Human Genome Epidemiology Literature Finder
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Records 1 - 30 (of 47 Records) |
| Query Trace: Alzheimer Disease and APP[original query] |
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| Evidence against a role for rare ADAM10 mutations in sporadic Alzheimer disease. Neurobiology of aging 2012 Feb 33 (2): 416-417.e3. Cai Guiqing, Atzmon Gil, Naj Adam C, Beecham Gary W, Barzilai Nir, Haines Jonathan L, Sano Mary, Pericak-Vance Margaret, Buxbaum Joseph |
| 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 |
| Loss of function of ATXN1 increases amyloid beta-protein levels by potentiating beta-secretase processing of beta-amyloid precursor protein. The Journal of biological chemistry 2010 1 285 (12): 8515-26. Zhang Can, Browne Andrew, Child Daniel, Divito Jason R, Stevenson Jesse A, Tanzi Rudolph |
| 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 |
| d-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 |
| The MAPT H1 haplotype is associated with tangle-predominant dementia. Acta neuropathologica 2012 Nov 124 (5): 693-704. Santa-Maria Ismael, Haggiagi Aya, Liu Xinmin, Wasserscheid Jessica, Nelson Peter T, Dewar Ken, Clark Lorraine N, Crary John |
| Identification of Alzheimer disease-associated variants in genes that regulate retromer function. Neurobiology of aging 2012 Sep 33 (9): 2231.e15-2231.e30. Vardarajan Badri N, Bruesegem Sophia Y, Harbour Michael E, Inzelberg Rivka, Friedland Robert, St George-Hyslop Peter, Seaman Matthew N J, Farrer Lindsay |
| 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 |
| APP mutations in the Aß coding region are associated with abundant cerebral deposition of Aß38. 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 |
| 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 |
| Independent and epistatic effects of variants in VPS10-d receptors on Alzheimer disease risk and processing of the amyloid precursor protein (APP). Translational psychiatry 2013 3 e256. Reitz C, Tosto G, Vardarajan B, Rogaeva E, Ghani M, Rogers R S, Conrad C, Haines J L, Pericak-Vance M A, Fallin M D, Foroud T, Farrer L A, Schellenberg G D, George-Hyslop P S, Mayeux R, |
| 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 |
| PLXNA4 is associated with Alzheimer disease and modulates tau phosphorylation. Annals of neurology 2014 Sep 76 (3): 379-92. Jun Gyungah, Asai Hirohide, Zeldich Ella, Drapeau Elodie, Chen CiDi, Chung Jaeyoon, Park Jong-Ho, Kim Sehwa, Haroutunian Vahram, Foroud Tatiana, Kuwano Ryozo, Haines Jonathan L, Pericak-Vance Margaret A, Schellenberg Gerard D, Lunetta Kathryn L, Kim Jong-Won, Buxbaum Joseph D, Mayeux Richard, Ikezu Tsuneya, Abraham Carmela R, Farrer Lindsay |
A genome-wide association meta-analysis of plasma Aß peptides concentrations in the elderly.
Molecular psychiatry 2014 Dec 19 (12): 1326-35. Chouraki V, De Bruijn R F A G, Chapuis J, Bis J C, Reitz C, Schraen S, Ibrahim-Verbaas C A, Grenier-Boley B, Delay C, Rogers R, Demiautte F, Mounier A, Fitzpatrick A L, , Berr C, Dartigues J-F, Uitterlinden A G, Hofman A, Breteler M, Becker J T, Lathrop M, Schupf N, Alpérovitch A, Mayeux R, van Duijn C M, Buée L, Amouyel P, Lopez O L, Ikram M A, Tzourio C, Lambert J |
| 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 |
| [Association between exon polymorphisms of BACE2 gene with Alzheimer disease]. Zhonghua yi xue za zhi 2014 Aug 94 (29): 2274-8. Yu Yueyi, Jia Jianpi |
| Coding mutations in SORL1 and Alzheimer disease. Annals of neurology 2015 Feb 77 (2): 215-27. Vardarajan Badri N, Zhang Yalun, Lee Joseph H, Cheng Rong, Bohm Christopher, Ghani Mahdi, Reitz Christiane, Reyes-Dumeyer Dolly, Shen Yufeng, Rogaeva Ekaterina, St George-Hyslop Peter, Mayeux Richa |
| De novo deleterious genetic variations target a biological network centered on Aß peptide in early-onset Alzheimer disease. Molecular psychiatry 2015 Sep 20 (9): 1046-56. Rovelet-Lecrux A, Charbonnier C, Wallon D, Nicolas G, Seaman M N J, Pottier C, Breusegem S Y, Mathur P P, Jenardhanan P, Le Guennec K, Mukadam A S, Quenez O, Coutant S, Rousseau S, Richard A-C, Boland A, Deleuze J-F, Frebourg T, Hannequin D, Campion |
| Seizures in dominantly inherited Alzheimer disease. Neurology 2016 Aug 87 (9): 912-9. Zarea Aline, Charbonnier Camille, Rovelet-Lecrux Anne, Nicolas Gaël, Rousseau Stéphane, Borden Alaina, Pariente Jeremie, Le Ber Isabelle, Pasquier Florence, Formaglio Maite, Martinaud Olivier, Rollin-Sillaire Adeline, Sarazin Marie, Croisile Bernard, Boutoleau-Bretonnière Claire, Ceccaldi Mathieu, Gabelle Audrey, Chamard Ludivine, Blanc Frédéric, Sellal François, Paquet Claire, Campion Dominique, Hannequin Didier, Wallon David, |
| Presymptomatic cortical thinning in familial Alzheimer disease: A longitudinal MRI study. Neurology 2016 Oct . Weston Philip S J, Nicholas Jennifer M, Lehmann Manja, Ryan Natalie S, Liang Yuying, Macpherson Kirsty, Modat Marc, Rossor Martin N, Schott Jonathan M, Ourselin Sebastien, Fox Nick |
| 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 |
| Integrative Analysis to Identify Common Genetic Markers of Metabolic Syndrome, Dementia, and Diabetes. Medical science monitor : international medical journal of experimental and clinical research 2017 12 23 5885-5891. Zhang Weihong, Xin Linlin, Lu Yi |
| Serum neurofilament light in familial Alzheimer disease: A marker of early neurodegeneration. Neurology 2017 10 89 (21): 2167-2175. Weston Philip S J, Poole Teresa, Ryan Natalie S, Nair Akshay, Liang Yuying, Macpherson Kirsty, Druyeh Ronald, Malone Ian B, Ahsan R Laila, Pemberton Hugh, Klimova Jana, Mead Simon, Blennow Kaj, Rossor Martin N, Schott Jonathan M, Zetterberg Henrik, Fox Nick |
| 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, |
| 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 |
| Association of Early-Onset Alzheimer Disease With Elevated Low-Density Lipoprotein Cholesterol Levels and Rare Genetic Coding Variants of APOB. JAMA neurology 2019 May . Wingo Thomas S, Cutler David J, Wingo Aliza P, Le Ngoc-Anh, Rabinovici Gil D, Miller Bruce L, Lah James J, Levey Allan |
| Alternative splicing in a presenilin 2 variant associated with Alzheimer disease. Annals of clinical and translational neurology 2019 4 6 (4): 762-777. Braggin Jacquelyn E, Bucks Stephanie A, Course Meredith M, Smith Carole L, Sopher Bryce, Osnis Leah, Shuey Kiel D, Domoto-Reilly Kimiko, Caso Christina, Kinoshita Chizuru, Scherpelz Kathryn P, Cross Chloe, Grabowski Thomas, Nik Seyyed H M, Newman Morgan, Garden Gwenn A, Leverenz James B, Tsuang Debby, Latimer Caitlin, Gonzalez-Cuyar Luis F, Keene Christopher Dirk, Morrison Richard S, Rhoads Kristoffer, Wijsman Ellen M, Dorschner Michael O, Lardelli Michael, Young Jessica E, Valdmanis Paul N, Bird Thomas D, Jayadev Sum |
| SORL1 genetic variants and Alzheimer disease risk: a literature review and meta-analysis of sequencing data. Acta neuropathologica 2019 Mar . Campion Dominique, Charbonnier Camille, Nicolas Ga |
| 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 |
| Endoplasmic reticulum stress induces Alzheimer disease-like phenotypes in the neuron derived from the induced pluripotent stem cell with D678H mutation on amyloid precursor protein. Journal of neurochemistry 2022 8 163 (1): 26-39. Devina Tania, Wong Yu-Hui, Hsiao Chiao-Wan, Li Yu-Jui, Lien Cheng-Chang, Cheng Irene Han-J |
- Page last reviewed:Feb 1, 2023
- Page last updated:May 22, 2023
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