Results 21 to 30 of about 339,190 (282)

Replication of the Association Between Keratoconus and Polymorphisms in PNPLA2 and MAML2 in a Han Chinese Population

open access: yesFrontiers in Genetics, 2020
Keratoconus (KC) is a complex ocular disease that is affected by both genetic and non-genetic triggers. A recent genome-wide association study (GWAS) identified a genome-wide significant locus for KC in the region of PNPLA2 (rs61876744), as well as a ...
Jing Zhang   +11 more
doaj   +1 more source

Body weights in Han Chinese populations

open access: yesChinese Science Bulletin, 2014
The body weights of 26,954 Han Chinese adults in 67 areas (16,503 in rural areas and 10,451 in urban areas) across China were measured from 2009 to 2013. The results showed that in China, the three areas (north China, northeast China, and Jianghuai Plain) were with the greatest body weight. Northwest Han Chinese populations were heavier.
Yonglan Li   +11 more
openaire   +1 more source

Association between STAT4 gene polymorphism and type 2 diabetes risk in Chinese Han population

open access: yesBMC Medical Genomics, 2021
Background Evidence from genetic epidemiology indicates that type 2 diabetes (T2D) has a strong genetic basis. Activated STAT4 has an inflammatory effect, and STAT4 is an important mediator of inflammation in diabetes.
Jiaqi Cui   +12 more
doaj   +1 more source

Genome-wide association study of serum tumor markers in Southern Chinese Han population

open access: yesBMC Cancer, 2022
Background Serum indicators AFP, CA50, CA125, CA153, CA19-9, CEA, f-PSA, SCC-Ag have been confirmed as tumor markers (TMs). We conducted a genome-wide association study on 8 tumor markers of our 427 Han population in southern China, in order to identify ...
Xiukuan Li   +13 more
doaj   +1 more source

Spectrum of malignancies among the population of adults living with HIV infection in China: A nationwide follow-up study, 2008-2011. [PDF]

open access: yes, 2019
BackgroundAlthough increasingly studied in high-income countries, there is a paucity of data from the Chinese population on the patterns of cancer among people living with HIV (PLHIV).MethodsWe conducted a nationwide follow-up study using routinely ...
Detels, Roger   +7 more
core   +2 more sources

Tuberculosis risk-associated single nucleotide polymorphisms do not show association with leprosy in Chinese population

open access: yesInternational Journal of Infectious Diseases, 2015
Objective: Leprosy and tuberculosis (TB) are chronic granulomatous infectious diseases. As well as pathogen and environmental factors, host genetic factors make a substantial contribution to susceptibility to both diseases.
Chuan Wang   +7 more
doaj   +1 more source

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]

open access: yesPLoS 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   +1 more source

Association Between Snoring and Diabetes Among Pre- and Postmenopausal Women

open access: yesInternational Journal of General Medicine, 2022
Yun Yuan,1 Fan Zhang,1 Jingfu Qiu,1 Liling Chen,2 Meng Xiao,1 Wenge Tang,2 Qinwen Luo,1 Xianbin Ding,2 Xiaojun Tang1 1School of Public Health and Management, Medical and Social Development Research Center, Chongqing Medical University, Chongqing, 400016,
Yuan Y   +8 more
doaj  

POLG Mutations Are Probably Rare in the Han Chinese Population [PDF]

open access: yesChinese Medical Sciences Journal, 2020
Objective Mutations in polymerase gamma gene (POLG) are believed to be an important cause of early and juvenile onset of non-syndromic intractable epilepsy. The aim of this study is to investigate the incidence/prevalence of POLG pathogenic variants in epilespy patients of Han population through sequencing it.Methods Han Chinese patients with seizures ...
Kun Fang, Yang   +7 more
openaire   +2 more sources

The LRRK2 Arg1628Pro variant is a risk factor for Parkinson's disease in the Chinese population [PDF]

open access: yes, 2008
The c.G4883C variant in the leucine-rich repeat kinase 2 (LRRK2) gene (protein effect: Arg1628Pro) has been recently proposed as a second risk factor for sporadic Parkinson's disease in the Han Chinese population (after the Gly2385Arg variant).
A Fonzo Di   +32 more
core   +4 more sources

Home - About - Disclaimer - Privacy