Human Genome Epidemiology Literature Finder
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Records 1 - 24 (of 24 Records) |
| Query Trace: Movement Disorders and GBA[original query] |
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| Fighting the risk of developing Parkinson's disease; clinical counseling for first degree relatives of patients with Parkinson's disease. Journal of the neurological sciences 2011 Jun . Giladi N, Mirelman A, Thaler A, Bar-Shira A, Gurevich T, Orr-Urtreger A |
| Genetic association study of glucocerebrosidase gene L444P mutation in essential tremor and multiple system atrophy in mainland China. Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia 2012 Nov . Sun QY, Guo JF, Han WW, Zuo X, Wang L, Yao LY, Pan Q, Xia K, Yan XX, Tang BS |
| Genotype and phenotype in Parkinson's disease: lessons in heterogeneity from deep brain stimulation. Movement disorders : official journal of the Movement Disorder Society 2013 Sep 28 (10): 1370-5. Angeli Aikaterina, Mencacci Niccolo E, Duran Raquel, Aviles-Olmos Iciar, Kefalopoulou Zinovia, Candelario Joseph, Rusbridge Sarah, Foley Jennifer, Pradhan Priyanka, Jahanshahi Marjan, Zrinzo Ludvic, Hariz Marwan, Wood Nicholas W, Hardy John, Limousin Patricia, Foltynie T |
| GBA-Associated Parkinson's Disease: Progression in a Deep Brain Stimulation Cohort. Journal of Parkinson's disease 2017 8 7 (4): 635-644. Lythe Vanessa, Athauda Dilan, Foley Jennifer, Mencacci Niccolò E, Jahanshahi Marjan, Cipolotti Lisa, Hyam Jonathan, Zrinzo Ludvic, Hariz Marwan, Hardy John, Limousin Patricia, Foltynie T |
| PREDICT-PD: An online approach to prospectively identify risk indicators of Parkinson's disease. Movement disorders : official journal of the Movement Disorder Society 2017 Jan . Noyce Alastair J, R'Bibo Lea, Peress Luisa, Bestwick Jonathan P, Adams-Carr Kerala L, Mencacci Niccolo E, Hawkes Christopher H, Masters Joseph M, Wood Nicholas, Hardy John, Giovannoni Gavin, Lees Andrew J, Schrag Anet |
| Utility and implications of exome sequencing in early-onset Parkinson's disease. Movement disorders : official journal of the Movement Disorder Society 2019 01 34 (1): 133-137. Trinh Joanne, Lohmann Katja, Baumann Hauke, Balck Alexander, Borsche Max, Brüggemann Norbert, Dure Leon, Dean Marissa, Volkmann Jens, Tunc Sinem, Prasuhn Jannik, Pawlack Heike, Imhoff Sophie, Lill Christina M, Kasten Meike, Bauer Peter, Rolfs Arndt, , Klein Christi |
| Evolution of prodromal parkinsonian features in a cohort of GBA mutation-positive individuals: a 6-year longitudinal study. Journal of neurology, neurosurgery, and psychiatry 2019 6 90 (10): 1091-1097. Avenali Micol, Toffoli Marco, Mullin Stephen, McNeil Alisdair, Hughes Derralynn A, Mehta A, Blandini Fabio, Schapira Anthony H |
| A clinical and genetic study of early-onset and familial parkinsonism in taiwan: An integrated approach combining gene dosage analysis and next-generation sequencing. Movement disorders : official journal of the Movement Disorder Society 2019 2 34 (4): 506-515. Lin Chin-Hsien, Chen Pei-Lung, Tai Chun-Hwei, Lin Hang-I, Chen Chih-Shan, Chen Meng-Ling, Wu Ruey-Me |
| Clinical and dopamine transporter imaging characteristics of non-manifest LRRK2 and GBA mutation carriers in the Parkinson's Progression Markers Initiative (PPMI): a cross-sectional study. The Lancet. Neurology 2019 11 19 (1): 71-80. Simuni Tanya, Uribe Liz, Cho Hyunkeun Ryan, Caspell-Garcia Chelsea, Coffey Christopher S, Siderowf Andrew, Trojanowski John Q, Shaw Leslie M, Seibyl John, Singleton Andrew, Toga Arthur W, Galasko Doug, Foroud Tatiana, Tosun Duygu, Poston Kathleen, Weintraub Daniel, Mollenhauer Brit, Tanner Caroline M, Kieburtz Karl, Chahine Lana M, Reimer Alyssa, Hutten Samantha J, Bressman Susan, Marek Kenneth, |
| GBA Variants in Parkinson's Disease: Clinical, Metabolomic, and Multimodal Neuroimaging Phenotypes. Movement disorders : official journal of the Movement Disorder Society 2020 8 35 (12): 2201-2210. Greuel Andrea, Trezzi Jean-Pierre, Glaab Enrico, Ruppert Marina C, Maier Franziska, Jäger Christian, Hodak Zdenka, Lohmann Katja, Ma Yilong, Eidelberg David, Timmermann Lars, Hiller Karsten, Tittgemeyer Marc, Drzezga Alexander, Diederich Nico, Eggers Carst |
| Common Variants Coregulate Expression of GBA and Modifier Genes to Delay Parkinson's Disease Onset. Movement disorders : official journal of the Movement Disorder Society 2020 6 35 (8): 1346-1356. Schierding William, Farrow Sophie, Fadason Tayaza, Graham Oscar E E, Pitcher Toni L, Qubisi Sara, Davidson Alan J, Perry Jo K, Anderson Tim J, Kennedy Martin A, Cooper Antony, O'Sullivan Justin |
| Clinical and Dopamine Transporter Imaging Characteristics of Leucine Rich Repeat Kinase 2 (LRRK2) and Glucosylceramidase Beta (GBA) Parkinson's Disease Participants in the Parkinson's Progression Markers Initiative: A Cross-Sectional Study. Movement disorders : official journal of the Movement Disorder Society 2020 2 35 (5): 833-844. Simuni Tanya, Brumm Michael C, Uribe Liz, Caspell-Garcia Chelsea, Coffey Christopher S, Siderowf Andrew, Alcalay Roy N, Trojanowski John Q, Shaw Leslie M, Seibyl John, Singleton Andrew, Toga Arthur W, Galasko Doug, Foroud Tatiana, Nudelman Kelly, Tosun-Turgut Duygu, Poston Kathleen, Weintraub Daniel, Mollenhauer Brit, Tanner Caroline M, Kieburtz Karl, Chahine Lana M, Reimer Alyssa, Hutten Samantha, Bressman Susan, Marek Kenneth, |
| Glucocerebrosidase Activity is not Associated with Parkinson's Disease Risk or Severity. Movement disorders : official journal of the Movement Disorder Society 2021 Sep . Omer Nurit, Giladi Nir, Gurevich Tanya, Bar-Shira Anat, Gana-Weisz Mali, Glinka Tal, Goldstein Orly, Kestenbaum Meir, Cedarbaum Jesse M, Mabrouk Omar S, Fraser Kyle B, Shirvan Julia C, Orr-Urtreger Avi, Mirelman Anat, Thaler Avn |
| Glucocerebrosidase Mutations and Motor Reserve in Parkinson's Disease. Journal of Parkinson's disease 2021 8 11 (4): 1715-1724. Chung Seok Jong, Lee Phil Hyu, Sohn Young H, Kim Yun Joo |
| Accelerating Medicines Partnership: Parkinson's Disease. Genetic Resource. Movement disorders : official journal of the Movement Disorder Society 2021 5 36 (8): 1795-1804. Iwaki Hirotaka, Leonard Hampton L, Makarious Mary B, Bookman Matt, Landin Barry, Vismer David, Casey Bradford, Gibbs J Raphael, Hernandez Dena G, Blauwendraat Cornelis, Vitale Daniel, Song Yeajin, Kumar Dinesh, Dalgard Clifton L, Sadeghi Mahdiar, Dong Xianjun, Misquitta Leonie, Scholz Sonja W, Scherzer Clemens R, Nalls Mike A, Biswas Shameek, Singleton Andrew B, , , |
| Intronic Haplotypes in the GBA Gene Do Not Predict Age at Diagnosis of Parkinson's Disease. Movement disorders : official journal of the Movement Disorder Society 2021 May . Toffoli Marco, Higgins Abigail, Lee Chiao, Koletsi Sofia, Chen Xiao, Eberle Michael, Sedlazeck Fritz J, Mullin Stephen, Proukakis Christos, Schapira Anthony H |
| Association of Dual LRRK2 G2019S and GBA Variations With Parkinson Disease Progression. JAMA network open 2021 Apr 4 (4): e215845. Ortega Roberto A, Wang Cuiling, Raymond Deborah, Bryant Nicole, Scherzer Clemens R, Thaler Avner, Alcalay Roy N, West Andrew B, Mirelman Anat, Kuras Yuliya, Marder Karen S, Giladi Nir, Ozelius Laurie J, Bressman Susan B, Saunders-Pullman Rach |
| Cytokines and Gaucher Biomarkers in Glucocerebrosidase Carriers with and Without Parkinson Disease. Movement disorders : official journal of the Movement Disorder Society 2021 Feb . Galper Jasmin, Balwani Manisha, Fahn Stanley, Waters Cheryl, Krohn Lynne, Gan-Or Ziv, Dzamko Nicolas, Alcalay Roy |
| The Association Between Lysosomal Storage Disorder Genes and Parkinson's Disease: A Large Cohort Study in Chinese Mainland Population. Frontiers in aging neuroscience 2021 12 13 749109. Zhao Yu-Wen, Pan Hong-Xu, Liu Zhenhua, Wang Yige, Zeng Qian, Fang Zheng-Huan, Luo Teng-Fei, Xu Kun, Wang Zheng, Zhou Xun, He Runcheng, Li Bin, Zhao Guihu, Xu Qian, Sun Qi-Ying, Yan Xin-Xiang, Tan Jie-Qiong, Li Jin-Chen, Guo Ji-Feng, Tang Bei-S |
| Neuroimaging in Glucocerebrosidase-Associated Parkinsonism: A Systematic Review. Movement disorders : official journal of the Movement Disorder Society 2022 5 37 (7): 1375-1393. Filippi Massimo, Balestrino Roberta, Basaia Silvia, Agosta Federi |
| Role of Lysosomal Gene Variants in Modulating GBA-Associated Parkinson's Disease Risk. Movement disorders : official journal of the Movement Disorder Society 2022 3 37 (6): 1202-1210. Straniero Letizia, Rimoldi Valeria, Monfrini Edoardo, Bonvegna Salvatore, Melistaccio Giada, Lake Julie, Soldà Giulia, Aureli Massimo, Shankaracharya , Keagle Pamela, Foroud Tatiana, Landers John E, Blauwendraat Cornelis, Zecchinelli Anna, Cilia Roberto, Di Fonzo Alessio, Pezzoli Gianni, Duga Stefano, Asselta Rosan |
| GBA and APOE Impact Cognitive Decline in Parkinson's Disease: A 10-Year Population-Based Study. Movement disorders : official journal of the Movement Disorder Society 2022 2 37 (5): 1016-1027. Szwedo Aleksandra A, Dalen Ingvild, Pedersen Kenn Freddy, Camacho Marta, Bäckström David, Forsgren Lars, Tzoulis Charalampos, Winder-Rhodes Sophie, Hudson Gavin, Liu Ganqiang, Scherzer Clemens R, Lawson Rachael A, Yarnall Alison J, Williams-Gray Caroline H, Macleod Angus D, Counsell Carl E, Tysnes Ole-Bjørn, Alves Guido, Maple-Grødem Jodi, |
| The genetic spectrum of a cohort of patients clinically diagnosed as Parkinson's disease in mainland China. NPJ Parkinson's disease 2023 5 9 (1): 76. Yi-Min Sun, Xin-Yue Zhou, Xiao-Niu Liang, Jin-Ran Lin, Yi-Dan Xu, Chen Chen, Si-Di Wei, Qi-Si Chen, Feng-Tao Liu, Jue Zhao, Yi-Lin Tang, Bo Shen, Lin-Hua Gan, Boxun Lu, Zheng-Tong Ding, Yu An, Jian-Jun Wu, Jian Wa |
| Levodopa-induced dyskinesia in early-onset Parkinson's disease (EOPD) associates with glucocerebrosidase mutation: A next-generation sequencing study in EOPD patients in Thailand. PloS one 2023 10 18 (10): e0293516. Sekh Thanprasertsuk, Prasit Phowthongkum, Thitipong Hopetrungraung, Chalalai Poorirerngpoom, Tikumphorn Sathirapatya, Patsorn Wichit, Onanong Phokaewvarangkul, Kornkiat Vongpaisarnsin, Saknan Bongsebandhu-Phubhakdi, Roongroj Bhidayasi |
- Page last reviewed:Feb 1, 2024
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