Centre d'Information et de documentation du CRA Rhône-Alpes
CRA
Informations pratiques
-
Adresse
Centre d'information et de documentation
du CRA Rhône-Alpes
Centre Hospitalier le Vinatier
bât 211
95, Bd Pinel
69678 Bron CedexHoraires
Lundi au Vendredi
9h00-12h00 13h30-16h00Contact
Tél: +33(0)4 37 91 54 65
Mail
Fax: +33(0)4 37 91 54 37
-
Détail de l'auteur
Auteur HuaiTing GU |
Documents disponibles écrits par cet auteur (2)
Faire une suggestion Affiner la recherche
Association analysis of two synapse-related gene mutations with autism spectrum disorder in a Chinese population / Fang HOU in Research in Autism Spectrum Disorders, 53 (September 2018)
[article]
Titre : Association analysis of two synapse-related gene mutations with autism spectrum disorder in a Chinese population Type de document : Texte imprimé et/ou numérique Auteurs : Fang HOU, Auteur ; Li LI, Auteur ; Jianhua GONG, Auteur ; Yanlin CHEN, Auteur ; Jia WANG, Auteur ; Lingfei LIU, Auteur ; Xiu LUO, Auteur ; HuaiTing GU, Auteur ; Jiajia ZHANG, Auteur ; Ranran SONG, Auteur Article en page(s) : p.67-72 Langues : Anglais (eng) Mots-clés : Polymorphism Autism spectrum disorder Index. décimale : PER Périodiques Résumé : Background Autism spectrum disorder (ASD) is a complex neurodevelopmental disorder with a strong genetic basis. Recently, synaptic abnormality has been proved to have a strong association with the etiology of ASD. PSD95 and DLGAP2 are the members of postsynaptic scaffolding proteins that play crucial roles in synaptic plasticity and function. This study evaluated the association of the genetic variants in PSD95 and DLGAP2 with ASD. Methods We performed a case-control study in a Chinese population with samples of 529 cases and 1923 controls. We extracted genomic DNA from oral swabs and determined the SNP genotypes by using a PCR-RFLP assay. Results We sequenced five SNPs (rs7005715, rs2301963 and rs2906569 in DLGAP2; rs2521985 and rs2017365 in PSD95). Genetic analysis suggested the GA genotype and GG genotype of rs7005715 were significantly associated with increased risk of ASD (respectively: OR?=?1.357, 95%CI?=?1.103–1.669, P?=?0.016; OR?=?1.860, 95%CI?=?1.359–2.551, P?0.001). The dominant model (OR?=?1.444, 95%CI?=?1.186–1.758, P?0.001) and recessive model (OR?=?1.597, 95%CI?=?1.187–2.149, P?=?0.011) also showed the same trend. We did not detect any significant association between other SNPs and ASD. Conclusions The genetic variant of rs7005715 in DLGAP2 increased susceptibility to the risk of ASD in a Chinese Han population. En ligne : https://doi.org/10.1016/j.rasd.2018.06.005 Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=368
in Research in Autism Spectrum Disorders > 53 (September 2018) . - p.67-72[article] Association analysis of two synapse-related gene mutations with autism spectrum disorder in a Chinese population [Texte imprimé et/ou numérique] / Fang HOU, Auteur ; Li LI, Auteur ; Jianhua GONG, Auteur ; Yanlin CHEN, Auteur ; Jia WANG, Auteur ; Lingfei LIU, Auteur ; Xiu LUO, Auteur ; HuaiTing GU, Auteur ; Jiajia ZHANG, Auteur ; Ranran SONG, Auteur . - p.67-72.
Langues : Anglais (eng)
in Research in Autism Spectrum Disorders > 53 (September 2018) . - p.67-72
Mots-clés : Polymorphism Autism spectrum disorder Index. décimale : PER Périodiques Résumé : Background Autism spectrum disorder (ASD) is a complex neurodevelopmental disorder with a strong genetic basis. Recently, synaptic abnormality has been proved to have a strong association with the etiology of ASD. PSD95 and DLGAP2 are the members of postsynaptic scaffolding proteins that play crucial roles in synaptic plasticity and function. This study evaluated the association of the genetic variants in PSD95 and DLGAP2 with ASD. Methods We performed a case-control study in a Chinese population with samples of 529 cases and 1923 controls. We extracted genomic DNA from oral swabs and determined the SNP genotypes by using a PCR-RFLP assay. Results We sequenced five SNPs (rs7005715, rs2301963 and rs2906569 in DLGAP2; rs2521985 and rs2017365 in PSD95). Genetic analysis suggested the GA genotype and GG genotype of rs7005715 were significantly associated with increased risk of ASD (respectively: OR?=?1.357, 95%CI?=?1.103–1.669, P?=?0.016; OR?=?1.860, 95%CI?=?1.359–2.551, P?0.001). The dominant model (OR?=?1.444, 95%CI?=?1.186–1.758, P?0.001) and recessive model (OR?=?1.597, 95%CI?=?1.187–2.149, P?=?0.011) also showed the same trend. We did not detect any significant association between other SNPs and ASD. Conclusions The genetic variant of rs7005715 in DLGAP2 increased susceptibility to the risk of ASD in a Chinese Han population. En ligne : https://doi.org/10.1016/j.rasd.2018.06.005 Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=368 Neurexin gene family variants as risk factors for autism spectrum disorder / Jia WANG in Autism Research, 11-1 (January 2018)
[article]
Titre : Neurexin gene family variants as risk factors for autism spectrum disorder Type de document : Texte imprimé et/ou numérique Auteurs : Jia WANG, Auteur ; Jianhua GONG, Auteur ; Li LI, Auteur ; Yanlin CHEN, Auteur ; Lingfei LIU, Auteur ; HuaiTing GU, Auteur ; Xiu LUO, Auteur ; Fang HOU, Auteur ; Jiajia ZHANG, Auteur ; Ranran SONG, Auteur Article en page(s) : p.37-43 Langues : Anglais (eng) Index. décimale : PER Périodiques Résumé : Increasing evidence suggests that abnormal synaptic function leads to neuronal developmental disorders and is an important component of the etiology of autism spectrum disorder (ASD). Neurexins are presynaptic cell?adhesion molecules that affect the function of synapses and mediate the conduction of nerve signals. Thus, neurexins are attractive candidate genes for autism. Since gene families have greater power to reveal genetic association than single genes, we designed this case?control study to investigate six genetic variants in three neurexin genes (NRXN1, NRXN2, and NRXN3) in a Chinese population including 529 ASD patients and 1,923 healthy controls. We found that two SNPs were significantly associated with ASD after false discovery rate (FDR) adjustment for multiple comparisons. The NRXN2 rs12273892 polymorphism T allele and AT genotype were significantly associated with increased risk of ASD (respectively: OR?=?1.328, 95% CI?=?1.133–1.557, P?0.001; OR?=?1.528; 95% CI?=?1.249–1.868, P?0.001). The dominant model showed the same association (OR?=?1.495, 95% CI?=?1.231–1.816, P?0.001). The NRXN3 rs12879016 polymorphism played a significant role in ASD susceptibility under the dominant model (OR?=?0.747, 95% CI= 0.615–0.908, P?=?0.023), with the same trend detected for the G allele and GT genotype (respectively: OR?=?0.811, 95% CI?=?0.699–0.941, P?=?0.036; OR?=?0.755, 95% CI?=?0.615–0.928, P?=?0.035). In conclusion, this study supports the importance of two genetic variants in the neurexin gene family in ASD susceptibility in China. Autism Res 2018, 11: 37–43. © 2017 International Society for Autism Research, Wiley Periodicals, Inc. Lay Summary Autism spectrum disorder (ASD) is a neurodevelopmental disorder that is highly heritable, and studies have found a number of candidate genes that might contribute to ASD. Neurexins are presynaptic cell?adhesion molecules that affect the function of synapses and mediate the conduction of nerve signals, and they play an important role in normal brain development and become candidate genes for autism. The purpose of our study is to explore the association between variants of the neurexins gene family and ASD in a Chinese population through a case?control study. En ligne : https://doi.org/10.1002/aur.1881 Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=333
in Autism Research > 11-1 (January 2018) . - p.37-43[article] Neurexin gene family variants as risk factors for autism spectrum disorder [Texte imprimé et/ou numérique] / Jia WANG, Auteur ; Jianhua GONG, Auteur ; Li LI, Auteur ; Yanlin CHEN, Auteur ; Lingfei LIU, Auteur ; HuaiTing GU, Auteur ; Xiu LUO, Auteur ; Fang HOU, Auteur ; Jiajia ZHANG, Auteur ; Ranran SONG, Auteur . - p.37-43.
Langues : Anglais (eng)
in Autism Research > 11-1 (January 2018) . - p.37-43
Index. décimale : PER Périodiques Résumé : Increasing evidence suggests that abnormal synaptic function leads to neuronal developmental disorders and is an important component of the etiology of autism spectrum disorder (ASD). Neurexins are presynaptic cell?adhesion molecules that affect the function of synapses and mediate the conduction of nerve signals. Thus, neurexins are attractive candidate genes for autism. Since gene families have greater power to reveal genetic association than single genes, we designed this case?control study to investigate six genetic variants in three neurexin genes (NRXN1, NRXN2, and NRXN3) in a Chinese population including 529 ASD patients and 1,923 healthy controls. We found that two SNPs were significantly associated with ASD after false discovery rate (FDR) adjustment for multiple comparisons. The NRXN2 rs12273892 polymorphism T allele and AT genotype were significantly associated with increased risk of ASD (respectively: OR?=?1.328, 95% CI?=?1.133–1.557, P?0.001; OR?=?1.528; 95% CI?=?1.249–1.868, P?0.001). The dominant model showed the same association (OR?=?1.495, 95% CI?=?1.231–1.816, P?0.001). The NRXN3 rs12879016 polymorphism played a significant role in ASD susceptibility under the dominant model (OR?=?0.747, 95% CI= 0.615–0.908, P?=?0.023), with the same trend detected for the G allele and GT genotype (respectively: OR?=?0.811, 95% CI?=?0.699–0.941, P?=?0.036; OR?=?0.755, 95% CI?=?0.615–0.928, P?=?0.035). In conclusion, this study supports the importance of two genetic variants in the neurexin gene family in ASD susceptibility in China. Autism Res 2018, 11: 37–43. © 2017 International Society for Autism Research, Wiley Periodicals, Inc. Lay Summary Autism spectrum disorder (ASD) is a neurodevelopmental disorder that is highly heritable, and studies have found a number of candidate genes that might contribute to ASD. Neurexins are presynaptic cell?adhesion molecules that affect the function of synapses and mediate the conduction of nerve signals, and they play an important role in normal brain development and become candidate genes for autism. The purpose of our study is to explore the association between variants of the neurexins gene family and ASD in a Chinese population through a case?control study. En ligne : https://doi.org/10.1002/aur.1881 Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=333