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Journal article
Book chapter / Article in edited volumes
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Abstract

Journal

Correction: Comprehensive analysis of CNOT3-related neurodevelopmental disorders: phenotypic and genotypic characterization (European Journal of Human Genetics, (2025), 33, 8, (989-996), 10.1038/s41431-025-01884-z) (2026) Engel C, Rendek M, Assoumani J, Argilli E, Ariani F, Avice-Denizet AL, Bijlsma EK, et al. Journal article, Erratum GTV segmentation in MRI guided radiotherapy with promptable foundation models (2025) Julius Blöcker T, Delopoulos N, Palacios MA, Klüter S, Hörner-Rieber J, Rippke C, Placidi L, et al. Journal article Mitigating climate change in sports league: A scenario-based analysis of travel distances in women's and men's amateur soccer in Germany (2025) Abu-Omar K, Völk T, Tcymbal A, Resch J, Özer D, Gelius P, Messing S, Ziemainz H Journal article Why is ultrasound needed in inflammatory bowel disease? (2025) Petersen F, Höpfner M, Jenssen C, Nürnberg D, Strobel D, Vogelpohl J, Dietrich CF Journal article, Review article Aprocitentan in Patients With Chronic Kidney Disease and Resistant Hypertension (2025) Rossignol P, Clozel M, Dreier RF, Flack JM, Flamion B, Mann J, Narkiewicz K, et al. Journal article Towards measuring astrophysical third-order correlation functions with the H.E.S.S. optical intensity interferometer (2025) Zmija A, Anton G, Ingenhütt C, Mitchell A, Saha P, Silva Batista P, Vogel N, et al. Journal article Discovering non-associated pressure-sensitive plasticity models with EUCLID (2025) Xu H, Flaschel M, De Lorenzis L Journal article In Vitro Performance Assessment of a Bioprosthetic Individualized Aortic Valve Prosthesis for Infants and Toddlers (2025) Smid CC, Haselmann C, Irani SK, Cesnjevar R, Schweiger M, Pappas GA Journal article Preferred working time models and equal opportunities in gynecology and obstetrics: a sub-analysis of the trinational FARBEN survey focusing on German participants from Western and Eastern federal states (2025) Tauber N, Banys-Paluchowski M, Becker C, Foessleitner P, Göpfert M, Hartmann S, Kiblawi R, et al. Journal article Generation of two iPSC lines from patients with Aicardi-Goutières syndrome carrying either biallelic ADAR1 mutations (PC138) or a heterozygous IFIH1 mutation (PC139) (2025) Zerad L, Didry-Barca B, Banal C, Onteniente B, Lefort N, Lepelley A, Seabra L, et al. Journal article