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Dao, Kim; Shechtman, Svetlana; Weber-Schoendorfer, Corinna; Diav-Citrin, Orna; Murad, Reem Hegla; Berlin, Maya; Hazan, Ariela; Richardson, Jonathan L; Eleftheriou, Georgios; Rousson, Valentin; Diezi, Leonore; Haefliger, David; Simões-Wüst, Ana Paula; Addor, Marie-Claude; Baud, David; Lamine, Faiza; Panchaud, Alice; Buclin, Thierry; Girardin, François R and Winterfeld, Ursula (2024). Use of GLP1 receptor agonists in early pregnancy and reproductive safety: a multicentre, observational, prospective cohort study based on the databases of six Teratology Information Services. BMJ open, 14(4), e083550. BMJ Publishing Group 10.1136/bmjopen-2023-083550
Dao, Kim; Shechtman, Svetlana; Diav-Citrin, Orna; George, Nathan; Richardson, Jonathan Luke; Rollason, Victoria; Pistelli, Alessandra; Eleftheriou, Georgios; Berlin, Maya; Ekobena, Pierre; Rousson, Valentin; Addor, Marie-Claude; Baud, David; Buclin, Thierry; Panchaud, Alice; Winterfeld, Ursula (2023). Reproductive Safety of Trazodone After Maternal Exposure in Early Pregnancy: A Comparative ENTIS Cohort Study. Journal of clinical psychopharmacology, 43(1), pp. 12-19. Wolters Kluwer Health 10.1097/JCP.0000000000001630
Papuc, Sorina M; Abela, Lucia; Steindl, Katharina; Begemann, Anaïs; Simmons, Thomas L; Schmitt, Bernhard; Zweier, Markus; Oneda, Beatrice; Socher, Eileen; Crowther, Lisa M; Wohlrab, Gabriele; Gogoll, Laura; Poms, Martin; Seiler, Michelle; Papik, Michael; Baldinger, Rosa; Baumer, Alessandra; Asadollahi, Reza; Kroell-Seger, Judith; Schmid, Regula; ... (2019). The role of recessive inheritance in early-onset epileptic encephalopathies: a combined whole-exome sequencing and copy number study. European journal of human genetics, 27(3), pp. 408-421. Nature Publishing Group 10.1038/s41431-018-0299-8
Magyar, István; Colman, Dvora; Arnold, Eliane; Baumgartner, Daniela; Bottani, Armand; Fokstuen, Siv; Addor, Marie-Claude; Berger, Wolfgang; Carrel, Thierry; Steinmann, Beat; Mátyás, Gábor (2009). Quantitative sequence analysis of FBN1 premature termination codons provides evidence for incomplete NMD in leukocytes. Human mutation, 30(9), pp. 1355-64. Hoboken, N.J.: Wiley-Blackwell 10.1002/humu.21058
