134 related articles for article (PubMed ID: 20468065)
1. Association of ZDHHC8 polymorphisms with smooth pursuit eye movement abnormality.
Shin HD; Park BL; Bae JS; Park TJ; Chun JY; Park CS; Sohn JW; Kim BJ; Kang YH; Kim JW; Kim KH; Shin TM; Woo SI
Am J Med Genet B Neuropsychiatr Genet; 2010 Sep; 153B(6):1167-72. PubMed ID: 20468065
[TBL] [Abstract][Full Text] [Related]
2. Association analysis of COMT polymorphisms with schizophrenia and smooth pursuit eye movement abnormality.
Park BL; Shin HD; Cheong HS; Park CS; Sohn JW; Kim BJ; Seo HK; Kim JW; Kim KH; Shin TM; Choi IG; Kim SG; Woo SI
J Hum Genet; 2009 Dec; 54(12):709-12. PubMed ID: 19881467
[TBL] [Abstract][Full Text] [Related]
3. Association of RANBP1 haplotype with smooth pursuit eye movement abnormality.
Cheong HS; Park BL; Kim EM; Park CS; Sohn JW; Kim BJ; Kim JW; Kim KH; Shin TM; Choi IG; Han SW; Hwang J; Koh I; Shin HD; Woo SI
Am J Med Genet B Neuropsychiatr Genet; 2011 Jan; 156B(1):67-71. PubMed ID: 21184585
[TBL] [Abstract][Full Text] [Related]
4. Case-control study and transmission disequilibrium test provide consistent evidence for association between schizophrenia and genetic variation in the 22q11 gene ZDHHC8.
Chen WY; Shi YY; Zheng YL; Zhao XZ; Zhang GJ; Chen SQ; Yang PD; He L
Hum Mol Genet; 2004 Dec; 13(23):2991-5. PubMed ID: 15489219
[TBL] [Abstract][Full Text] [Related]
5. Neuregulin 3 does not confer risk for schizophrenia and smooth pursuit eye movement abnormality in a Korean population.
Pasaje CF; Bae JS; Park BL; Cheong HS; Kim JH; Park TJ; Lee JS; Kim Y; Park CS; Kim BJ; Cha B; Kim JW; Choi WH; Shin TM; Choi IG; Hwang J; Shin HD; Woo SI
Genes Brain Behav; 2011 Nov; 10(8):828-33. PubMed ID: 21762460
[TBL] [Abstract][Full Text] [Related]
6. ZDHHC8 as a candidate gene for schizophrenia: analysis of a putative functional intronic marker in case-control and family-based association studies.
Faul T; Gawlik M; Bauer M; Jung S; Pfuhlmann B; Jabs B; Knapp M; Stöber G
BMC Psychiatry; 2005 Oct; 5():35. PubMed ID: 16225675
[TBL] [Abstract][Full Text] [Related]
7. The ZDHHC8 gene did not associate with bipolar disorder or schizophrenia.
Otani K; Ujike H; Tanaka Y; Morita Y; Kishimoto M; Morio A; Uchida N; Nomura A; Kuroda S
Neurosci Lett; 2005 Dec; 390(3):166-70. PubMed ID: 16150541
[TBL] [Abstract][Full Text] [Related]
8. No association was found between a functional SNP in ZDHHC8 and schizophrenia in a Japanese case-control population.
Saito S; Ikeda M; Iwata N; Suzuki T; Kitajima T; Yamanouchi Y; Kinoshita Y; Takahashi N; Inada T; Ozaki N
Neurosci Lett; 2005 Feb; 374(1):21-4. PubMed ID: 15631889
[TBL] [Abstract][Full Text] [Related]
9. ZDHHC8 single nucleotide polymorphism rs175174 is not associated with psychiatric features of the 22q11 deletion syndrome or schizophrenia.
Demily C; Legallic S; Bou J; Houy-Durand E; Van Amelsvoort T; Zinkstok J; Manouvrier-Hanue S; Vogels A; Drouin-Garraud V; Philip N; Philippe A; Héron D; Sarda P; Petit M; Thibaut F; Frébourg T; Campion D
Psychiatr Genet; 2007 Oct; 17(5):311-2. PubMed ID: 17728672
[No Abstract] [Full Text] [Related]
10. Testing for genetic association between the ZDHHC8 gene locus and susceptibility to schizophrenia: An integrated analysis of multiple datasets.
Xu M; St Clair D; He L
Am J Med Genet B Neuropsychiatr Genet; 2010 Oct; 153B(7):1266-75. PubMed ID: 20661937
[TBL] [Abstract][Full Text] [Related]
11. Genetic association analysis of ERBB4 polymorphisms with the risk of schizophrenia and SPEM abnormality in a Korean population.
Bae JS; Pasaje CF; Park BL; Cheong HS; Kim JH; Kim JY; Shin JG; Park CS; Kim BJ; Lee CS; Lee M; Choi WH; Shin TM; Hwang J; Shin HD; Woo SI
Brain Res; 2012 Jul; 1466():146-51. PubMed ID: 22634065
[TBL] [Abstract][Full Text] [Related]
12. Lack of association of the RTN4R genetic variations with risk of schizophrenia and SPEM abnormality in a Korean population.
Pasaje CF; Bae JS; Park BL; Park CS; Kim BJ; Lee CS; Kim JW; Choi WH; Shin TM; Koh IS; Choi IG; Woo SL; Shin HD
Psychiatry Res; 2011 Sep; 189(2):312-4. PubMed ID: 21377214
[TBL] [Abstract][Full Text] [Related]
13. Lack of associations of neuregulin 1 variations with schizophrenia and smooth pursuit eye movement abnormality in a Korean population.
Kim JH; Park BL; Pasaje CF; Bae JS; Park CS; Cha B; Kim BJ; Lee M; Choi WH; Shin TM; Choi IG; Hwang J; Koh I; Woo SI; Shin HD
J Mol Neurosci; 2012 Mar; 46(3):476-82. PubMed ID: 21858616
[TBL] [Abstract][Full Text] [Related]
14. Investigating the potential genetic association between RANBP9 polymorphisms and the risk of schizophrenia.
Bae JS; Kim JY; Park BL; Cheong HS; Kim JH; Namgoong S; Kim JO; Park CS; Kim BJ; Lee CS; Lee M; Choi WH; Shin TM; Hwang J; Shin HD; Woo SI
Mol Med Rep; 2015 Apr; 11(4):2975-80. PubMed ID: 25482375
[TBL] [Abstract][Full Text] [Related]
15. Association analysis of PDE4B polymorphisms with schizophrenia and smooth pursuit eye movement abnormality in a Korean population.
Bae JS; Park BL; Cheong HS; Kim JH; Kim JY; Namgoong S; Kim JO; Park CS; Kim BJ; Lee CS; Kim JW; Choi WH; Shin TM; Hwang J; Koh IS; Shin HD; Woo SI
Gen Physiol Biophys; 2015 Jul; 34(3):277-84. PubMed ID: 25926551
[TBL] [Abstract][Full Text] [Related]
16. ZDHHC8 gene may play a role in cortical volumes of patients with schizophrenia.
Ota VK; Gadelha A; Assunção IB; Santoro ML; Christofolini DM; Bellucco FT; Santos-Filho AF; Ottoni GL; Lara DR; Mari JJ; Melaragno MI; Smith MA; Bressan RA; Belangero SI; Jackowski AP
Schizophr Res; 2013 Apr; 145(1-3):33-5. PubMed ID: 23403413
[TBL] [Abstract][Full Text] [Related]
17. An in-depth analysis reveals two new genetic variants on 22q11.2 associated with vitiligo in the Chinese Han population.
Tang X; Cheng H; Cheng L; Liang B; Chen M; Zheng X; Xiao F
Mol Biol Rep; 2021 Aug; 48(8):5955-5964. PubMed ID: 34350550
[TBL] [Abstract][Full Text] [Related]
18. Schizophrenia-related neuregulin-1 single-nucleotide polymorphisms lead to deficient smooth eye pursuit in a large sample of young men.
Smyrnis N; Kattoulas E; Stefanis NC; Avramopoulos D; Stefanis CN; Evdokimidis I
Schizophr Bull; 2011 Jul; 37(4):822-31. PubMed ID: 19965935
[TBL] [Abstract][Full Text] [Related]
19. HTF9C gene of 22q11.21 region associates with schizophrenia having deficit-sustained attention.
Liu YL; Fann CS; Liu CM; Chang CC; Yang WC; Wu JY; Hung SI; Chan HY; Chen JJ; Hsieh MH; Hwang TJ; Faraone SV; Tsuang MT; Chen WJ; Hwu HG
Psychiatr Genet; 2007 Dec; 17(6):333-8. PubMed ID: 18075473
[TBL] [Abstract][Full Text] [Related]
20. Lack of association between COMT Val158Met and ZDHHC8 rs175174 polymorphisms and susceptibility to schizophrenia in a Brazilian population.
Moraes LS; Santos ACC; Ferreira-Fernandes H; Yoshioka FKN; Teixeira SS; Guimarães AC; da Rocha CAM; Rey JA; Pinto GR; Burbano RR
Psychiatr Genet; 2017 Oct; 27(5):197-198. PubMed ID: 28562378
[No Abstract] [Full Text] [Related]
[Next] [New Search]
