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Targeted Oncology|April 20, 2023
A Systematic Evaluation of Cost-Saving Dosing Regimens for Therapeutic Antibodies and Antibody-Drug Conjugates for the Treatment of Lung CancerRob Ter Heine, Michel M van den Heuvel, Berber Piet, et al.
Frontiers in Pediatrics|July 12, 2021
Prevention of Neural Tube Defects in Europe: A Public Health FailureJoan K Morris, Marie-Claude Addor, Elisa Ballardini, et al.
Nature Nanotechnology|April 10, 2023
Expansion-enhanced super-resolution radial fluctuations enable nanoscale molecular profiling of pathology specimensDominik Kylies, Marina Zimmermann, Fabian Haas, et al.
European Journal of Human Genetics : EJHG|November 29, 2017
HUWE1 variants cause dominant X-linked intellectual disability: a clinical study of 21 patientsStéphanie Moortgat, Siren Berland, Ingvild Aukrust, et al.
Molecular Syndromology|November 4, 2010
IRF6 Screening of Syndromic and a priori Non-Syndromic Cleft Lip and Palate Patients: Identification of a New Type of Minor VWS SignL Desmyter, M Ghassibe, N Revencu, et al.
Physical Review Letters|October 16, 2020
First Germanium-Based Constraints on Sub-MeV Dark Matter with the EDELWEISS ExperimentQ Arnaud, E Armengaud, C Augier, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|March 8, 2011
Paper 6: EUROCAT member registries: organization and activitiesRuth Greenlees, Amanda Neville, Marie-Claude Addor, et al.
The Journal of Clinical Investigation|April 4, 2023
Accumulation of α-synuclein mediates podocyte injury in Fabry nephropathyFabian Braun, Ahmed Abed, Dominik Sellung, et al.
American Journal of Medical Genetics. Part A|December 30, 2022
Amniotic band syndrome and limb body wall complex in Europe 1980-2019Jorieke E H Bergman, Ingeborg Barišić, Marie-Claude Addor, et al.
Nature Communications|August 14, 2023
An integrated organoid omics map extends modeling potential of kidney diseaseMoritz Lassé, Jamal El Saghir, Celine C Berthier, et al.
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