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Nature Medicine|August 28, 2023
Cell-free DNA methylome analysis for early preeclampsia predictionMarie De Borre, Huiwen Che, Qian Yu, et al.Cancer Discovery|January 24, 2025
Prenatal Exposure to Chemotherapy Increases the Mutation Burden in Human Neonatal Hematopoietic Stem CellsIlana Struys, Carolina Velázquez, Joske Ubels, et al.American Journal of Human Genetics|May 25, 2010
Haploinsufficiency of TAB2 causes congenital heart defects in humansBernard Thienpont, Litu Zhang, Alex V Postma, et al.Nature|August 18, 2016
Tumour hypoxia causes DNA hypermethylation by reducing TET activityBernard Thienpont, Jessica Steinbacher, Hui Zhao, et al.Clinical Chemistry|June 17, 2008
State-of-the-art of serum testosterone measurement by isotope dilution-liquid chromatography-tandem mass spectrometryLinda M Thienpont, Katleen Van Uytfanghe, Stuart Blincko, et al.Biorxiv : the Preprint Server for Biology|February 6, 2026
Synthetic Hybrid Receptors for Safer and Programmable T Cell TherapyMaxwell G Foisey, Julie Garcia, Xun Li, et al.Genome Medicine|August 30, 2020
Systems genetics analysis identifies calcium-signaling defects as novel cause of congenital heart diseaseJose M G Izarzugaza, Sabrina G Ellesøe, Canan Doganli, et al.Frontiers in Pediatrics|February 22, 2021
Health Literacy and Quality of Life in Young Adults From The Belgian Crohn's Disease Registry Compared to Type 1 Diabetes MellitusConstance Carels, Lucas Wauters, An Outtier, et al.Nature|June 20, 2020
Publisher Correction: IGF1R is an entry receptor for respiratory syncytial virusCameron D Griffiths, Leanne M Bilawchuk, John E McDonough, et al.The Journal of Clinical Investigation|May 3, 2017
Comparative oncogenomics identifies tyrosine kinase FES as a tumor suppressor in melanomaMichael Olvedy, Julie C Tisserand, Flavie Luciani, et al.Pageof 56