troakes Claire, Al-Sarraj Safa, Asmann Yan, Miller Bruce L, Graff-Radford Neill R, Boeve Bradley F, Seeley William W, Mackenzie Ian R A, van Swieten John C, Dickson Dennis W, Biernacka Joanna M, Rademakers Ro |
| Systematic Review and Meta-Analyses of Aminopeptidases as Prognostic Biomarkers in Amyotrophic Lateral Sclerosis. International journal of molecular sciences 2023 4 24 (8): . Bárbara Teruel-Peña, José Luís Gómez-Urquiza, Nora Suleiman-Martos, Isabel Prieto, Francisco José García-Cózar, Manuel Ramírez-Sánchez, Carmen Fernández-Martos, Germán Domínguez-Ví |
| Whole-exome sequencing reveals the genomic profile and IL6ST mutations as a prognostic biomarker of paraneoplastic pemphigus associated unicentric Castleman disease. The Journal of investigative dermatology 2023 10 . Sai Wang, Rui Wang, Panpan Shang, Xuejun Zhu, Xixue Chen, Guohong Zhang, Mingyue Wa |
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