S Mortlock

No ORCID on file · 4 papers in corpus · active 2019-2022

Study types

  • article 2
  • erratum 1
  • review 1

Condition tags

  • endometriosis 4
  • mesh:D004715 3
erratum 2022
Author Correction: Genome-wide association and epidemiological analyses reveal common genetic origins between uterine leiomyomata and endometriosis
Nature communications ·doi:10.1038/s41467-022-33222-y
article 2020
Genetic risk factors for endometriosis near estrogen receptor 1 and coexpression of genes in this region in endometrium
Molecular human reproduction ·doi:10.1093/molehr/gaaa082

The etiology and pathogenesis of endometriosis are complex with both genetic and environmental factors contributing to disease risk. Genome-wide association studies (GWAS) have identified multiple signals in the estrogen receptor 1 (ESR1) r…

article 2019
Generation of immortalized human endometrial stromal cell lines with different endometriosis risk genotypes
Molecular human reproduction ·doi:10.1093/molehr/gaz006

Endometriotic lesions are composed in part of endometrial-like stromal cells, however, there is a shortage of immortalized human endometrial stromal cultures available for research. As genetic factors play a role in endometriosis risk, it i…

review 2019
Genome-wide association and epidemiological analyses reveal common genetic origins between uterine leiomyomata and endometriosis
Nature communications ·doi:10.1038/s41467-019-12536-4

Abstract Uterine leiomyomata (UL) are the most common neoplasms of the female reproductive tract and primary cause for hysterectomy, leading to considerable morbidity and high economic burden. Here we conduct a GWAS meta-analysis in 35,474 …