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 *

464 related articles for article (PubMed ID: 30911827)

  • 1. SORL1 genetic variants and Alzheimer disease risk: a literature review and meta-analysis of sequencing data.
    Campion D; Charbonnier C; Nicolas G
    Acta Neuropathol; 2019 Aug; 138(2):173-186. PubMed ID: 30911827
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Contribution to Alzheimer's disease risk of rare variants in TREM2, SORL1, and ABCA7 in 1779 cases and 1273 controls.
    Bellenguez C; Charbonnier C; Grenier-Boley B; Quenez O; Le Guennec K; Nicolas G; Chauhan G; Wallon D; Rousseau S; Richard AC; Boland A; Bourque G; Munter HM; Olaso R; Meyer V; Rollin-Sillaire A; Pasquier F; Letenneur L; Redon R; Dartigues JF; Tzourio C; Frebourg T; Lathrop M; Deleuze JF; Hannequin D; Genin E; Amouyel P; Debette S; Lambert JC; Campion D;
    Neurobiol Aging; 2017 Nov; 59():220.e1-220.e9. PubMed ID: 28789839
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Characterization of pathogenic SORL1 genetic variants for association with Alzheimer's disease: a clinical interpretation strategy.
    Holstege H; van der Lee SJ; Hulsman M; Wong TH; van Rooij JG; Weiss M; Louwersheimer E; Wolters FJ; Amin N; Uitterlinden AG; Hofman A; Ikram MA; van Swieten JC; Meijers-Heijboer H; van der Flier WM; Reinders MJ; van Duijn CM; Scheltens P
    Eur J Hum Genet; 2017 Aug; 25(8):973-981. PubMed ID: 28537274
    [TBL] [Abstract][Full Text] [Related]  

  • 4. From Common to Rare Variants: The Genetic Component of Alzheimer Disease.
    Nicolas G; Charbonnier C; Campion D
    Hum Hered; 2016; 81(3):129-141. PubMed ID: 28002825
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Impaired SorLA maturation and trafficking as a new mechanism for SORL1 missense variants in Alzheimer disease.
    Rovelet-Lecrux A; Feuillette S; Miguel L; Schramm C; Pernet S; Quenez O; Ségalas-Milazzo I; Guilhaudis L; Rousseau S; Riou G; Frébourg T; Campion D; Nicolas G; Lecourtois M
    Acta Neuropathol Commun; 2021 Dec; 9(1):196. PubMed ID: 34922638
    [TBL] [Abstract][Full Text] [Related]  

  • 6. SorLA Protective Function Is Restored by Improving SorLA Protein Maturation in a Subset of Alzheimer's Disease-Associated SORL1 Missense Variants.
    Miguel L; Gervais J; Nicolas G; Lecourtois M
    J Alzheimers Dis; 2023; 94(4):1343-1349. PubMed ID: 37424467
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A comprehensive study of the genetic impact of rare variants in SORL1 in European early-onset Alzheimer's disease.
    Verheijen J; Van den Bossche T; van der Zee J; Engelborghs S; Sanchez-Valle R; Lladó A; Graff C; Thonberg H; Pastor P; Ortega-Cubero S; Pastor MA; Benussi L; Ghidoni R; Binetti G; Clarimon J; Lleó A; Fortea J; de Mendonça A; Martins M; Grau-Rivera O; Gelpi E; Bettens K; Mateiu L; Dillen L; Cras P; De Deyn PP; Van Broeckhoven C; Sleegers K
    Acta Neuropathol; 2016 Aug; 132(2):213-224. PubMed ID: 27026413
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Association between genetic variants in sortilin-related receptor 1 (SORL1) and Alzheimer's disease in adults with Down syndrome.
    Lee JH; Chulikavit M; Pang D; Zigman WB; Silverman W; Schupf N
    Neurosci Lett; 2007 Sep; 425(2):105-9. PubMed ID: 17826910
    [TBL] [Abstract][Full Text] [Related]  

  • 9. SORL1 rare variants: a major risk factor for familial early-onset Alzheimer's disease.
    Nicolas G; Charbonnier C; Wallon D; Quenez O; Bellenguez C; Grenier-Boley B; Rousseau S; Richard AC; Rovelet-Lecrux A; Le Guennec K; Bacq D; Garnier JG; Olaso R; Boland A; Meyer V; Deleuze JF; Amouyel P; Munter HM; Bourque G; Lathrop M; Frebourg T; Redon R; Letenneur L; Dartigues JF; Génin E; Lambert JC; Hannequin D; Campion D;
    Mol Psychiatry; 2016 Jun; 21(6):831-6. PubMed ID: 26303663
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Genetic Study of Alzheimer's Disease in Saudi Population.
    El Bitar F; Qadi N; Al Rajeh S; Majrashi A; Abdulaziz S; Majrashi N; Al Inizi M; Taher A; Al Tassan N
    J Alzheimers Dis; 2019; 67(1):231-242. PubMed ID: 30636737
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Impact of SORL1 single nucleotide polymorphisms on Alzheimer's disease cerebrospinal fluid markers.
    Alexopoulos P; Guo LH; Kratzer M; Westerteicher C; Kurz A; Perneczky R
    Dement Geriatr Cogn Disord; 2011; 32(3):164-70. PubMed ID: 21997402
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Meta-analysis of the Association between Alzheimer Disease and Variants in GAB2, PICALM, and SORL1.
    Wang Z; Lei H; Zheng M; Li Y; Cui Y; Hao F
    Mol Neurobiol; 2016 Nov; 53(9):6501-6510. PubMed ID: 26611835
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Biallelic Loss of Function of SORL1 in an Early Onset Alzheimer's Disease Patient.
    Le Guennec K; Tubeuf H; Hannequin D; Wallon D; Quenez O; Rousseau S; Richard AC; Deleuze JF; Boland A; Frebourg T; Gaildrat P; Campion D; Martins A; Nicolas G
    J Alzheimers Dis; 2018; 62(2):821-831. PubMed ID: 29480197
    [TBL] [Abstract][Full Text] [Related]  

  • 14. An alternative transcript of the Alzheimer's disease risk gene SORL1 encodes a truncated receptor.
    Blechingberg J; Poulsen ASA; Kjølby M; Monti G; Allen M; Ivarsen AK; Lincoln SJ; Thotakura G; Vægter CB; Ertekin-Taner N; Nykjær A; Andersen OM
    Neurobiol Aging; 2018 Nov; 71():266.e11-266.e24. PubMed ID: 30078640
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Identification and description of three families with familial Alzheimer disease that segregate variants in the SORL1 gene.
    Thonberg H; Chiang HH; Lilius L; Forsell C; Lindström AK; Johansson C; Björkström J; Thordardottir S; Sleegers K; Van Broeckhoven C; Rönnbäck A; Graff C
    Acta Neuropathol Commun; 2017 Jun; 5(1):43. PubMed ID: 28595629
    [TBL] [Abstract][Full Text] [Related]  

  • 16. SORL1 Variants in Familial Alzheimer's Disease.
    Gómez-Tortosa E; Ruggiero M; Sainz MJ; Villarejo-Galende A; Prieto-Jurczynska C; Venegas Pérez B; Ordás C; Agüero P; Guerrero-López R; Pérez-Pérez J
    J Alzheimers Dis; 2018; 61(4):1275-1281. PubMed ID: 29376855
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Novel Rare SORL1 Variants in Early-Onset Dementia.
    Korpioja A; Krüger J; Koivuluoma S; Pylkäs K; Moilanen V; Helisalmi S; Hiltunen M; Remes AM
    J Alzheimers Dis; 2021; 82(2):761-770. PubMed ID: 34092641
    [TBL] [Abstract][Full Text] [Related]  

  • 18. An updated meta-analysis of the association between SORL1 variants and the risk for sporadic Alzheimer's disease.
    Jin C; Liu X; Zhang F; Wu Y; Yuan J; Zhu J; Zhang F; Wang G; Cheng Z
    J Alzheimers Dis; 2013; 37(2):429-37. PubMed ID: 23948893
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Coding mutations in SORL1 and Alzheimer disease.
    Vardarajan BN; Zhang Y; Lee JH; Cheng R; Bohm C; Ghani M; Reitz C; Reyes-Dumeyer D; Shen Y; Rogaeva E; St George-Hyslop P; Mayeux R
    Ann Neurol; 2015 Feb; 77(2):215-27. PubMed ID: 25382023
    [TBL] [Abstract][Full Text] [Related]  

  • 20. SORL1 genetic variants and cerebrospinal fluid biomarkers of Alzheimer’s disease.
    Guo LH; Westerteicher C; Wang XH; Kratzer M; Tsolakidou A; Jiang M; Grimmer T; Laws SM; Alexopoulos P; Bujo H; Kurz A; Perneczky R
    Eur Arch Psychiatry Clin Neurosci; 2012 Sep; 262(6):529-34. PubMed ID: 22286501
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 24.