Human Genome Epidemiology Literature Finder
Records 1 - 15 (of 15 Records) |
Query Trace: Dementia and HTT[original query] |
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Genetic correlates of behavioral endophenotypes in Alzheimer disease: role of COMT, 5-HTTLPR and APOE polymorphisms. Neurobiology of aging 2006 Nov 27 (11): 1595-603. Borroni B, Grassi M, Agosti C, Costanzi C, Archetti S, Franzoni S, Caltagirone C, Di Luca M, Caimi L, Padovani |
Association study of the 5-HTTLPR polymorphism and depression in 75-Year-Old nondemented subjects from the Vienna Transdanube Aging (VITA) study. The Journal of clinical psychiatry 2006 Sep 67 (9): 1373-8. Grünblatt Edna, Löffler Christiane, Zehetmayer Sonja, Jungwirth Susanne, Tragl Karl-Heinz, Riederer Peter, Fischer Pet |
Serotonin transporter gene polymorphism and BPSD in mild Alzheimer's disease. Journal of Alzheimer's disease : JAD 2007 Nov 12 (3): 245-53. Ueki Akinori, Ueno Hideo, Sato Noriko, Shinjo Hidetaka, Morita Yosh |
Risk variants in the S100B gene predict elevated S100B serum concentrations in healthy individuals. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2010 Jan 153B (1): 291-7. Hohoff Christa, Ponath Gerald, Freitag Christine M, Kästner Florian, Krakowitzky Petra, Domschke Katharina, Koelkebeck Katja, Kipp Frank, von Eiff Christof, Deckert Jürgen, Rothermundt Matthi |
The role of tau in the pathological process and clinical expression of Huntington's disease. Brain : a journal of neurology 2015 Jul 138 (Pt 7): 1907-18. Vuono Romina, Winder-Rhodes Sophie, de Silva Rohan, Cisbani Giulia, Drouin-Ouellet Janelle, , Spillantini Maria G, Cicchetti Francesca, Barker Roger |
Defining neurodegeneration on Guam by targeted genomic sequencing. Annals of neurology 2015 Mar 77 (3): 458-68. Steele John C, Guella Ilaria, Szu-Tu Chelsea, Lin Michelle K, Thompson Christina, Evans Daniel M, Sherman Holly E, Vilariño-Güell Carles, Gwinn Katrina, Morris Huw, Dickson Dennis W, Farrer Matthew |
Repeat length variations in ATXN1 and AR modify disease expression in Alzheimer's disease. Neurobiology of aging 2018 Sep . Gardiner Sarah L, Harder Aster V E, Campman Yvonne J M, Trompet Stella, Gussekloo Jacobijn, van Belzen Martine J, Boogaard Merel W, Roos Raymund A C, Jansen Iris E, Pijnenburg Yolande A L, Scheltens Philip, van der Flier Wiesje M, Aziz N Ahm |
Role for ATXN1, ATXN2, and HTT intermediate repeats in frontotemporal dementia and Alzheimer's disease. Neurobiology of aging 2019 Nov . Rosas Irene, Martínez Carmen, Clarimón Jordi, Lleó Alberto, Illán-Gala Ignacio, Dols-Icardo Oriol, Borroni Barbara, Almeida Maria Rosário, van der Zee Julie, Van Broeckhoven Christine, Bruni Amalia C, Anfossi Maria, Bernardi Livia, Maletta Raffaele, Serpente María, Galimberti Daniela, Scarpini Elio, Rossi Giacomina, Caroppo Paola, Benussi Luisa, Ghidoni Roberta, Binetti Giuliano, Nacmias Benedetta, Sorbi Sandro, Piaceri Irene, Bagnoli Silvia, Antonell Anna, Sánchez-Valle Raquel, De la Casa-Fages Beatriz, Grandas Francisco, Diez-Fairen Mónica, Pastor Pau, Ferrari Raffaele, Álvarez Victoria, Menéndez-González Manu |
The role of genetics in neurodegenerative dementia: a large cohort study in South China. NPJ genomic medicine 2021 8 6 (1): 69. Jiao Bin, Liu Hui, Guo Lina, Xiao Xuewen, Liao Xinxin, Zhou Yafang, Weng Ling, Zhou Lu, Wang Xin, Jiang Yaling, Yang Qijie, Zhu Yuan, Zhou Lin, Zhang Weiwei, Wang Junling, Yan Xinxiang, Li Jinchen, Tang Beisha, Shen |
Intermediate and Expanded HTT Alleles and the Risk for ?-Synucleinopathies. Movement disorders : official journal of the Movement Disorder Society 2022 7 37 (9): 1841-1849. Pérez-Oliveira Sergio, Álvarez Ignacio, Rosas Irene, Menendez-González Manuel, Blázquez-Estrada Marta, Aguilar Miquel, Corte Daniela, Buongiorno Mariateresa, Molina-Porcel Laura, Aldecoa Iban, Martí María J, Sánchez-Juan Pascual, Infante Jon, González-Aramburu Isabel, García-González Pablo, Rosende-Roca Maitée, Boada Mercè, Ruiz Agustín, Periñán María Teresa, Macías-García Daniel, Muñoz-Delgado Laura, Gómez-Garre Pilar, Mir Pablo, Clarimón Jordi, Lleo Alberto, Alcolea Daniel, De la Casa-Fages Beatriz, Duarte Israel, Álvarez Victoria, Pastor P |
C9orf72 hexanucleotide repeat expansion found in suspected spinobulbar muscular atrophy (SBMA). Neurologia i neurochirurgia polska 2022 6 56 (3): 276-280. Radziwonik Wiktoria, Elert-Dobkowska Ewelina, Tomczuk Filip, Wozniak Aleksandra, Sobanska Anna, Stepniak Iwona, Koziorowski Dariusz, Zaremba Jacek, Su?ek An |
Intermediate alleles of HTT: A new pathway in longevity. Journal of the neurological sciences 2022 5 438 120274. Ingannato Assunta, Bagnoli Silvia, Bessi Valentina, Ferrari Camilla, Mazzeo Salvatore, Sorbi Sandro, Nacmias Benedet |
Analysis of HTT CAG repeat expansion in Italian patients with amyotrophic lateral sclerosis. Annals of clinical and translational neurology 2022 10 9 (11): 1820-1825. Manini Arianna, Gagliardi Delia, Meneri Megi, Antognozzi Sara, Del Bo Roberto, Scaglione Cesa, Comi Giacomo Pietro, Corti Stefania, Ronchi Dar |
A mother and her daughter carrying a pathogenic expansion of the HTT gene with a phenotype encompassing motor neuron disease and Huntington's disease. Clinical genetics 2023 12 . Antonio Canosa, Sara Cabras, Francesca Di Pede, Umberto Manera, Rosario Vasta, Cristina Moglia, Andrea Calvo, Salvatore Gallone, Adriano Ch |
Reduced-penetrance Huntington's disease-causing alleles with 39 CAG trinucleotide repeats could be a genetic factor of amyotrophic lateral sclerosis. Journal of the Chinese Medical Association : JCMA 2023 1 86 (1): 47-51. Jih Kang-Yang, Lai Kuan-Lin, Lin Kon-Ping, Liao Yi-Chu, Lee Yi-Chu |
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- Page last updated:Apr 22, 2024
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