These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

284 related articles for article (PubMed ID: 30917570)

  • 1. Analysis of 50 Neurodegenerative Genes in Clinically Diagnosed Early-Onset Alzheimer's Disease.
    Giau VV; Senanarong V; Bagyinszky E; An SSA; Kim S
    Int J Mol Sci; 2019 Mar; 20(6):. PubMed ID: 30917570
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Genetic analyses of early-onset Alzheimer's disease using next generation sequencing.
    Giau VV; Bagyinszky E; Yang YS; Youn YC; An SSA; Kim SY
    Sci Rep; 2019 Jun; 9(1):8368. PubMed ID: 31182772
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Gene mutations in a Han Chinese Alzheimer's disease cohort.
    Ma L; Zhang J; Shi Y; Wang W; Ren Z; Xia M; Zhang Y; Yang M
    Brain Behav; 2019 Jan; 9(1):e01180. PubMed ID: 30549411
    [TBL] [Abstract][Full Text] [Related]  

  • 4.
    Giau VV; Bagyinszky E; Youn YC; An SSA; Kim S
    Int J Mol Sci; 2019 Sep; 20(19):. PubMed ID: 31557888
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Screening of dementia genes by whole-exome sequencing in Spanish patients with early-onset dementia: likely pathogenic, uncertain significance and risk variants.
    Ramos-Campoy O; Antonell A; Falgàs N; Balasa M; Borrego-Écija S; Rodríguez-Santiago B; Datta D; Armengol L; Fernández-Villullas G; Bosch B; Olives J; Muñoz-García C; Castellví M; Tort-Merino A; Sánchez-Valle R; Lladó A
    Neurobiol Aging; 2020 Sep; 93():e1-e9. PubMed ID: 32317127
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Mutation analysis of disease causing genes in patients with early onset or familial forms of Alzheimer's disease and frontotemporal dementia.
    Pagnon de la Vega M; Näslund C; Brundin R; Lannfelt L; Löwenmark M; Kilander L; Ingelsson M; Giedraitis V
    BMC Genomics; 2022 Feb; 23(1):99. PubMed ID: 35120450
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A genetic screen of the mutations in the Korean patients with early-onset Alzheimer's disease.
    An SS; Park SA; Bagyinszky E; Bae SO; Kim YJ; Im JY; Park KW; Park KH; Kim EJ; Jeong JH; Kim JH; Han HJ; Choi SH; Kim S
    Clin Interv Aging; 2016; 11():1817-1822. PubMed ID: 28008242
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Molecular Genetics of Early- and Late-Onset Alzheimer's Disease.
    Uddin MS; Hasana S; Hossain MF; Islam MS; Behl T; Perveen A; Hafeez A; Ashraf GM
    Curr Gene Ther; 2021; 21(1):43-52. PubMed ID: 33231156
    [TBL] [Abstract][Full Text] [Related]  

  • 9. APP, PSEN1, and PSEN2 mutations in early-onset Alzheimer disease: A genetic screening study of familial and sporadic cases.
    Lanoiselée HM; Nicolas G; Wallon D; Rovelet-Lecrux A; Lacour M; Rousseau S; Richard AC; Pasquier F; Rollin-Sillaire A; Martinaud O; Quillard-Muraine M; 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; Félician O; Godefroy O; Formaglio M; Croisile B; Auriacombe S; Chamard L; Vincent JL; Sauvée M; Marelli-Tosi C; Gabelle A; Ozsancak C; Pariente J; Paquet C; Hannequin D; Campion D;
    PLoS Med; 2017 Mar; 14(3):e1002270. PubMed ID: 28350801
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Mutation Analysis of the Genes Linked to Early Onset Alzheimer's Disease and Frontotemporal Lobar Degeneration.
    Luukkainen L; Helisalmi S; Kytövuori L; Ahmasalo R; Solje E; Haapasalo A; Hiltunen M; Remes AM; Krüger J
    J Alzheimers Dis; 2019; 69(3):775-782. PubMed ID: 31127772
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. Genetic screening in early-onset Alzheimer's disease identified three novel presenilin mutations.
    Wong TH; Seelaar H; Melhem S; Rozemuller AJM; van Swieten JC
    Neurobiol Aging; 2020 Feb; 86():201.e9-201.e14. PubMed ID: 30797548
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Rare variants in APP, PSEN1 and PSEN2 increase risk for AD in late-onset Alzheimer's disease families.
    Cruchaga C; Haller G; 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;
    PLoS One; 2012; 7(2):e31039. PubMed ID: 22312439
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Pathogenic variants in the Longitudinal Early-onset Alzheimer's Disease Study cohort.
    Nudelman KNH; Jackson T; Rumbaugh M; Eloyan A; Abreu M; Dage JL; Snoddy C; Faber KM; Foroud T; Hammers DB; ; Taurone A; Thangarajah M; Aisen P; Beckett L; Kramer J; Koeppe R; Kukull WA; Murray ME; Toga AW; Vemuri P; Atri A; Day GS; Duara R; Graff-Radford NR; Honig LS; Jones DT; Masdeu JC; Mendez M; Musiek E; Onyike CU; Riddle M; Rogalski E; Salloway S; Sha SJ; Turner RS; Wingo TS; Wolk DA; Carrillo MC; Dickerson BC; Rabinovici GD; Apostolova LG;
    Alzheimers Dement; 2023 Nov; 19 Suppl 9(Suppl 9):S64-S73. PubMed ID: 37801072
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Exome sequencing identifies 2 novel presenilin 1 mutations (p.L166V and p.S230R) in British early-onset Alzheimer's disease.
    Sassi C; Guerreiro R; Gibbs R; Ding J; Lupton MK; Troakes C; Lunnon K; Al-Sarraj S; Brown KS; Medway C; Lord J; Turton J; Mann D; Snowden J; Neary D; Harris J; Bras J; ; Morgan K; Powell JF; Singleton A; Hardy J
    Neurobiol Aging; 2014 Oct; 35(10):2422.e13-6. PubMed ID: 24880964
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Pilot whole-exome sequencing of a German early-onset Alzheimer's disease cohort reveals a substantial frequency of PSEN2 variants.
    Blauwendraat C; Wilke C; Jansen IE; Schulte C; Simón-Sánchez J; Metzger FG; Bender B; Gasser T; Maetzler W; Rizzu P; Heutink P; Synofzik M
    Neurobiol Aging; 2016 Jan; 37():208.e11-208.e17. PubMed ID: 26522186
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Clinical and neuroimaging characterization of Chinese dementia patients with PSEN1 and PSEN2 mutations.
    Shi Z; Wang Y; Liu S; Liu M; Liu S; Zhou Y; Wang J; Cai L; Huo YR; Gao S; Ji Y
    Dement Geriatr Cogn Disord; 2015; 39(1-2):32-40. PubMed ID: 25323700
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Evaluation of the Clinical Features Accompanied by the Gene Mutations: The 2 Novel PSEN1 Variants in a Turkish Early-onset Alzheimer Disease Cohort.
    Eryilmaz IE; Bakar M; Egeli U; Cecener G; Yurdacan B; Colak DK; Tunca B
    Alzheimer Dis Assoc Disord; 2021 Jul-Sep 01; 35(3):214-222. PubMed ID: 33769986
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. Genetic analysis of Vietnamese patients with early-onset Alzheimer's disease.
    Tong TM; Dao TTH; Doan LP; Nguyen DT; Nguyen QT; Do TT; Truong KD; Phan MD; Nguyen HN; Tran TC; Giang H
    Int J Neurosci; 2022 Dec; 132(12):1190-1197. PubMed ID: 33397166
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 15.