BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

490 related articles for article (PubMed ID: 21895634)

  • 1. Recent genomic advances in schizophrenia.
    Doherty JL; O'Donovan MC; Owen MJ
    Clin Genet; 2012 Feb; 81(2):103-9. PubMed ID: 21895634
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Schizophrenia genetics: advancing on two fronts.
    Owen MJ; Williams HJ; O'Donovan MC
    Curr Opin Genet Dev; 2009 Jun; 19(3):266-70. PubMed ID: 19345090
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Schizophrenia genetics: new insights from new approaches.
    Williams HJ; Owen MJ; O'Donovan MC
    Br Med Bull; 2009; 91():61-74. PubMed ID: 19443537
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Autism genetics: emerging data from genome-wide copy-number and single nucleotide polymorphism scans.
    Weiss LA
    Expert Rev Mol Diagn; 2009 Nov; 9(8):795-803. PubMed ID: 19895225
    [TBL] [Abstract][Full Text] [Related]  

  • 5. The role of DNA copy number variation in schizophrenia.
    Tam GW; Redon R; Carter NP; Grant SG
    Biol Psychiatry; 2009 Dec; 66(11):1005-12. PubMed ID: 19748074
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Disentangling the myriad genomics of complex disorders, specifically focusing on autism, epilepsy, and schizophrenia.
    Poot M; van der Smagt JJ; Brilstra EH; Bourgeron T
    Cytogenet Genome Res; 2011; 135(3-4):228-40. PubMed ID: 22085975
    [TBL] [Abstract][Full Text] [Related]  

  • 7. New technologies provide insights into genetic basis of psychiatric disorders and explain their co-morbidity.
    Rudan I
    Psychiatr Danub; 2010 Jun; 22(2):190-2. PubMed ID: 20562745
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. Copy number variation and psychiatric disease risk.
    Levy RJ; Xu B; Gogos JA; Karayiorgou M
    Methods Mol Biol; 2012; 838():97-113. PubMed ID: 22228008
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Genome arrays for the detection of copy number variations in idiopathic mental retardation, idiopathic generalized epilepsy and neuropsychiatric disorders: lessons for diagnostic workflow and research.
    Hochstenbach R; Buizer-Voskamp JE; Vorstman JA; Ophoff RA
    Cytogenet Genome Res; 2011; 135(3-4):174-202. PubMed ID: 22056632
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Schizophrenia genetics: progress, at last.
    Mulle JG
    Curr Opin Genet Dev; 2012 Jun; 22(3):238-44. PubMed ID: 22424801
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Detection and characterization of copy number variation in autism spectrum disorder.
    Marshall CR; Scherer SW
    Methods Mol Biol; 2012; 838():115-35. PubMed ID: 22228009
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Association of common copy number variants at the glutathione S-transferase genes and rare novel genomic changes with schizophrenia.
    Rodríguez-Santiago B; Brunet A; Sobrino B; Serra-Juhé C; Flores R; Armengol L; Vilella E; Gabau E; Guitart M; Guillamat R; Martorell L; Valero J; Gutiérrez-Zotes A; Labad A; Carracedo A; Estivill X; Pérez-Jurado LA
    Mol Psychiatry; 2010 Oct; 15(10):1023-33. PubMed ID: 19528963
    [TBL] [Abstract][Full Text] [Related]  

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

  • 15. [The etiology of schizophrenia].
    Gejman PV; Sanders AR
    Medicina (B Aires); 2012; 72(3):227-34. PubMed ID: 22763160
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. Why schizophrenia genetics needs epigenetics: a review.
    Maric NP; Svrakic DM
    Psychiatr Danub; 2012 Mar; 24(1):2-18. PubMed ID: 22447077
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Genome-wide survey implicates the influence of copy number variants (CNVs) in the development of early-onset bipolar disorder.
    Priebe L; Degenhardt FA; Herms S; Haenisch B; Mattheisen M; Nieratschker V; Weingarten M; Witt S; Breuer R; Paul T; Alblas M; Moebus S; Lathrop M; Leboyer M; Schreiber S; Grigoroiu-Serbanescu M; Maier W; Propping P; Rietschel M; Nöthen MM; Cichon S; Mühleisen TW
    Mol Psychiatry; 2012 Apr; 17(4):421-32. PubMed ID: 21358712
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Dissecting the many genetic faces of schizophrenia.
    Rujescu D; Collier DA
    Epidemiol Psichiatr Soc; 2009; 18(2):91-5. PubMed ID: 19526738
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Clinical significance of rare copy number variations in epilepsy: a case-control survey using microarray-based comparative genomic hybridization.
    Striano P; Coppola A; Paravidino R; Malacarne M; Gimelli S; Robbiano A; Traverso M; Pezzella M; Belcastro V; Bianchi A; Elia M; Falace A; Gazzerro E; Ferlazzo E; Freri E; Galasso R; Gobbi G; Molinatto C; Cavani S; Zuffardi O; Striano S; Ferrero GB; Silengo M; Cavaliere ML; Benelli M; Magi A; Piccione M; Dagna Bricarelli F; Coviello DA; Fichera M; Minetti C; Zara F
    Arch Neurol; 2012 Mar; 69(3):322-30. PubMed ID: 22083797
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 25.