279 related articles for article (PubMed ID: 19913623)
21. The influence of schizophrenia-related neuregulin-1 polymorphisms on sensorimotor gating in healthy males.
Roussos P; Giakoumaki SG; Adamaki E; Bitsios P
Biol Psychiatry; 2011 Mar; 69(5):479-86. PubMed ID: 21035784
[TBL] [Abstract][Full Text] [Related]
22. Mixture model clustering of phenotype features reveals evidence for association of DTNBP1 to a specific subtype of schizophrenia.
Wessman J; Paunio T; Tuulio-Henriksson A; Koivisto M; Partonen T; Suvisaari J; Turunen JA; Wedenoja J; Hennah W; Pietiläinen OP; Lönnqvist J; Mannila H; Peltonen L
Biol Psychiatry; 2009 Dec; 66(11):990-6. PubMed ID: 19782967
[TBL] [Abstract][Full Text] [Related]
23. Less efficient information transfer in Cys-allele carriers of DISC1: a brain network study based on diffusion MRI.
Li Y; Liu B; Hou B; Qin W; Wang D; Yu C; Jiang T
Cereb Cortex; 2013 Jul; 23(7):1715-23. PubMed ID: 22693340
[TBL] [Abstract][Full Text] [Related]
24. Genetic variation in COMT and PRODH is associated with brain anatomy in patients with schizophrenia.
Zinkstok J; Schmitz N; van Amelsvoort T; Moeton M; Baas F; Linszen D
Genes Brain Behav; 2008 Feb; 7(1):61-9. PubMed ID: 17504246
[TBL] [Abstract][Full Text] [Related]
25. The effect of COMT, BDNF, 5-HTT, NRG1 and DTNBP1 genes on hippocampal and lateral ventricular volume in psychosis.
Dutt A; McDonald C; Dempster E; Prata D; Shaikh M; Williams I; Schulze K; Marshall N; Walshe M; Allin M; Collier D; Murray R; Bramon E
Psychol Med; 2009 Nov; 39(11):1783-97. PubMed ID: 19573260
[TBL] [Abstract][Full Text] [Related]
26. A functional polymorphism in the disrupted-in schizophrenia 1 gene is associated with chronic fatigue syndrome.
Fukuda S; Hashimoto R; Ohi K; Yamaguti K; Nakatomi Y; Yasuda Y; Kamino K; Takeda M; Tajima S; Kuratsune H; Nishizawa Y; Watanabe Y
Life Sci; 2010 May; 86(19-20):722-5. PubMed ID: 20227423
[TBL] [Abstract][Full Text] [Related]
27. Association of DISC1 with autism and Asperger syndrome.
Kilpinen H; Ylisaukko-Oja T; Hennah W; Palo OM; Varilo T; Vanhala R; Nieminen-von Wendt T; von Wendt L; Paunio T; Peltonen L
Mol Psychiatry; 2008 Feb; 13(2):187-96. PubMed ID: 17579608
[TBL] [Abstract][Full Text] [Related]
28. Molecular mechanism of schizophrenia with reference to disrupted-in-schizophrenia 1 (DISC1).
Matsuzaki S; Tohyama M
Neurochem Int; 2007; 51(2-4):165-72. PubMed ID: 17664024
[TBL] [Abstract][Full Text] [Related]
29. Is neuregulin 1 involved in determining cerebral volumes in schizophrenia? Preliminary results showing a decrease in superior temporal gyrus volume.
Tosato S; Bellani M; Bonetto C; Ruggeri M; Perlini C; Lasalvia A; Marinelli V; Rambaldelli G; Cristofalo D; Bertani M; Zanoni M; Lazzarotto L; Cerini R; Pozzi Mucelli R; Tansella M; Dazzan P; Di Forti M; Murray RM; Collier DA; Brambilla P
Neuropsychobiology; 2012; 65(3):119-25. PubMed ID: 22378022
[TBL] [Abstract][Full Text] [Related]
30. Impact of schizophrenia candidate genes on schizotypy and cognitive endophenotypes at the population level.
Stefanis NC; Trikalinos TA; Avramopoulos D; Smyrnis N; Evdokimidis I; Ntzani EE; Ioannidis JP; Stefanis CN
Biol Psychiatry; 2007 Oct; 62(7):784-92. PubMed ID: 17336946
[TBL] [Abstract][Full Text] [Related]
31. Heritability of changes in brain volume over time in twin pairs discordant for schizophrenia.
Brans RG; van Haren NE; van Baal GC; Schnack HG; Kahn RS; Hulshoff Pol HE
Arch Gen Psychiatry; 2008 Nov; 65(11):1259-68. PubMed ID: 18981337
[TBL] [Abstract][Full Text] [Related]
32. Schizophrenia: genes at last?
Owen MJ; Craddock N; O'Donovan MC
Trends Genet; 2005 Sep; 21(9):518-25. PubMed ID: 16009449
[TBL] [Abstract][Full Text] [Related]
33. Low-activity allele of Catechol-O-Methyltransferase (COMTL) is associated with increased lateral ventricles in patients with first episode non-affective psychosis.
Crespo-Facorro B; Roiz-Santiáñez R; Pelayo-Terán JM; Pérez-Iglesias R; Carrasco-Marín E; Mata I; González-Mandly A; Jorge R; Vázquez-Barquero JL
Prog Neuropsychopharmacol Biol Psychiatry; 2007 Oct; 31(7):1514-8. PubMed ID: 17706335
[TBL] [Abstract][Full Text] [Related]
34. An exploratory association study of the influence of dysbindin and neuregulin polymorphisms on brain morphometry in patients with schizophrenia and healthy subjects from South India.
Thirunavukkarasu P; Vijayakumari AA; John JP; Halahalli HN; Paul P; Sen S; Purushottam M; Jain S
Asian J Psychiatr; 2014 Aug; 10():62-8. PubMed ID: 25042954
[TBL] [Abstract][Full Text] [Related]
35. Lack of association to a NRG1 missense polymorphism in schizophrenia or bipolar disorder in a Costa Rican population.
Moon E; Rollins B; Mesén A; Sequeira A; Myers RM; Akil H; Watson SJ; Barchas J; Jones EG; Schatzberg A; Bunney WE; DeLisi LE; Byerley W; Vawter MP
Schizophr Res; 2011 Sep; 131(1-3):52-7. PubMed ID: 21745728
[TBL] [Abstract][Full Text] [Related]
36. DISC1 is associated with cortical thickness and neural efficiency.
Brauns S; Gollub RL; Roffman JL; Yendiki A; Ho BC; Wassink TH; Heinz A; Ehrlich S
Neuroimage; 2011 Aug; 57(4):1591-600. PubMed ID: 21642004
[TBL] [Abstract][Full Text] [Related]
37. Biological validation of increased schizophrenia risk with NRG1, ERBB4, and AKT1 epistasis via functional neuroimaging in healthy controls.
Nicodemus KK; Law AJ; Radulescu E; Luna A; Kolachana B; Vakkalanka R; Rujescu D; Giegling I; Straub RE; McGee K; Gold B; Dean M; Muglia P; Callicott JH; Tan HY; Weinberger DR
Arch Gen Psychiatry; 2010 Oct; 67(10):991-1001. PubMed ID: 20921115
[TBL] [Abstract][Full Text] [Related]
38. Association of DISC1 gene with schizophrenia in families from two distinct French and Algerian populations.
Lepagnol-Bestel AM; Dubertret C; Benmessaoud D; Simonneau M; Adès J; Kacha F; Hamdani N; Gorwood P; Ramoz N
Psychiatr Genet; 2010 Dec; 20(6):298-303. PubMed ID: 20505556
[TBL] [Abstract][Full Text] [Related]
39. Functional genomics in postmortem human brain: abnormalities in a DISC1 molecular pathway in schizophrenia.
Lipska BK; Mitkus SN; Mathew SV; Fatula R; Hyde TM; Weinberger DR; Kleinman JE
Dialogues Clin Neurosci; 2006; 8(3):353-7. PubMed ID: 17117617
[TBL] [Abstract][Full Text] [Related]
40. A neuregulin 1 transmembrane domain mutation causes imbalanced glutamatergic and dopaminergic receptor expression in mice.
Newell KA; Karl T; Huang XF
Neuroscience; 2013 Sep; 248():670-80. PubMed ID: 23811072
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
