Results 11 to 20 of about 92,663 (299)
Forensic characterization and genetic polymorphisms of 19 X-chromosomal STRs in 1344 Han Chinese individuals and comprehensive population relationship analyses among 20 Chinese groups. [PDF]
PLoS ONE, 2018 X-chromosomal short tandem repeats (X-STRs) may assist resolution of complex forensic kinship cases and complement autosomal and Y-chromosomal STRs in routine forensic practice and population genetics.
Pengyu Chen +8 more
doaj +2 more sources
Molecular Genetics & Genomic Medicine, 2019 Background It is meaningful to expand the available population information on forensic medicine and to investigate the genetic characteristics of Han population from Jilin Province, Northeast China.
Xiao‐ming Xu +5 more
doaj +2 more sources
The association analysis polymorphism of CDKAL1 and diabetic retinopathy in Chinese Han population [PDF]
International Journal of Ophthalmology, 2016 AIM: To identify the contribution of CDKAL1 to the development of diabetic retinopathy (DR) in Chinese population. METHODS: A case-control study was performed to investigate the genetic association between DR and polymorphic variants of CDKAL1 in ...
Nai-Jia Liu +10 more
doaj +2 more sources
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 +2 more sources
Genetic variants at 20p11 confer risk to androgenetic alopecia in the Chinese Han population. [PDF]
PLoS ONE, 2013 BACKGROUND: Androgenetic alopecia (AGA) is a well-characterized type of progressive hair loss commonly seen in men, with different prevalences in different ethnic populations. It is generally considered to be a polygenic heritable trait.
Bo Liang +21 more
doaj +2 more sources
Wilson Disease in the South Chinese Han Population [PDF]
Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques, 2014 Purpose:To prospectively investigate the incidence and prevalence of Wilson disease (WD) in Chinese Han population in Anhui Province, to analyze the genetic mutations in individuals with WD, and to provide basic epidemiological data regarding WD in this Chinese Han population.Methods:Between November 2008 and June 2010, individuals aged from 7 to 75 ...
Nan, Cheng +7 more
openaire +2 more sources
BMC Medical Genomics, 2022 Objectives The purpose of this study was to investigate the association of PNPLA3 single nucleotide polymorphisms (SNPs) (rs738409 C > G, rs3747207 G > A, rs4823173 G > A, and rs2896019 T > G) with hepatocellular carcinoma (HCC) susceptibility.
Dongwei Gong +5 more
doaj +1 more source
BMC Medical Genomics, 2023 Purpose The research aimed to detect the association between single nucleotide polymorphisms (SNPs) in CYP4V2 gene and coronary heart disease (CHD) risk. Methods This case–control study included 487 CHD subjects and 487 healthy individuals.
Kang Huang +9 more
doaj +1 more source
Association of rs662799 in APOA5 with CAD in Chinese Han population [PDF]
BMC Cardiovascular Disorders, 2018 CAD (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. However, the results are inconsistent.
Hua Chen +6 more
openaire +3 more sources
Environmental Health and Preventive Medicine, 2020 Background We aim to explore the association between self-reported snoring and hypertension among adults aged 30–79 in Chongqing, China. Methods A total of 23,342 individuals aged 30–79 were included at baseline from August 2018 to January 2019, and the ...
Meng Xiao +11 more
doaj +1 more source