Disease: Autistic Disorder ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder 		0.380 Biomarker disease CTD_human Our results strengthen the case for a more detailed study of the role of RELN and GRIK2 in autism susceptibility, as well as identifying two new potential candidate genes, MKL2 and SND1. 20442744 2010
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder 		0.380 Biomarker disease BEFREE Previous studies implicated GluK2 in autism. 20863077 2010
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder 		0.380 Biomarker disease BEFREE Our results strengthen the case for a more detailed study of the role of RELN and GRIK2 in autism susceptibility, as well as identifying two new potential candidate genes, MKL2 and SND1. 20442744 2010
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder 		0.380 GeneticVariation disease BEFREE Therefore in the present study, we have performed genetic analysis of three markers of GluR6 (SNP1: rs2227281, SNP2: rs2227283, SNP3: rs2235076) for possible association with autism through population, and family-based (TDT and HHRR) approaches. 17712621 2007
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder 		0.380 GeneticVariation disease LHGDN Therefore in the present study, we have performed genetic analysis of three markers of GluR6 (SNP1: rs2227281, SNP2: rs2227283, SNP3: rs2235076) for possible association with autism through population, and family-based (TDT and HHRR) approaches. 17712621 2007
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder 		0.380 GeneticVariation disease LHGDN Our data on altered functional properties of GluR6(M836I) provide a functional basis for the postulated linkage of GluR6 to autism. 17167233 2006
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder 		0.380 GeneticVariation disease BEFREE Our data on altered functional properties of GluR6(M836I) provide a functional basis for the postulated linkage of GluR6 to autism. 17167233 2006
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder 		0.380 GeneticVariation disease BEFREE Only the GRIK2 SNP I867, recently associated with autism, was less transmitted than expected (p < 0.03), supporting a functional role for this variant. 15094479 2004
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder 		0.380 GeneticVariation disease BEFREE Our results suggested that GluR6 is in linkage disequilibrium with autism. 15389769 2004
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder 		0.380 GeneticVariation disease BEFREE These results are similar to the maternal GRIK2 transmission disequilibrium previously reported for autism, and support the presence of a susceptibility gene for schizophrenia at 6q16. 15305151 2004
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder 		0.380 GeneticVariation disease LHGDN Furthermore, TDT analysis (with only one affected proband per family) showed significant association between GluR6 and autism (TDT association P = 0.008). 11920157 2002
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder 		0.380 Biomarker disease CTD_human Furthermore, TDT analysis (with only one affected proband per family) showed significant association between GluR6 and autism (TDT association P = 0.008). 11920157 2002
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder 		0.380 Biomarker disease BEFREE Furthermore, TDT analysis (with only one affected proband per family) showed significant association between GluR6 and autism (TDT association P = 0.008). 11920157 2002