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 *

197 related articles for article (PubMed ID: 16894060)

  • 1. Genetic association and brain morphology studies and the chromosome 8p22 pericentriolar material 1 (PCM1) gene in susceptibility to schizophrenia.
    Gurling HM; Critchley H; Datta SR; McQuillin A; Blaveri E; Thirumalai S; Pimm J; Krasucki R; Kalsi G; Quested D; Lawrence J; Bass N; Choudhury K; Puri V; O'Daly O; Curtis D; Blackwood D; Muir W; Malhotra AK; Buchanan RW; Good CD; Frackowiak RS; Dolan RJ
    Arch Gen Psychiatry; 2006 Aug; 63(8):844-54. PubMed ID: 16894060
    [TBL] [Abstract][Full Text] [Related]  

  • 2. A threonine to isoleucine missense mutation in the pericentriolar material 1 gene is strongly associated with schizophrenia.
    Datta SR; McQuillin A; Rizig M; Blaveri E; Thirumalai S; Kalsi G; Lawrence J; Bass NJ; Puri V; Choudhury K; Pimm J; Crombie C; Fraser G; Walker N; Curtis D; Zvelebil M; Pereira A; Kandaswamy R; St Clair D; Gurling HM
    Mol Psychiatry; 2010 Jun; 15(6):615-28. PubMed ID: 19048012
    [TBL] [Abstract][Full Text] [Related]  

  • 3. No association between the PCM1 gene and schizophrenia: a multi-center case-control study and a meta-analysis.
    Hashimoto R; Ohi K; Yasuda Y; Fukumoto M; Yamamori H; Kamino K; Morihara T; Iwase M; Kazui H; Numata S; Ikeda M; Ueno S; Ohmori T; Iwata N; Ozaki N; Takeda M
    Schizophr Res; 2011 Jun; 129(1):80-4. PubMed ID: 21481569
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Recruitment of PCM1 to the centrosome by the cooperative action of DISC1 and BBS4: a candidate for psychiatric illnesses.
    Kamiya A; Tan PL; Kubo K; Engelhard C; Ishizuka K; Kubo A; Tsukita S; Pulver AE; Nakajima K; Cascella NG; Katsanis N; Sawa A
    Arch Gen Psychiatry; 2008 Sep; 65(9):996-1006. PubMed ID: 18762586
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Genomewide genetic linkage analysis confirms the presence of susceptibility loci for schizophrenia, on chromosomes 1q32.2, 5q33.2, and 8p21-22 and provides support for linkage to schizophrenia, on chromosomes 11q23.3-24 and 20q12.1-11.23.
    Gurling HM; Kalsi G; Brynjolfson J; Sigmundsson T; Sherrington R; Mankoo BS; Read T; Murphy P; Blaveri E; McQuillin A; Petursson H; Curtis D
    Am J Hum Genet; 2001 Mar; 68(3):661-73. PubMed ID: 11179014
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Linkage evidence of schizophrenia to loci near neuregulin 1 gene on chromosome 8p21 in Taiwanese families.
    Liu CM; Hwu HG; Fann CS; Lin CY; Liu YL; Ou-Yang WC; Lee SF
    Am J Med Genet B Neuropsychiatr Genet; 2005 Apr; 134B(1):79-83. PubMed ID: 15704228
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Family-based linkage disequilibrium mapping using SNP marker haplotypes: application to a potential locus for schizophrenia at chromosome 22q11.
    Li T; Ball D; Zhao J; Murray RM; Liu X; Sham PC; Collier DA
    Mol Psychiatry; 2000 Jan; 5(1):77-84. PubMed ID: 10673772
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Linkage and association studies of prostate cancer susceptibility: evidence for linkage at 8p22-23.
    Xu J; Zheng SL; Hawkins GA; Faith DA; Kelly B; Isaacs SD; Wiley KE; Chang B; Ewing CM; Bujnovszky P; Carpten JD; Bleecker ER; Walsh PC; Trent JM; Meyers DA; Isaacs WB
    Am J Hum Genet; 2001 Aug; 69(2):341-50. PubMed ID: 11443539
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Neuregulin-1 haplotype HAP(ICE) is associated with lower hippocampal volumes in schizophrenic patients and in non-affected family members.
    Gruber O; Falkai P; Schneider-Axmann T; Schwab SG; Wagner M; Maier W
    J Psychiatr Res; 2008 Nov; 43(1):1-6. PubMed ID: 18291420
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Fine mapping by genetic association implicates the chromosome 1q23.3 gene UHMK1, encoding a serine/threonine protein kinase, as a novel schizophrenia susceptibility gene.
    Puri V; McQuillin A; Choudhury K; Datta S; Pimm J; Thirumalai S; Krasucki R; Lawrence J; Quested D; Bass N; Moorey H; Morgan J; Punukollu B; Kandasami G; Curtis D; Gurling H
    Biol Psychiatry; 2007 Apr; 61(7):873-9. PubMed ID: 16978587
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Linkage and association of schizophrenia with genetic variations in the locus of neuregulin 1 in Korean population.
    Kim JW; Lee YS; Cho EY; Jang YL; Park DY; Choi KS; Jeun HO; Cho SH; Jang SY; Hong KS
    Am J Med Genet B Neuropsychiatr Genet; 2006 Apr; 141B(3):281-6. PubMed ID: 16526041
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Linkage disequilibrium analyses in the Costa Rican population suggests discrete gene loci for schizophrenia at 8p23.1 and 8q13.3.
    Walss-Bass C; Montero AP; Armas R; Dassori A; Contreras SA; Liu W; Medina R; Levinson D; Pereira M; Atmella I; NeSmith L; Leach R; Almasy L; Raventos H; Escamilla MA
    Psychiatr Genet; 2006 Aug; 16(4):159-68. PubMed ID: 16829783
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Neuroanatomical and behavioral deficits in mice haploinsufficient for Pericentriolar material 1 (Pcm1).
    Zoubovsky S; Oh EC; Cash-Padgett T; Johnson AW; Hou Z; Mori S; Gallagher M; Katsanis N; Sawa A; Jaaro-Peled H
    Neurosci Res; 2015 Sep; 98():45-9. PubMed ID: 25697395
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Gene brain structure relationships: arbitrary assumptions of heterogeneity generate unfalsifiable claims.
    Crow TJ; DeLisi L
    Arch Gen Psychiatry; 2007 Sep; 64(9):1097-8; author reply 1098-9. PubMed ID: 17768277
    [No Abstract]   [Full Text] [Related]  

  • 15. Evidence for rare and common genetic risk variants for schizophrenia at protein kinase C, alpha.
    Carroll LS; Williams NM; Moskvina V; Russell E; Norton N; Williams HJ; Peirce T; Georgieva L; Dwyer S; Grozeva D; Greene E; Farmer A; McGuffin P; Morris DW; Corvin A; Gill M; Rujescu D; Sham P; Holmans P; Jones I; Kirov G; Craddock N; O'Donovan MC; Owen MJ
    Mol Psychiatry; 2010 Nov; 15(11):1101-11. PubMed ID: 19786960
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Association study of neuregulin 1 gene with schizophrenia.
    Yang JZ; Si TM; Ruan Y; Ling YS; Han YH; Wang XL; Zhou M; Zhang HY; Kong QM; Liu C; Zhang DR; Yu YQ; Liu SZ; Ju GZ; Shu L; Ma DL; Zhang D
    Mol Psychiatry; 2003 Jul; 8(7):706-9. PubMed ID: 12874607
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A transmission disequilibrium and linkage analysis of D22S278 marker alleles in 574 families: further support for a susceptibility locus for schizophrenia at 22q12. Schizophrenia Collaborative Linkage Group for Chromosome 22.
    Schizophr Res; 1998 Jul; 32(2):115-21. PubMed ID: 9713907
    [TBL] [Abstract][Full Text] [Related]  

  • 18. The DISC1 Ser704Cys substitution affects centrosomal localization of its binding partner PCM1 in glia in human brain.
    Eastwood SL; Walker M; Hyde TM; Kleinman JE; Harrison PJ
    Hum Mol Genet; 2010 Jun; 19(12):2487-96. PubMed ID: 20360304
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Four polymorphisms of the pericentriolar material 1 (PCM1) gene are not associated with schizophrenia in a Japanese population.
    Sakamoto S; Takaki M; Okahisa Y; Mizuki Y; Kodama M; Ujike H; Uchitomi Y
    Psychiatry Res; 2014 May; 216(2):288-9. PubMed ID: 24576429
    [No Abstract]   [Full Text] [Related]  

  • 20. Cognitive and magnetic resonance imaging brain morphometric correlates of brain-derived neurotrophic factor Val66Met gene polymorphism in patients with schizophrenia and healthy volunteers.
    Ho BC; Milev P; O'Leary DS; Librant A; Andreasen NC; Wassink TH
    Arch Gen Psychiatry; 2006 Jul; 63(7):731-40. PubMed ID: 16818862
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.