HuGE Literature Finder
Records 1-30
|
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 |
|
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 |
|
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 |
|
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 |
|
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 |
|
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, |
|
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 |
|
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 |
|
High-resolution arrays reveal burden of copy number variations on Parkinson disease genes associated with increased disease risk in random cohorts.
Neurological research 2016 Jul 1-11. Murthy Megha N, Veerappa Avinash M, Seshachalam Keshava B, Ramachandra Nallur |
|
Urinary LRRK2 phosphorylation predicts parkinsonian phenotypes in G2019S LRRK2 carriers.
Neurology 2016 Mar 86 (11): 994-9. Fraser Kyle B, Moehle Mark S, Alcalay Roy N, West Andrew B, |
|
A Personalized Approach to Parkinson's Disease Patients Based on Founder Mutation Analysis.
Frontiers in neurology 2016 7 71. Giladi Nir, Mirelman Anat, Thaler Avner, Orr-Urtreger A |
|
Greater motor progression in patients with Parkinson disease who carry LRRK2 risk variants.
Neurology 2015 Sep 85 (12): 1039-42. Oosterveld Linda P, Allen John C, Ng Ebonne Y L, Seah Soo-Hoon, Tay Kay-Yaw, Au Wing-Lok, Tan Eng-King, Tan Louis C |
|
Novel recruitment strategy to enrich for LRRK2 mutation carriers.
Molecular genetics & genomic medicine 2015 Sep 3 (5): 404-12. Foroud Tatiana, Smith Danielle, Jackson Jacqueline, Verbrugge Jennifer, Halter Cheryl, Wetherill Leah, Sims Katherine, Xin Winnie, Arnedo Vanessa, Lasch Shirley, Marek Kenneth, |
|
LRRK2 mutations in Parkinson disease; a sex effect or lack thereof? A meta-analysis.
Parkinsonism & related disorders 2015 Jul 21 (7): 778-82. Gan-Or Ziv, Leblond Claire S, Mallett Victoria, Orr-Urtreger Avi, Dion Patrick A, Rouleau Guy |
|
Clinical correlations with Lewy body pathology in LRRK2-related Parkinson disease.
JAMA neurology 2015 Jan 72 (1): 100-5. Kalia Lorraine V, Lang Anthony E, Hazrati Lili-Naz, Fujioka Shinsuke, Wszolek Zbigniew K, Dickson Dennis W, Ross Owen A, Van Deerlin Vivianna M, Trojanowski John Q, Hurtig Howard I, Alcalay Roy N, Marder Karen S, Clark Lorraine N, Gaig Carles, Tolosa Eduardo, Ruiz-Martínez Javier, Marti-Masso Jose F, Ferrer Isidre, López de Munain Adolfo, Goldman Samuel M, Schüle Birgitt, Langston J William, Aasly Jan O, Giordana Maria T, Bonifati Vincenzo, Puschmann Andreas, Canesi Margherita, Pezzoli Gianni, Maues De Paula Andre, Hasegawa Kazuko, Duyckaerts Charles, Brice Alexis, Stoessl A Jon, Marras Conn |
|
Higher frequency of certain cancers in LRRK2 G2019S mutation carriers with Parkinson disease: a pooled analysis.
JAMA neurology 2015 Jan 72 (1): 58-65. Agalliu Ilir, San Luciano Marta, Mirelman Anat, Giladi Nir, Waro Bjorg, Aasly Jan, Inzelberg Rivka, Hassin-Baer Sharon, Friedman Eitan, Ruiz-Martinez Javier, Marti-Masso Jose Felix, Orr-Urtreger Avi, Bressman Susan, Saunders-Pullman Rach |
|
Reorganization of corticostriatal circuits in healthy G2019S LRRK2 carriers.
Neurology 2015 Jan 84 (4): 399-406. Helmich Rick C, Thaler Avner, van Nuenen Bart F L, Gurevich Tanya, Mirelman Anat, Marder Karen S, Bressman Susan, Orr-Urtreger Avi, Giladi Nir, Bloem Bastiaan R, Toni Ivan, |
|
Analysis of the LRRK2 p.G2019S mutation in Colombian Parkinson's Disease Patients.
Colombia me?dica (Cali, Colombia) 2015 46 (3): 117-21. Duque Andrés Felipe, Lopez Juan Carlos, Benitez Bruno, Hernandez Helena, Yunis Juan José, Fernandez William, Arboleda Humberto, Arboleda Gonza |
|
Sleep Disorders in Parkinsonian and Nonparkinsonian LRRK2 Mutation Carriers.
PloS one 2015 10 (7): e0132368. Pont-Sunyer Claustre, Iranzo Alex, Gaig Carles, Fernández-Arcos Ana, Vilas Dolores, Valldeoriola Francesc, Compta Yaroslau, Fernández-Santiago Ruben, Fernández Manel, Bayés Angels, Calopa Matilde, Casquero Pilar, de Fàbregues Oriol, Jaumà Serge, Puente Victor, Salamero Manel, José Martí Maria, Santamaría Joan, Tolosa Edua |
|
Disease penetrance of late-onset parkinsonism: a meta-analysis.
JAMA neurology 2014 Dec 71 (12): 1535-9. Trinh Joanne, Guella Ilaria, Farrer Matthew Jam |
Genome-wide mapping of IBD segments in an Ashkenazi PD cohort identifies associated haplotypes.
Human molecular genetics 2014 Sep 23 (17): 4693-702. Vacic Vladimir, Ozelius Laurie J, Clark Lorraine N, Bar-Shira Anat, Gana-Weisz Mali, Gurevich Tanya, Gusev Alexander, Kedmi Merav, Kenny Eimear E, Liu Xinmin, Mejia-Santana Helen, Mirelman Anat, Raymond Deborah, Saunders-Pullman Rachel, Desnick Robert J, Atzmon Gil, Burns Edward R, Ostrer Harry, Hakonarson Hakon, Bergman Aviv, Barzilai Nir, Darvasi Ariel, Peter Inga, Guha Saurav, Lencz Todd, Giladi Nir, Marder Karen, Pe'er Itsik, Bressman Susan B, Orr-Urtreger A |
|
Comparative study of Parkinson's disease and leucine-rich repeat kinase 2 p.G2019S parkinsonism.
Neurobiology of aging 2014 May 35 (5): 1125-31. Trinh Joanne, Amouri Rim, Duda John E, Morley James F, Read Matthew, Donald Alan, Vilariño-Güell Carles, Thompson Christina, Szu Tu Chelsea, Gustavsson Emil K, Ben Sassi Samia, Hentati Emna, Zouari Mourad, Farhat Emna, Nabli Fatma, Hentati Faycel, Farrer Matthew |
|
DNAJC13 mutations in Parkinson disease.
Human molecular genetics 2014 Apr 23 (7): 1794-801. Vilariño-Güell Carles, Rajput Alex, Milnerwood Austen J, Shah Brinda, Szu-Tu Chelsea, Trinh Joanne, Yu Irene, Encarnacion Mary, Munsie Lise N, Tapia Lucia, Gustavsson Emil K, Chou Patrick, Tatarnikov Igor, Evans Daniel M, Pishotta Frederick T, Volta Mattia, Beccano-Kelly Dayne, Thompson Christina, Lin Michelle K, Sherman Holly E, Han Heather J, Guenther Bruce L, Wasserman Wyeth W, Bernard Virginie, Ross Colin J, Appel-Cresswell Silke, Stoessl A Jon, Robinson Christopher A, Dickson Dennis W, Ross Owen A, Wszolek Zbigniew K, Aasly Jan O, Wu Ruey-Meei, Hentati Faycal, Gibson Rachel A, McPherson Peter S, Girard Martine, Rajput Michele, Rajput Ali H, Farrer Matthew |
|
Cognitive and Antipsychotic Medication Use in Monoallelic GBA-Related Parkinson Disease.
JIMD reports 2014 16 31-8. Barrett M J, Shanker V L, Severt W L, Raymond D, Gross S J, Schreiber-Agus N, Kornreich R, Ozelius L J, Bressman S B, Saunders-Pullman |
|
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 |
|
Parkinson disease phenotype in Ashkenazi Jews with and without LRRK2 G2019S mutations.
Movement disorders : official journal of the Movement Disorder Society 2013 Dec 28 (14): 1966-71. Alcalay Roy N, Mirelman Anat, Saunders-Pullman Rachel, Tang Ming-X, Mejia Santana Helen, Raymond Deborah, Roos Ernest, Orbe-Reilly Martha, Gurevich Tanya, Bar Shira Anat, Gana Weisz Mali, Yasinovsky Kira, Zalis Maayan, Thaler Avner, Deik Andres, Barrett Matthew James, Cabassa Jose, Groves Mark, Hunt Ann L, Lubarr Naomi, San Luciano Marta, Miravite Joan, Palmese Christina, Sachdev Rivka, Sarva Harini, Severt Lawrence, Shanker Vicki, Swan Matthew Carrington, Soto-Valencia Jeannie, Johannes Brooke, Ortega Robert, Fahn Stanley, Cote Lucien, Waters Cheryl, Mazzoni Pietro, Ford Blair, Louis Elan, Levy Oren, Rosado Llency, Ruiz Diana, Dorovski Tsvyatko, Pauciulo Michael, Nichols William, Orr-Urtreger Avi, Ozelius Laurie, Clark Lorraine, Giladi Nir, Bressman Susan, Marder Karen |
|
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 |
|
Analysis of Leucine-rich repeat kinase 2 (LRRK2) and Parkinson protein 2 (parkin, PARK2) genes mutations in Slovak Parkinson disease patients.
General physiology and biophysics 2013 Mar 32 (1): 55-66. Bognar Csaba, Baldovic Marian, Benetin Jan, Kadasi Ludovit, Zatkova Andr |
|
Olfaction and imaging biomarkers in premotor LRRK2 G2019S-associated Parkinson disease.
Neurology 2013 Feb 80 (7): 621-6. Sierra Maria, Sánchez-Juan Pascual, Martínez-Rodríguez María Isabel, González-Aramburu Isabel, García-Gorostiaga Inés, Quirce María Remedios, Palacio Enrique, Carril José Manuel, Berciano José, Combarros Onofre, Infante J |
- Page last reviewed:Oct 1, 2020
- Page last updated:Jun 09, 2021
- Content source: