F. Mondon

No ORCID on file · 7 papers in corpus · active 2008-2015

Study types

  • article 7

Condition tags

  • endometriosis 7
  • die_deep_infiltrating 2
  • infertility 1
  • endometrioma 1
article 2015
BioMed research international ·doi:10.1155/2015/461024

Characterizing genetic contributions to endometriosis might help to shorten the time to diagnosis, especially in the most severe forms, but represents a challenge. Previous genome-wide association studies (GWAS) made no distinction between …

article 2011
·doi:10.1016/j.jmig.2011.08.499
article 2010
·doi:10.1016/j.jmig.2010.08.261
article 2010
Gynecologie, obstetrique & fertilite ·doi:10.1016/j.gyobfe.2010.05.005
article 2010
Molecular endocrinology (Baltimore, Md.) ·doi:10.1210/me.2010-0160

Several lines of evidence indicate that endometriosis could be partially due to selective epigenetic deregulations. Promoter hypermethylation of some key genes, such as progesterone receptor and aromatase, has been associated with the silen…

article 2009
·doi:10.1016/j.jmig.2009.08.130
article 2008
Molecular endocrinology (Baltimore, Md.) ·doi:10.1210/me.2008-0322

Endometriosis is a common gynecological disorder characterized by pain and infertility, where the lesions disseminate everywhere in the body with a preference for the pelvis. In that, it could be regarded as a benign metastatic disease, bec…