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| A comprehensive analysis of copy number variation in a Turkish dementia cohort. Human genomics 2021 Jul 15 (1): 48. Dehghani Nadia, Guven Gamze, Kun-Rodrigues Celia, Gouveia Catarina, Foster Kalina, Hanagasi Hasmet, Lohmann Ebba, Samanci Bedia, Gurvit Hakan, Bilgic Basar, Bras Jose, Guerreiro Ri |
| Genetics Contributes to Concomitant Pathology and Clinical Presentation in Dementia with Lewy Bodies. Journal of Alzheimer's disease : JAD 2021 Jul . van der Lee Sven J, van Steenoven Inger, van de Beek Marleen, Tési Niccolo, Jansen Iris E, van Schoor Natasja M, Reinders Marcel J T, Huisman Martijn, Scheltens Philip, Teunissen Charlotte E, Holstege Henne, van der Flier Wiesje M, Lemstra Afina |
| Retinal Thickness Predicts the Risk of Cognitive Decline in Parkinson Disease. Annals of neurology 2020 Oct . Murueta-Goyena Ane, Del Pino Rocío, Galdós Marta, Arana Begoña, Acera Marian, Carmona-Abellán Mar, Fernández-Valle Tamara, Tijero Beatriz, Lucas-Jiménez Olaia, Ojeda Natalia, Ibarretxe-Bilbao Naroa, Peña Javier, Cortes Jesus, Ayala Unai, Barrenechea Maitane, Gómez-Esteban Juan Carlos, Gabilondo Iñi |
| Fine-Mapping of SNCA in Rapid Eye Movement Sleep Behavior Disorder and Overt Synucleinopathies. Annals of neurology 2020 Jan . Krohn Lynne, Wu Richard Yj, Heilbron Karl, Ruskey Jennifer A, Laurent Sandra B, Blauwendraat Cornelis, Alam Armaghan, Arnulf Isabelle, Hu Michele T M, Dauvilliers Yves, Högl Birgit, Toft Mathias, Bjørnarå Kari Anne, Stefani Ambra, Holzknecht Evi, Monaca Christelle Charley, Beatriz Abril, Plazzi Giuseppe, Antelmi Elena, Ferini-Strambi Luigi, Young Peter, Heidbreder Anna, Cochen De Cock Valérie, Mollenhauer Brit, Sixel-Döring Friederike, Trenkwalder Claudia, Sonka Karel, Kemlink David, Figorilli Michela, Puligheddu Monica, Dijkstra Femke, Viaene Mineke, Oertel Wolfang, Toffoli Marco, Gigli Gian Luigi, Valente Mariarosaria, Gagnon Jean-François, Nalls Mike A, Singleton Andrew B, , Desautels Alex, Montplaisir Jacques Y, Cannon Paul, Ross Owen A, Boeve Bradley F, Dupré Nicolas, Fon Edward A, Postuma Ronald B, Pihlstrøm Lasse, Rouleau Guy A, Gan-Or Z |
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 |
| Dementia with lewy bodies: GBA1 mutations are associated with cerebrospinal fluid alpha-synuclein profile. Movement disorders : official journal of the Movement Disorder Society 2019 Jun . Lerche Stefanie, Machetanz Gerrit, Wurster Isabel, Roeben Benjamin, Zimmermann Milan, Pilotto Andrea, Preische Oliver, Stransky Elke, Deuschle Christian, Hauser Ann-Kathrin, Schulte Claudia, Lachmann Ingolf, Waniek Katharina, Gasser Thomas, Berg Daniela, Maetzler Walter, Brockmann Kathr |
| Alpha-synuclein gene polymorphism affects risk of dementia in Han Chinese with Parkinson's disease. Neuroscience letters 2019 May 706 146-150. Zheng Jinhua, Zang Qiuling, Hu Fengyun, Wei Hongen, Ma Jianjun, Xu Yanmi |
| A comprehensive screening of copy number variability in dementia with Lewy bodies. Neurobiology of aging 2019 03 75 223.e1-223.e10. Kun-Rodrigues Celia, Orme Tatiana, Carmona Susana, Hernandez Dena G, Ross Owen A, Eicher John D, Shepherd Claire, Parkkinen Laura, Darwent Lee, Heckman Michael G, Scholz Sonja W, Troncoso Juan C, Pletnikova Olga, Dawson Ted, Rosenthal Liana, Ansorge Olaf, Clarimon Jordi, Lleo Alberto, Morenas-Rodriguez Estrella, Clark Lorraine, Honig Lawrence S, Marder Karen, Lemstra Afina, Rogaeva Ekaterina, St George-Hyslop Peter, Londos Elisabet, Zetterberg Henrik, Barber Imelda, Braae Anne, Brown Kristelle, Morgan Kevin, Troakes Claire, Al-Sarraj Safa, Lashley Tammaryn, Holton Janice, Compta Yaroslau, Van Deerlin Vivianna, Serrano Geidy E, Beach Thomas G, Lesage Suzanne, Galasko Douglas, Masliah Eliezer, Santana Isabel, Pastor Pau, Diez-Fairen Monica, Aguilar Miquel, Tienari Pentti J, Myllykangas Liisa, Oinas Minna, Revesz Tamas, Lees Andrew, Boeve Brad F, Petersen Ronald C, Ferman Tanis J, Escott-Price Valentina, Graff-Radford Neill, Cairns Nigel J, Morris John C, Pickering-Brown Stuart, Mann David, Halliday Glenda M, Hardy John, Trojanowski John Q, Dickson Dennis W, Singleton Andrew, Stone David J, Guerreiro Rita, Bras Jo |
| INDEL Length and Haplotypes in the ß-Synuclein Gene: A Key to Differentiate Dementia with Lewy Bodies? Journal of Alzheimer's disease : JAD 2018 Jul . Gámez-Valero Ana, Canet-Pons Julia, Urbizu Aintzane, Anillo Ana, Santos Cristina, Ariza Aurelio, Beyer Katr |
| 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 |
| Investigating the genetic architecture of dementia with Lewy bodies: a two-stage genome-wide association study.
The Lancet. Neurology 2018 Jan 17 (1): 64-74. Guerreiro Rita, Ross Owen A, Kun-Rodrigues Celia, Hernandez Dena G, Orme Tatiana, Eicher John D, Shepherd Claire E, Parkkinen Laura, Darwent Lee, Heckman Michael G, Scholz Sonja W, Troncoso Juan C, Pletnikova Olga, Ansorge Olaf, Clarimon Jordi, Lleo Alberto, Morenas-Rodriguez Estrella, Clark Lorraine, Honig Lawrence S, Marder Karen, Lemstra Afina, Rogaeva Ekaterina, St George-Hyslop Peter, Londos Elisabet, Zetterberg Henrik, Barber Imelda, Braae Anne, Brown Kristelle, Morgan Kevin, Troakes Claire, Al-Sarraj Safa, Lashley Tammaryn, Holton Janice, Compta Yaroslau, Van Deerlin Vivianna, Serrano Geidy E, Beach Thomas G, Lesage Suzanne, Galasko Douglas, Masliah Eliezer, Santana Isabel, Pastor Pau, Diez-Fairen Monica, Aguilar Miquel, Tienari Pentti J, Myllykangas Liisa, Oinas Minna, Revesz Tamas, Lees Andrew, Boeve Brad F, Petersen Ronald C, Ferman Tanis J, Escott-Price Valentina, Graff-Radford Neill, Cairns Nigel J, Morris John C, Pickering-Brown Stuart, Mann David, Halliday Glenda M, Hardy John, Trojanowski John Q, Dickson Dennis W, Singleton Andrew, Stone David J, Bras Jo |
| The Length of SNCA Rep1 Microsatellite May Influence Cognitive Evolution in Parkinson's Disease. Frontiers in neurology 2018 9 213. Corrado Lucia, De Marchi Fabiola, Tunesi Sara, Oggioni Gaia Donata, Carecchio Miryam, Magistrelli Luca, Tesei Silvana, Riboldazzi Giulio, Di Fonzo Alessio, Locci Clarissa, Trezzi Ilaria, Zangaglia Roberta, Cereda Cristina, D'Alfonso Sandra, Magnani Corrado, Comi Giacomo P, Bono Giorgio, Pacchetti Claudio, Cantello Roberto, Goldwurm Stefano, Comi Cristofo |
| Genetic factors influencing frontostriatal dysfunction and the development of dementia in Parkinson's disease. PloS one 2017 12 (4): e0175560. Huertas Ismael, Jesús Silvia, García-Gómez Francisco Javier, Lojo José Antonio, Bernal-Bernal Inmaculada, Bonilla-Toribio Marta, Martín-Rodriguez Juan Francisco, García-Solís David, Gómez-Garre Pilar, Mir Pab |
| Elevated mRNA Expression and Low Methylation of SNCA in Japanese Alzheimer's Disease Subjects. Journal of Alzheimer's disease : JAD 2016 Oct 54 (4): 1349-1357. Yoshino Yuta, Mori Takaaki, Yoshida Taku, Yamazaki Kiyohiro, Ozaki Yuki, Sao Tomoko, Funahashi Yu, Iga Jun-Ichi, Ueno Shu-Ic |
| Regional expression of the MAPT gene is associated with loss of hubs in brain networks and cognitive impairment in Parkinson disease and progressive supranuclear palsy. Neurobiology of aging 2016 Sep 48 153-160. Rittman Timothy, Rubinov Mikail, Vértes Petra E, Patel Ameera X, Ginestet Cedric E, Ghosh Boyd C P, Barker Roger A, Spillantini Maria Grazia, Bullmore Edward T, Rowe James |
| TREM2 p.R47H substitution is not associated with dementia with Lewy bodies. Neurology. Genetics 2016 Aug 2 (4): e85. Walton Ronald L, Soto-Ortolaza Alexandra I, Murray Melissa E, Lorenzo-Betancor Oswaldo, Ogaki Kotaro, Heckman Michael G, Rayaprolu Sruti, Rademakers Rosa, Ertekin-Taner Nilüfer, Uitti Ryan J, van Gerpen Jay A, Wszolek Zbigniew K, Smith Glenn E, Kantarci Kejal, Lowe Val J, Parisi Joseph E, Jones David T, Savica Rodolfo, Graff-Radford Jonathan, Knopman David S, Petersen Ronald C, Graff-Radford Neill R, Ferman Tanis J, Dickson Dennis W, Boeve Bradley F, Ross Owen A, Labbé Catheri |
| a-synuclein genetic variability: A biomarker for dementia in Parkinson disease. Annals of neurology 2016 Apr . Guella Ilaria, Evans Daniel M, Szu-Tu Chelsea, Nosova Ekaterina, Bortnick Stephanie F, , Goldman Jennifer G, Dalrymple-Alford John, Geurtsen Gert J, Litvan Irene, Ross Owen A, Middleton Lefkos T, Parkkinen Laura, Farrer Matthew |
| Genetic analysis implicates APOE, SNCA and suggests lysosomal dysfunction in the etiology of dementia with Lewy bodies. Human molecular genetics 2014 Dec 23 (23): 6139-46. Bras Jose, Guerreiro Rita, Darwent Lee, Parkkinen Laura, Ansorge Olaf, Escott-Price Valentina, Hernandez Dena G, Nalls Michael A, Clark Lorraine N, Honig Lawrence S, Marder Karen, Van Der Flier Wiesje M, Lemstra Afina, Scheltens Philip, Rogaeva Ekaterina, St George-Hyslop Peter, Londos Elisabet, Zetterberg Henrik, Ortega-Cubero Sara, Pastor Pau, Ferman Tanis J, Graff-Radford Neill R, Ross Owen A, Barber Imelda, Braae Anne, Brown Kristelle, Morgan Kevin, Maetzler Walter, Berg Daniela, Troakes Claire, Al-Sarraj Safa, Lashley Tammaryn, Compta Yaroslau, Revesz Tamas, Lees Andrew, Cairns Nigel, Halliday Glenda M, Mann David, Pickering-Brown Stuart, Dickson Dennis W, Singleton Andrew, Hardy Jo |
| APOE, MAPT, and SNCA genes and cognitive performance in Parkinson disease. JAMA neurology 2014 Nov 71 (11): 1405-12. Mata Ignacio F, Leverenz James B, Weintraub Daniel, Trojanowski John Q, Hurtig Howard I, Van Deerlin Vivianna M, Ritz Beate, Rausch Rebecca, Rhodes Shannon L, Factor Stewart A, Wood-Siverio Cathy, Quinn Joseph F, Chung Kathryn A, Peterson Amie L, Espay Alberto J, Revilla Fredy J, Devoto Johnna, Hu Shu-Ching, Cholerton Brenna A, Wan Jia Y, Montine Thomas J, Edwards Karen L, Zabetian Cyrus |
| Analysis of Parkinson's disease brain-derived DNA for alpha-synuclein coding somatic mutations. Movement disorders : official journal of the Movement Disorder Society 2014 Jul 29 (8): 1060-4. Proukakis Christos, Shoaee Maryiam, Morris James, Brier Timothy, Kara Eleanna, Sheerin Una-Marie, Charlesworth Gavin, Tolosa Eduardo, Houlden Henry, Wood Nicholas W, Schapira Anthony |
| Does a-synuclein have a dual and opposing effect in preclinical vs. clinical Parkinson's disease? Parkinsonism & related disorders 2014 Jun 20 (6): 584-9; discussion 584. Markopoulou Katerina, Biernacka Joanna M, Armasu Sebastian M, Anderson Kari J, Ahlskog J Eric, Chase Bruce A, Chung Sun Ju, Cunningham Julie M, Farrer Matthew, Frigerio Roberta, Maraganore Demetrius |
| An evaluation of the impact of MAPT, SNCA and APOE on the burden of Alzheimer's and Lewy body pathology. Journal of neurology, neurosurgery, and psychiatry 2012 Apr 83 (4): 424-9. Wider Christian, Ross Owen A, Nishioka Kenya, Heckman Michael G, Vilariño-Güell Carles, Jasinska-Myga Barbara, Erketin-Taner Nilufer, Rademakers Rosa, Graff-Radford Neill R, Mash Deborah C, Papapetropoulos Spiridon, Duara Ranjan, Uchikado Hirotake, Wszolek Zbigniew K, Farrer Matthew J, Dickson Dennis |
| Association of alpha-, beta-, and gamma-Synuclein with diffuse lewy body disease. Archives of neurology 2010 Aug 67 (8): 970-5. Nishioka Kenya, Wider Christian, Vilariño-Güell Carles, Soto-Ortolaza Alexandra I, Lincoln Sarah J, Kachergus Jennifer M, Jasinska-Myga Barbara, Ross Owen A, Rajput Alex, Robinson Christopher A, Ferman Tanis J, Wszolek Zbigniew K, Dickson Dennis W, Farrer Matthew |
| Alpha-synuclein promoter haplotypes and dementia in Parkinson's disease. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2008 Apr 147 (3): 403-7. De Marco E V, Tarantino P, Rocca F E, Provenzano G, Civitelli D, De Luca V, Annesi F, Carrideo S, Cirò Candiano I C, Romeo N, Nicoletti G, Marconi R, Novellino F, Morelli M, Quattrone A, Annesi |
| Genetic association study of synphilin-1 in idiopathic Parkinson's disease. BMC medical genetics 2008 9 (1): 19. Myhre Ronny, Klungland Helge, Farrer Matthew J, Aasly Jan |
| Tau and alpha-synuclein in susceptibility to, and dementia in, Parkinson's disease. Annals of neurology 2007 Aug 62 (2): 145-53. Goris An, Williams-Gray Caroline H, Clark Graeme R, Foltynie Thomas, Lewis Simon J G, Brown Joanne, Ban Maria, Spillantini Maria G, Compston Alastair, Burn David J, Chinnery Patrick F, Barker Roger A, Sawcer Stephen |
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- Page last updated:Jun 28, 2022
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