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Clinical Genetics|October 30, 2020
WDR34, a candidate gene for non-syndromic rod-cone dystrophyMaria Solaguren-Beascoa, Kinga M Bujakowska, Cécile Méjécase, et al.Human Molecular Genetics|August 30, 2014
Mutations in IFT172 cause isolated retinal degeneration and Bardet-Biedl syndromeKinga M Bujakowska, Qi Zhang, Anna M Siemiatkowska, et al.Scientific Reports|April 27, 2021
Gene network and biological pathways associated with susceptibility to differentiated thyroid carcinomaOm Kulkarni, Pierre-Emmanuel Sugier, Julie Guibon, et al.International Journal of Cancer|December 28, 2020
Gene- and pathway-level analyses of iCOGS variants highlight novel signaling pathways underlying familial breast cancer susceptibilityChristine Lonjou, Séverine Eon-Marchais, Thérèse Truong, et al.International Journal of Cancer|October 11, 2018
Familial breast cancer and DNA repair genes: Insights into known and novel susceptibility genes from the GENESIS study, and implications for multigene panel testingElodie Girard, Séverine Eon-Marchais, Robert Olaso, et al.Pageof 2