Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 42 Records) |
Query Trace: Dementia and LRRK2[original query] |
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Cognitive and behavioral symptoms in Parkinson's disease patients with the G2019S and R1441G mutations of the LRRK2 gene. Parkinsonism & related disorders 2015 May 21 (5): 494-9. Somme Johanne Hatteland, Molano Salazar Ana, Gonzalez Amaia, Tijero Beatriz, Berganzo Koldo, Lezcano Elena, Fernandez Martinez Manuel, Zarranz Juan Jose, Gómez-Esteban Juan Carl |
Cognitive profile of LRRK2-related Parkinson's disease. Movement disorders : official journal of the Movement Disorder Society 2015 Apr 30 (5): 728-33. Srivatsal Sindhu, Cholerton Brenna, Leverenz James B, Wszolek Zbigniew K, Uitti Ryan J, Dickson Dennis W, Weintraub Daniel, Trojanowski John Q, Van Deerlin Vivianna M, Quinn Joseph F, Chung Kathryn A, Peterson Amie L, Factor Stewart A, Wood-Siverio Cathy, Goldman Jennifer G, Stebbins Glenn T, Bernard Bryan, Ritz Beate, Rausch Rebecca, Espay Alberto J, Revilla Fredy J, Devoto Johnna, Rosenthal Liana S, Dawson Ted M, Albert Marilyn S, Mata Ignacio F, Hu Shu-Ching, Montine Kathleen S, Johnson Catherine, Montine Thomas J, Edwards Karen L, Zhang Jing, Zabetian Cyrus |
Clinical heterogeneity of LRRK2 p.I2012T mutation. Parkinsonism & related disorders 2016 Sep . Fan Tian-Sin, Wu Ruey-Meei, Chen Pei-Lung, Chen Ta-Fu, Li Huei-Ying, Lin Yin-Hung, Chen Chien-Yu, Chen Meng-Ling, Tai Chun-Hwei, Lin Hang-I, Lin Chin-Hsi |
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 |
High Frequency of GBA Gene Mutations in Dementia With Lewy Bodies Among Ashkenazi Jews. JAMA neurology 2016 Oct . Shiner Tamara, Mirelman Anat, Gana Weisz Mali, Bar-Shira Anat, Ash Elissa, Cialic Ron, Nevler Naomi, Gurevich Tanya, Bregman Noa, Orr-Urtreger Avi, Giladi N |
Cognitive profile and 18F-fluorodeoxyglucose PET study in LRRK2-related Parkinson's disease. Parkinsonism & related disorders 2017 12 47 80-83. De Rosa Anna, Peluso Silvio, De Lucia Natascia, Russo Paola, Annarumma Ida, Esposito Marcello, Manganelli Fiore, Brunetti Arturo, De Michele Giuseppe, Pappatà Sabi |
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 |
Cognition among individuals along a spectrum of increased risk for Parkinson's disease. PloS one 2018 13 (8): e0201964. Chahine Lana M, Urbe Liz, Caspell-Garcia Chelsea, Aarsland Dag, Alcalay Roy, Barone Paolo, Burn David, Espay Alberto J, Hamilton Jamie L, Hawkins Keith A, Lasch Shirley, Leverenz James B, Litvan Irene, Richard Irene, Siderowf Andrew, Coffey Christopher S, Simuni Tanya, Weintraub Daniel, |
Pooled-DNA target sequencing of Parkinson genes reveals novel phenotypic associations in Spanish population. Neurobiology of aging 2018 May . Diez-Fairen Monica, Benitez Bruno A, Ortega-Cubero Sara, Lorenzo-Betancor Oswaldo, Cruchaga Carlos, Lorenzo Elena, Samaranch Lluis, Carcel Maria, Obeso Jose A, Rodriguez-Oroz Maria Cruz, Aguilar Miquel, Coria Francisco, Pastor Maria A, Pastor P |
Cerebral Imaging Markers of GBA and LRRK2 Related Parkinson's Disease and Their First-Degree Unaffected Relatives. Brain topography 2018 May . Thaler Avner, Kliper Efrat, Maidan Inbal, Herman Talia, Rosenberg-Katz Keren, Bregman Noa, Gurevich Tanya, Shiner Tamara, Hausdorff Jeffrey M, Orr-Urtreger Avi, Giladi Nir, Mirelman An |
LRRK2 protective haplotype and full sequencing study in REM sleep behavior disorder. Parkinsonism & related disorders 2018 Mar . Ouled Amar Bencheikh Bouchra, Ruskey Jennifer A, Arnulf Isabelle, Dauvilliers Yves, Monaca Christelle Charley, De Cock Valérie Cochen, Gagnon Jean-François, Spiegelman Dan, Hu Michele T M, Högl Birgit, Stefani Ambra, Ferini-Strambi Luigi, Plazzi Giuseppe, Antelmi Elena, Young Peter, Heidbreder Anna, Mollenhauer Brit, Sixel-Döring Friederike, Trenkwalder Claudia, Oertel Wolfgang, Montplaisir Jacques Y, Postuma Ronald B, Rouleau Guy A, Gan-Or Z |
Carriers of both GBA and LRRK2 mutations, compared to carriers of either, in Parkinson's disease: Risk estimates and genotype-phenotype correlations. Parkinsonism & related disorders 2019 May 62 179-184. Yahalom Gilad, Greenbaum Lior, Israeli-Korn Simon, Fay-Karmon Tsvia, Livneh Vered, Ruskey Jennifer A, Roncière Léanne, Alam Armaghan, Gan-Or Ziv, Hassin-Baer Shar |
Immune-related genetic enrichment in frontotemporal dementia: An analysis of genome-wide association studies. PLoS medicine 2018 1 15 (1): e1002487. Broce Iris, Karch Celeste M, Wen Natalie, Fan Chun C, Wang Yunpeng, Tan Chin Hong, Kouri Naomi, Ross Owen A, Höglinger Günter U, Muller Ulrich, Hardy John, , Momeni Parastoo, Hess Christopher P, Dillon William P, Miller Zachary A, Bonham Luke W, Rabinovici Gil D, Rosen Howard J, Schellenberg Gerard D, Franke Andre, Karlsen Tom H, Veldink Jan H, Ferrari Raffaele, Yokoyama Jennifer S, Miller Bruce L, Andreassen Ole A, Dale Anders M, Desikan Rahul S, Sugrue Leo |
Mutation and association analyses of dementia-causal genes in Han Chinese patients with early-onset and familial Alzheimer's disease. Journal of psychiatric research 2019 4 113 141-147. Wang Guihong, Zhang Deng-Feng, Jiang Hong-Yan, Fan Yu, Ma Lingyan, Shen Zonglin, Bi Rui, Xu Min, Tan Liwen, Shan Baoci, Yao Yong-Gang, Feng T |
Analysis of 50 Neurodegenerative Genes in Clinically Diagnosed Early-Onset Alzheimer's Disease. International journal of molecular sciences 2019 Mar 20 (6): . Giau Vo Van, Senanarong Vorapun, Bagyinszky Eva, An Seong Soo A, Kim SangY |
Genetic modifiers of risk and age at onset in GBA associated Parkinson's disease and Lewy body dementia.
Brain : a journal of neurology 2019 Nov . Blauwendraat Cornelis, Reed Xylena, Krohn Lynne, Heilbron Karl, Bandres-Ciga Sara, Tan Manuela, Gibbs J Raphael, Hernandez Dena G, Kumaran Ravindran, Langston Rebekah, Bonet-Ponce Luis, Alcalay Roy N, Hassin-Baer Sharon, Greenbaum Lior, Iwaki Hirotaka, Leonard Hampton L, Grenn Francis P, Ruskey Jennifer A, Sabir Marya, Ahmed Sarah, Makarious Mary B, Pihlstrøm Lasse, Toft Mathias, van Hilten Jacobus J, Marinus Johan, Schulte Claudia, Brockmann Kathrin, Sharma Manu, Siitonen Ari, Majamaa Kari, Eerola-Rautio Johanna, Tienari Pentti J, Team The andMe Research, Pantelyat Alexander, Hillis Argye E, Dawson Ted M, Rosenthal Liana S, Albert Marilyn S, Resnick Susan M, Ferrucci Luigi, Morris Christopher M, Pletnikova Olga, Troncoso Juan, Grosset Donald, Lesage Suzanne, Corvol Jean-Christophe, Brice Alexis, Noyce Alastair J, Masliah Eliezer, Wood Nick, Hardy John, Shulman Lisa M, Jankovic Joseph, Shulman Joshua M, Heutink Peter, Gasser Thomas, Cannon Paul, Scholz Sonja W, Morris Huw, Cookson Mark R, Nalls Mike A, Gan-Or Ziv, Singleton Andrew |
Association of rare variants in neurodegenerative genes with familial Alzheimer's disease. Annals of clinical and translational neurology 2020 Sep . Zhang Weiwei, Jiao Bin, Xiao Tingting, Liu Xixi, Liao Xinxin, Xiao Xuewen, Guo Lina, Yuan Zhenhua, Yan Xinxiang, Tang Beisha, Shen |
Role of LRRK2 variant p.Gly2019Ser in patients with Parkinsonism. The Indian journal of medical research 2020 Jun 151 (6): 592-597. Sadhukhan Dipanwita, Biswas Arindam, Bhaduri Arunima, Sarkar Neelanjana, Biswas Atanu, Das Shyamal K, Banerjee Tapas K, Ray Kunal, Ray Jhar |
Mutation Analysis of the Genes Associated with Parkinson's Disease in a Finnish Cohort of Early-Onset Dementia. Journal of Alzheimer's disease : JAD 2020 6 76 (3): 955-965. Luukkainen Laura, Huttula Samuli, Väyrynen Henri, Helisalmi Seppo, Kytövuori Laura, Haapasalo Annakaisa, Hiltunen Mikko, Remes Anne M, Krüger Johan |
Identification of susceptibility loci for cognitive impairment in a cohort of Han Chinese patients with Parkinson's disease. Neuroscience letters 2020 May 135034. Liu Hong-Jun, Li Xiao-Yan, Chen Hui, Yu Hui-Li, Tao Qing-Qing, Wu Zhi-Yi |
Clinicopathologic and genetic features of multiple system atrophy with Lewy body disease. Brain pathology (Zurich, Switzerland) 2020 4 30 (4): 766-778. Koga Shunsuke, Li Fuyao, Zhao Na, Roemer Shanu F, Ferman Tanis J, Wernick Anna I, Walton Ronald L, Faroqi Ayman H, Graff-Radford Neill R, Cheshire William P, Ross Owen A, Dickson Dennis |
A Specific Diplotype H1j/H2 of the MAPT Gene Could Be Responsible for Parkinson's Disease with Dementia. Case reports in genetics 2020 2020 8813344. Smaili Imane, Hajjaj Imane, Razine Rachid, Tibar Houyam, Salmi Ayyoub, Bouslam Naima, Moussa Ahmed, Regragui Wafa, Bouhouche Ahm |
[Plasma Exosomes in Inherited Forms of Parkinson's Disease]. Molekuliarnaia biologiia 2021 4 55 (2): 338-345. Kulabukhova D G, Garaeva L A, Emelyanov A K, Senkevich K A, Gracheva E V, Miliukhina I V, Varfolomeeva E Y, Timofeeva A A, Schwartsman A L, Shtam T A, Pchelina S |
Genetic study of young-onset dementia using targeted gene panel sequencing in Taiwan. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2021 Feb . Hsu Jung-Lung, Lin Chin-Hsien, Chen Pei-Lung, Lin Kun-Ju, Chen Ta- |
Association between CSF alpha-synuclein seeding activity and genetic status in Parkinson's disease and dementia with Lewy bodies. Acta neuropathologica communications 2021 Oct 9 (1): 175. Brockmann Kathrin, Quadalti Corinne, Lerche Stefanie, Rossi Marcello, Wurster Isabel, Baiardi Simone, Roeben Benjamin, Mammana Angela, Zimmermann Milan, Hauser Ann-Kathrin, Deuschle Christian, Schulte Claudia, Waniek Katharina, Lachmann Ingolf, Sjödin Simon, Brinkmalm Ann, Blennow Kaj, Zetterberg Henrik, Gasser Thomas, Parchi Pie |
Serum MicroRNAs Predict Isolated Rapid Eye Movement Sleep Behavior Disorder and Lewy Body Diseases. Movement disorders : official journal of the Movement Disorder Society 2022 8 37 (10): 2086-2098. Soto Marta, Iranzo Alex, Lahoz Sara, Fernández Manel, Serradell Mónica, Gaig Carles, Melón Paula, Martí Maria-Jose, Santamaría Joan, Camps Jordi, Fernández-Santiago Rubén, Ezquerra Mar |
Gene Panel Sequencing Analysis Revealed a Strong Contribution of Rare Coding Variants to the Risk of Parkinson's Disease in Sporadic Moroccan Patients. Journal of molecular neuroscience : MN 2023 5 . Imane Smaili, Houyam Tibar, Mounia Rahmani, Najlaa Machkour, Rachid Razine, Hajar Naciri Darai, Naima Bouslam, Ali Benomar, Wafa Regragui, Ahmed Bouhouc |
Gene Expression Profiling as a Novel Diagnostic Tool for Neurodegenerative Disorders. International journal of molecular sciences 2023 3 24 (6): . Martínez-Iglesias Olaia, Naidoo Vinogran, Carril Juan Carlos, Seoane Silvia, Cacabelos Natalia, Cacabelos Ram |
Investigation of the genetic aetiology of Lewy body diseases with and without dementia. medRxiv : the preprint server for health sciences 2023 11 . Lesley Wu, Raquel Real, Alejandro Martinez, Ruth Chia, Michael A Lawton, Maryam Shoai, Catherine Bresner, Leon Hubbard, Cornelis Blauwendraat, Andrew B Singleton, Mina Ryten, Sonja W Scholz, Bryan J Traynor, Nigel Williams, Michele T M Hu, Yoav Ben-Shlomo, Donald G Grosset, John Hardy, Huw R Morris, |
Genetic overlap between ALS and other neurodegenerative or neuromuscular disorders. Amyotrophic lateral sclerosis & frontotemporal degeneration 2023 10 1-11. Cathrine Goberg Olsen, Øyvind Løvold Busk, Øystein Lunde Holla, Kristian Tveten, Trygve Holmøy, Ole-Bjørn Tysnes, Helle Høy |
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- Page last updated:Mar 25, 2024
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