HuGE Literature Finder
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| Effects of ApoE genotype on clinical phenotypes in early-onset and late-onset Alzheimer's disease in China: Data from the PUMCH dementia cohort. Brain and behavior 2021 Sep e2373. Dong Liling, Li Jie, Liu Caiyan, Mao Chenhui, Wang Jie, Lei Dan, Huang Xinying, Chu Shanshan, Hou Bo, Feng Feng, Sha Longze, Xu Qi, Gao Ji |
| 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- |
| Genetic analysis of Vietnamese patients with early-onset Alzheimer's disease. The International journal of neuroscience 2021 Jan 1-10. Tong Trang Mai, Dao Thuy Thi Hong, Doan Loc Phuoc, Nguyen Dat Thanh, Nguyen Quynh-Tho Thi, Do Thanh-Thuy Thi, Truong Kiet Dinh, Phan Minh-Duy, Nguyen Hoai-Nghia, Tran Thang Cong, Giang H |
| The APOE e4 exerts differential effects on familial and other subtypes of Alzheimer's disease. Alzheimer's & dementia : the journal of the Alzheimer's Association 2020 Sep . Jia Longfei, Xu Hui, Chen Shuoqi, Wang Xiu, Yang Jianwei, Gong Min, Wei Cuibai, Tang Yi, Qu Qiumin, Chu Lan, Shen Lu, Zhou Chunkui, Wang Qi, Zhao Tan, Zhou Aihong, Li Ying, Li Fangyu, Li Yan, Jin Hongmei, Qin Qi, Jiao Haishan, Li Yan, Zhang Heng, Lyu Diyang, Shi Yuqing, Song Yang, Jia Jianpi |
| Association Between Visual Memory and In Vivo Amyloid and Tau Pathology in Preclinical Autosomal Dominant Alzheimer's Disease. Journal of the International Neuropsychological Society : JINS 2020 Aug 1-9. Bocanegra Yamile, Fox-Fuller Joshua T, Baena Ana, Guzmán-Vélez Edmarie, Vila-Castelar Clara, Martínez Jairo, Torrico-Teave Heirangi, Lopera Francisco, Quiroz Yakeel |
| Screening of dementia genes by whole-exome sequencing in Spanish patients with early-onset dementia: likely pathogenic, uncertain significance and risk variants. Neurobiology of aging 2020 Feb . Ramos-Campoy Oscar, Antonell Anna, Falgàs Neus, Balasa Mircea, Borrego-Écija Sergi, Rodríguez-Santiago Benjamín, Datta Debayan, Armengol Lluís, Fernández-Villullas Guadalupe, Bosch Beatriz, Olives Jaume, Muñoz-García Cristina, Castellví Magdalena, Tort-Merino Adrià, Sánchez-Valle Raquel, Lladó Albe |
| Genetic screening of a large series of North American sporadic and familial frontotemporal dementia cases. Alzheimer's & dementia : the journal of the Alzheimer's Association 2020 Jan 16 (1): 118-130. Ramos Eliana Marisa, Dokuru Deepika Reddy, Van Berlo Victoria, Wojta Kevin, Wang Qing, Huang Alden Y, Deverasetty Sandeep, Qin Yue, van Blitterswijk Marka, Jackson Jazmyne, Appleby Brian, Bordelon Yvette, Brannelly Patrick, Brushaber Danielle E, Dickerson Bradford, Dickinson Susan, Domoto-Reilly Kimiko, Faber Kelley, Fields Julie, Fong Jamie, Foroud Tatiana, Forsberg Leah K, Gavrilova Ralitza, Ghoshal Nupur, Goldman Jill, Graff-Radford Jonathan, Graff-Radford Neill, Grant Ian, Grossman Murray, Heuer Hilary W, Hsiung Ging-Yuek R, Huey Edward, Irwin David, Kantarci Kejal, Karydas Anna, Kaufer Daniel, Kerwin Diana, Knopman David, Kornak John, Kramer Joel H, Kremers Walter, Kukull Walter, Litvan Irene, Ljubenkov Peter, Lungu Codrin, Mackenzie Ian, Mendez Mario F, Miller Bruce L, Onyike Chiadi, Pantelyat Alexander, Pearlman Rodney, Petrucelli Len, Potter Madeline, Rankin Katherine P, Rascovsky Katya, Roberson Erik D, Rogalski Emily, Shaw Leslie, Syrjanen Jeremy, Tartaglia Maria Carmela, Tatton Nadine, Taylor Joanne, Toga Arthur, Trojanowski John Q, Weintraub Sandra, Wong Bonnie, Wszolek Zbigniew, Rademakers Rosa, Boeve Brad F, Rosen Howard J, Boxer Adam L, , Coppola Giovan |
| Genetic Analysis of Chinese Patients with Early-Onset Dementia Using Next-Generation Sequencing. Clinical interventions in aging 2020 15 1831-1839. Han Li-Hong, Xue Yan-Yan, Zheng Yi-Cen, Li Xiao-Yan, Lin Rong-Rong, Wu Zhi-Ying, Tao Qing-Qi |
| Mutation Analysis of the Genes Linked to Early Onset Alzheimer's Disease and Frontotemporal Lobar Degeneration. Journal of Alzheimer's disease : JAD 2019 May . Luukkainen Laura, Helisalmi Seppo, Kytövuori Laura, Ahmasalo Riitta, Solje Eino, Haapasalo Annakaisa, Hiltunen Mikko, Remes Anne M, Krüger Johan |
| 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 Study of Alzheimer's Disease in Saudi Population. Journal of Alzheimer's disease : JAD 2019 67 (1): 231-242. El Bitar Fadia, Qadi Najeeb, Al Rajeh Saad, Majrashi Amna, Abdulaziz Sara, Majrashi Nada, Al Inizi Maznah, Taher Asma, Al Tassan Na |
| The Whole Exome Sequencing Clarifies the Genotype- Phenotype Correlations in Patients with Early-Onset Dementia. Aging and disease 2018 Aug 9 (4): 696-705. Xu Yangqi, Liu Xiaoli, Shen Junyi, Tian Wotu, Fang Rong, Li Binyin, Ma Jianfang, Cao Li, Chen Shengdi, Li Guanjun, Tang Huido |
| Clinical exome sequencing in dementias: a preliminary study. Psychiatria Danubina 2018 Jun 30 (2): 216-219. Zalar Bojan, Maver Aleš, Kovanda Ana, Peterlin Ana, Peterlin Bor |
| Genetic Variation in Genes Underlying Diverse Dementias May Explain a Small Proportion of Cases in the Alzheimer's Disease Sequencing Project. Dementia and geriatric cognitive disorders 2018 Feb 45 (1): 1-17. Blue Elizabeth E, Bis Joshua C, Dorschner Michael O, Tsuang Debby W, Barral Sandra M, Beecham Gary, Below Jennifer E, Bush William S, Butkiewicz Mariusz, Cruchaga Carlos, DeStefano Anita, Farrer Lindsay A, Goate Alison, Haines Jonathan, Jaworski Jim, Jun Gyungah, Kunkle Brian, Kuzma Amanda, Lee Jenny J, Lunetta Kathryn L, Ma Yiyi, Martin Eden, Naj Adam, Nato Alejandro Q, Navas Patrick, Nguyen Hiep, Reitz Christiane, Reyes Dolly, Salerno William, Schellenberg Gerard D, Seshadri Sudha, Sohi Harkirat, Thornton Timothy A, Valadares Otto, van Duijn Cornelia, Vardarajan Badri N, Wang Li-San, Boerwinkle Eric, Dupuis Josée, Pericak-Vance Margaret A, Mayeux Richard, Wijsman Ellen M, |
| 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 |
| Mutation burden profile in familial Alzheimer's disease cases from India. Neurobiology of aging 2017 Dec . Syama Adhikarla, Sen Somdatta, Kota Lakshmi Narayanan, Viswanath Biju, Purushottam Meera, Varghese Mathew, Jain Sanjeev, Panicker Mitradas M, Mukherjee Odi |
| Population-based Study of Risk Polymorphisms Associated with Vascular Disorders and Dementia. Current genomics 2017 Oct 18 (5): 430-441. Teijido Óscar, Carril Juan Carlos, Cacabelos Ram |
| The wide genetic landscape of clinical frontotemporal dementia: systematic combined sequencing of 121 consecutive subjects. Genetics in medicine : official journal of the American College of Medical Genetics 2017 Jul . Blauwendraat Cornelis, Wilke Carlo, Simón-Sánchez Javier, Jansen Iris E, Reifschneider Anika, Capell Anja, Haass Christian, Castillo-Lizardo Melissa, Biskup Saskia, Maetzler Walter, Rizzu Patrizia, Heutink Peter, Synofzik Matth |
| Next-generation sequencing reveals substantial genetic contribution to dementia with Lewy bodies. Neurobiology of disease 2016 Jun 94 55-62. Geiger Joshua T, Ding Jinhui, Crain Barbara, Pletnikova Olga, Letson Christopher, Dawson Ted M, Rosenthal Liana S, Pantelyat Alexander, Gibbs J Raphael, Albert Marilyn S, Hernandez Dena G, Hillis Argye E, Stone David J, Singleton Andrew B, , Hardy John A, Troncoso Juan C, Scholz Sonja |
| [Significance and progress of DIAN/A4/API]. Nihon rinsho. Japanese journal of clinical medicine 2016 Mar 74 (3): 417-22. Shimada Hiroyu |
| Cognitive Decline in a Colombian Kindred With Autosomal Dominant Alzheimer Disease: A Retrospective Cohort Study. JAMA neurology 2016 Feb . Aguirre-Acevedo Daniel C, Lopera Francisco, Henao Eliana, Tirado Victoria, Muñoz Claudia, Giraldo Margarita, Bangdiwala Shrikant I, Reiman Eric M, Tariot Pierre N, Langbaum Jessica B, Quiroz Yakeel T, Jaimes Fabi |
| Novel PSEN1 mutations (H214N and R220P) associated with familial Alzheimer's disease identified by targeted exome sequencing. Neurobiology of aging 2016 Feb . Piccoli Elena, Rossi Giacomina, Rossi Tommaso, Pelliccioni Giuseppe, D'Amato Ilaria, Tagliavini Fabrizio, Di Fede Giusep |
| Plasma Phospholipid and Sphingolipid Alterations in Presenilin1 Mutation Carriers: A Pilot Study. Journal of Alzheimer's disease : JAD 2016 Jan . Chatterjee Pratishtha, Lim Wei L F, Shui Guanghou, Gupta Veer B, James Ian, Fagan Anne M, Xiong Chengjie, Sohrabi Hamid R, Taddei Kevin, Brown Belinda M, Benzinger Tammie, Masters Colin, Snowden Stuart G, Wenk Marcus R, Bateman Randall J, Morris John C, Martins Ralph |
| Presenilin E318G variant and Alzheimer's disease risk: the Cache County study. BMC genomics 2016 17 Suppl 3 438. Hippen Ariel A, Ebbert Mark T W, Norton Maria C, Tschanz JoAnn T, Munger Ronald G, Corcoran Christopher D, Kauwe John S |
| Diagnostic accuracy of CERAD total score in a Colombian cohort with mild cognitive impairment and Alzheimer's disease affected by E280A mutation on presenilin-1 gene. International psychogeriatrics / IPA 2015 Oct 1-8. Aguirre-Acevedo Daniel Camilo, Jaimes-Barragán Fabian, Henao Eliana, Tirado Victoria, Muñoz Claudia, Reiman Eric M, Tariot Pierre N, Langbaum Jessica B, Lopera Francis |
| Evaluating pathogenic dementia variants in posterior cortical atrophy. Neurobiology of aging 2015 Oct . Carrasquillo Minerva M, Barber Imelda, Lincoln Sarah J, Murray Melissa E, Camsari Gamze Balci, Khan Qurat Ul Ain, Nguyen Thuy, Ma Li, Bisceglio Gina D, Crook Julia E, Younkin Steven G, Dickson Dennis W, Boeve Bradley F, Graff-Radford Neill R, Morgan Kevin, Ertekin-Taner Nilüf |
| Rare variants in ß-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 |
| Disease-related mutations among Caribbean Hispanics with familial dementia. Molecular genetics & genomic medicine 2014 Sep 2 (5): 430-7. Lee Joseph H, Kahn Amanda, Cheng Rong, Reitz Christiane, Vardarajan Badri, Lantigua Rafael, Medrano Martin, Jiménez-Velázquez Ivonne Z, Williamson Jennifer, Nagy Peter, Mayeux Richa |
- Page last reviewed:Oct 1, 2021
- Page last updated:Oct 20, 2021
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