Human Genome Epidemiology Literature Finder
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Records 1 - 30 (of 100 Records) |
| Query Trace: Parkinson Disease and LRRK2[original query] |
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| Parkinson disease-associated LRRK2 G2019S transgene disrupts marrow myelopoiesis and peripheral Th17 response. Journal of leukocyte biology 2017 10 102 (4): 1093-1102. Park Jeongho, Lee Jang-Won, Cooper Scott C, Broxmeyer Hal E, Cannon Jason R, Kim Chang |
| Association of LRRK2 Haplotype With Age at Onset in Parkinson Disease. JAMA neurology 2017 11 75 (1): 127-128. Xiao Bin, Deng Xiao, Ng Ebonne Yu-Lin, Allen John Carson, Lim Shen-Yang, Ahmad-Annuar Azlina, Tan Eng-Ki |
| The heterozygous R1441C mutation of leucine-rich repeat kinase 2 gene in a Chinese patient with Parkinson disease: A five-year follow-up and literatures review. Journal of the neurological sciences 2017 Feb 373 23-26. Peng Fang, Sun Yi-Min, Chen Chen, Luo Su-Shan, Li Da-Ke, Wang Yi-Xuan, Yang Ke, Liu Feng-Tao, Zuo Chuan-Tao, Ding Zheng-Tong, An Yu, Wu Jian-Jun, Wang Ji |
| 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, |
| Motor and non-motor features of Parkinson's disease in LRRK2 G2019S carriers versus matched controls. Journal of the neurological sciences 2018 4 388 203-207. Gunzler Steven A, Riley David E, Chen Shu G, Tatsuoka Curtis M, Johnson William M, Mieyal John J, Walter Ellen M, Whitney Christina M, Feng I Jung, Owusu-Dapaah Harry, Mittal Shivam O, Wilson-Delfosse Amy |
| LRRK2-associated Parkinson's disease patients have better stereopsis than idiopathic Parkinson disease. Clinical neurology and neurosurgery 2018 Apr 169 174-177. Sun Liang, Chan P |
| Leucine rich repeat kinase 2 (LRRK2) GLY2019SER mutation is absent in a second cohort of Nigerian Africans with Parkinson disease. PloS one 2018 13 (12): e0207984. Okubadejo Njideka U, Rizig Mie, Ojo Oluwadamilola O, Jonvik Hallgeir, Oshinaike Olajumoke, Brown Emmeline, Houlden Hen |
| Progression in the LRRK2-Asssociated Parkinson Disease Population. JAMA neurology 2018 1 75 (3): 312-319. Saunders-Pullman Rachel, Mirelman Anat, Alcalay Roy N, Wang Cuiling, Ortega Roberto A, Raymond Deborah, Mejia-Santana Helen, Orbe-Reilly Martha, Johannes Brooke A, Thaler Avner, Ozelius Laurie, Orr-Urtreger Avi, Marder Karen S, Giladi Nir, Bressman Susan B, |
| 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 |
| Genetic risk of Parkinson disease and progression:: An analysis of 13 longitudinal cohorts. Neurology. Genetics 2019 Aug 5 (4): e348. Iwaki Hirotaka, Blauwendraat Cornelis, Leonard Hampton L, Liu Ganqiang, Maple-Grødem Jodi, Corvol Jean-Christophe, Pihlstrøm Lasse, van Nimwegen Marlies, Hutten Samantha J, Nguyen Khanh-Dung H, Rick Jacqueline, Eberly Shirley, Faghri Faraz, Auinger Peggy, Scott Kirsten M, Wijeyekoon Ruwani, Van Deerlin Vivianna M, Hernandez Dena G, Day-Williams Aaron G, Brice Alexis, Alves Guido, Noyce Alastair J, Tysnes Ole-Bjørn, Evans Jonathan R, Breen David P, Estrada Karol, Wegel Claire E, Danjou Fabrice, Simon David K, Ravina Bernard, Toft Mathias, Heutink Peter, Bloem Bastiaan R, Weintraub Daniel, Barker Roger A, Williams-Gray Caroline H, van de Warrenburg Bart P, Van Hilten Jacobus J, Scherzer Clemens R, Singleton Andrew B, Nalls Mike |
| Network abnormalities among non-manifesting Parkinson disease related LRRK2 mutation carriers. Human brain mapping 2019 2 40 (8): 2546-2555. Jacob Yael, Rosenberg-Katz Keren, Gurevich Tanya, Helmich Rick C, Bloem Bastiaan R, Orr-Urtreger Avi, Giladi Nir, Mirelman Anat, Hendler Talma, Thaler Avn |
| Association of Subthalamic Deep Brain Stimulation With Motor, Functional, and Pharmacologic Outcomes in Patients With Monogenic Parkinson Disease: A Systematic Review and Meta-analysis. JAMA network open 2019 Feb 2 (2): e187800. Artusi Carlo Alberto, Dwivedi Alok K, Romagnolo Alberto, Pal Gian, Kauffman Marcelo, Mata Ignacio, Patel Dhiren, Vizcarra Joaquin A, Duker Andrew, Marsili Luca, Cheeran Binith, Woo Daniel, Contarino Maria Fiorella, Verhagen Leonard, Lopiano Leonardo, Espay Alberto J, Fasano Alfonso, Merola Aristi |
| Gender differences in prevalence of LRRK2-associated Parkinson disease: A meta-analysis of observational studies. Neuroscience letters 2019 Nov 134609. Chen Weiyao, Yan Xuejing, Lv Hong, Liu Yang, He Zhiyi, Luo Xiaogua |
| Somatic Mutations in LRRK2 Identify a Subset of Invasive Mammary Carcinomas Associated with High Mutation Burden. The American journal of pathology 2020 Sep . Parrilla Castellar Edgardo R, Plichta Jennifer K, Davis Richard, Gonzalez-Hunt Claudia, Sanders Laurie |
| 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 |
| Novel Variants in LRRK2 and GBA Identified in Latino Parkinson Disease Cohort Enriched for Caribbean Origin. Frontiers in neurology 2020 12 11 573733. Nuytemans Karen, Rajabli Farid, Bussies Parker L, Celis Katrina, Scott William K, Singer Carlos, Luca Corneliu C, Vinuela Angel, Pericak-Vance Margaret A, Vance Jeff |
| Association of caffeine and related analytes with resistance to Parkinson disease among LRRK2 mutation carriers: A metabolomic study. Neurology 2020 10 95 (24): e3428-e3437. Crotty Grace F, Maciuca Romeo, Macklin Eric A, Wang Junhua, Montalban Manuel, Davis Sonnet S, Alkabsh Jamal I, Bakshi Rachit, Chen Xiqun, Ascherio Alberto, Astarita Giuseppe, Huntwork-Rodriguez Sarah, Schwarzschild Michael |
| 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 |
| Identification of LRRK2 missense variants in the accelerating medicines partnership Parkinson's disease cohort. Human molecular genetics 2021 2 30 (6): 454-466. Bryant Nicole, Malpeli Nicole, Ziaee Julia, Blauwendraat Cornelis, Liu Zhiyong, , West Andrew |
| Peripheral synucleinopathy in Parkinson disease with LRRK2 G2385R variants. Annals of clinical and translational neurology 2021 Feb . Yang Jing, Wang Hao, Yuan Yanpeng, Fan Shiheng, Li Lanjun, Jiang Chenyang, Mao Chengyuan, Shi Changhe, Xu Yumi |
| 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 |
| Genetic factors affecting dopaminergic deterioration during the premotor stage of Parkinson disease. NPJ Parkinson's disease 2021 11 7 (1): 104. Lee Myung Jun, Pak Kyoungjune, Kim Han-Kyeol, Nudelman Kelly N, Kim Jong Hun, Kim Yun Hak, Kang Junho, Baek Min Seok, Lyoo Chul Hyou |
| 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 |
| Genetic variations in GBA1 and LRRK2 genes: Biochemical and clinical consequences in Parkinson disease. Frontiers in neurology 2022 8 13 971252. Smith Laura J, Lee Chiao-Yin, Menozzi Elisa, Schapira Anthony H |
| Elevated Urinary Rab10 Phosphorylation in Idiopathic Parkinson Disease. Movement disorders : official journal of the Movement Disorder Society 2022 5 37 (7): 1454-1464. Wang Shijie, Unnithan Shakthi, Bryant Nicole, Chang Allison, Rosenthal Liana S, Pantelyat Alexander, Dawson Ted M, Al-Khalidi Hussein R, West Andrew |
| Penetrance of Parkinson disease LRRK2 G2385R-associated variant in the Chinese population. European journal of neurology 2022 May . Wang Pei, Cui Peijing, Luo Qi, Chen Jie, Tang Huidong, Zhang Lina, Chen Shengdi, Ma Jianfa |
| 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 |
| Validity of the Short Weekly Calendar Planning Activity in patients with Parkinson disease and nonmanifesting LRRK2 and GBA carriers. European journal of neurology 2024 5 e16327. Tamara Schejter-Margalit, Noam Ben Binyamin, Avner Thaler, Inbal Maidan, Jesse M Cedarbaum, Avi Orr-Urtreger, Mali Gana Weisz, Orly Goldstein, Nir Giladi, Anat Mirelman, Rachel Kizo |
| Understanding Parkinson disease in Spain: Genetic and clinical insights. European journal of neurology 2024 11 e16499. Pilar Gómez-Garre, Miguel Martín-Bórnez, Laura Muñoz-Delgado, Rafael Díaz-Belloso, María Teresa Periñán, Marta Bonilla-Toribio, Dolores Buiza-Rueda, Daniel Macías-García, Silvia Jesús, Astrid Adarmes-Gómez, Elena Ojeda, Antonio Luque-Ambrosiani, Sergio García-Díaz, Rocío Pineda Sánchez, Fátima Carrillo, Pablo M |
- Page last reviewed:Feb 1, 2024
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