|
rs1861972
|
|
|
0.070 |
GeneticVariation |
BEFREE |
Here, we have investigated the association of five markers [rs3735653 (C/T) in exon 1; rs34808376 (GC/-) and rs6150410 (CGCATCCCC/-) in promoter region; rs1861972 (A/G) and rs1861973 (C/T) in the intron] of the gene with autism and ASD in Indian population using family-based approach.
|
20050924 |
2010 |
|
rs1861972
|
|
|
0.070 |
GeneticVariation |
BEFREE |
The haplotype A-C of rs1861972 and rs1861973 is the core element of the observed haplotype association in this study, which plays a role as a protective factor against autism; in addition, the haplotype G-A-C is less frequent in male cases compared to controls (38.64 vs. 52.51%), which plausibly modulate disease vulnerability to autism.
|
20523082 |
2010 |
|
rs1861972
|
|
|
0.070 |
GeneticVariation |
BEFREE |
Two SNPs (rs1861972, rs1861973) at the EN2 gene that have been reported to be associated with autism underwent analysis among our studied cohorts.
|
18424904 |
2008 |
|
rs1861972
|
|
|
0.070 |
GeneticVariation |
BEFREE |
Two recent studies have demonstrated that two intronic SNPs (rs1861972, rs1861973) in the EN2 gene are significantly associated with autism.
|
17948901 |
2008 |
|
rs1861972
|
|
|
0.070 |
GeneticVariation |
BEFREE |
Since the associated SNPs were in high linkage disequilibrium and shared similar minor allele frequencies, we chose to test whether one of the SNPs (rs1861972) was associated with autism in three recruiting sites from the NIH Collaborative Programs of Excellence in Autism (CPEA) network.
|
17948868 |
2008 |
|
rs1861972
|
|
|
0.070 |
GeneticVariation |
BEFREE |
Our previous research involving 167 nuclear families from the Autism Genetic Resource Exchange (AGRE) demonstrated that two intronic SNPs, rs1861972 and rs1861973, in the homeodomain transcription factor gene ENGRAILED 2 (EN2) are significantly associated with autism spectrum disorder (ASD).
|
16252243 |
2005 |
|
rs1861972
|
|
|
0.070 |
GeneticVariation |
BEFREE |
Two intronic SNPs (rs1861972 and rs1861973) demonstrated significant association with autism (rs1861972, P=0.0018; rs1861973, P=0.0003; haplotype, P=0.000005).
|
15024396 |
2004 |
|
rs1861973
|
|
|
0.060 |
GeneticVariation |
BEFREE |
The haplotype A-C of rs1861972 and rs1861973 is the core element of the observed haplotype association in this study, which plays a role as a protective factor against autism; in addition, the haplotype G-A-C is less frequent in male cases compared to controls (38.64 vs. 52.51%), which plausibly modulate disease vulnerability to autism.
|
20523082 |
2010 |
|
rs1861973
|
|
|
0.060 |
GeneticVariation |
BEFREE |
While Del-T haplotype formed from rs34808376-rs1861973 markers showed increased non-transmission, the Ins-C showed significant transmission suggesting protective effect and risk, respectively, conferred by these haplotypes in autism etiology.
|
20050924 |
2010 |
|
rs1861973
|
|
|
0.060 |
GeneticVariation |
BEFREE |
Two recent studies have demonstrated that two intronic SNPs (rs1861972, rs1861973) in the EN2 gene are significantly associated with autism.
|
17948901 |
2008 |
|
rs1861973
|
|
|
0.060 |
GeneticVariation |
BEFREE |
Two SNPs (rs1861972, rs1861973) at the EN2 gene that have been reported to be associated with autism underwent analysis among our studied cohorts.
|
18424904 |
2008 |
|
rs1861973
|
|
|
0.060 |
GeneticVariation |
BEFREE |
Our previous research involving 167 nuclear families from the Autism Genetic Resource Exchange (AGRE) demonstrated that two intronic SNPs, rs1861972 and rs1861973, in the homeodomain transcription factor gene ENGRAILED 2 (EN2) are significantly associated with autism spectrum disorder (ASD).
|
16252243 |
2005 |
|
rs1861973
|
|
|
0.060 |
GeneticVariation |
BEFREE |
Two intronic SNPs (rs1861972 and rs1861973) demonstrated significant association with autism (rs1861972, P=0.0018; rs1861973, P=0.0003; haplotype, P=0.000005).
|
15024396 |
2004 |
|
rs3735653
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Here, we have investigated the association of five markers [rs3735653 (C/T) in exon 1; rs34808376 (GC/-) and rs6150410 (CGCATCCCC/-) in promoter region; rs1861972 (A/G) and rs1861973 (C/T) in the intron] of the gene with autism and ASD in Indian population using family-based approach.
|
20050924 |
2010 |
|
rs3824068
|
|
|
0.010 |
GeneticVariation |
BEFREE |
However, when haplotypes were constructed with multiple markers, a number of haplotypes including three two-marker haplotypes, nine three-marker haplotypes, one four-marker haplotype, and one six-marker haplotype, all of which contain the major allele A of rs3824068, displayed significantly associated with autism.
|
17948901 |
2008 |