HuGE Literature Finder
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| Genetic landscape of early-onset dementia in Hungary. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 2022 Jun . Csaban Dora, Illes Anett, Renata Toth-Bencsik, Balicza Peter, Pentelenyi Klara, Molnar Viktor, Gezsi Andras, Grosz Zoltan, Gal Aniko, Kovacs Tibor, Klivenyi Peter, Molnar Maria Jud |
| A Young Man with Cognitive Impairment and a Heart Condition. Journal of Alzheimer's disease : JAD 2022 7 89 (2): 405-410. Russo Mirella, Santilli Matteo, De Rosa Matteo A, Calisi Dario, Dono Fedele, Mattoli Maria Vittoria, Bonanni Laura, Onofrj Marco, Sensi Stefano |
| 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 |
| 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- |
| Analysis of Genotype-Phenotype Correlations in Patients With Degenerative Dementia Through the Whole Exome Sequencing. Frontiers in aging neuroscience 2021 11 13 745407. Sun Lin, Zhang Jianye, Su Ning, Zhang Shaowei, Yan Feng, Lin Xiang, Yu Jie, Li Wei, Li Xia, Xiao Shi |
| 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 |
| Analysis of neurodegenerative disease-causing genes in dementia with Lewy bodies. Acta neuropathologica communications 2020 Jan 8 (1): 5. Orme Tatiana, Hernandez Dena, Ross Owen A, Kun-Rodrigues Celia, Darwent Lee, Shepherd Claire E, Parkkinen Laura, Ansorge Olaf, Clark Lorraine, Honig Lawrence S, Marder Karen, Lemstra Afina, Rogaeva Ekaterina, St George-Hyslop Peter, Londos Elisabet, Zetterberg Henrik, Morgan Kevin, Troakes Claire, Al-Sarraj Safa, Lashley Tammaryn, Holton Janice, Compta Yaroslau, Van Deerlin Vivianna, Trojanowski John Q, Serrano Geidy E, Beach Thomas G, Lesage Suzanne, Galasko Douglas, Masliah Eliezer, Santana Isabel, Pastor Pau, 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, Stone David J, Dickson Dennis W, Hardy John, Singleton Andrew, Guerreiro Rita, Bras Jo |
| Genetics of dementia: insights from Latin America. Dementia & neuropsychologia 2020 9 14 (3): 223-236. Ramos Claudia, Aguillon David, Cordano Christian, Lopera Francis |
| 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 screening in early-onset Alzheimer's disease identified three novel presenilin mutations. Neurobiology of aging 2019 2 86 201.e9-201.e14. Wong Tsz Hang, Seelaar Harro, Melhem Shamiram, Rozemuller Annemieke J M, van Swieten John |
| Genome sequencing for early-onset or atypical dementia: high diagnostic yield and frequent observation of multiple contributory alleles. Cold Spring Harbor molecular case studies 2019 12 5 (6): . Cochran J Nicholas, McKinley Emily C, Cochran Meagan, Amaral Michelle D, Moyers Bryan A, Lasseigne Brittany N, Gray David E, Lawlor James M J, Prokop Jeremy W, Geier Ethan G, Holt James M, Thompson Michelle L, Newberry J Scott, Yokoyama Jennifer S, Worthey Elizabeth A, Geldmacher David S, Love Marissa Natelson, Cooper Gregory M, Myers Richard M, Roberson Erik |
| 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 |
| Genetics of dementia in a Finnish cohort. European journal of human genetics : EJHG 2018 Feb . Pasanen Petra, Myllykangas Liisa, Pöyhönen Minna, Kiviharju Anna, Siitonen Maija, Hardy John, Bras Jose, Paetau Anders, Tienari Pentti J, Guerreiro Rita, Verkkoniemi-Ahola Au |
| Pleiotropic Effects of Variants in Dementia Genes in Parkinson Disease. Frontiers in neuroscience 2018 12 230. Ibanez Laura, Dube Umber, Davis Albert A, Fernandez Maria V, Budde John, Cooper Breanna, Diez-Fairen Monica, Ortega-Cubero Sara, Pastor Pau, Perlmutter Joel S, Cruchaga Carlos, Benitez Bruno |
| Genetic compendium of 1511 human brains available through the UK Medical Research Council Brain Banks Network Resource. Genome research 2016 Dec . Keogh Michael J, Wei Wei, Wilson Ian, Coxhead Jon, Ryan Sarah, Rollinson Sara, Griffin Helen, Kurzawa-Akanbi Marzena, Santibanez-Koref Mauro, Talbot Kevin, Turner Martin R, McKenzie Chris-Anne, Troakes Claire, Attems Johannes, Smith Colin, Al Sarraj Safa, Morris Chris M, Ansorge Olaf, Pickering-Brown Stuart, Ironside James W, Chinnery Patrick |
| Rare variants in ?-Amyloid precursor protein (APP) and Parkinson's disease. European journal of human genetics : EJHG 2015 Oct 23 (10): 1328-33. Schulte Eva C, Fukumori Akio, Mollenhauer Brit, Hor Hyun, Arzberger Thomas, Perneczky Robert, Kurz Alexander, Diehl-Schmid Janine, Hüll Michael, Lichtner Peter, Eckstein Gertrud, Zimprich Alexander, Haubenberger Dietrich, Pirker Walter, Brücke Thomas, Bereznai Benjamin, Molnar Maria J, Lorenzo-Betancor Oswaldo, Pastor Pau, Peters Annette, Gieger Christian, Estivill Xavier, Meitinger Thomas, Kretzschmar Hans A, Trenkwalder Claudia, Haass Christian, Winkelmann Julia |
| Systematic review and meta-analysis of Japanese familial Alzheimer's disease and FTDP-17. Journal of human genetics 2015 May 60 (5): 281-3. Kasuga Kensaku, Kikuchi Masataka, Tokutake Takayoshi, Nakaya Akihiro, Tezuka Toshiyuki, Tsukie Tamao, Hara Norikazu, Miyashita Akinori, Kuwano Ryozo, Ikeuchi Takes |
| Clinical and neuroimaging characterization of Chinese dementia patients with PSEN1 and PSEN2 mutations. Dementia and geriatric cognitive disorders 2015 39 (1-2): 32-40. Shi Zhihong, Wang Ying, Liu Shuai, Liu Mengyuan, Liu Shuling, Zhou Yuying, Wang Jinhuan, Cai Li, Huo Ya Ruth, Gao Shuo, Ji Yo |
| Investigating the role of rare coding variability in Mendelian dementia genes (APP, PSEN1, PSEN2, GRN, MAPT, and PRNP) in late-onset Alzheimer's disease. Neurobiology of aging 2014 Dec 35 (12): 2881.e1-6. Sassi Celeste, Guerreiro Rita, Gibbs Raphael, Ding Jinhui, Lupton Michelle K, Troakes Claire, Al-Sarraj Safa, Niblock Michael, Gallo Jean-Marc, Adnan Jihad, Killick Richard, Brown Kristelle S, Medway Christopher, Lord Jenny, Turton James, Bras Jose, , Morgan Kevin, Powell John F, Singleton Andrew, Hardy Jo |
| Exome sequencing identifies 2 novel presenilin 1 mutations (p.L166V and p.S230R) in British early-onset Alzheimer's disease. Neurobiology of aging 2014 Oct 35 (10): 2422.e13-6. Sassi Celeste, Guerreiro Rita, Gibbs Raphael, Ding Jinhui, Lupton Michelle K, Troakes Claire, Lunnon Katie, Al-Sarraj Safa, Brown Kristelle S, Medway Chirstopher, Lord Jenny, Turton James, Mann David, Snowden Julie, Neary David, Harris Jeniffer, Bras Jose, , Morgan Kevin, Powell John F, Singleton Andrew, Hardy Jo |
| C9ORF72 repeat expansions and other FTD gene mutations in a clinical AD patient series from Mayo Clinic. American journal of neurodegenerative disease 2012 1 (1): 1. Wojtas A, Heggeli KA, Finch N, Baker M, Dejesus-Hernandez M, Younkin SG, Dickson DW, Graff-Radford NR, Rademakers R |
| Pooled-DNA sequencing identifies novel causative variants in PSEN1, GRN and MAPT in a clinical early-onset and familial Alzheimer's disease Ibero-American cohort. Alzheimer's research & therapy 2012 4 (4): 34. Jin Sheng Chih, Pastor Pau, Cooper Breanna, Cervantes Sebastian, Benitez Bruno A, Razquin Cristina, Goate Alison, , Cruchaga Carl |
| Prevalence of pathogenic mutations in an Italian clinical series of patients with familial dementia. Current Alzheimer research 2004 Aug 1 (3): 215-8. Signorini S, Ghidoni R, Barbiero L, Benussi L, Binetti |
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- Page last updated:Mar 22, 2023
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