386 related articles for article (PubMed ID: 33464407)
21. Alzheimer's Disease: An Updated Overview of Its Genetics.
Andrade-Guerrero J; Santiago-Balmaseda A; Jeronimo-Aguilar P; Vargas-Rodríguez I; Cadena-Suárez AR; Sánchez-Garibay C; Pozo-Molina G; Méndez-Catalá CF; Cardenas-Aguayo MD; Diaz-Cintra S; Pacheco-Herrero M; Luna-Muñoz J; Soto-Rojas LO
Int J Mol Sci; 2023 Feb; 24(4):. PubMed ID: 36835161
[TBL] [Abstract][Full Text] [Related]
22. Mutation profile of APP, PSEN1, and PSEN2 in Chinese familial Alzheimer's disease.
Gao Y; Ren RJ; Zhong ZL; Dammer E; Zhao QH; Shan S; Zhou Z; Li X; Zhang YQ; Cui HL; Hu YB; Chen SD; Chen JJ; Guo QH; Wang G
Neurobiol Aging; 2019 May; 77():154-157. PubMed ID: 30822634
[TBL] [Abstract][Full Text] [Related]
23. Comprehensive Screening for Disease Risk Variants in Early-Onset Alzheimer's Disease Genes in African Americans Identifies Novel PSEN Variants.
N'Songo A; Carrasquillo MM; Wang X; Nguyen T; Asmann Y; Younkin SG; Allen M; Duara R; Custo MT; Graff-Radford N; Ertekin-Taner N
J Alzheimers Dis; 2017; 56(4):1215-1222. PubMed ID: 28106563
[TBL] [Abstract][Full Text] [Related]
24. Genetics of early-onset Alzheimer dementia.
Rademakers R; Cruts M; Van Broeckhoven C
ScientificWorldJournal; 2003 Jun; 3():497-519. PubMed ID: 12847300
[TBL] [Abstract][Full Text] [Related]
25. Screening of dementia genes by whole-exome sequencing in early-onset Alzheimer disease: input and lessons.
Nicolas G; Wallon D; Charbonnier C; Quenez O; Rousseau S; Richard AC; Rovelet-Lecrux A; Coutant S; Le Guennec K; Bacq D; Garnier JG; Olaso R; Boland A; Meyer V; Deleuze JF; Munter HM; Bourque G; Auld D; Montpetit A; Lathrop M; Guyant-Maréchal L; Martinaud O; Pariente J; Rollin-Sillaire A; Pasquier F; Le Ber I; Sarazin M; Croisile B; Boutoleau-Bretonnière C; Thomas-Antérion C; Paquet C; Sauvée M; Moreaud O; Gabelle A; Sellal F; Ceccaldi M; Chamard L; Blanc F; Frebourg T; Campion D; Hannequin D
Eur J Hum Genet; 2016 May; 24(5):710-6. PubMed ID: 26242991
[TBL] [Abstract][Full Text] [Related]
26. Amyloid-β
Perrone F; Bjerke M; Hens E; Sieben A; Timmers M; De Roeck A; Vandenberghe R; Sleegers K; Martin JJ; De Deyn PP; Engelborghs S; van der Zee J; Van Broeckhoven C; Cacace R;
Alzheimers Res Ther; 2020 Sep; 12(1):108. PubMed ID: 32917274
[TBL] [Abstract][Full Text] [Related]
27. A Possible Pathogenic PSEN2 Gly56Ser Mutation in a Korean Patient with Early-Onset Alzheimer's Disease.
Shim KH; Kang MJ; Bae H; Kim D; Park J; An SA; Jeong DE
Int J Mol Sci; 2022 Mar; 23(6):. PubMed ID: 35328387
[TBL] [Abstract][Full Text] [Related]
28. The Genetics of Alzheimer's Disease in the Chinese Population.
Gan CL; Zhang T; Lee TH
Int J Mol Sci; 2020 Mar; 21(7):. PubMed ID: 32235595
[TBL] [Abstract][Full Text] [Related]
29. Early-onset Alzheimer's disease in two Iranian families: a genetic study.
Noroozian M; Azadfar P; Akbari L; Sadeghi A; Houshmand M; Vousooghi N; Zarrindast MR; Minagar A
Dement Geriatr Cogn Disord; 2014; 38(5-6):330-6. PubMed ID: 25138979
[TBL] [Abstract][Full Text] [Related]
30. Investigating the role of rare coding variability in Mendelian dementia genes (APP, PSEN1, PSEN2, GRN, MAPT, and PRNP) in late-onset Alzheimer's disease.
Sassi C; Guerreiro R; Gibbs R; Ding J; Lupton MK; Troakes C; Al-Sarraj S; Niblock M; Gallo JM; Adnan J; Killick R; Brown KS; Medway C; Lord J; Turton J; Bras J; ; Morgan K; Powell JF; Singleton A; Hardy J
Neurobiol Aging; 2014 Dec; 35(12):2881.e1-2881.e6. PubMed ID: 25104557
[TBL] [Abstract][Full Text] [Related]
31. Mutational analysis in early-onset familial Alzheimer's disease in Mainland China.
Jiao B; Tang B; Liu X; Xu J; Wang Y; Zhou L; Zhang F; Yan X; Zhou Y; Shen L
Neurobiol Aging; 2014 Aug; 35(8):1957.e1-6. PubMed ID: 24650794
[TBL] [Abstract][Full Text] [Related]
32. Epidemiology and etiology of Alzheimer's disease: from genetic to non-genetic factors.
Jiang T; Yu JT; Tian Y; Tan L
Curr Alzheimer Res; 2013 Oct; 10(8):852-67. PubMed ID: 23919770
[TBL] [Abstract][Full Text] [Related]
33. Identification of the Third Case of PSEN1 Tyr389His Variant in Early-Onset Alzheimer's Disease in Korea.
Shim KH; Kang S; An SSA; Kang MJ
Int J Mol Sci; 2022 Dec; 23(24):. PubMed ID: 36555832
[TBL] [Abstract][Full Text] [Related]
34. PSEN2 Thr421Met Mutation in a Patient with Early Onset Alzheimer's Disease.
Yang Y; Bagyinszky E; An SSA; Kim S
Int J Mol Sci; 2022 Nov; 23(21):. PubMed ID: 36362122
[TBL] [Abstract][Full Text] [Related]
35. Genetic testing in familial and young-onset Alzheimer's disease: mutation spectrum in a Serbian cohort.
Dobricic V; Stefanova E; Jankovic M; Gurunlian N; Novakovic I; Hardy J; Kostic V; Guerreiro R
Neurobiol Aging; 2012 Jul; 33(7):1481.e7-12. PubMed ID: 22221884
[TBL] [Abstract][Full Text] [Related]
36. Causative Mutations and Genetic Risk Factors in Sporadic Early Onset Alzheimer's Disease Before 51 Years.
Lacour M; Quenez O; Rovelet-Lecrux A; Salomon B; Rousseau S; Richard AC; Quillard-Muraine M; Pasquier F; Rollin-Sillaire A; Martinaud O; Zarea A; de la Sayette V; Boutoleau-Bretonniere C; Etcharry-Bouyx F; Chauviré V; Sarazin M; le Ber I; Epelbaum S; Jonveaux T; Rouaud O; Ceccaldi M; Godefroy O; Formaglio M; Croisile B; Auriacombe S; Magnin E; Sauvée M; Marelli C; Gabelle A; Pariente J; Paquet C; Boland A; Deleuze JF; Campion D; Hannequin D; Nicolas G; Wallon D;
J Alzheimers Dis; 2019; 71(1):227-243. PubMed ID: 31381512
[TBL] [Abstract][Full Text] [Related]
37. Early-onset autosomal dominant Alzheimer disease: prevalence, genetic heterogeneity, and mutation spectrum.
Campion D; Dumanchin C; Hannequin D; Dubois B; Belliard S; Puel M; Thomas-Anterion C; Michon A; Martin C; Charbonnier F; Raux G; Camuzat A; Penet C; Mesnage V; Martinez M; Clerget-Darpoux F; Brice A; Frebourg T
Am J Hum Genet; 1999 Sep; 65(3):664-70. PubMed ID: 10441572
[TBL] [Abstract][Full Text] [Related]
38. Genes associated with Alzheimer's disease: an overview and current status.
Giri M; Zhang M; Lü Y
Clin Interv Aging; 2016; 11():665-81. PubMed ID: 27274215
[TBL] [Abstract][Full Text] [Related]
39. Contribution of homozygous and compound heterozygous missense mutations in VWA2 to Alzheimer's disease.
Hoogmartens J; Hens E; Engelborghs S; Vandenberghe R; De Deyn PP; Cacace R; Van Broeckhoven C;
Neurobiol Aging; 2021 Mar; 99():100.e17-100.e23. PubMed ID: 33023779
[TBL] [Abstract][Full Text] [Related]
40. Presenilin-1 (PSEN1) Mutations: Clinical Phenotypes beyond Alzheimer's Disease.
Yang Y; Bagyinszky E; An SSA
Int J Mol Sci; 2023 May; 24(9):. PubMed ID: 37176125
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
