Lack of association of the RTN4R genetic variations with risk of schizophrenia and SPEM abnormality in a Korean population

Charisse Flerida A. Pasaje, Joon Seol Bae, Byung Lae Park, Chul Soo Park, Bong Jo Kim, Cheol Soon Lee, Jae Won Kim, Woo Hyuk Choi, Tae Min Shin, InSong Koh, Ihn Geun Choi, Sung ll Woo, Hyoung Doo Shin

Research output: Contribution to journalArticle

3 Citations (Scopus)

Abstract

This study examined the association of the reticulon 4 receptor (RTN4R) gene with schizophrenia and smooth pursuit eye movement (SPEM) abnormality in a Korean population. Although we failed to provide convincing evidence that RTN4R is associated with schizophrenia development and SPEM impairment, our findings may be useful for further genetic studies.

Original languageEnglish
Pages (from-to)312-314
Number of pages3
JournalPsychiatry Research
Volume189
Issue number2
DOIs
StatePublished - 2011 Sep 30

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Eye Abnormalities
Smooth Pursuit
Eye Movements
Schizophrenia
Population
Genes
Nogo Receptor 1

Keywords

  • RTN4R
  • Schizophrenia
  • Single nucleotide polymorphism

Cite this

Pasaje, C. F. A., Bae, J. S., Park, B. L., Park, C. S., Kim, B. J., Lee, C. S., ... Shin, H. D. (2011). Lack of association of the RTN4R genetic variations with risk of schizophrenia and SPEM abnormality in a Korean population. Psychiatry Research, 189(2), 312-314. https://doi.org/10.1016/j.psychres.2011.02.006
Pasaje, Charisse Flerida A. ; Bae, Joon Seol ; Park, Byung Lae ; Park, Chul Soo ; Kim, Bong Jo ; Lee, Cheol Soon ; Kim, Jae Won ; Choi, Woo Hyuk ; Shin, Tae Min ; Koh, InSong ; Choi, Ihn Geun ; Woo, Sung ll ; Shin, Hyoung Doo. / Lack of association of the RTN4R genetic variations with risk of schizophrenia and SPEM abnormality in a Korean population. In: Psychiatry Research. 2011 ; Vol. 189, No. 2. pp. 312-314.
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abstract = "This study examined the association of the reticulon 4 receptor (RTN4R) gene with schizophrenia and smooth pursuit eye movement (SPEM) abnormality in a Korean population. Although we failed to provide convincing evidence that RTN4R is associated with schizophrenia development and SPEM impairment, our findings may be useful for further genetic studies.",
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Pasaje, CFA, Bae, JS, Park, BL, Park, CS, Kim, BJ, Lee, CS, Kim, JW, Choi, WH, Shin, TM, Koh, I, Choi, IG, Woo, SL & Shin, HD 2011, 'Lack of association of the RTN4R genetic variations with risk of schizophrenia and SPEM abnormality in a Korean population', Psychiatry Research, vol. 189, no. 2, pp. 312-314. https://doi.org/10.1016/j.psychres.2011.02.006

Lack of association of the RTN4R genetic variations with risk of schizophrenia and SPEM abnormality in a Korean population. / Pasaje, Charisse Flerida A.; Bae, Joon Seol; Park, Byung Lae; Park, Chul Soo; Kim, Bong Jo; Lee, Cheol Soon; Kim, Jae Won; Choi, Woo Hyuk; Shin, Tae Min; Koh, InSong; Choi, Ihn Geun; Woo, Sung ll; Shin, Hyoung Doo.

In: Psychiatry Research, Vol. 189, No. 2, 30.09.2011, p. 312-314.

Research output: Contribution to journalArticle

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AU - Bae, Joon Seol

AU - Park, Byung Lae

AU - Park, Chul Soo

AU - Kim, Bong Jo

AU - Lee, Cheol Soon

AU - Kim, Jae Won

AU - Choi, Woo Hyuk

AU - Shin, Tae Min

AU - Koh, InSong

AU - Choi, Ihn Geun

AU - Woo, Sung ll

AU - Shin, Hyoung Doo

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KW - RTN4R

KW - Schizophrenia

KW - Single nucleotide polymorphism

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