Human Genome Epidemiology Literature Finder
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Records 1 - 27 (of 27 Records) |
| Query Trace: Parkinson Disease and MAPT[original query] |
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| Linkage disequilibrium and association of MAPT H1 in Parkinson disease. American journal of human genetics 2004 Oct 75 (4): 669-77. Skipper Lisa, Wilkes Kristen, Toft Mathias, Baker Matthew, Lincoln Sarah, Hulihan Mary, Ross Owen A, Hutton Mike, Aasly Jan, Farrer Matth |
| Haplotypes and gene expression implicate the MAPT region for Parkinson disease: the GenePD Study. Neurology 2008 May . Tobin JE, Latourelle JC, Lew MF, Klein C, Suchowersky O, Shill HA, Golbe LI, Mark MH, Growdon JH, Wooten GF, Racette BA, Perlmutter JS, Watts R, Guttman M, Baker KB, Goldwurm S, Pezzoli G, Singer C, Saint-Hilaire MH, Hendricks AE, Williamson S, Nagle MW, Wilk JB, Massood T, Laramie JM, Destefano AL, Litvan I, Nicholson G, Corbett A, Isaacson S, Burn DJ, Chinnery PF, Pramstaller PP, Sherman S, Al-Hinti J, Drasby E, Nance M, Moller AT, Ostergaard K, Roxburgh R, Snow B, Slevin JT, Cambi F, Gusella JF, Myers RH |
Genomewide association study for susceptibility genes contributing to familial Parkinson disease.
Human genetics 2009 Jan 124 (6): 593-605. Pankratz Nathan, Wilk Jemma B, Latourelle Jeanne C, DeStefano Anita L, Halter Cheryl, Pugh Elizabeth W, Doheny Kimberly F, Gusella James F, Nichols William C, Foroud Tatiana, Myers Richard H, |
| A comprehensive analysis of deletions, multiplications, and copy number variations in PARK2. Neurology 2010 Sep 75 (13): 1189-94. Kay D M, Stevens C F, Hamza T H, Montimurro J S, Zabetian C P, Factor S A, Samii A, Griffith A, Roberts J W, Molho E S, Higgins D S, Gancher S, Moses L, Zareparsi S, Poorkaj P, Bird T, Nutt J, Schellenberg G D, Payami |
| SNCA, MAPT, and GSK3B in Parkinson disease: a gene-gene interaction study. European journal of neurology : the official journal of the European Federation of Neurological Societies 2010 Dec . Wider C, Vilariño-Güell C, Heckman MG, Jasinska-Myga B, Ortolaza-Soto AI, Diehl NN, Crook JE, Cobb SA, Bacon JA, Aasly JO, Gibson JM, Lynch T, Uitti RJ, Wszolek ZK, Farrer MJ, Ross OA |
| Family-based association analysis of the MAPT gene in Parkinson disease. Journal of applied genetics 2010 51 (4): 509-14. Wang K S, Mullersman J E, Liu X |
| Genome-wide association study confirms SNPs in SNCA and the MAPT region as common risk factors for Parkinson disease.
Annals of human genetics 2010 Mar 74 (2): 97-109. Edwards Todd L, Scott William K, Almonte Cherylyn, Burt Amber, Powell Eric H, Beecham Gary W, Wang Liyong, Züchner Stephan, Konidari Ioanna, Wang Gaofeng, Singer Carlos, Nahab Fatta, Scott Burton, Stajich Jeffrey M, Pericak-Vance Margaret, Haines Jonathan, Vance Jeffery M, Martin Eden |
| Genome-wide association study identifies candidate genes for Parkinson's disease in an Ashkenazi Jewish population.
BMC medical genetics 2011 12 (1): 104. Liu Xinmin, Cheng Rong, Verbitsky Miguel, Kisselev Sergey, Browne Andrew, Mejia-Sanatana Helen, Louis Elan D, Cote Lucien J, Andrews Howard, Waters Cheryl, Ford Blair, Frucht Steven, Fahn Stanley, Marder Karen, Clark Lorraine N, Lee Joseph |
| [Analysis of single nucleotide polymorphism rs415430 in the WNT3 gene in the Russian population with the Parkinson disease]. Molekuliarnaia genetika, mikrobiologiia i virusologiia 2011 (2): 3-4. Filatova E V, Shadrina M I, Fedotova E Iu, Slominski? P A, Illarioshkin S N, Ivanova-Smolenskaia I A, Limborskaia S |
| Independent and joint effects of the MAPT and SNCA genes in Parkinson disease. Annals of neurology 2011 May 69 (5): 778-92. Elbaz Alexis, Ross Owen A, Ioannidis John P A, Soto-Ortolaza Alexandra I, Moisan Frédéric, Aasly Jan, Annesi Grazia, Bozi Maria, Brighina Laura, Chartier-Harlin Marie-Christine, Destée Alain, Ferrarese Carlo, Ferraris Alessandro, Gibson J Mark, Gispert Suzana, Hadjigeorgiou Georgios M, Jasinska-Myga Barbara, Klein Christine, Krüger Rejko, Lambert Jean-Charles, Lohmann Katja, van de Loo Simone, Loriot Marie-Anne, Lynch Timothy, Mellick George D, Mutez Eugénie, Nilsson Christer, Opala Grzegorz, Puschmann Andreas, Quattrone Aldo, Sharma Manu, Silburn Peter A, Stefanis Leonidas, Uitti Ryan J, Valente Enza Maria, Vilariño-Güell Carles, Wirdefeldt Karin, Wszolek Zbigniew K, Xiromerisiou Georgia, Maraganore Demetrius M, Farrer Matthew J, |
| SNCA and MAPT genes: Independent and joint effects in Parkinson disease in the Italian population. Parkinsonism & related disorders 2012 Mar 18 (3): 257-62. Trotta Luca, Guella Ilaria, Soldà Giulia, Sironi Francesca, Tesei Silvana, Canesi Margherita, Pezzoli Gianni, Goldwurm Stefano, Duga Stefano, Asselta Rosan |
| Investigation of c9orf72 in 4 neurodegenerative disorders. Archives of neurology 2012 Dec 69 (12): 1583-90. Xi Zhengrui, Zinman Lorne, Grinberg Yakov, Moreno Danielle, Sato Christine, Bilbao Juan M, Ghani Mahdi, Hernández Isabel, Ruiz Agustín, Boada Mercè, Morón Francisco J, Lang Anthony E, Marras Connie, Bruni Amalia, Colao Rosanna, Maletta Raffaele G, Puccio Gianfranco, Rainero Innocenzo, Pinessi Lorenzo, Galimberti Daniela, Morrison Karen E, Moorby Catriona, Stockton Joanne D, Masellis Mario, Black Sandra E, Hazrati Lili-Naz, Liang Yan, van Haersma de With Jan, Fornazzari Luis, Villagra Roque, Rojas-Garcia Ricardo, Clarimón Jordi, Mayeux Richard, Robertson Janice, St George-Hyslop Peter, Rogaeva Ekateri |
| An exploratory analysis on gene-environment interactions for Parkinson disease. Neurobiology of aging 2012 Oct 33 (10): 2528.e1-6. Gao Jianjun, Nalls Michael A, Shi Min, Joubert Bonnie R, Hernandez Dena G, Huang Xuemei, Hollenbeck Albert, Singleton Andrew B, Chen Hongl |
| The MAPT H1 haplotype is associated with tangle-predominant dementia. Acta neuropathologica 2012 Nov 124 (5): 693-704. Santa-Maria Ismael, Haggiagi Aya, Liu Xinmin, Wasserscheid Jessica, Nelson Peter T, Dewar Ken, Clark Lorraine N, Crary John |
| Large-scale replication and heterogeneity in Parkinson disease genetic loci. Neurology 2012 Aug 79 (7): 659-67. Sharma Manu, Ioannidis John P A, Aasly Jan O, Annesi Grazia, Brice Alexis, Van Broeckhoven Christine, Bertram Lars, Bozi Maria, Crosiers David, Clarke Carl, Facheris Maurizio, Farrer Matthew, Garraux Gaetan, Gispert Suzana, Auburger Georg, Vilariño-Güell Carles, Hadjigeorgiou Georgios M, Hicks Andrew A, Hattori Nobutaka, Jeon Beom, Lesage Suzanne, Lill Christina M, Lin Juei-Jueng, Lynch Timothy, Lichtner Peter, Lang Anthony E, Mok Vincent, Jasinska-Myga Barbara, Mellick George D, Morrison Karen E, Opala Grzegorz, Pramstaller Peter P, Pichler Irene, Park Sung Sup, Quattrone Aldo, Rogaeva Ekaterina, Ross Owen A, Stefanis Leonidas, Stockton Joanne D, Satake Wataru, Silburn Peter A, Theuns Jessie, Tan Eng-King, Toda Tatsushi, Tomiyama Hiroyuki, Uitti Ryan J, Wirdefeldt Karin, Wszolek Zbigniew, Xiromerisiou Georgia, Yueh Kuo-Chu, Zhao Yi, Gasser Thomas, Maraganore Demetrius, Krüger Rejko, |
| APOE, MAPT, and SNCA genes and cognitive performance in Parkinson disease. JAMA neurology 2014 Nov 71 (11): 1405-12. Mata Ignacio F, Leverenz James B, Weintraub Daniel, Trojanowski John Q, Hurtig Howard I, Van Deerlin Vivianna M, Ritz Beate, Rausch Rebecca, Rhodes Shannon L, Factor Stewart A, Wood-Siverio Cathy, Quinn Joseph F, Chung Kathryn A, Peterson Amie L, Espay Alberto J, Revilla Fredy J, Devoto Johnna, Hu Shu-Ching, Cholerton Brenna A, Wan Jia Y, Montine Thomas J, Edwards Karen L, Zabetian Cyrus |
| Genome-wide mapping of IBD segments in an Ashkenazi PD cohort identifies associated haplotypes.
Human molecular genetics 2014 Sep 23 (17): 4693-702. Vacic Vladimir, Ozelius Laurie J, Clark Lorraine N, Bar-Shira Anat, Gana-Weisz Mali, Gurevich Tanya, Gusev Alexander, Kedmi Merav, Kenny Eimear E, Liu Xinmin, Mejia-Santana Helen, Mirelman Anat, Raymond Deborah, Saunders-Pullman Rachel, Desnick Robert J, Atzmon Gil, Burns Edward R, Ostrer Harry, Hakonarson Hakon, Bergman Aviv, Barzilai Nir, Darvasi Ariel, Peter Inga, Guha Saurav, Lencz Todd, Giladi Nir, Marder Karen, Pe'er Itsik, Bressman Susan B, Orr-Urtreger A |
| Association of Parkinson disease risk loci with mild parkinsonian signs in older persons. JAMA neurology 2014 Apr 71 (4): 429-35. Shulman Joshua M, Yu Lei, Buchman Aron S, Evans Denis A, Schneider Julie A, Bennett David A, De Jager Philip |
| Genome-wide Meta-analysis on the Sense of Smell Among US Older Adults.
Medicine 2015 Nov 94 (47): e1892. Dong Jing, Yang Jingyun, Tranah Greg, Franceschini Nora, Parimi Neeta, Alkorta-Aranburu Gorka, Xu Zongli, Alonso Alvaro, Cummings Steven R, Fornage Myriam, Huang Xuemei, Kritchevsky Stephen, Liu Yongmei, London Stephanie, Niu Liang, Wilson Robert S, De Jager Philip L, Yu Lei, Singleton Andrew B, Harris Tamara, Mosley Thomas H, Pinto Jayant M, Bennett David A, Chen Hongl |
| Variants in GBA, SNCA, and MAPT influence Parkinson disease risk, age at onset, and progression. Neurobiology of aging 2015 Sep . Davis Albert A, Andruska Kristin M, Benitez Bruno A, Racette Brad A, Perlmutter Joel S, Cruchaga Carl |
| The effect of MAPT haplotype on neocortical Lewy body pathology in Parkinson disease. Journal of neural transmission (Vienna, Austria : 1996) 2016 Apr . Robakis Daphne, Cortes Etty, Clark Lorraine N, Vonsattel Jean Paul G, Virmani Tuhin, Alcalay Roy N, Crary John F, Levy Oren |
| Regional expression of the MAPT gene is associated with loss of hubs in brain networks and cognitive impairment in Parkinson disease and progressive supranuclear palsy. Neurobiology of aging 2016 Sep 48 153-160. Rittman Timothy, Rubinov Mikail, Vértes Petra E, Patel Ameera X, Ginestet Cedric E, Ghosh Boyd C P, Barker Roger A, Spillantini Maria Grazia, Bullmore Edward T, Rowe James |
| Regional Overlap of Pathologies in Lewy Body Disorders. Journal of neuropathology and experimental neurology 2017 Mar 76 (3): 216-224. Colom-Cadena Martí, Grau-Rivera Oriol, Planellas Lluís, Cerquera Catalina, Morenas Estrella, Helgueta Sergio, Muñoz Laia, Kulisevsky Jaime, Martí Maria Jose, Tolosa Eduard, Clarimon Jordi, Lleó Alberto, Gelpi Ell |
| Selective Genetic Overlap Between Amyotrophic Lateral Sclerosis and Diseases of the Frontotemporal Dementia Spectrum. JAMA neurology 2018 Jul 75 (7): 860-875. Karch Celeste M, Wen Natalie, Fan Chun C, Yokoyama Jennifer S, Kouri Naomi, Ross Owen A, Höglinger Gunter, Müller Ulrich, Ferrari Raffaele, Hardy John, Schellenberg Gerard D, Sleiman Patrick M, Momeni Parastoo, Hess Christopher P, Miller Bruce L, Sharma Manu, Van Deerlin Vivianna, Smeland Olav B, Andreassen Ole A, Dale Anders M, Desikan Rahul S, |
| Diagnosis Across the Spectrum of Progressive Supranuclear Palsy and Corticobasal Syndrome. JAMA neurology 2019 12 77 (3): 377-387. Jabbari Edwin, Holland Negin, Chelban Viorica, Jones P Simon, Lamb Ruth, Rawlinson Charlotte, Guo Tong, Costantini Alyssa A, Tan Manuela M X, Heslegrave Amanda J, Roncaroli Federico, Klein Johannes C, Ansorge Olaf, Allinson Kieren S J, Jaunmuktane Zane, Holton Janice L, Revesz Tamas, Warner Thomas T, Lees Andrew J, Zetterberg Henrik, Russell Lucy L, Bocchetta Martina, Rohrer Jonathan D, Williams Nigel M, Grosset Donald G, Burn David J, Pavese Nicola, Gerhard Alexander, Kobylecki Christopher, Leigh P Nigel, Church Alistair, Hu Michele T M, Woodside John, Houlden Henry, Rowe James B, Morris Huw |
| Genome-wide association study stratified by MAPT haplotypes identifies potential novel loci in Parkinson's disease. medRxiv : the preprint server for health sciences 2023 6 . Konstantin Senkevich, Sara Bandres-Ciga, Alejandro Cisterna-García, Eric Yu, Bernabe I Bustos, Lynne Krohn, Steven J Lubbe, Juan A Botía, , Ziv Gan- |
| Genome-wide analyses reveal a potential role for the MAPT, MOBP, and APOE loci in sporadic frontotemporal dementia. American journal of human genetics 2024 6 . Claudia Manzoni, Demis A Kia, Raffaele Ferrari, Ganna Leonenko, Beatrice Costa, Valentina Saba, Edwin Jabbari, Manuela Mx Tan, Diego Albani, Victoria Alvarez, Ignacio Alvarez, Ole A Andreassen, Antonella Angiolillo, Andrea Arighi, Matt Baker, Luisa Benussi, Valentina Bessi, Giuliano Binetti, Daniel J Blackburn, Merce Boada, Bradley F Boeve, Sergi Borrego-Ecija, Barbara Borroni, Geir Bråthen, William S Brooks, Amalia C Bruni, Paola Caroppo, Sara Bandres-Ciga, Jordi Clarimon, Rosanna Colao, Carlos Cruchaga, Adrian Danek, Sterre Cm de Boer, Itziar de Rojas, Alfonso di Costanzo, Dennis W Dickson, Janine Diehl-Schmid, Carol Dobson-Stone, Oriol Dols-Icardo, Aldo Donizetti, Elise Dopper, Elisabetta Durante, Camilla Ferrari, Gianluigi Forloni, Francesca Frangipane, Laura Fratiglioni, Milica G Kramberger, Daniela Galimberti, Maurizio Gallucci, Pablo García-González, Roberta Ghidoni, Giorgio Giaccone, Caroline Graff, Neill R Graff-Radford, Jordan Grafman, Glenda M Halliday, Dena G Hernandez, Lena E Hjermind, John R Hodges, Guy Holloway, Edward D Huey, Ignacio Illán-Gala, Keith A Josephs, David S Knopman, Mark Kristiansen, John B Kwok, Isabelle Leber, Hampton L Leonard, Ilenia Libri, Alberto Lleo, Ian R Mackenzie, Gaganjit K Madhan, Raffaele Maletta, Marta Marquié, Ales Maver, Manuel Menendez-Gonzalez, Graziella Milan, Bruce L Miller, Christopher M Morris, Huw R Morris, Benedetta Nacmias, Judith Newton, Jørgen E Nielsen, Christer Nilsson, Valeria Novelli, Alessandro Padovani, Suvankar Pal, Florence Pasquier, Pau Pastor, Robert Perneczky, Borut Peterlin, Ronald C Petersen, Olivier Piguet, Yolande Al Pijnenburg, Annibale A Puca, Rosa Rademakers, Innocenzo Rainero, Lianne M Reus, Anna Mt Richardson, Matthias Riemenschneider, Ekaterina Rogaeva, Boris Rogelj, Sara Rollinson, Howard Rosen, Giacomina Rossi, James B Rowe, Elisa Rubino, Agustin Ruiz, Erika Salvi, Raquel Sanchez-Valle, Sigrid Botne Sando, Alexander F Santillo, Jennifer A Saxon, Johannes Cm Schlachetzki, Sonja W Scholz, Harro Seelaar, William W Seeley, Maria Serpente, Sandro Sorbi, Sabrina Sordon, Peter St George-Hyslop, Jennifer C Thompson, Christine Van Broeckhoven, Vivianna M Van Deerlin, Sven J Van der Lee, John Van Swieten, Fabrizio Tagliavini, Julie van der Zee, Arianna Veronesi, Emilia Vitale, Maria Landqvist Waldo, Jennifer S Yokoyama, Mike A Nalls, Parastoo Momeni, Andrew B Singleton, John Hardy, Valentina Escott-Pri |
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