HuGE Literature Finder
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Records 1-100
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An updated analysis with 45,078 subjects confirms the association between SNCA rs11931074 and Parkinson's disease.
Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 2018 Aug . Liu Xu, Zhu Ruixia, Xiao Tongling, Li Qu, Zhu Ying, He Zhi |
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Evaluation of FGF 20 variants for susceptibility to Parkinson's disease in Eastern Indians.
Neuroscience letters 2018 Mar 675 68-73. Sadhukhan Dipanwita, Das Gautami, Biswas Arindam, Ghosh Soumitra, Das Shyamal K, Ray Kunal, Ray Jhar |
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Risk variants of the a-synuclein locus and REM sleep behavior disorder in Parkinson's disease: a genetic association study.
BMC neurology 2018 Feb 18 (1): 20. Bjørnarå Kari Anne, Pihlstrøm Lasse, Dietrichs Espen, Toft Mathi |
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Investigating the genetic architecture of dementia with Lewy bodies: a two-stage genome-wide association study.
The Lancet. Neurology 2018 Jan 17 (1): 64-74. Guerreiro Rita, Ross Owen A, Kun-Rodrigues Celia, Hernandez Dena G, Orme Tatiana, Eicher John D, Shepherd Claire E, Parkkinen Laura, Darwent Lee, Heckman Michael G, Scholz Sonja W, Troncoso Juan C, Pletnikova Olga, Ansorge Olaf, Clarimon Jordi, Lleo Alberto, Morenas-Rodriguez Estrella, Clark Lorraine, Honig Lawrence S, Marder Karen, Lemstra Afina, Rogaeva Ekaterina, St George-Hyslop Peter, Londos Elisabet, Zetterberg Henrik, Barber Imelda, Braae Anne, Brown Kristelle, Morgan Kevin, Troakes Claire, Al-Sarraj Safa, Lashley Tammaryn, Holton Janice, Compta Yaroslau, Van Deerlin Vivianna, Serrano Geidy E, Beach Thomas G, Lesage Suzanne, Galasko Douglas, Masliah Eliezer, Santana Isabel, Pastor Pau, Diez-Fairen Monica, Aguilar Miquel, Tienari Pentti J, Myllykangas Liisa, Oinas Minna, Revesz Tamas, Lees Andrew, Boeve Brad F, Petersen Ronald C, Ferman Tanis J, Escott-Price Valentina, Graff-Radford Neill, Cairns Nigel J, Morris John C, Pickering-Brown Stuart, Mann David, Halliday Glenda M, Hardy John, Trojanowski John Q, Dickson Dennis W, Singleton Andrew, Stone David J, Bras Jo |
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Analysis of age-related changes in psychosine metabolism in the human brain.
PloS one 2018 13 (2): e0193438. Marshall Michael S, Jakubauskas Benas, Bogue Wil, Stoskute Monika, Hauck Zane, Rue Emily, Nichols Matthew, DiAntonio Lisa L, van Breemen Richard B, Kordower Jeffrey H, Saavedra-Matiz Carlos A, Bongarzone Ernesto |
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Insufficient evidence for pathogenicity of SNCA His50Gln (H50Q) in Parkinson's disease.
Neurobiology of aging 2018 04 64 159.e5-159.e8. Blauwendraat Cornelis, Kia Demis A, Pihlstrøm Lasse, Gan-Or Ziv, Lesage Suzanne, Gibbs J Raphael, Ding Jinhui, Alcalay Roy N, Hassin-Baer Sharon, Pittman Alan M, Brooks Janet, Edsall Connor, Chung Sun Ju, Goldwurm Stefano, Toft Mathias, Schulte Claudia, , Hernandez Dena, Singleton Andrew B, Nalls Mike A, Brice Alexis, Scholz Sonja W, Wood Nicholas |
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Role of LRRK2 and SNCA in autosomal dominant Parkinson's disease in Turkey.
Parkinsonism & related disorders 2017 Dec . Kessler Christoph, Atasu Burcu, Hanagasi Hasmet, Simón-Sánchez Javier, Hauser Ann-Kathrin, Pak Meltem, Bilgic Basar, Erginel-Unaltuna Nihan, Gurvit Hakan, Gasser Thomas, Lohmann Eb |
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Association between SNCA rs2736990 polymorphism and Parkinson's disease: a meta-analysis.
Neuroscience letters 2017 Aug 658 102-107. Fang Jinni, Hou Binghui, Liu Hongxin, Zhang Xiaona, Wang Jing, Zhou Chang, Xie An |
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Association between gene polymorphism and depression in Parkinson's disease: A case-control study.
Journal of the neurological sciences 2017 Apr 375 231-234. Zheng Jinhua, Yang Xinglong, Zhao Quanzhen, Tian Sijia, Huang Hongyan, Chen Yalan, Xu Yanmi |
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SNCA 3'UTR genetic variants in patients with Parkinson's disease and REM sleep behavior disorder.
Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 2017 Apr . Toffoli M, Dreussi E, Cecchin E, Valente M, Sanvilli N, Montico M, Gagno S, Garziera M, Polano M, Savarese M, Calandra-Buonaura G, Placidi F, Terzaghi M, Toffoli G, Gigli G |
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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 |
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TMEM230 in Parkinson's disease.
Neurobiology of aging 2017 Mar . Ibanez Laura, Dube Umber, Budde John, Black Kathleen, Medvedeva Alexandra, Davis Albert A, Perlmutter Joel S, Benitez Bruno A, Cruchaga Carl |
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Analysis of the prion protein gene in multiple system atrophy.
Neurobiology of aging 2017 Jan 49 216.e15-216.e18. Chelban Viorica, Manole Andreea, Pihlstrøm Lasse, Schottlaender Lucia, Efthymiou Stephanie, OConnor Emer, Meissner Wassilios G, Holton Janice L, Houlden Hen |
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Neuropathological and genetic correlates of survival and dementia onset in synucleinopathies: a retrospective analysis.
The Lancet. Neurology 2017 Jan 16 (1): 55-65. Irwin David J, Grossman Murray, Weintraub Daniel, Hurtig Howard I, Duda John E, Xie Sharon X, Lee Edward B, Van Deerlin Vivianna M, Lopez Oscar L, Kofler Julia K, Nelson Peter T, Jicha Gregory A, Woltjer Randy, Quinn Joseph F, Kaye Jeffery, Leverenz James B, Tsuang Debby, Longfellow Katelan, Yearout Dora, Kukull Walter, Keene C Dirk, Montine Thomas J, Zabetian Cyrus P, Trojanowski John |
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Autosomal dominant Parkinson's disease: Incidence of mutations in LRRK2, SNCA, VPS35 and GBA genes in Brazil.
Neuroscience letters 2016 Dec 635 67-70. Abreu Gabriella de M, Valença Débora Cristina T, Campos Mário, da Silva Camilla P, Pereira João S, Araujo Leite Marco A, Rosso Ana Lucia, Nicaretta Denise H, Vasconcellos Luiz Felipe R, da Silva Delson José, Della Coletta Marcus V, Dos Santos Jussara M, Gonçalves Andressa P, Santos-Rebouças Cíntia B, Pimentel Márcia M |
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[Frequency of single nucleotide polymorphisms and alpha-synuclein haplotypes associated with sporadic Parkinson's disease in the Mexican population].
Revista de neurologia 2016 Oct 63 (8): 345-350. Davila-Ortiz de Montellano D J, Rodriguez-Violante M, Fresan A, Monroy-Jaramillo N, Yescas-Gomez |
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Aging modifies the effect of GCH1 RS11158026 on DAT uptake and Parkinson's disease clinical severity.
Neurobiology of aging 2016 Oct 50 39-46. Webb Joseph, Willette Auriel |
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Lack of RAB39B mutations in early-onset and familial Parkinson's disease in a Taiwanese cohort.
Neurobiology of aging 2016 Oct . Lin Hsien-Han, Wu Ruey-Meei, Lin Han-I, Chen Meng-Ling, Tai Chun-Hwei, Lin Chin-Hsi |
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Oligomeric ?-synuclein and glucocerebrosidase activity levels in GBA-associated Parkinson's disease.
Neuroscience letters 2016 Oct . Pchelina S, Emelyanov A, Baydakova G, Andoskin P, Senkevich K, Nikolaev M, Miliukhina I, Yakimovskii A, Timofeeva A, Fedotova E, Abramycheva N, Usenko T, Kulabukhova D, Lavrinova A, Kopytova A, Garaeva L, Nuzhnyi E, Illarioshkin S, Zakharova |
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SNCA mutation p.Ala53Glu is derived from a common founder in the Finnish population.
Neurobiology of aging 2016 Oct . Pasanen Petra, Palin Eino, Pohjolan-Pirhonen Risto, Pöyhönen Minna, Rinne Juha O, Päivärinta Markku, Martikainen Mika H, Kaasinen Valtteri, Hietala Marja, Gardberg Maria, Saukkonen Anna Maija, Eerola-Rautio Johanna, Kaakkola Seppo, Lyytinen Jukka, Tienari Pentti J, Paetau Anders, Suomalainen Anu, Myllykangas Lii |
A genome-wide association study in multiple system atrophy.
Neurology 2016 Sep . Sailer Anna, Scholz Sonja W, Nalls Michael A, Schulte Claudia, Federoff Monica, Price T Ryan, Lees Andrew, Ross Owen A, Dickson Dennis W, Mok Kin, Mencacci Niccolo E, Schottlaender Lucia, Chelban Viorica, Ling Helen, O'Sullivan Sean S, Wood Nicholas W, Traynor Bryan J, Ferrucci Luigi, Federoff Howard J, Mhyre Timothy R, Morris Huw R, Deuschl Günther, Quinn Niall, Widner Hakan, Albanese Alberto, Infante Jon, Bhatia Kailash P, Poewe Werner, Oertel Wolfgang, Höglinger Günter U, Wüllner Ullrich, Goldwurm Stefano, Pellecchia Maria Teresa, Ferreira Joaquim, Tolosa Eduardo, Bloem Bastiaan R, Rascol Olivier, Meissner Wassilios G, Hardy John A, Revesz Tamas, Holton Janice L, Gasser Thomas, Wenning Gregor K, Singleton Andrew B, Houlden Henry, |
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Association between common genetic risk variants and depression in Parkinson's disease: A dPD study in Chinese.
Parkinsonism & related disorders 2016 Sep . Dan Xiaojuan, Wang Chaodong, Zhang Jinglin, Gu Zhuqin, Zhou Yongtao, Ma Jinghong, Chan P |
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Parkinson's disease: SNCA-, PARK2-, and LRRK2- targeting microRNAs elevated in cingulate gyrus.
Parkinsonism & related disorders 2016 Sep . Tatura Roman, Kraus Theo, Giese Armin, Arzberger Thomas, Buchholz Malte, Höglinger Günter, Müller Ulri |
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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 |
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SNCA rs356182 variant increases risk of sporadic Parkinson's disease in ethnic Chinese.
Journal of the neurological sciences 2016 Sep 368 231-4. Cheng Lan, Wang Ling, Li Nan-Nan, Yu Wen-Juan, Sun Xiao-Yi, Li Jun-Ying, Zhou Dong, Peng Ro |
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LRRK2 variation and dementia with Lewy bodies.
Parkinsonism & related disorders 2016 Jul . Heckman Michael G, Soto-Ortolaza Alexandra I, Sanchez Contreras Monica Y, Murray Melissa E, Pedraza Otto, Diehl Nancy N, Walton Ronald, Labbé Catherine, Lorenzo-Betancor Oswaldo, Uitti Ryan J, van Gerpen Jay, Ertekin-Taner Nilüfer, Smith Glenn E, Kantarci Kejal, Savica Rodolfo, Jones David T, Graff-Radford Jonathan, Knopman David S, Lowe Val J, Jack Clifford R, Petersen Ronald C, Parisi Joseph E, Rademakers Rosa, Wszolek Zbigniew K, Graff-Radford Neill R, Ferman Tanis J, Dickson Dennis W, Boeve Bradley F, Ross Owen |
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The rs3857059 variant of the SNCA gene is associated with Parkinson's disease in Mexican Mestizos.
Arquivos de neuro-psiquiatria 2016 Jun 74 (6): 445-9. García S, Chavira-Hernández G, Gallegos-Arreola M P, Dávila-Maldonado L, García Martínez F, Montes Almanza L A, Palma-Flores C, Mondragón-Terán P, Alcaraz Estrada S L, López-Hernández L |
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?-synuclein genetic variability: A biomarker for dementia in Parkinson's 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 |
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Cerebrospinal fluid biomarkers and clinical features in leucine-rich repeat kinase 2 (LRRK2) mutation carriers.
Movement disorders : official journal of the Movement Disorder Society 2016 Apr . Vilas Dolores, Shaw Leslie M, Taylor Peggy, Berg Daniela, Brockmann Kathrin, Aasly Jan, Marras Connie, Pont-Sunyer Claustre, Ríos José, Marek Ken, Tolosa Eduar |
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SEPT14 Is Associated with a Reduced Risk for Parkinson's Disease and Expressed in Human Brain.
Journal of molecular neuroscience : MN 2016 Apr . Rozenkrantz Liron, Gan-Or Ziv, Gana-Weisz Mali, Mirelman Anat, Giladi Nir, Bar-Shira Anat, Orr-Urtreger A |
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Exonic rearrangements in the known Parkinson's disease-causing genes are a rare cause of the disease in South African patients.
Neuroscience letters 2016 Mar 619 168-171. van der Merwe Celia, Carr Jonathan, Glanzmann Brigitte, Bardien Sora |
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Involvement of Gaucher Disease Mutations in Parkinson Disease.
Current protein & peptide science 2016 Mar . Vilageliu Lluïsa, Grinberg Dani |
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Synaptotagmin XI in Parkinson's disease: New evidence from an association study in Spain and Mexico.
Journal of the neurological sciences 2016 Mar 362 321-5. Sesar Angel, Cacheiro Pilar, López-López Marisol, Camiña-Tato Montserrat, Quintáns Beatriz, Monroy-Jaramillo Nancy, Alonso-Vilatela María-Elisa, Cebrián Ernesto, Yescas-Gómez Petra, Ares Begoña, Rivas María-Teresa, Castro Alfonso, Carracedo Angel, Sobrido María-Jes |
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FBXO7 mutations in Parkinson's disease and multiple system atrophy.
Neurobiology of aging 2016 Jan . Conedera Silvio, Apaydin Hulya, Li Yuanzhe, Yoshino Hiroyo, Ikeda Aya, Matsushima Takashi, Funayama Manabu, Nishioka Kenya, Hattori Nobuta |
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The analysis of association between SNCA, HUSEYO and CSMD1 gene variants and Parkinson's disease in Iranian population.
Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 2016 Jan . Shahmohammadibeni Neda, Rahimi-Aliabadi Simin, Jamshidi Javad, Emamalizadeh Babak, Shahmohammadibeni Hossein Ali, Zare Bidoki Alireza, Akhavan-Niaki Haleh, Eftekhari Hajar, Abdollahi Shokoufeh, Shekari Khaniani Mahmoud, Shahmohammadibeni Mahnaz, Fazeli Atena, Motallebi Marzieh, Taghavi Shaghayegh, Ahmadifard Azadeh, Shafiei Zarneh Amir Ehtesham, Andarva Monavvar, Dadkhah Tahereh, Khademi Ehteram, Alehabib Elham, Rahimi Mahnoosh, Tafakhori Abbas, Atakhorrami Minoo, Darvish Hosse |
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[SNCA rs356219 AND rs356165 VARIANTS ARE ASSOCIATED WITH PARKINSON'S DISEASE AND INCREASED ALPHA-SYNUCLEIN GENE EXPRESSION IN THE CD45(+)-BLOOD CELLS].
Tsitologiia 2016 58 (2): 99-104. Emelyanov A K, Andoskin P A, Miliukhina I V, Timofeeva A A, Yakimovskii A F, Senkevich K A, Nikolaev M A, Pchelina S |
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Genetic causes of Parkinson's disease in the Maltese: a study of selected mutations in LRRK2, MTHFR, QDPR and SPR.
BMC medical genetics 2016 17 (1): 65. Zahra Charmaine, Tabone Christine, Camilleri Graziella, Felice Alex E, Farrugia Rosienne, Bezzina Wettinger Stephan |
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Resequencing analysis of five Mendelian genes and the top genes from genome-wide association studies in Parkinson's Disease.
Molecular neurodegeneration 2016 11 (1): 29. Benitez Bruno A, Davis Albert A, Jin Sheng Chih, Ibanez Laura, Ortega-Cubero Sara, Pastor Pau, Choi Jiyoon, Cooper Breanna, Perlmutter Joel S, Cruchaga Carl |
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Salivary total ?-synuclein, oligomeric ?-synuclein and SNCA variants in Parkinson's disease patients.
Scientific reports 2016 6 28143. Kang Wenyan, Chen Wei, Yang Qiong, Zhang Lina, Zhang Linyuan, Wang Xiaoying, Dong Fangyi, Zhao Yang, Chen Shuai, Quinn Thomas J, Zhang Jing, Chen Shengdi, Liu J |
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Variants in the SNCA gene associate with motor progression while variants in the MAPT gene associate with the severity of Parkinson's disease.
Parkinsonism & related disorders 2015 Dec . Wang Gang, Huang Yue, Wei Chen , Chen Shuai, Wang Ying, Xiao Qin, Liu Jun, Fung Victor S C, Halliday Glenda, Chen Sheng |
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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 |
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SNCA rs3822086 C>T Polymorphism Increases the Susceptibility to Parkinson's Disease in a Chinese Han Population.
Genetic testing and molecular biomarkers 2015 Sep 19 (9): 481-7. Jian Chong-Dong, Huang Jian-Min, Meng Lan-Qing, Li Xue-Bin, Huang Rui-Ya, Shi Sheng-Liang, Wu Yuan, Qin Chao, Chen Jin, Zhang Yan-Mei, Wang Shuang, Feng Yin-Ling, Zhou Sheng-Ni |
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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 |
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SNP rs11931074 of the SNCA gene may not be associated with multiple system atrophy in Chinese population.
The International journal of neuroscience 2015 Aug 125 (8): 612-5. Sun ZhanFang, Xiang XiaoShuang, Tang BeiSha, Chen Zhao, Peng HuiRong, Xia Kun, Jiang Ho |
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A cytosine-thymine (CT)-rich haplotype in intron 4 of SNCA confers risk for Lewy body pathology in Alzheimer's disease and affects SNCA expression.
Alzheimer's & dementia : the journal of the Alzheimer's Association 2015 Jun . Lutz Michael W, Saul Robert, Linnertz Colton, Glenn Omolara-Chinue, Roses Allen D, Chiba-Falek Orn |
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Alpha-synuclein A53T mutation is not frequent on a sample of Brazilian Parkinson's disease patients.
Arquivos de neuro-psiquiatria 2015 Jun 73 (6): 506-9. Longo Gabriela S, Pinhel Marcela A S, Gregório Michele L, Oliveira Bruno A P, Quinhoneiro Driele C G, Tognola Waldir A, Oliveira Fábio N, Cezario Sabrina M, Sado Caroline L, Nakazone Marcelo A, Calastri Maria C J, Souza Dorotéia R |
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Hyposmia correlates with SNCA variant and non-motor symptoms in Chinese patients with Parkinson's disease.
Parkinsonism & related disorders 2015 Jun 21 (6): 610-4. Chen Wei, Kang Wen-Yan, Chen Shuai, Wang Ying, Xiao Qin, Wang Gang, Liu Jun, Chen Sheng- |
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Parkinson disease: ?-synuclein mutational screening and new clinical insight into the p.E46K mutation.
Parkinsonism & related disorders 2015 Jun 21 (6): 586-9. Pimentel Márcia M G, Rodrigues Fabíola C, Leite Marco Antônio A, Campos Júnior Mário, Rosso Ana Lucia, Nicaretta Denise H, Pereira João S, Silva Delson José, Della Coletta Marcus V, Vasconcellos Luiz Felipe R, Abreu Gabriella M, Dos Santos Jussara M, Santos-Rebouças Cíntia |
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Head injury, ?-synuclein genetic variability and Parkinson's disease.
European journal of neurology : the official journal of the European Federation of Neurological Societies 2015 May 22 (5): 874-8. Lee P C, Bordelon Y, Bronstein J, Sinsheimer J S, Farrer M, Ritz |
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Polygenic determinants of Parkinson's disease in a Chinese population.
Neurobiology of aging 2015 Apr 36 (4): 1765.e1-6. Guo Ji-Feng, Li Kai, Yu Ri-Li, Sun Qi-Yin, Wang Lei, Yao Ling-Yan, Hu Ya-Cen, Lv Zhan-Yun, Luo Lin-Zi, Shen Lu, Jiang Hong, Yan Xin-Xiang, Pan Qian, Xia Kun, Tang Bei-S |
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Alpha-synuclein (SNCA) polymorphisms and susceptibility to Parkinson's disease: a meta-analysis.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2015 Mar 168B (2): 123-34. Han Wei, Liu Yingli, Mi Yingjun, Zhao Jing, Liu Dianwu, Tian Qingb |
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Head injury, potential interaction with genes, and risk for Parkinson's disease.
Parkinsonism & related disorders 2015 Mar 21 (3): 292-6. Gao Jianjun, Liu Rui, Zhao Edward, Huang Xuemei, Nalls Michael A, Singleton Andrew B, Chen Hongl |
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Identification of candidate genes for Parkinson's disease through blood transcriptome analysis in LRRK2-G2019S carriers, idiopathic cases, and controls.
Neurobiology of aging 2015 Feb 36 (2): 1105-9. Infante Jon, Prieto Carlos, Sierra María, Sánchez-Juan Pascual, González-Aramburu Isabel, Sánchez-Quintana Coro, Berciano José, Combarros Onofre, Sainz Jes |
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Motor phenotype of LRRK2-associated Parkinson's disease: a tunisian longitudinal study.
Movement disorders : official journal of the Movement Disorder Society 2015 Feb 30 (2): 253-8. Nabli Fatma, Ben Sassi Samia, Amouri Rim, Duda John E, Farrer Matthew J, Hentati Fayç |
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Association of the COQ2 V393A Variant with Parkinson's Disease: A Case-Control Study and Meta-Analysis.
PloS one 2015 10 (6): e0130970. Yang Xinglong, Xi Jing, Zhao Quanzhen, Jia Hua, An Ran, Liu Zhuolin, Xu Yanmi |
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Did ?-Synuclein and Glucocerebrosidase Coevolve? Implications for Parkinson's Disease.
PloS one 2015 10 (7): e0133863. Gruschus James |
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Genetic Variants of SNCA Are Associated with Susceptibility to Parkinson's Disease but Not Amyotrophic Lateral Sclerosis or Multiple System Atrophy in a Chinese Population.
PloS one 2015 10 (7): e0133776. Chen YongPing, Wei Qian-Qian, Ou RuWei, Cao Bei, Chen XuePing, Zhao Bi, Guo XiaoYan, Yang Yuan, Chen Ke, Wu Ying, Song Wei, Shang Hui-Fa |
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Phosphorylated ?-synuclein in Parkinson's disease: correlation depends on disease severity.
Acta neuropathologica communications 2015 3 7. Stewart Tessandra, Sossi Vesna, Aasly Jan O, Wszolek Zbigniew K, Uitti Ryan J, Hasegawa Kazuko, Yokoyama Teruo, Zabetian Cyrus P, Leverenz James B, Stoessl Alexander Jon, Wang Yu, Ginghina Carmen, Liu Changqin, Cain Kevin C, Auinger Peggy, Kang Un Jung, Jensen Poul Henning, Shi Min, Zhang Ji |
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Selective loss of glucocerebrosidase activity in sporadic Parkinson's disease and dementia with Lewy bodies.
Molecular neurodegeneration 2015 10 15. Chiasserini Davide, Paciotti Silvia, Eusebi Paolo, Persichetti Emanuele, Tasegian Anna, Kurzawa-Akanbi Marzena, Chinnery Patrick F, Morris Christopher M, Calabresi Paolo, Parnetti Lucilla, Beccari Tomma |
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SNCA Gene, but Not MAPT, Influences Onset Age of Parkinson's Disease in Chinese and Australians.
BioMed research international 2015 2015 135674. Huang Yue, Wang Gang, Rowe Dominic, Wang Ying, Kwok John B J, Xiao Qin, Mastaglia Frank, Liu Jun, Chen Sheng-Di, Halliday Glen |
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Disease penetrance of late-onset parkinsonism: a meta-analysis.
JAMA neurology 2014 Dec 71 (12): 1535-9. Trinh Joanne, Guella Ilaria, Farrer Matthew Jam |
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Genetic analysis implicates APOE, SNCA and suggests lysosomal dysfunction in the etiology of dementia with Lewy bodies.
Human molecular genetics 2014 Dec 23 (23): 6139-46. Bras Jose, Guerreiro Rita, Darwent Lee, Parkkinen Laura, Ansorge Olaf, Escott-Price Valentina, Hernandez Dena G, Nalls Michael A, Clark Lorraine N, Honig Lawrence S, Marder Karen, Van Der Flier Wiesje M, Lemstra Afina, Scheltens Philip, Rogaeva Ekaterina, St George-Hyslop Peter, Londos Elisabet, Zetterberg Henrik, Ortega-Cubero Sara, Pastor Pau, Ferman Tanis J, Graff-Radford Neill R, Ross Owen A, Barber Imelda, Braae Anne, Brown Kristelle, Morgan Kevin, Maetzler Walter, Berg Daniela, Troakes Claire, Al-Sarraj Safa, Lashley Tammaryn, Compta Yaroslau, Revesz Tamas, Lees Andrew, Cairns Nigel, Halliday Glenda M, Mann David, Pickering-Brown Stuart, Dickson Dennis W, Singleton Andrew, Hardy Jo |
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SNCA variants rs2736990 and rs356220 as risk factors for Parkinson's disease but not for amyotrophic lateral sclerosis and multiple system atrophy in a Chinese population.
Neurobiology of aging 2014 Dec 35 (12): 2882.e1-6. Guo Xiao Yan, Chen Yong Ping, Song Wei, Zhao Bi, Cao Bei, Wei Qian Qian, Ou Ru Wei, Yang Yuan, Yuan Li Xing, Shang Hui-Fa |
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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 |
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?-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 |
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Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease.
Nature genetics 2014 Sep 46 (9): 989-93. Nalls Mike A, Pankratz Nathan, Lill Christina M, Do Chuong B, Hernandez Dena G, Saad Mohamad, DeStefano Anita L, Kara Eleanna, Bras Jose, Sharma Manu, Schulte Claudia, Keller Margaux F, Arepalli Sampath, Letson Christopher, Edsall Connor, Stefansson Hreinn, Liu Xinmin, Pliner Hannah, Lee Joseph H, Cheng Rong, , , , , , , , , , , , , Ikram M Arfan, Ioannidis John P A, Hadjigeorgiou Georgios M, Bis Joshua C, Martinez Maria, Perlmutter Joel S, Goate Alison, Marder Karen, Fiske Brian, Sutherland Margaret, Xiromerisiou Georgia, Myers Richard H, Clark Lorraine N, Stefansson Kari, Hardy John A, Heutink Peter, Chen Honglei, Wood Nicholas W, Houlden Henry, Payami Haydeh, Brice Alexis, Scott William K, Gasser Thomas, Bertram Lars, Eriksson Nicholas, Foroud Tatiana, Singleton Andrew |
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The PD-associated alpha-synuclein promoter Rep1 allele 2 shows diminished frequency in restless legs syndrome.
Neurogenetics 2014 Aug 15 (3): 189-92. Lahut Suna, Vadasz David, Depboylu Candan, Ries Vincent, Krenzer Martina, Stiasny-Kolster Karin, Basak A Nazli, Oertel Wolfgang H, Auburger Geo |
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Alpha-synuclein repeat variants and survival in Parkinson's disease.
Movement disorders : official journal of the Movement Disorder Society 2014 Jul 29 (8): 1053-7. Chung Sun Ju, Biernacka Joanna M, Armasu Sebastian M, Anderson Kari, Frigerio Roberta, Aasly Jan O, Annesi Grazia, Bentivoglio Anna Rita, Brighina Laura, Chartier-Harlin Marie-Christine, Goldwurm Stefano, Hadjigeorgiou Georgios, Jasinska-Myga Barbara, Jeon Beom Seok, Kim Yun Joong, Krüger Rejko, Lesage Suzanne, Markopoulou Katerina, Mellick George, Morrison Karen E, Puschmann Andreas, Tan Eng-King, Crosiers David, Theuns Jessie, Van Broeckhoven Christine, Wirdefeldt Karin, Wszolek Zbigniew K, Elbaz Alexis, Maraganore Demetrius M, |
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Analysis of Parkinson's disease brain-derived DNA for alpha-synuclein coding somatic mutations.
Movement disorders : official journal of the Movement Disorder Society 2014 Jul 29 (8): 1060-4. Proukakis Christos, Shoaee Maryiam, Morris James, Brier Timothy, Kara Eleanna, Sheerin Una-Marie, Charlesworth Gavin, Tolosa Eduardo, Houlden Henry, Wood Nicholas W, Schapira Anthony |
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Does ?-synuclein have a dual and opposing effect in preclinical vs. clinical Parkinson's disease?
Parkinsonism & related disorders 2014 Jun 20 (6): 584-9; discussion 584. Markopoulou Katerina, Biernacka Joanna M, Armasu Sebastian M, Anderson Kari J, Ahlskog J Eric, Chase Bruce A, Chung Sun Ju, Cunningham Julie M, Farrer Matthew, Frigerio Roberta, Maraganore Demetrius |
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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 |
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Protective effect of LRRK2 p.R1398H on risk of Parkinson's disease is independent of MAPT and SNCA variants.
Neurobiology of aging 2014 Jan 35 (1): 266.e5-14. Heckman Michael G, Elbaz Alexis, Soto-Ortolaza Alexandra I, Serie Daniel J, Aasly Jan O, Annesi Grazia, Auburger Georg, Bacon Justin A, Boczarska-Jedynak Magdalena, Bozi Maria, Brighina Laura, Chartier-Harlin Marie-Christine, Dardiotis Efthimios, Destée Alain, Ferrarese Carlo, Ferraris Alessandro, Fiske Brian, Gispert Suzana, Hadjigeorgiou Georgios M, Hattori Nobutaka, Ioannidis John P A, Jasinska-Myga Barbara, Jeon Beom S, Kim Yun Joong, Klein Christine, Kruger Rejko, Kyratzi Elli, Lin Chin-Hsien, Lohmann Katja, Loriot Marie-Anne, Lynch Timothy, Mellick George D, Mutez Eugénie, Opala Grzegorz, Park Sung Sup, Petrucci Simona, Quattrone Aldo, Sharma Manu, Silburn Peter A, Sohn Young Ho, Stefanis Leonidas, Tadic Vera, Tomiyama Hiroyuki, Uitti Ryan J, Valente Enza Maria, Vassilatis Demetrios K, Vilariño-Güell Carles, White Linda R, Wirdefeldt Karin, Wszolek Zbigniew K, Wu Ruey-Meei, Xiromerisiou Georgia, Maraganore Demetrius M, Farrer Matthew J, Ross Owen A, |
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Comparable autoantibody serum levels against amyloid- and inflammation-associated proteins in Parkinson's disease patients and controls.
PloS one 2014 9 (2): e88604. Maetzler Walter, Apel Anja, Langkamp Markus, Deuschle Christian, Dilger Sarah Selina, Stirnkorb Johannes Georg, Schulte Claudia, Schleicher Erwin, Gasser Thomas, Berg Danie |
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Identification of a novel Parkinson's disease locus via stratified genome-wide association study.
BMC genomics 2014 15 (1): 118. Hill-Burns Erin M, Wissemann William T, Hamza Taye H, Factor Stewart A, Zabetian Cyrus P, Payami Hayd |
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Low prevalence of most frequent pathogenic variants of six PARK genes in sporadic Parkinson's disease.
Folia neuropathologica / Association of Polish Neuropathologists and Medical Research Centre, Polish Academy of Sciences 2014 52 (1): 22-9. García Silvia, López-Hernández Luz Berenice, Suarez-Cuenca Juan Antonio, Solano-Rojas Marlene, Gallegos-Arreola Martha P, Gama-Moreno Olga, Valdez-Anguiano Paulina, Canto Patricia, Dávila-Maldonado Luis, Cuevas-García Carlos F, Coral-Vázquez Ramón Mauric |
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Confluence of ?-synuclein, tau, and ?-amyloid pathologies in dementia with Lewy bodies.
Journal of neuropathology and experimental neurology 2013 Dec 72 (12): 1203-12. Colom-Cadena Martí, Gelpi Ellen, Charif Sara, Belbin Olivia, Blesa Rafael, Martí Maria J, Clarimón Jordi, Lleó Alber |
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Genetic assessment of familial and early-onset Parkinson's disease in a Greek population.
European journal of neurology : the official journal of the European Federation of Neurological Societies 2013 Dec . Bozi M, Papadimitriou D, Antonellou R, Moraitou M, Maniati M, Vassilatis DK, Papageorgiou SG, Leonardos A, Tagaris G, Malamis G, Theofilopoulos D, Kamakari S, Stamboulis E, Hadjigeorgiou GM, Athanassiadou A, Michelakakis H, Papadimitriou A, Gasser T, Stefanis L |
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Alzheimer's disease and Parkinson's disease genome-wide association study top hits and risk of Parkinson's disease in Korean population.
Neurobiology of aging 2013 Nov 34 (11): 2695.e1-7. Chung Sun Ju, Jung Yusun, Hong Myunghee, Kim Mi Jung, You Sooyeoun, Kim Young Jin, Kim Juyeon, Song Kyuyou |
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Analysis of genome-wide association study-linked loci in Parkinson's disease of Mainland China.
Movement disorders : official journal of the Movement Disorder Society 2013 Nov 28 (13): 1892-5. Liu Jun, Xiao Qin, Wang Ying, Xu Zhi-Min, Wang Ying, Yang Qiong, Wang Gang, Tan Yu-Yan, Ma Jian-Fang, Zhang Jin, Huang Wei, Chen Sheng- |
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Association between early-onset Parkinson disease and 22q11.2 deletion syndrome: identification of a novel genetic form of Parkinson disease and its clinical implications.
JAMA neurology 2013 Nov 70 (11): 1359-66. Butcher Nancy J, Kiehl Tim-Rasmus, Hazrati Lili-Naz, Chow Eva W C, Rogaeva Ekaterina, Lang Anthony E, Bassett Anne |
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Novel A18T and pA29S substitutions in ?-synuclein may be associated with sporadic Parkinson's disease.
Parkinsonism & related disorders 2013 Nov 19 (11): 1057-60. Hoffman-Zacharska Dorota, Koziorowski Dariusz, Ross Owen A, Milewski Micha?, Pozna?ski Jaros?aw, Jurek Marta, Wszolek Zbigniew K, Soto-Ortolaza Alexandra, S?awek Jaros?aw, Janik Piotr, Jamrozik Zygmunt, Potulska-Chromik Anna, Jasi?ska-Myga Barbara, Opala Grzegorz, Krygowska-Wajs Anna, Czy?ewski Krzysztof, Dickson Dennis W, Bal Jerzy, Friedman Andrz |
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High-resolution survey in familial Parkinson disease genes reveals multiple independent copy number variation events in PARK2.
Human mutation 2013 Aug 34 (8): 1071-4. Wang Liyong, Nuytemans Karen, Bademci Guney, Jauregui Cherylyn, Martin Eden R, Scott William K, Vance Jeffery M, Zuchner Steph |
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SNCA: major genetic modifier of age at onset of Parkinson's disease.
Movement disorders : official journal of the Movement Disorder Society 2013 Aug 28 (9): 1217-21. Brockmann Kathrin, Schulte Claudia, Hauser Ann-Kathrin, Lichtner Peter, Huber Heiko, Maetzler Walter, Berg Daniela, Gasser Thom |
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SNCA rs356219 variant increases risk of sporadic Parkinson's disease in ethnic Chinese.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2013 Jul 162B (5): 452-6. Li Nan-Nan, Mao Xue-Ye, Chang Xue-Li, Zhao Dong-Mei, Zhang Jin-Hong, Liao Qiao, Yu Wen-Juan, Tan Eng-King, Peng Ro |
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Genetic susceptibility loci, environmental exposures, and Parkinson's disease: a case-control study of gene-environment interactions.
Parkinsonism & related disorders 2013 Jun 19 (6): 595-9. Chung Sun Ju, Armasu Sebastian M, Anderson Kari J, Biernacka Joanna M, Lesnick Timothy G, Rider David N, Cunningham Julie M, Ahlskog J Eric, Frigerio Roberta, Maraganore Demetrius |
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MAPT H1 haplotype is associated with enhanced ?-synuclein deposition in dementia with Lewy bodies.
Neurobiology of aging 2013 Mar 34 (3): 936-42. Colom-Cadena Martí, Gelpi Ellen, Martí María J, Charif Sara, Dols-Icardo Oriol, Blesa Rafael, Clarimón Jordi, Lleó Alber |
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Low CSF Levels of Both ?-Synuclein and the ?-Synuclein Cleaving Enzyme Neurosin in Patients with Synucleinopathy.
PloS one 2013 8 (1): 1. Wennström M, Surova Y, Hall S, Nilsson C, Minthon L, Boström F, Hansson O, Nielsen HM |
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P268S in NOD2 associates with susceptibility to Parkinson's disease in Chinese population.
Behavioral and brain functions : BBF 2013 9 (1): 19. Ma Qilin, An Xingkai, Li Zhiming, Zhang Huanjing, Huang Wenqing, Cai Liangliang, Hu Peng, Lin Qing, Tzeng Chi-Me |
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[Analysis of the rs12720208 single-nucleotide polymorphism of the FGF20 gene in Russian patients with sporadic Parkinson's disease].
Genetika 2012 Dec 48 (12): 1437-9. Ustinova V V, Shadrina M I, Fedotova E Iu, Illarioshkin S N, Limborskaia S A, Slominski? P |
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Variants in the 3'UTR of SNCA do not affect miRNA-433 binding and alpha-synuclein expression.
European journal of human genetics : EJHG 2012 Dec 20 (12): 1265-9. Schmitt Ina, Wüllner Ullrich, van Rooyen Jan Pierre, Khazneh Hassan, Becker Julian, Volk Alexander, Kubisch Christian, Becker Tim, Kostic Vladimir S, Klein Christine, Ramirez Alfre |
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Genetic variants of SNCA and LRRK2 genes are associated with sporadic PD susceptibility: A replication study in a Taiwanese cohort.
Parkinsonism & related disorders 2012 Nov . Wu-Chou YH, Chen YT, Yeh TH, Chang HC, Weng YH, Lai SC, Huang CL, Chen RS, Huang YZ, Chen CC, Hung J, Chuang WL, Lin WY, Chen CH, Lu CS |
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Supportive evidence for 11 loci from genome-wide association studies in Parkinson's disease.
Neurobiology of aging 2012 Nov . Pihlstrøm L, Axelsson G, Bjørnarå KA, Dizdar N, Fardell C, Forsgren L, Holmberg B, Larsen JP, Linder J, Nissbrandt H, Tysnes OB, Ohman E, Dietrichs E, Toft M |
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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 |
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GBA mutations increase risk for Lewy body disease with and without Alzheimer disease pathology.
Neurology 2012 Oct . Tsuang D, Leverenz JB, Lopez OL, Hamilton RL, Bennett DA, Schneider JA, Buchman AS, Larson EB, Crane PK, Kaye JA, Kramer P, Woltjer R, Kukull W, Nelson PT, Jicha GA, Neltner JH, Galasko D, Masliah E, Trojanowski JQ, Schellenberg GD, Yearout D, Huston H, Fritts-Penniman A, Mata IF, Wan JY, Edwards KL, Montine TJ, Zabetian CP |
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Age at onset in LRRK2-associated PD is modified by SNCA variants.
Journal of molecular neuroscience : MN 2012 Sep 48 (1): 245-7. Botta-Orfila Teresa, Ezquerra Mario, Pastor Pau, Fernández-Santiago Rubén, Pont-Sunyer Claustre, Compta Yaroslau, Lorenzo-Betancor Oswaldo, Samaranch Lluis, Martí Maria José, Valldeoriola Francesc, Calopa Matilde, Fernández Manel, Aguilar Miquel, de Fabregas Oriol, Hernández-Vara Jorge, Tolosa Edua |
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Penetrance of LRRK2 G2385R and R1628P is modified by common PD-associated genetic variants.
Parkinsonism & related disorders 2012 Sep 18 (8): 958-63. Wang Chaodong, Cai Yanning, Zheng Zheng, Tang Bei-Sha, Xu Yanming, Wang Tao, Ma Jinghong, Chen Sheng-Di, Langston J William, Tanner Caroline M, Chan Piu, |
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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, |
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A search for SNCA 3' UTR variants identified SNP rs356165 as a determinant of disease risk and onset age in Parkinson's disease.
Journal of molecular neuroscience : MN 2012 Jul 47 (3): 425-30. Cardo Lucía F, Coto Eliecer, de Mena Lorena, Ribacoba René, Lorenzo-Betancor Oswaldo, Pastor Pau, Samaranch Lluis, Mata Ignacio F, Díaz Marta, Moris Germán, Menéndez Manuel, Corao Ana I, Alvarez Victor |
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UCHL1 S18Y variant is a risk factor for Parkinson's disease in Japan.
BMC neurology 2012 Jul 12 (1): 1. Miyake Y, Tanaka K, Fukushima W, Kiyohara C, Sasaki S, Tsuboi Y, Yamada T, Oeda T, Shimada H, Kawamura N, Sakae N, Fukuyama H, Hirota Y, Nagai M, Study Group TF |
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SNP rs356219 of the ?-synuclein (SNCA) gene is associated with Parkinson's disease in a Chinese Han population.
Parkinsonism & related disorders 2012 Jun 18 (5): 632-4. Pan Fenghua, Dong Hairong, Ding Haixia, Ye Min, Liu Weiguo, Wu Yanfeng, Zhang Xueling, Chen Zhuoyou, Luo Yang, Ding Xinshe |
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