HuGE Literature Finder
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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, |
Genetic determinants of survival in progressive supranuclear palsy: a genome-wide association study.
![]() The Lancet. Neurology 2020 12 20 (2): 107-116. Jabbari Edwin, Koga Shunsuke, Valentino Rebecca R, Reynolds Regina H, Ferrari Raffaele, Tan Manuela M X, Rowe James B, Dalgard Clifton L, Scholz Sonja W, Dickson Dennis W, Warner Thomas T, Revesz Tamas, Höglinger Günter U, Ross Owen A, Ryten Mina, Hardy John, Shoai Maryam, Morris Huw R, |
Frequency of Loss of Function Variants in LRRK2 in Parkinson Disease. JAMA neurology 2018 Jul . Blauwendraat Cornelis, Reed Xylena, Kia Demis A, Gan-Or Ziv, Lesage Suzanne, Pihlstrøm Lasse, Guerreiro Rita, Gibbs J Raphael, Sabir Marya, Ahmed Sarah, Ding Jinhui, Alcalay Roy N, Hassin-Baer Sharon, Pittman Alan M, Brooks Janet, Edsall Connor, Hernandez Dena G, Chung Sun Ju, Goldwurm Stefano, Toft Mathias, Schulte Claudia, Bras Jose, Wood Nicholas W, Brice Alexis, Morris Huw R, Scholz Sonja W, Nalls Mike A, Singleton Andrew B, Cookson Mark R, |
Survival rates among Parkinson's disease patients who carry mutations in the LRRK2 and GBA genes. Movement disorders : official journal of the Movement Disorder Society 2018 10 33 (10): 1656-1660. Thaler Avner, Kozlovski Tal, Gurevich Tanya, Bar-Shira Anat, Gana-Weisz Mali, Orr-Urtreger Avi, Giladi Nir, Mirelman An |
Whole-exome sequencing of the BDR cohort: evidence to support the role of the PILRA gene in Alzheimer's disease. Neuropathology and applied neurobiology 2017 Nov . Patel T, Brookes K J, Turton J, Chaudhury S, Guetta-Baranes T, Guerreiro R, Bras J, Hernandez D, Singleton A, Francis P T, Hardy J, Morgan |
Penetrance estimate of LRRK2 p.G2019S mutation in individuals of non-Ashkenazi Jewish ancestry. Movement disorders : official journal of the Movement Disorder Society 2017 Jun . Lee Annie J, Wang Yuanjia, Alcalay Roy N, Mejia-Santana Helen, Saunders-Pullman Rachel, Bressman Susan, Corvol Jean-Christophe, Brice Alexis, Lesage Suzanne, Mangone Graziella, Tolosa Eduardo, Pont-Sunyer Claustre, Vilas Dolores, Schüle Birgitt, Kausar Farah, Foroud Tatiana, Berg Daniela, Brockmann Kathrin, Goldwurm Stefano, Siri Chiara, Asselta Rosanna, Ruiz-Martinez Javier, Mondragón Elisabet, Marras Connie, Ghate Taneera, Giladi Nir, Mirelman Anat, Marder Karen, |
Parkinson-Related LRRK2 Mutation R1628P Enables Cdk5 Phosphorylation of LRRK2 and Upregulates Its Kinase Activity. PloS one 2016 11 (3): e0149739. Shu Yang, Ming Jie, Zhang Pei, Wang Qingzhi, Jiao Fengjuan, Tian |
Disease penetrance of late-onset parkinsonism: a meta-analysis. JAMA neurology 2014 Dec 71 (12): 1535-9. Trinh Joanne, Guella Ilaria, Farrer Matthew Jam |
LRRK2 variant associated with Alzheimer's disease. Neurobiology of aging 2011 Nov 32 (11): 1990-3. Zhao Yi, Ho P, Yih Yuen, Chen C, Lee W L, Tan E |
Structural imaging in the presymptomatic stage of genetically determined parkinsonism. Neurobiology of disease 2010 Sep 39 (3): 402-8. Reetz Kathrin, Tadic Vera, Kasten Meike, Brüggemann Norbert, Schmidt Alexander, Hagenah Johann, Pramstaller Peter P, Ramirez Alfredo, Behrens Maria I, Siebner Hartwig R, Klein Christine, Binkofski Ferdina |
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- Page last updated:Mar 30, 2023
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