HuGE Literature Finder
Records 1-30
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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 |
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Mutation profile of APP, PSEN1, and PSEN2 in Chinese familial Alzheimer's disease.
Neurobiology of aging 2019 Jan 77 154-157. Gao Ying, Ren Ru-Jing, Zhong Zi-Lin, Dammer Eric, Zhao Qian-Hua, Shan Shan, Zhou Zheng, Li Xia, Zhang Yue-Qi, Cui Hai-Lun, Hu Yong-Bo, Chen Sheng-Di, Chen Jian-Jun, Guo Qi-Hao, Wang Ga |
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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 |
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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 |
Genome-wide Network-assisted Association and Enrichment Study of Amyloid Imaging Phenotype in Alzheimer's Disease.
Current Alzheimer research 2019 16 (13): 1163-1174. Li Jin, Chen Feng, Zhang Qiushi, Meng Xianglian, Yao Xiaohui, Risacher Shannon L, Yan Jingwen, Saykin Andrew J, Liang Hong, Shen Li, |
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A Genome-Wide Association Study of ?-Synuclein Levels in Cerebrospinal Fluid.
Neurotoxicity research 2018 Jun . Zhong Xiao-Ling, Li Jie-Qiong, Sun Li, Li Ya-Qing, Wang Hui-Fu, Cao Xi-Peng, Tan Chen-Chen, Wang Ling, Tan Lan, Yu Jin-Tai, |
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Genome-wide association study identified ATP6V1H locus influencing cerebrospinal fluid BACE activity.
BMC medical genetics 2018 May 19 (1): 75. Hu Hao, Li Haiyan, Li Jieqiong, Yu Jintai, Tan Lan, |
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Patterns and severity of vascular amyloid in Alzheimer's disease associated with duplications and missense mutations in APP gene, Down syndrome and sporadic Alzheimer's disease.
Acta neuropathologica 2018 May . Mann David M A, Davidson Yvonne S, Robinson Andrew C, Allen Nancy, Hashimoto Tadafumi, Richardson Anna, Jones Matthew, Snowden Julie S, Pendleton Neil, Potier Marie-Claude, Laquerrière Annie, Prasher Vee, Iwatsubo Takeshi, Strydom And |
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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 |
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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 |
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Early-Onset Alzheimer Disease and Candidate Risk Genes Involved in Endolysosomal Transport.
JAMA neurology 2017 Jul . Kunkle Brian W, Vardarajan Badri N, Naj Adam C, Whitehead Patrice L, Rolati Sophie, Slifer Susan, Carney Regina M, Cuccaro Michael L, Vance Jeffery M, Gilbert John R, Wang Li-San, Farrer Lindsay A, Reitz Christiane, Haines Jonathan L, Beecham Gary W, Martin Eden R, Schellenberg Gerard D, Mayeux Richard P, Pericak-Vance Margaret |
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Lower functional connectivity of default mode network in cognitively normal young adults with mutation of APP, presenilins and APOE e4.
Brain imaging and behavior 2017 Jun 11 (3): 818-828. Su Yun Yan, Zhang Xiao Dong, Schoepf U Joseph, Varga-Szemes Akos, Stubenrauch Andrew, Liang Xue, Zheng Li Juan, Zheng Gang, Kong Xiang, Xu Qiang, Wang Shou Ju, Qi Rong Feng, Lu Guang Ming, Zhang Long Jia |
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Candidate gene analysis for Alzheimer's disease in adults with Down syndrome.
Neurobiology of aging 2017 May . Lee Joseph H, Lee Annie J, Dang Lam-Ha, Pang Deborah, Kisselev Sergey, Krinsky-McHale Sharon J, Zigman Warren B, Luchsinger José A, Silverman Wayne, Tycko Benjamin, Clark Lorraine N, Schupf Nico |
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Comprehensive Screening for Disease Risk Variants in Early-Onset Alzheimer's Disease Genes in African Americans Identifies Novel PSEN Variants.
Journal of Alzheimer's disease : JAD 2017 Jan . N'Songo Aurelie, Carrasquillo Minerva M, Wang Xue, Nguyen Thuy, Asmann Yan, Younkin Steven G, Allen Mariet, Duara Ranjan, Custo Maria T Greig, Graff-Radford Neill, Ertekin-Taner Nilüf |
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SORL1 variants across Alzheimer's disease European American cohorts.
European journal of human genetics : EJHG 2016 Sep . Fernández Maria Victoria, Black Kathleen, Carrell David, Saef Ben, Budde John, Deming Yuetiva, Howells Bill, Del-Aguila Jorge L, Ma Shengmei, Bi Catherine, Norton Joanne, Chasse Rachel, Morris John, Goate Alison, Cruchaga Carlos, |
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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 |
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Dura mater is a potential source of A? seeds.
Acta neuropathologica 2016 Mar . Kovacs Gabor G, Lutz Mirjam I, Ricken Gerda, Ströbel Thomas, Höftberger Romana, Preusser Matthias, Regelsberger Günther, Hönigschnabl Selma, Reiner Angelika, Fischer Peter, Budka Herbert, Hainfellner Johannes |
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Family-based association analyses of imputed genotypes reveal genome-wide significant association of Alzheimer's disease with OSBPL6, PTPRG, and PDCL3.
Molecular psychiatry 2016 Feb . Herold C, Hooli B V, Mullin K, Liu T, Roehr J T, Mattheisen M, Parrado A R, Bertram L, Lange C, Tanzi R |
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Influence of Coding Variability in APP-A? Metabolism Genes in Sporadic Alzheimer's Disease.
PloS one 2016 11 (6): e0150079. Sassi Celeste, Ridge Perry G, Nalls Michael A, Gibbs Raphael, Ding Jinhui, Lupton Michelle K, Troakes Claire, Lunnon Katie, Al-Sarraj Safa, Brown Kristelle S, Medway Christopher, Lord Jenny, Turton James, , Morgan Kevin, Powell John F, Kauwe John S, Cruchaga Carlos, Bras Jose, Goate Alison M, Singleton Andrew B, Guerreiro Rita, Hardy Jo |
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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 |
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Genetic determinants of white matter hyperintensities and amyloid angiopathy in familial Alzheimer's disease.
Neurobiology of aging 2015 Sep . Ryan Natalie S, Biessels Geert-Jan, Kim Lois, Nicholas Jennifer M, Barber Philip A, Walsh Phoebe, Gami Priya, Morris Huw R, Bastos-Leite António J, Schott Jonathan M, Beck Jon, Mead Simon, Chavez-Gutierrez Lucia, de Strooper Bart, Rossor Martin N, Revesz Tamas, Lashley Tammaryn, Fox Nick |
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Cerebrospinal fluid A?42 levels and APP processing pathway genes in Parkinson's disease.
Movement disorders : official journal of the Movement Disorder Society 2015 Jun 30 (7): 936-44. Bekris Lynn M, Tsuang Debby W, Peskind Elaine R, Yu Chang E, Montine Thomas J, Zhang Jing, Zabetian Cyrus P, Leverenz James |
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Genetic association between APP, ADAM10 gene polymorphism, and sporadic alzheimer's disease in the Chinese population.
Neurotoxicity research 2015 Apr 27 (3): 284-91. Zeng Fan, Shen Cheng, Liu Yu-Hui, Li Jing, Zhu Jie, Wang Ye-Ran, Yan Jia-Chuan, Gao Chang-Yue, Zhou Hua-Dong, Deng Juan, Wang Yan-Jia |
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Rarity of the Alzheimer disease-protective APP A673T variant in the United States.
JAMA neurology 2015 Feb 72 (2): 209-16. Wang Li-San, Naj Adam C, Graham Robert R, Crane Paul K, Kunkle Brian W, Cruchaga Carlos, Murcia Josue D Gonzalez, Cannon-Albright Lisa, Baldwin Clinton T, Zetterberg Henrik, Blennow Kaj, Kukull Walter A, Faber Kelley M, Schupf Nicole, Norton Maria C, Tschanz JoAnn T, Munger Ronald G, Corcoran Christopher D, Rogaeva Ekaterina, , Lin Chiao-Feng, Dombroski Beth A, Cantwell Laura B, Partch Amanda, Valladares Otto, Hakonarson Hakon, St George-Hyslop Peter, Green Robert C, Goate Alison M, Foroud Tatiana M, Carney Regina M, Larson Eric B, Behrens Timothy W, Kauwe John S K, Haines Jonathan L, Farrer Lindsay A, Pericak-Vance Margaret A, Mayeux Richard, Schellenberg Gerard D, , Albert Marilyn S, Albin Roger L, Apostolova Liana G, Arnold Steven E, Barber Robert, Barmada Michael, Barnes Lisa L, Beach Thomas G, Becker James T, Beecham Gary W, Beekly Duane, Bennett David A, Bigio Eileen H, Bird Thomas D, Blacker Deborah, Boeve Bradley F, Bowen James D, Boxer Adam, Burke James R, Buxbaum Joseph D, Cairns Nigel J, Cao Chuanhai, Carlson Chris S, Carroll Steven L, Chui Helena C, Clark David G, Cribbs David H, Crocco Elizabeth A, DeCarli Charles, DeKosky Steven T, Demirci F Yesim, Dick Malcolm, Dickson Dennis W, Duara Ranjan, Ertekin-Taner Nilufer, Fallon Kenneth B, Farlow Martin R, Ferris Steven, Frosch Matthew P, Galasko Douglas R, Ganguli Mary, Gearing Marla, Geschwind Daniel H, Ghetti Bernardino, Gilbert John R, Glass Jonathan D, Graff-Radford Neill R, Growdon John H, Hamilton Ronald L, Hamilton-Nelson Kara L, Harrell Lindy E, Head Elizabeth, Honig Lawrence S, Hulette Christine M, Hyman Bradley T, Jarvik Gail P, Jicha Gregory A, Jin Lee-Way, Jun Gyungah, Jun Gyungah, Kamboh M Ilyas, Karydas Anna, Kaye Jeffrey A, Kim Ronald, Koo Edward H, Kowall Neil W, Kramer Joel H, LaFerla Frank M, Lah James J, Leverenz James B, Levey Allan I, Li Gei, Lieberman Andrew P, Lopez Oscar L, Lunetta Kathryn L, Lyketsos Constantine G, Mack Wendy J, Marson Daniel C, Martin Eden R, Martiniuk Frank, Mash Deborah C, Masliah Eliezer, McCormick Wayne C, McCurry Susan M, McDavid Andrew N, McKee Ann C, Mesulam W Marsel, Miller Bruce L, Miller Carol A, Miller Joshua W, Montine Thomas J, Morris John C, Murrell Jill R, Olichney John M, Parisi Joseph E, Perry William, Peskind Elaine, Petersen Ronald C, Pierce Aimee, Poon Wayne W, Potter Huntington, Quinn Joseph F, Raj Ashok, Raskind Murray, Reiman Eric M, Reisberg Barry, Reitz Christiane, Ringman John M, Roberson Erik D, Rosen Howard J, Rosenberg Roger N, Sano Mary, Saykin Andrew J, Schneider Julie A, Schneider Lon S, Seeley William W, Smith Amanda G, Sonnen Joshua A, Spina Salvatore, Stern Robert A, Tanzi Rudolph E, Thornton-Wells Tricia A, Trojanowski John Q, Troncoso Juan C, Tsuang Debby W, Van Deerlin Vivianna M, Van Eldik Linda J, Vardarajan Badri N, Vinters Harry V, Vonsattel Jean Paul, Weintraub Sandra, Welsh-Bohmer Kathleen A, Williamson Jennifer, Wishnek Sarah, Woltjer Randall L, Wright Clinton B, Younkin Steven G, Yu Chang-En, Yu L |
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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 |
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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 |
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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 |
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Investigation of an amyloid precursor protein protective mutation (A673T) in a North American case-control sample of late-onset Alzheimer's disease.
Neurobiology of aging 2014 Jul 35 (7): 1779.e15-6. Bamne Mikhil N, Demirci F Yesim, Berman Sarah, Snitz Beth E, Rosenthal Samantha L, Wang Xingbin, Lopez Oscar L, Kamboh M Ily |
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Absence of A673T variant in APP gene indicates an alternative protective mechanism contributing to longevity in Chinese individuals.
Neurobiology of aging 2014 Apr 35 (4): 935.e11-2. Liu Yao-Wen, He Yong-Han, Zhang Yun-Xia, Cai Wang-Wei, Yang Li-Qin, Xu Liang-You, Kong Qing-Pe |
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Interactions between GSK3? and amyloid genes explain variance in amyloid burden.
Neurobiology of aging 2014 Mar 35 (3): 460-5. Hohman Timothy J, Koran Mary Ellen I, Thornton-Wells Tricia A, |
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Clinical and psychological characteristics of the initial cohort of the Dominantly Inherited Alzheimer Network (DIAN).
Neuropsychology 2014 Jan 28 (1): 19-29. Storandt Martha, Balota David A, Aschenbrenner Andrew J, Morris John |
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Absence of A673T amyloid-? precursor protein variant in Alzheimer's disease and other neurological diseases.
Neurobiology of aging 2013 Oct 34 (10): 2441.e7-8. Ting Simon Kang Seng, Chong Mei-Sian, Kandiah Nagaendran, Hameed Shahul, Tan Louis, Au Wing-Lok, Prakash Kumar M, Pavanni Ratnagopal, Lee Tih-Shih, Foo Jia-Nee, Bei Jin-Xin, Yu Xue-Qing, Liu Jian-Jun, Zhao Yi, Lee Wei-Ling, Tan Eng-Ki |
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Genetic susceptibility for Alzheimer disease neuritic plaque pathology.
JAMA neurology 2013 Sep 70 (9): 1150-7. Shulman Joshua M, Chen Kewei, Keenan Brendan T, Chibnik Lori B, Fleisher Adam, Thiyyagura Pradeep, Roontiva Auttawut, McCabe Cristin, Patsopoulos Nikolaos A, Corneveaux Jason J, Yu Lei, Huentelman Matthew J, Evans Denis A, Schneider Julie A, Reiman Eric M, De Jager Philip L, Bennett David |
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A genome-wide study shows a limited contribution of rare copy number variants to Alzheimer's disease risk.
Human molecular genetics 2013 Feb 22 (4): 816-24. Chapman Jade, Rees Elliott, Harold Denise, Ivanov Dobril, Gerrish Amy, Sims Rebecca, Hollingworth Paul, Stretton Alexandra, , Holmans Peter, Owen Michael J, O'Donovan Michael C, Williams Julie, Kirov Geor |
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The PSEN1, p.E318G variant increases the risk of Alzheimer's disease in APOE-?4 carriers.
PLoS genetics 2013 9 (8): e1003685. Benitez Bruno A, Karch Celeste M, Cai Yefei, Jin Sheng Chih, Cooper Breanna, Carrell David, Bertelsen Sarah, Chibnik Lori, Schneider Julie A, Bennett David A, , , Fagan Anne M, Holtzman David, Morris John C, Goate Alison M, Cruchaga Carl |
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APP mutations in the A? coding region are associated with abundant cerebral deposition of A?38.
Acta neuropathologica 2012 Dec 124 (6): 809-21. Moro Maria Luisa, Giaccone Giorgio, Lombardi Raffaella, Indaco Antonio, Uggetti Andrea, Morbin Michela, Saccucci Stefania, Di Fede Giuseppe, Catania Marcella, Walsh Dominic M, Demarchi Andrea, Rozemuller Annemieke, Bogdanovic Nenad, Bugiani Orso, Ghetti Bernardino, Tagliavini Fabriz |
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Role of common and rare APP DNA sequence variants in Alzheimer disease.
Neurology 2012 Apr 78 (16): 1250-7. Hooli B V, Mohapatra G, Mattheisen M, Parrado A R, Roehr J T, Shen Y, Gusella J F, Moir R, Saunders A J, Lange C, Tanzi R E, Bertram |
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Rare Variants in APP, PSEN1 and PSEN2 Increase Risk for AD in Late-Onset Alzheimer's Disease Families.
PloS one 2012 7 (2): 2. Cruchaga C, Chakraverty S, Mayo K, Vallania FL, Mitra RD, Faber K, Williamson J, Bird T, Diaz-Arrastia R, Foroud TM, Boeve BF, Graff-Radford NR, St Jean P, Lawson M, Ehm MG, Mayeux R, Goate AM |
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?-Catenin is genetically and biologically associated with cortical cataract and future Alzheimer-related structural and functional brain changes.
PloS one 2012 7 (9): e43728. Jun Gyungah, Moncaster Juliet A, Koutras Carolina, Seshadri Sudha, Buros Jacqueline, McKee Ann C, Levesque Georges, Wolf Philip A, St George-Hyslop Peter, Goldstein Lee E, Farrer Lindsay |
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The role of variation at A?PP, PSEN1, PSEN2, and MAPT in late onset Alzheimer's disease.
Journal of Alzheimer's disease : JAD 2012 28 (2): 377-87. Gerrish Amy, Russo Giancarlo, Richards Alexander, Moskvina Valentina, Ivanov Dobril, Harold Denise, Sims Rebecca, Abraham Richard, Hollingworth Paul, Chapman Jade, Hamshere Marian, Pahwa Jaspreet Singh, Dowzell Kimberley, Williams Amy, Jones Nicola, Thomas Charlene, Stretton Alexandra, Morgan Angharad R, Lovestone Simon, Powell John, Proitsi Petroula, Lupton Michelle K, Brayne Carol, Rubinsztein David C, Gill Michael, Lawlor Brian, Lynch Aoibhinn, Morgan Kevin, Brown Kristelle S, Passmore Peter A, Craig David, McGuinness Bernadette, Todd Stephen, Johnston Janet A, Holmes Clive, Mann David, Smith A David, Love Seth, Kehoe Patrick G, Hardy John, Mead Simon, Fox Nick, Rossor Martin, Collinge John, Maier Wolfgang, Jessen Frank, Kölsch Heike, Heun Reinhard, Schürmann Britta, van den Bussche Hendrik, Heuser Isabella, Kornhuber Johannes, Wiltfang Jens, Dichgans Martin, Frölich Lutz, Hampel Harald, Hüll Michael, Rujescu Dan, Goate Alison M, Kauwe John S K, Cruchaga Carlos, Nowotny Petra, Morris John C, Mayo Kevin, Livingston Gill, Bass Nicholas J, Gurling Hugh, McQuillin Andrew, Gwilliam Rhian, Deloukas Panagiotis, Davies Gail, Harris Sarah E, Starr John M, Deary Ian J, Al-Chalabi Ammar, Shaw Christopher E, Tsolaki Magda, Singleton Andrew B, Guerreiro Rita, Mühleisen Thomas W, Nöthen Markus M, Moebus Susanne, Jöckel Karl-Heinz, Klopp Norman, Wichmann H-Erich, Carrasquillo Minerva M, Pankratz V Shane, Younkin Steven G, Jones Lesley, Holmans Peter A, O'Donovan Michael C, Owen Michael J, Williams Jul |
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Amyloid precursor protein gene (APP) variation in late-onset Alzheimer's disease.
Journal of molecular neuroscience : MN 2011 Sep 45 (1): 5-9. Miar Ana, Alvarez Victoria, Corao Ana I, Díaz Marta, Alonso Belén, Martínez Carmen, Calatayud María T, Menéndez Manuel, Morís Germán, Coto Eliec |
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Amyloid precursor protein (APP) processing genes and cerebrospinal fluid APP cleavage product levels in Alzheimer's disease.
Neurobiology of aging 2011 Mar 32 (3): 556.e13-23. Bekris L M, Galloway N M, Millard S, Lockhart D, Li G, Galasko D R, Farlow M R, Clark C M, Quinn J F, Kaye J A, Schellenberg G D, Leverenz J B, Seubert P, Tsuang D W, Peskind E R, Yu C |
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No association of psychosis in Alzheimer disease with neurodegenerative pathway genes.
Neurobiology of aging 2011 Mar 32 (3): 555.e9-11. DeMichele-Sweet Mary Ann A, Klei Lambertus, Devlin Bernie, Ferrell Robert E, Weamer Elise A, Emanuel James E, Lopez Oscar L, Sweet Robert |
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APOE and A?PP gene variation in cortical and cerebrovascular amyloid-? pathology and Alzheimer's disease: a population-based analysis.
Journal of Alzheimer's disease : JAD 2011 26 (2): 377-85. Peuralinna Terhi, Tanskanen Maarit, Mäkelä Mira, Polvikoski Tuomo, Paetau Anders, Kalimo Hannu, Sulkava Raimo, Hardy John, Lai Shiao-Lin, Arepalli Sampath, Hernandez Dena, Traynor Bryan J, Singleton Andrew, Tienari Pentti J, Myllykangas Lii |
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Genetic screening of Alzheimer's disease genes in Iberian and African samples yields novel mutations in presenilins and APP.
Neurobiology of aging 2010 May 31 (5): 725-31. Guerreiro Rita Joao, Baquero Miquel, Blesa Rafael, Boada Mercè, Brás Jose Miguel, Bullido Maria J, Calado Ana, Crook Richard, Ferreira Carla, Frank Ana, Gómez-Isla Teresa, Hernández Isabel, Lleó Alberto, Machado Alvaro, Martínez-Lage Pablo, Masdeu José, Molina-Porcel Laura, Molinuevo José L, Pastor Pau, Pérez-Tur Jordi, Relvas Rute, Oliveira Catarina Resende, Ribeiro Maria Helena, Rogaeva Ekaterina, Sa Alfredo, Samaranch Lluís, Sánchez-Valle Raquel, Santana Isabel, Tàrraga Lluís, Valdivieso Fernando, Singleton Andrew, Hardy John, Clarimón Jor |
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High striatal amyloid beta-peptide deposition across different autosomal Alzheimer disease mutation types.
Archives of neurology 2009 Dec 66 (12): 1537-44. Villemagne Victor L, Ataka Suzuka, Mizuno Toshiki, Brooks William S, Wada Yasuhiro, Kondo Masaki, Jones Gareth, Watanabe Yasuyoshi, Mulligan Rachel, Nakagawa Masanori, Miki Takami, Shimada Hiroyuki, O'Keefe Graeme J, Masters Colin L, Mori Hiroshi, Rowe Christopher |
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PSEN1 polymorphisms alter the rate of cognitive decline in sporadic Alzheimer's disease patients.
Neurobiology of aging 2009 Dec 30 (12): 1992-9. Belbin Olivia, Beaumont Helen, Warden Donald, Smith A David, Kalsheker Noor, Morgan Kev |
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APP and BACE1 miRNA genetic variability has no major role in risk for Alzheimer disease.
Human mutation 2009 Aug 30 (8): 1207-13. Bettens Karolien, Brouwers Nathalie, Engelborghs Sebastiaan, Van Miegroet Helen, De Deyn Peter P, Theuns Jessie, Sleegers Kristel, Van Broeckhoven Christi |
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Novel polymorphisms of the amyloid precursor protein (APP) gene in Chinese/Taiwanese patients with Alzheimer's disease.
Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia 2009 Feb 16 (2): 259-63. Thajeb Peterus, Wang Pei, Chien Chung-Liang, Harrigan Rosan |
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AbetaPP A713T mutation in late onset Alzheimer's disease with cerebrovascular lesions.
Journal of Alzheimer's disease : JAD 2009 17 (2): 383-9. Bernardi Livia, Geracitano Silvana, Colao Rosanna, Puccio Gianfranco, Gallo Maura, Anfossi Maria, Frangipane Francesca, Curcio Sabrina A M, Mirabelli Maria, Tomaino Carmine, Vasso Franca, Smirne Nicoletta, Maletta Raffaele, Bruni Amalia |
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Genetic association between low-density lipoprotein receptor-related protein gene polymorphisms and Alzheimer's disease in Chinese Han population.
Neuroscience letters 2008 Oct 444 (1): 109-11. Zhou Yong-Tao, Zhang Zhen-Xin, Chan Piu, He Xiao-Ming, Tang Mou-Ni, Wu Cheng-Bin, Hong Zh |
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Promoter polymorphisms which modulate APP expression may increase susceptibility to Alzheimer's disease.
Neurobiology of aging 2008 Feb 29 (2): 194-202. Lv Haiyan, Jia Longfei, Jia Jianpi |
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Increased prevalence of significant recurrent headache in preclinical familial Alzheimer's disease mutation carriers.
Dementia and geriatric cognitive disorders 2008 25 (4): 380-4. Ringman John M, Romano Joseph D, Medina Luis D, Rodriguez-Agudelo Yaneth, Schaffer Barbara, Varpetian Arousiak, Ortiz Freddy, Fitten L Jamie, Cummings Jeffrey L, Baloh Robert |
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The extended tau haplotype and the age of onset of dementia in Down syndrome.
Dementia and geriatric cognitive disorders 2008 26 (3): 199-202. Jones Emma L, Margallo-Lana Marisa, Prasher Vee P, Ballard Clive |
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Association studies testing for risk for late-onset Alzheimer's disease with common variants in the beta-amyloid precursor protein (APP).
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2007 Jun 144B (4): 469-74. Nowotny Petra, Simcock Xavier, Bertelsen Sarah, Hinrichs Anthony L, Kauwe John S K, Mayo Kevin, Smemo Scott, Morris John C, Goate Alis |
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A mutation screening by DHPLC of PSEN1 and APP genes reveals no significant variation associated with the sporadic late-onset form of Alzheimer's disease.
Neuroscience letters 2007 May 418 (3): 282-5. Scacchi Renato, Gambina Giuseppe, Moretto Giuseppe, Corbo Rosa Mar |
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Variations in the APP gene promoter region and risk of Alzheimer disease.
Neurology 2007 Feb 68 (9): 684-7. Guyant-Maréchal L, Rovelet-Lecrux A, Goumidi L, Cousin E, Hannequin D, Raux G, Penet C, Ricard S, Macé S, Amouyel P, Deleuze J-F, Frebourg T, Brice A, Lambert J-C, Campion |
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A genetic association analysis of cognitive ability and cognitive ageing using 325 markers for 109 genes associated with oxidative stress or cognition.
BMC genetics 2007 8 (1): 43. Harris Sarah E, Fox Helen, Wright Alan F, Hayward Caroline, Starr John M, Whalley Lawrence J, Deary Ian |
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Promoter mutations that increase amyloid precursor-protein expression are associated with Alzheimer disease.
American journal of human genetics 2006 Jun 78 (6): 936-46. Theuns Jessie, Brouwers Nathalie, Engelborghs Sebastiaan, Sleegers Kristel, Bogaerts Veerle, Corsmit Ellen, De Pooter Tim, van Duijn Cornelia M, De Deyn Peter P, Van Broeckhoven Christi |
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Genetic study of Sardinian patients with Alzheimer's disease.
Neuroscience letters 2006 May 398 (1-2): 124-8. Piscopo Paola, Manfredi Antonella, Malvezzi-Campeggi Lorenzo, Crestini Alessio, Spadoni Ornella, Cherchi Rossella, Deiana Emiliano, Piras Maria Rita, Confaloni Annamar |
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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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Mutations in presenilin 1, presenilin 2 and amyloid precursor protein genes in patients with early-onset Alzheimer's disease in Poland.
Experimental neurology 2003 Dec 184 (2): 991-6. Zekanowski Cezary, Styczy?ska Maria, Pep?o?ska Beata, Gabryelewicz Tomasz, Religa Dorota, Ilkowski Jan, Kijanowska-Ha?adyna Beata, Kotapka-Minc S?awomira, Mikkelsen Sanne, Pfeffer Anna, Barczak Anna, ?uczywek Elzbieta, Wasiak Bogus?aw, Chodakowska-Zebrowska Ma?gorzata, Gustaw Katarzyna, ?aczkowski Jaros?aw, Sobów Tomasz, Ku?nicki Jacek, Barcikowska Mar |
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A novel mutation in the PSEN2 gene (T430M) associated with variable expression in a family with early-onset Alzheimer disease.
Archives of neurology 2003 Aug 60 (8): 1149-51. Ezquerra Mario, Lleó Alberto, Castellví Magda, Queralt Rosa, Santacruz Pilar, Pastor Pau, Molinuevo José Luis, Blesa Rafael, Oliva Rafa |
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Joint analysis of candidate genes related to Alzheimer's disease in a Spanish population.
Psychiatric genetics 2003 Jun 13 (2): 85-90. Clarimón Jordi, Bertranpetit Jaume, Calafell Francesc, Boada Mercè, Tàrraga Lluís, Comas Dav |
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Systematic genetic study of Alzheimer disease in Latin America: mutation frequencies of the amyloid beta precursor protein and presenilin genes in Colombia.
American journal of medical genetics 2001 Oct 103 (2): 138-43. Arango D, Cruts M, Torres O, Backhovens H, Serrano M L, Villareal E, Montañes P, Matallana D, Cano C, Van Broeckhoven C, Jacquier |
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Molecular genetic analysis of the APP, PSEN1, and PSEN2 genes in Finnish patients with early-onset Alzheimer disease and frontotemporal lobar degeneration.
Alzheimer disease and associated disorders 0 26 (3): 272-6. Krüger Johanna, Moilanen Virpi, Majamaa Kari, Remes Anne |
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