Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 44 Records) |
Query Trace: Parkinson Disease and SNCA[original query] |
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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 |
SNCA variant associated with Parkinson disease and plasma alpha-synuclein level. Archives of neurology 2010 Nov 67 (11): 1350-6. Mata Ignacio F, Shi Min, Agarwal Pinky, Chung Kathryn A, Edwards Karen L, Factor Stewart A, Galasko Douglas R, Ginghina Carmen, Griffith Alida, Higgins Donald S, Kay Denise M, Kim Hojoong, Leverenz James B, Quinn Joseph F, Roberts John W, Samii Ali, Snapinn Katherine W, Tsuang Debby W, Yearout Dora, Zhang Jing, Payami Haydeh, Zabetian Cyrus |
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 |
Copy number variation in familial Parkinson disease. PloS one 2011 6 (8): e20988. Pankratz Nathan, Dumitriu Alexandra, Hetrick Kurt N, Sun Mei, Latourelle Jeanne C, Wilk Jemma B, Halter Cheryl, Doheny Kimberly F, Gusella James F, Nichols William C, Myers Richard H, Foroud Tatiana, DeStefano Anita L, |
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 |
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 |
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 |
Genetic analysis of SNCA coding mutation in Chinese Han patients with Parkinson disease. Acta neurologica Belgica 2015 Sep 115 (3): 267-71. Deng Sheng, Deng Xiong, Yuan Lamei, Song Zhi, Yang Zhijian, Xiong Wei, Deng H |
a-Synuclein rs356219 polymorphisms in patients with Gaucher disease and Parkinson disease. Neuroscience letters 2014 Sep 580 104-7. Altarescu Gheona, Ioscovich Daniel, Alcalay Roy N, Zimran Ari, Elstein Debor |
Epitope Mapping of Antibodies to Alpha-Synuclein in LRRK2 Mutation Carriers, Idiopathic Parkinson Disease Patients, and Healthy Controls. Frontiers in aging neuroscience 2014 6 169. Alvarez-Castelao Beatriz, Gorostidi Ana, Ruíz-Martínez Javier, López de Munain Adolfo, Castaño José |
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 |
Disease penetrance of late-onset parkinsonism: a meta-analysis. JAMA neurology 2014 Dec 71 (12): 1535-9. Trinh Joanne, Guella Ilaria, Farrer Matthew Jam |
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 |
TREM2 p.R47H substitution is not associated with dementia with Lewy bodies. Neurology. Genetics 2016 Aug 2 (4): e85. Walton Ronald L, Soto-Ortolaza Alexandra I, Murray Melissa E, Lorenzo-Betancor Oswaldo, Ogaki Kotaro, Heckman Michael G, Rayaprolu Sruti, Rademakers Rosa, Ertekin-Taner Nilüfer, Uitti Ryan J, van Gerpen Jay A, Wszolek Zbigniew K, Smith Glenn E, Kantarci Kejal, Lowe Val J, Parisi Joseph E, Jones David T, Savica Rodolfo, Graff-Radford Jonathan, Knopman David S, Petersen Ronald C, Graff-Radford Neill R, Ferman Tanis J, Dickson Dennis W, Boeve Bradley F, Ross Owen A, Labbé Catheri |
a-synuclein genetic variability: A biomarker for dementia in Parkinson disease. Annals of neurology 2016 Apr . Guella Ilaria, Evans Daniel M, Szu-Tu Chelsea, Nosova Ekaterina, Bortnick Stephanie F, , Goldman Jennifer G, Dalrymple-Alford John, Geurtsen Gert J, Litvan Irene, Ross Owen A, Middleton Lefkos T, Parkkinen Laura, Farrer Matthew |
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 |
A comprehensive analysis of SNCA-related genetic risk in sporadic parkinson disease. Annals of neurology 2018 Jul 84 (1): 117-129. Pihlstrøm Lasse, Blauwendraat Cornelis, Cappelletti Chiara, Berge-Seidl Victoria, Langmyhr Margrete, Henriksen Sandra Pilar, van de Berg Wilma D J, Gibbs J Raphael, Cookson Mark R, , , Singleton Andrew B, Nalls Mike A, Toft Mathi |
Parkinson-Associated SNCA Enhancer Variants Revealed by Open Chromatin in Mouse Dopamine Neurons. American journal of human genetics 2018 12 103 (6): 874-892. McClymont Sarah A, Hook Paul W, Soto Alexandra I, Reed Xylena, Law William D, Kerans Samuel J, Waite Eric L, Briceno Nicole J, Thole Joey F, Heckman Michael G, Diehl Nancy N, Wszolek Zbigniew K, Moore Cedric D, Zhu Heng, Akiyama Jennifer A, Dickel Diane E, Visel Axel, Pennacchio Len A, Ross Owen A, Beer Michael A, McCallion Andrew |
Low prevalence of known pathogenic mutations in dominant PD genes: A Swedish multicenter study. Parkinsonism & related disorders 2019 Jul . Puschmann Andreas, Jiménez-Ferrer Itzia, Lundblad-Andersson Elin, Mårtensson Emma, Hansson Oskar, Odin Per, Widner Håkan, Brolin Kajsa, Mzezewa Ropafadzo, Kristensen Jonas, Soller Maria, Rödström Emil Ygland, Ross Owen A, Toft Mathias, Breedveld Guido J, Bonifati Vincenzo, Brodin Lovisa, Zettergren Anna, Sydow Olof, Linder Jan, Wirdefeldt Karin, Svenningsson Per, Nissbrandt Hans, Belin Andrea Carmine, Forsgren Lars, Swanberg Mar |
Integrated sequencing and array comparative genomic hybridization in familial Parkinson disease. Neurology. Genetics 2020 Oct 6 (5): e498. Robak Laurie A, Du Renqian, Yuan Bo, Gu Shen, Alfradique-Dunham Isabel, Kondapalli Vismaya, Hinojosa Evelyn, Stillwell Amanda, Young Emily, Zhang Chaofan, Song Xiaofei, Du Haowei, Gambin Tomasz, Jhangiani Shalini N, Coban Akdemir Zeynep, Muzny Donna M, Tejomurtula Anusha, Ross Owen A, Shaw Chad, Jankovic Joseph, Bi Weimin, Posey Jennifer E, Lupski James R, Shulman Joshua |
Metal Exposure and SNCA rs356219 Polymorphism Associated With Parkinson Disease and Parkinsonism. Frontiers in neurology 2020 12 11 556337. Lucchini Roberto G, Guazzetti Stefano, Renzetti Stefano, Broberg Karin, Caci Margherita, Covolo Loredana, Crippa Patrizia, Gelatti Umberto, Hashim Dana, Oppini Manuela, Pepe Fulvio, Pilotto Andrea, Passeri Chiara, Placidi Donatella, Rizzetti Maira Cristina, Turla Marinella, Wahlberg Karin, Padovani Alessand |
Fine-Mapping of SNCA in Rapid Eye Movement Sleep Behavior Disorder and Overt Synucleinopathies. Annals of neurology 2020 Jan . Krohn Lynne, Wu Richard Y J, Heilbron Karl, Ruskey Jennifer A, Laurent Sandra B, Blauwendraat Cornelis, Alam Armaghan, Arnulf Isabelle, Hu Michele T M, Dauvilliers Yves, Högl Birgit, Toft Mathias, Bjørnarå Kari Anne, Stefani Ambra, Holzknecht Evi, Monaca Christelle Charley, Abril Beatriz, Plazzi Giuseppe, Antelmi Elena, Ferini-Strambi Luigi, Young Peter, Heidbreder Anna, Cochen De Cock Valérie, Mollenhauer Brit, Sixel-Döring Friederike, Trenkwalder Claudia, Sonka Karel, Kemlink David, Figorilli Michela, Puligheddu Monica, Dijkstra Femke, Viaene Mineke, Oertel Wolfang, Toffoli Marco, Gigli Gian Luigi, Valente Mariarosaria, Gagnon Jean-François, Nalls Mike A, Singleton Andrew B, , Desautels Alex, Montplaisir Jacques Y, Cannon Paul, Ross Owen A, Boeve Bradley F, Dupré Nicolas, Fon Edward A, Postuma Ronald B, Pihlstrøm Lasse, Rouleau Guy A, Gan-Or Z |
Early-Onset Parkinson Disease Screening in Patients From Nigeria. Frontiers in neurology 2021 2 11 594927. Milanowski Lukasz M, Oshinaike Olajumoke, Broadway Benjamin J, Lindemann Jennifer A, Soto-Beasley Alexandra I, Walton Ronald L, Hanna Al-Shaikh Rana, Strongosky Audrey J, Fiesel Fabienne C, Ross Owen A, Springer Wolfdieter, Ogun Shamsideen Abayomi, Wszolek Zbigniew |
Biomarker characterization of clinical subtypes of Parkinson Disease. NPJ Parkinson's disease 2022 Aug 8 (1): 109. Deng Xiao, Saffari Seyed Ehsan, Liu Nan, Xiao Bin, Allen John Carson, Ng Samuel Yong Ern, Chia Nicole, Tan Yi Jayne, Choi Xinyi, Heng Dede Liana, Lo Yew-Long, Xu Zheyu, Tay Kay-Yaw, Au Wing-Lok, Ng Adeline, Tan Eng-King, Tan Louis C |
Genome-wide Association and Meta-analysis of Age at Onset in Parkinson Disease: Evidence From the COURAGE-PD Consortium.
Neurology 2022 8 99 (7): e698-e710. Grover Sandeep, Kumar Sreelatha Ashwin Ashok, Pihlstrom Lasse, Domenighetti Cloé, Schulte Claudia, Sugier Pierre-Emmanuel, Radivojkov-Blagojevic Milena, Lichtner Peter, Mohamed Océane, Portugal Berta, Landoulsi Zied, May Patrick, Bobbili Dheeraj, Edsall Connor, Bartusch Felix, Hanussek Maximilian, Krüger Jens, Hernandez Dena G, Blauwendraat Cornelis, Mellick George D, Zimprich Alexander, Pirker Walter, Tan Manuela, Rogaeva Ekaterina, Lang Anthony, Koks Sulev, Taba Pille, Lesage Suzanne, Brice Alexis, Corvol Jean-Christophe, Chartier-Harlin Marie-Christine, Mutez Eugenie, Brockmann Kathrin, Deutschländer Angela B, Hadjigeorgiou Georges M, Dardiotis Efthimos, Stefanis Leonidas, Simitsi Athina Maria, Valente Enza Maria, Petrucci Simona, Straniero Letizia, Zecchinelli Anna, Pezzoli Gianni, Brighina Laura, Ferrarese Carlo, Annesi Grazia, Quattrone Andrea, Gagliardi Monica, Burbulla Lena F, Matsuo Hirotaka, Kawamura Yusuke, Hattori Nobutaka, Nishioka Kenya, Chung Sun Ju, Kim Yun Joong, Pavelka Lukas, van de Warrenburg Bart P C, Bloem Bastiaan R, Singleton Andrew B, Aasly Jan, Toft Mathias, Guedes Leonor Correia, Ferreira Joaquim J, Bardien Soraya, Carr Jonathan, Tolosa Eduardo, Ezquerra Mario, Pastor Pau, Diez-Fairen Monica, Wirdefeldt Karin, Pedersen Nancy L, Ran Caroline, Belin Andrea C, Puschmann Andreas, Hellberg Clara, Clarke Carl E, Morrison Karen E, Krainc Dimitri, Farrer Matt J, Kruger Rejko, Elbaz Alexis, Gasser Thomas, Sharma Manu, |
Differences in Survival across Monogenic Forms of Parkinson's Disease. Annals of neurology 2023 3 . Lanore Aymeric, Casse Fanny, Tesson Christelle, Courtin Thomas, Menon Poornima Jayadev, Sambin Sara, Mangone Graziella, Mariani Louise-Laure, Lesage Suzanne, Brice Alexis, Elbaz Alexis, Corvol Jean-Christophe, |
Levodopa-carbidopa intestinal gel infusion (LCIG) in Parkinson disease with genetic mutations. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 2023 11 . R Balestrino, T Martone, M Toffoli, E Montanaro, M Fabbri, C A Artusi, A Romagnolo, M Zibetti, M Rizzone, S Goldwurm, L Lopiano, A H V Schapi |
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