Society for Reproductive Investigation (SRI) Annual Meeting
March 16-2016
Montreal, Canada
Whole exome sequencing of endometriosis patients uncovers mutations with large effects
K. Ward, R. Chettier, H.M. Albertsen
Four genes consistently associated with endometriosis suggest that aberrant epithelial-to-mesenchymal transition is an initiating factor in the pathogenesis of endometriosis
K. Ward, R. Chettier, H.M. Albertsen
Novel candidate genes for endometriosis were identified by exome analysis of high risk endometriosis families that share rare damaging variants in multiple families
Ward, R. Chettier, H.M. Albertsen
Key endometriosis genes show very low mutations rates indicating these genes have essential functions during embryonic development and suggests a role in endometriosis-related infertility
H.M. Albertsen, R. Chettier, K. Ward
Distant relative pair analysis identifies a DNA repair gene POLN associated with familial endometriosis
R. Chettier, H.M. Albertsen, K. Ward
Replication study implicates IL33 and PDE1C as candidate genes for endometriosis
K. Ward, R. Chettier, H.M. Albertsen