BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

276 related articles for article (PubMed ID: 36878965)

  • 1. The molecular pathology of schizophrenia: an overview of existing knowledge and new directions for future research.
    Nakamura T; Takata A
    Mol Psychiatry; 2023 May; 28(5):1868-1889. PubMed ID: 36878965
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Genetics of schizophrenia].
    Jitoku D; Yoshikawa T
    Nihon Rinsho; 2013 Apr; 71(4):599-604. PubMed ID: 23678585
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Genetic architecture of schizophrenia: a review of major advancements.
    Legge SE; Santoro ML; Periyasamy S; Okewole A; Arsalan A; Kowalec K
    Psychol Med; 2021 Oct; 51(13):2168-2177. PubMed ID: 33550997
    [TBL] [Abstract][Full Text] [Related]  

  • 4. The genetic architecture of schizophrenia: review of large-scale genetic studies.
    Kato H; Kimura H; Kushima I; Takahashi N; Aleksic B; Ozaki N
    J Hum Genet; 2023 Mar; 68(3):175-182. PubMed ID: 35821406
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Copy number variation in schizophrenia in Sweden.
    Szatkiewicz JP; O'Dushlaine C; Chen G; Chambert K; Moran JL; Neale BM; Fromer M; Ruderfer D; Akterin S; Bergen SE; Kähler A; Magnusson PK; Kim Y; Crowley JJ; Rees E; Kirov G; O'Donovan MC; Owen MJ; Walters J; Scolnick E; Sklar P; Purcell S; Hultman CM; McCarroll SA; Sullivan PF
    Mol Psychiatry; 2014 Jul; 19(7):762-73. PubMed ID: 24776740
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Genomic copy number variations: A breakthrough in our knowledge on schizophrenia etiology?
    Hosak L; Silhan P; Hosakova J
    Neuro Endocrinol Lett; 2012; 33(2):183-90. PubMed ID: 22592199
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Genetics of Schizophrenia: Ready to Translate?
    Foley C; Corvin A; Nakagome S
    Curr Psychiatry Rep; 2017 Sep; 19(9):61. PubMed ID: 28741255
    [TBL] [Abstract][Full Text] [Related]  

  • 8. After GWAS: searching for genetic risk for schizophrenia and bipolar disorder.
    Gershon ES; Alliey-Rodriguez N; Liu C
    Am J Psychiatry; 2011 Mar; 168(3):253-6. PubMed ID: 21285144
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Genome-wide investigation of rare structural variants identifies VIPR2 as a new candidate gene for schizophrenia.
    Nieratschker V; Meyer-Lindenberg A; Witt SH
    Expert Rev Neurother; 2011 Jul; 11(7):937-41. PubMed ID: 21721910
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Copy number variations in schizophrenia: critical review and new perspectives on concepts of genetics and disease.
    Bassett AS; Scherer SW; Brzustowicz LM
    Am J Psychiatry; 2010 Aug; 167(8):899-914. PubMed ID: 20439386
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [An analysis of the relationship between genetic factors and the risk of schizophrenia].
    Shmakova AA; Semina EV; Neyfeld EA; Tsygankov BD; Karagyaur MN
    Zh Nevrol Psikhiatr Im S S Korsakova; 2023; 123(2):26-36. PubMed ID: 36843456
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Systematic prioritization and integrative analysis of copy number variations in schizophrenia reveal key schizophrenia susceptibility genes.
    Luo X; Huang L; Han L; Luo Z; Hu F; Tieu R; Gan L
    Schizophr Bull; 2014 Nov; 40(6):1285-99. PubMed ID: 24664977
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Rare copy number variants: a point of rarity in genetic risk for bipolar disorder and schizophrenia.
    Grozeva D; Kirov G; Ivanov D; Jones IR; Jones L; Green EK; St Clair DM; Young AH; Ferrier N; Farmer AE; McGuffin P; Holmans PA; Owen MJ; O'Donovan MC; Craddock N;
    Arch Gen Psychiatry; 2010 Apr; 67(4):318-27. PubMed ID: 20368508
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Joint Contributions of Rare Copy Number Variants and Common SNPs to Risk for Schizophrenia.
    Bergen SE; Ploner A; Howrigan D; ; O'Donovan MC; Smoller JW; Sullivan PF; Sebat J; Neale B; Kendler KS
    Am J Psychiatry; 2019 Jan; 176(1):29-35. PubMed ID: 30392412
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Support for the N-methyl-D-aspartate receptor hypofunction hypothesis of schizophrenia from exome sequencing in multiplex families.
    Timms AE; Dorschner MO; Wechsler J; Choi KY; Kirkwood R; Girirajan S; Baker C; Eichler EE; Korvatska O; Roche KW; Horwitz MS; Tsuang DW
    JAMA Psychiatry; 2013 Jun; 70(6):582-90. PubMed ID: 23553203
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Search for risk genes in schizophrenia].
    Rujescu D
    Nervenarzt; 2017 Jul; 88(7):751-754. PubMed ID: 28429076
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Genome-wide analysis shows increased frequency of copy number variation deletions in Dutch schizophrenia patients.
    Buizer-Voskamp JE; Muntjewerff JW; ; Strengman E; Sabatti C; Stefansson H; Vorstman JA; Ophoff RA
    Biol Psychiatry; 2011 Oct; 70(7):655-62. PubMed ID: 21489405
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A New Method for Detecting Associations with Rare Copy-Number Variants.
    Tzeng JY; Magnusson PK; Sullivan PF; ; Szatkiewicz JP
    PLoS Genet; 2015 Oct; 11(10):e1005403. PubMed ID: 26431523
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Pathogenic rare copy number variants in community-based schizophrenia suggest a potential role for clinical microarrays.
    Costain G; Lionel AC; Merico D; Forsythe P; Russell K; Lowther C; Yuen T; Husted J; Stavropoulos DJ; Speevak M; Chow EW; Marshall CR; Scherer SW; Bassett AS
    Hum Mol Genet; 2013 Nov; 22(22):4485-501. PubMed ID: 23813976
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Characterization of Single Gene Copy Number Variants in Schizophrenia.
    Szatkiewicz JP; Fromer M; Nonneman RJ; Ancalade N; Johnson JS; Stahl EA; Rees E; Bergen SE; Hultman CM; Kirov G; O'Donovan M; Owen M; Holmans P; Sklar P; Sullivan PF; Purcell SM; Crowley JJ; Ruderfer DM
    Biol Psychiatry; 2020 Apr; 87(8):736-744. PubMed ID: 31767120
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 14.