Literature DB >> 16897606

No association between the genetic polymorphisms in the RTN4R gene and schizophrenia in the Chinese population.

J Meng1, Y Shi, X Zhao, S Guo, H Wang, Y Zheng, R Tang, G Feng, N Gu, H Liu, S Zhu, L He.   

Abstract

The RTN4R gene is located in the 22q11 region and it encodes a subunit of the receptor complex (RTN4R-p75NTR) which results in neuronal growth inhibitory signals in response to Nogo-66, MAG or OMG signaling. Previous studies have suggested that RTN4R might act as a potential candidate for schizophrenia susceptibility loci. We genotyped four SNPs within the gene and conducted a case-control study and TDT analysis, involving 707 schizophrenic patients, 689 controls and 372 unrelated small nuclear families with schizophrenic offspring in the Chinese population. We examined allele and genotype frequencies and haplotype distributions in both family- and nonfamily-based samples. Our results suggest that there is no significant association between the genetic polymorphisms and schizophrenia in the Han Chinese population.

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Year:  2006        PMID: 16897606     DOI: 10.1007/s00702-006-0538-y

Source DB:  PubMed          Journal:  J Neural Transm (Vienna)        ISSN: 0300-9564            Impact factor:   3.575


  35 in total

Review 1.  Problems of reporting genetic associations with complex outcomes.

Authors:  Helen M Colhoun; Paul M McKeigue; George Davey Smith
Journal:  Lancet       Date:  2003-03-08       Impact factor: 79.321

2.  An association study of PCQAP polymorphisms and schizophrenia.

Authors:  Harinder K Sandhu; Nancy Hollenbeck; Thomas H Wassink; Robert A Philibert
Journal:  Psychiatr Genet       Date:  2004-09       Impact factor: 2.458

3.  Confirmation and fine mapping of the chromosome 1 alcohol dependence risk locus.

Authors:  J Lappalainen; H R Kranzler; I Petrakis; L K Somberg; G Page; J H Krystal; J Gelernter
Journal:  Mol Psychiatry       Date:  2004-03       Impact factor: 15.992

4.  Case-control study and transmission disequilibrium test provide consistent evidence for association between schizophrenia and genetic variation in the 22q11 gene ZDHHC8.

Authors:  Wu-Yan Chen; Yong-Yong Shi; Yong-Lan Zheng; Xin-Zhi Zhao; Guang-Ji Zhang; Sheng-Qi Chen; Pei-Di Yang; Lin He
Journal:  Hum Mol Genet       Date:  2004-10-15       Impact factor: 6.150

5.  A highly significant association between a COMT haplotype and schizophrenia.

Authors:  Sagiv Shifman; Michal Bronstein; Meira Sternfeld; Anne Pisanté-Shalom; Efrat Lev-Lehman; Avraham Weizman; Ilya Reznik; Baruch Spivak; Nimrod Grisaru; Leon Karp; Richard Schiffer; Moshe Kotler; Rael D Strous; Marnina Swartz-Vanetik; Haim Y Knobler; Eilat Shinar; Jacques S Beckmann; Benjamin Yakir; Neil Risch; Naomi B Zak; Ariel Darvasi
Journal:  Am J Hum Genet       Date:  2002-10-25       Impact factor: 11.025

6.  Focal gray matter density changes in schizophrenia.

Authors:  H E Hulshoff Pol; H G Schnack; R C Mandl; N E van Haren; H Koning; D L Collins; A C Evans; R S Kahn
Journal:  Arch Gen Psychiatry       Date:  2001-12

7.  Genetic variation at the 22q11 PRODH2/DGCR6 locus presents an unusual pattern and increases susceptibility to schizophrenia.

Authors:  Hui Liu; Simon C Heath; Christina Sobin; J Louw Roos; Brandi L Galke; Maude L Blundell; Marge Lenane; Brian Robertson; Ellen M Wijsman; Judith L Rapoport; Joseph A Gogos; Maria Karayiorgou
Journal:  Proc Natl Acad Sci U S A       Date:  2002-03-12       Impact factor: 11.205

8.  Myelin-associated glycoprotein interacts with the Nogo66 receptor to inhibit neurite outgrowth.

Authors:  Marco Domeniconi; Zixuan Cao; Timothy Spencer; Rajeev Sivasankaran; Kevin Wang; Elena Nikulina; Noriko Kimura; Hong Cai; Kangwen Deng; Ying Gao; Zhigang He; Marie Filbin
Journal:  Neuron       Date:  2002-07-18       Impact factor: 17.173

Review 9.  White matter changes in schizophrenia: evidence for myelin-related dysfunction.

Authors:  Kenneth L Davis; Daniel G Stewart; Joseph I Friedman; Monte Buchsbaum; Philip D Harvey; Patrick R Hof; Joseph Buxbaum; Vahram Haroutunian
Journal:  Arch Gen Psychiatry       Date:  2003-05

Review 10.  The molecular genetics of schizophrenia: new findings promise new insights.

Authors:  M J Owen; N M Williams; M C O'Donovan
Journal:  Mol Psychiatry       Date:  2004-01       Impact factor: 15.992

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  7 in total

1.  Genetic variants of Nogo-66 receptor with possible association to schizophrenia block myelin inhibition of axon growth.

Authors:  Stéphane Budel; Thihan Padukkavidana; Betty P Liu; Zeny Feng; Fenghua Hu; Sam Johnson; Juha Lauren; James H Park; Aaron W McGee; Ji Liao; Althea Stillman; Ji-Eun Kim; Bao-Zhu Yang; Stefano Sodi; Joel Gelernter; Hongyu Zhao; Fuki Hisama; Amy F T Arnsten; Stephen M Strittmatter
Journal:  J Neurosci       Date:  2008-12-03       Impact factor: 6.167

Review 2.  Contribution of nonprimate animal models in understanding the etiology of schizophrenia.

Authors:  Noah L Lazar; Richard W J Neufeld; Donald P Cain
Journal:  J Psychiatry Neurosci       Date:  2011-07       Impact factor: 6.186

Review 3.  Copy number variation at 22q11.2: from rare variants to common mechanisms of developmental neuropsychiatric disorders.

Authors:  N Hiroi; T Takahashi; A Hishimoto; T Izumi; S Boku; T Hiramoto
Journal:  Mol Psychiatry       Date:  2013-08-06       Impact factor: 15.992

4.  Nogo Receptor 1 (RTN4R) as a candidate gene for schizophrenia: analysis using human and mouse genetic approaches.

Authors:  Ruby Hsu; Abigail Woodroffe; Wen-Sung Lai; Melloni N Cook; Jun Mukai; Jonathan P Dunning; Douglas J Swanson; J Louw Roos; Gonçalo R Abecasis; Maria Karayiorgou; Joseph A Gogos
Journal:  PLoS One       Date:  2007-11-28       Impact factor: 3.240

Review 5.  Nogo-A and Nogo-66 receptor in amyotrophic lateral sclerosis.

Authors:  Felicia Yu Hsuan Teng; Bor Luen Tang
Journal:  J Cell Mol Med       Date:  2008-04-15       Impact factor: 5.310

6.  Genetic variants in Nogo receptor signaling pathways may be associated with early life adversity in schizophrenia susceptibility.

Authors:  Jessica L Andrews; Francesca Fernandez-Enright
Journal:  BBA Clin       Date:  2014-12-09

7.  Identification of genetic variants of LGI1 and RTN4R (NgR1) linked to schizophrenia that are defective in NgR1-LGI1 signaling.

Authors:  Rhalena A Thomas; Amirthagowri Ambalavanan; Guy A Rouleau; Philip A Barker
Journal:  Mol Genet Genomic Med       Date:  2016-03-11       Impact factor: 2.183

  7 in total

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