Human Genome Epidemiology Literature Finder
Rare Diseases
Records 1 - 17 (of 17 Records) |
Query Trace: Familial Alzheimer Disease[original query] |
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Impact of DNA testing for early-onset familial Alzheimer disease and frontotemporal dementia. Archives of neurology 2001 Nov 58 (11): 1828-31. Steinbart E J, Smith C O, Poorkaj P, Bird T |
Familial Alzheimer disease among Caribbean Hispanics: a reexamination of its association with APOE. Archives of neurology 2002 1 59 (1): 87-91. Romas Stavra N, Santana Vincent, Williamson Jennifer, Ciappa Alejandra, Lee Joseph H, Rondon Haydee Z, Estevez Pedro, Lantigua Rafael, Medrano Martin, Torres Mayobanex, Stern Yaakov, Tycko Benjamin, Mayeux Richa |
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 |
Apolipoprotein E epsilon4 and age at onset of sporadic and familial Alzheimer disease in Caribbean Hispanics. Archives of neurology 2006 Nov 63 (11): 1586-90. Olarte Lucia, Schupf Nicole, Lee Joseph H, Tang Ming-Xin, Santana Vincent, Williamson Jennifer, Maramreddy Prashanthi, Tycko Benjamin, Mayeux Richa |
Familial Alzheimer disease in Latinos: interaction between APOE, stroke, and estrogen replacement. Neurology 2006 Jan 66 (1): 35-40. Rippon G A, Tang M X, Lee J H, Lantigua R, Medrano M, Mayeux |
Variability of age at onset in siblings with familial Alzheimer disease. Archives of neurology 2007 Dec 64 (12): 1743-8. Gómez-Tortosa Estrella, Barquero M Sagrario, Barón Manuel, Sainz M Jose, Manzano Sagrario, Payno Maria, Ros Raquel, Almaraz Carmen, Gómez-Garré Pilar, Jiménez-Escrig Adria |
The heritability of abstract reasoning in Caribbean Latinos with familial Alzheimer disease. Dementia and geriatric cognitive disorders 2007 24 (6): 411-7. Johnson Beverly, Santana Vincent, Schupf Nicole, Tang Ming-X, Stern Yaakov, Mayeux Richard, Lee Joseph |
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 |
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 |
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 |
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 |
Polygenic risk scores in familial Alzheimer disease. Neurology 2017 Feb . Tosto Giuseppe, Bird Thomas D, Tsuang Debby, Bennett David A, Boeve Bradley F, Cruchaga Carlos, Faber Kelley, Foroud Tatiana M, Farlow Martin, Goate Alison M, Bertlesen Sarah, Graff-Radford Neill R, Medrano Martin, Lantigua Rafael, Manly Jennifer, Ottman Ruth, Rosenberg Roger, Schaid Daniel J, Schupf Nicole, Stern Yaakov, Sweet Robert A, Mayeux Richa |
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 |
A rare loss-of-function variant of ADAM17 is associated with late-onset familial Alzheimer disease. Molecular psychiatry 2018 Jul . Hartl Daniela, May Patrick, Gu Wei, Mayhaus Manuel, Pichler Sabrina, Spaniol Christian, Glaab Enrico, Bobbili Dheeraj Reddy, Antony Paul, Koegelsberger Sandra, Kurz Alexander, Grimmer Timo, Morgan Kevin, Vardarajan Badri N, Reitz Christiane, Hardy John, Bras Jose, Guerreiro Rita, Balling Rudi, Schneider Jochen G, Riemenschneider Matthias, |
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 |
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 |
Polygenic risk score penetrance & recurrence risk in familial Alzheimer disease. Annals of clinical and translational neurology 2023 3 . Qiao Min, Lee Annie J, Reyes-Dumeyer Dolly, Tosto Giuseppe, Faber Kelley, Goate Alison, Renton Alan, Chao Michael, Boeve Brad, Cruchaga Carlos, Pericak-Vance Margaret, Haines Jonathan L, Rosenberg Roger, Tsuang Debby, Sweet Robert A, Bennett David A, Wilson Robert S, Foroud Tatiana, Mayeux Richard, Vardarajan Badri |
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- Page last updated:May 13, 2024
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