The single-nucleotide polymorphisms (SNPs) rs6700125 and rs6690993 in FGGY (FLJ10986) were recently reported to be a susceptibility factor for sporadic amyotrophic lateral sclerosis (SALS) in Caucasian populations in genome-wide association studies. However, no such association was observed in other independent genome-wide association studies or replication studies in a European cohort or 2 small sample sizes of Chinese patients. We performed a large case-control study in a cohort consisting of 963 SALS cases and 1039 control subjects to examine the association between the 2 reported SNPs in FGGY and amyotrophic lateral sclerosisin Chinese patients. Our results did not find the SNP rs6690993 in FGGY is associated with Chinese SALS and canno...
The cause of sporadic amyotrophic lateral sclerosis (ALS) is largely unknown, but genetic factors ar...
A linkage and association of the VEGF (vascular endothelial growth factor) C2578A polymorphism and a...
Cross-ethnic genetic studies can leverage power from differences in disease epidemiology and populat...
A genome-wide association study (GWAS) using pooled DNA samples from 386 sporadic ALS patients and 5...
Background: Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disease that primarily ...
We performed a replication study of the 2 genetic variants, rs2814707 on 9p21.2 and rs12608932 on 19...
To identify susceptibility genes for amyotrophic lateral sclerosis (ALS), we conducted a genome-wide...
Objective To identify the existence and distribution of C9ORF72 hexanucleotide(GGGGCC) repeat expans...
http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAM...
Single-nucleotide polymorphisms (SNPs) in the Nogo-A receptor gene (RTN4R) have been associated with...
Amyotrophic Lateral Sclerosis (ALS) is a rare neurodegenerative disease that affects motor neurons a...
The expansion of a noncoding hexanucleotide repeat (GGGGCC) in the chromosome 9 open reading frame (...
The cause of sporadic amyotrophic lateral sclerosis (ALS) is largely unknown, but genetic factors ar...
A recent genome-wide association study (GWAS) found significant association of six single nucleotide...
Objective To investigate whether GSTA1 , GSTO2 , and GSTZ1 are relevant to an increased risk of amyo...
The cause of sporadic amyotrophic lateral sclerosis (ALS) is largely unknown, but genetic factors ar...
A linkage and association of the VEGF (vascular endothelial growth factor) C2578A polymorphism and a...
Cross-ethnic genetic studies can leverage power from differences in disease epidemiology and populat...
A genome-wide association study (GWAS) using pooled DNA samples from 386 sporadic ALS patients and 5...
Background: Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disease that primarily ...
We performed a replication study of the 2 genetic variants, rs2814707 on 9p21.2 and rs12608932 on 19...
To identify susceptibility genes for amyotrophic lateral sclerosis (ALS), we conducted a genome-wide...
Objective To identify the existence and distribution of C9ORF72 hexanucleotide(GGGGCC) repeat expans...
http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAM...
Single-nucleotide polymorphisms (SNPs) in the Nogo-A receptor gene (RTN4R) have been associated with...
Amyotrophic Lateral Sclerosis (ALS) is a rare neurodegenerative disease that affects motor neurons a...
The expansion of a noncoding hexanucleotide repeat (GGGGCC) in the chromosome 9 open reading frame (...
The cause of sporadic amyotrophic lateral sclerosis (ALS) is largely unknown, but genetic factors ar...
A recent genome-wide association study (GWAS) found significant association of six single nucleotide...
Objective To investigate whether GSTA1 , GSTO2 , and GSTZ1 are relevant to an increased risk of amyo...
The cause of sporadic amyotrophic lateral sclerosis (ALS) is largely unknown, but genetic factors ar...
A linkage and association of the VEGF (vascular endothelial growth factor) C2578A polymorphism and a...
Cross-ethnic genetic studies can leverage power from differences in disease epidemiology and populat...