Hien Luong

No ORCID on file · 7 papers in corpus
observational 2016
Human Reproduction ·doi:10.1093/humrep/dew047

STUDY QUESTION: Do endometriosis risk-associated single nucleotide polymorphisms (SNPs) found at the 12q22 locus have effects on vezatin ( ITALIC! VEZT) expression? SUMMARY ANSWER: The original genome-wide association study (GWAS) SNP (rs1…

other 2016
Human molecular genetics ·doi:10.1093/hmg/ddw320

Genome-wide association studies (GWAS) have identified markers within the WNT4 region on chromosome 1p36.12 showing consistent and strong association with increasing endometriosis risk. Fine mapping using sequence and imputed genotype data …

2015
·doi:10.3978/j.issn.2305-5839.2015.ab028

Endometriosis is a common, chronic gynaecological disease characterised by pelvic pain and sub-fertility. It is a complex genetic disease affecting of 6-10% women of reproductive age and up to 50% of women with infertility. Evidence from ge…

2014
·doi:10.14264/uql.2014.293

I investigated two conditions affecting female reproductive health, dizygotic (DZ) twinning or double ovulation as a complex trait influencing fertility, and endometriosis with common symptoms of pain and infertility. Research questions and…

observational 2013
International journal of molecular epidemiology and genetics

Genome-wide association studies show strong evidence of association with endometriosis for markers on chromosome 1p36 spanning the potential candidate genes WNT4, CDC42 and LINC00339. WNT4 is involved in development of the uterus, and the e…

observational 2013

Genome-wide association studies show strong evidence of association with endometriosis for markers on chromosome 1p36 spanning the potential candidate genes WNT4, CDC42 and LINC00339. WNT4 is involved in development of the uterus, and the e…

observational 2012

Is there a contribution of the minor allele at the KRAS single nucleotide polymorphism (SNP) rs61764370 in the let-7 microRNA-binding site to endometriosis risk?