Center for Translational Research
About the Lab
The Délot Laboratory develops preclinical genomic and translational approaches to study the genetics and epigenetics of rare genetic pediatric disorders and differences between the sexes in health and disease.
Paucity and disparity of publicly available sex-disaggregated data for the COVID-19 epidemic hamper evidence-based decision-makingKocher K, Delot-Vilain A, Spence D, LoTempio J, Délot EC, in press in Archives of Sexual Behavior Arch Sex Behav DOI: 10.1007/s10508-020-01882-w January (2021)
nanotatoR: A tool for enhanced annotation of genomic structural variantsBhattacharya S, Barseghyan H, Délot EC, Vilain E BMC Genomics DOI: 10.1101/2020.08.18.254680 August (2020)
Genetics of disorders of sex development: The DSD-TRN experienceDélot EC, Papp JC; DSD-TRN Genetics Workgroup, Sandberg DE, Vilain E. PMID: 28476235; PMCID: PMC5714504 Endocrinol Metab Clin North Am 46(2):519-537. DOI: 10.1016/j.ecl.2017.01.015 March (2017)
Non-syndromic 46,XX testicular disorders of sex developmentEmmanuèle C Délot, PhD and Eric J Vilain, MD, PhD, FACMG. GeneReviews October (2003)