Results 41 to 50 of about 771,775 (343)
A single nucleotide polymorphism in the IL1RL1 gene is associated with Behcet’s disease in a Chinese Han population [PDF]
International Journal of Ophthalmology, 2021 AIM: To explore the association of single nucleotide polymorphisms (SNPs) in the IL33/IL1RL1 gene region with the susceptibility to Behcet's disease (BD) in a Chinese Han population. METHODS: A total of eight SNPs in the candidate gene region (rs11792633,
Xin-Shu Liu +9 more
doaj +1 more source
A sex-specific association of common variants of neuroligin genes (NLGN3 and NLGN4X) with autism spectrum disorders in a Chinese Han cohort [PDF]
, 2011 Background Synaptic genes, NLGN3 and NLGN4X, two homologous members of the neuroligin family, have been supposed as predisposition loci for autism spectrum disorders (ASDs), and defects of these two genes have been identified in a small ...
Jindan Yu +5 more
core +2 more sources
PLoS ONE, 2017 Background Somatic complaints are often the presenting symptoms of major depressive disorder (MDD) in the outpatient context, because this may go unrecognized. It is well understood that MDD carries an increased risk of suicide.
Hai-Yan Li +9 more
semanticscholar +1 more source
Translational Psychiatry, 2018 Cytogenetic studies suggested that chromosome 15q11-q13 might be a candidate region that increases the risk of autism. Previous association studies in Caucasian populations identified the risk variants of genes in this region. However, the association of
Linyan Wang +12 more
semanticscholar +1 more source
A functional polymorphism in the gene is associated with asthma in a Chinese Han Population [PDF]
, 2009 Background Mutation in SPINK5 causes Netherton syndrome, a rare recessive skin disease that is accompanied by severe atopic manifestations including atopic dermatitis, allergic rhinitis, asthma, high serum IgE and hypereosinophilia.
Qiji Liu +30 more
core +2 more sources
BioMed Research International, 2018 Aim To clarify the association between the single nucleotide polymorphisms (SNPs) in the NLRP1 and NLRP3 and Psoriasis Vulgaris (PsV) in the Chinese Han population.
Pei Yu +4 more
semanticscholar +1 more source
Haplotype diversity in mitochondrial genome in a Chinese Han population [PDF]
Journal of Human Genetics, 2016 Investigations into the use of mitochondrial genome (mtGenome) typing by massively parallel sequencing technologies are well underway in many areas, including forensic genetics. Previous studies have demonstrated that mtGenome sequencing data generated from Ion torrent personal genome machine (PGM) system were highly viable and reliable in forensic ...
Ke, Ma +5 more
openaire +2 more sources
Evaluation of genetic parameters of 23 autosomal STR loci in a Southern Chinese Han population
Annals of Human Biology, 2018 Aim: To evaluate the 23 autosomal short tandem repeat (STR) loci included in GoldenEye™ 25 A kit using forensic human identification and paternity testing.
Hai-xia Li +6 more
doaj +1 more source
Multiple genetic analyses for Chinese Hunan Han population via 46 A-STRs
Annals of Human Biology, 2022 Background Short tandem repeats (STRs) are important as common genetic markers in forensic identification and population genetics due to their highly polymorphic nature.
Yunying Zhang +7 more
doaj +1 more source
Association of rs662799 in APOA5 with CAD in Chinese Han population
BMC Cardiovascular Disorders, 2018 BackgroundCAD (Coronary Artery Disease) is a complex disease that influenced by various environmental and genetic factors. Previous studies have found many single nucleotide polymorphisms (SNPs) associated with the risk of CAD occurrence.
Hua Chen +6 more
semanticscholar +1 more source