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Investigation into the mechanical behavior of a polymer optical fiber embedded in a structural adhesive2021 International Journal of Adhesion and Adhesives article Engineering Advanced Fiber Optic Sensors
Josef Weiland, W. Bartholomee, Michael Luber, Alexander Schiebahn, Rainer Engelbrecht, Uwe Reisgen
9citations -
6 × 2 pt: Forecasting gains from joint weak lensing and galaxy clustering analyses with spectroscopic-photometric galaxy cross-correlations2025 Astronomy and Astrophysics article Physics and Astronomy Cosmology and Gravitation Theories Open access
Harry Johnston, Nora Elisa Chisari, Shahab Joudaki, Robert Reischke, Benjamin Stölzner, Arthur Loureiro, +22 more
8citations -
The phenotypic and genotypic spectrum of individuals with mono‐ or biallelic ANK3 variants2024 Clinical Genetics article Biochemistry, Genetics and Molecular Biology Genetics and Neurodevelopmental Disorders Open access
Francesca Furia, Amanda M. Levy, Miel Theunis, Michael J. Bamshad, Meghan N. Bartos, Emilia K. Bijlsma, +30 more
8citations -
Side-channel countermeasures utilizing dynamic logic reconfiguration: Protecting AES/Rijndael and Serpent encryption in hardware2020 Microprocessors and Microsystems article Computer Science Cryptographic Implementations and Security Open access cited by 3 patents
Petr Socha, Jan Brejník, Josep Balasch, Martin Novotný, Nele Mentens
8citations -
Prevalence of Clostridioides difficile in dogs (Canis familiaris) with gastrointestinal disorders in Rio de Janeiro2023 Anaerobe article Medicine Clostridium difficile and Clostridium perfringens research Open access
Suzana Martins Gomes Leite, Carlos Cotias, Kelly C. Rainha, Mayara Gil de Castro Santos, Bruno Penna, Renata Fernandes Ferreira de Moraes, +3 more
7citations -
Genetic variants, thrombocytopenia, and clinical phenotype of type 2B von Willebrand disease: a median 16-year follow-up study2024 Journal of Thrombosis and Haemostasis article Medicine Platelet Disorders and Treatments Open access
Calvin B. van Kwawegen, Ferdows Atiq, Dara Endenburg, Karin Fijnvandraat, Karin P. M. van Galen, Marjon H. Cnossen, +8 more
7citations -
PhenoScore: AI-based phenomics to quantify rare disease and genetic variation2022 medRxiv preprint Biochemistry, Genetics and Molecular Biology Genomics and Rare Diseases Open access
Alexander J.M. Dingemans, Max Hinne, Kim M. G. Truijen, Lia C. M. J. Goltstein, Jeroen van Reeuwijk, Nicole de Leeuw, +25 more
6citations -
KCNV2-associated retinopathy: genotype–phenotype correlations –KCNV2study group report 32023 British Journal of Ophthalmology article Biochemistry, Genetics and Molecular Biology Retinal Development and Disorders Open access
Thales A. C. de Guimarães, Michalis Georgiou, Anthony G. Robson, Kaoru Fujinami, Ajoy Vincent, Fadi Nasser, +30 more
6citations -
A Novel Approach to Justify Dissolution Differences in an Extended Release Drug Product using Physiologically Based Biopharmaceutics Modeling and Simulation2022 Journal of Pharmaceutical Sciences article Pharmacology, Toxicology and Pharmaceutics Drug Solubulity and Delivery Systems
Richa Aishwarya, Aditya Narasimha Murthy, Tausif Ahmed, Siddharth Chachad
6citations -
Growth charts for Marfan syndrome in the Netherlands and analysis of genotype–phenotype relationships2022 American Journal of Medical Genetics Part A article Biochemistry, Genetics and Molecular Biology Connective tissue disorders research Open access
Peter Lauffer, Gerard Pals, Aeilko Having Zwinderman, Floor A.M. Postema, Marieke J.H. Baars, Eelco Dulfer, +11 more
6citations -
Variant of the catalytic cysteine of UFSP2 leads to spondyloepimetaphyseal dysplasia type Di Rocco2023 Bone Reports article Biochemistry, Genetics and Molecular Biology Connective tissue disorders research Open access
Larissa Mattern, Matthias Begemann, Heide Delbrück, Petra Holschbach, Silvia Schröder, Ingo Kurth, +1 more
6citations -
Molecular differences in sequential extracts obtained by core flooding of the early mature ultra-tight Posidonia Shale2020 Marine and Petroleum Geology article Engineering Hydrocarbon exploration and reservoir analysis
Qian Zhang, Reinhard Fink, Sebastian Grohmann, Alireza Baniasad, Ralf Littke
6citations -
Reliability parameters of the Timed 25-Foot-Walk (T25FW) in patients with Multiple Sclerosis: Lower walking speed is associated with greater Smallest Detectable Change2024 Multiple Sclerosis and Related Disorders article Medicine Multiple Sclerosis Research Studies Open access
Daniëlla M. Oosterveer, Natasja Charon Wouda, Gerard Volker, Christel van den Berg, Berend Terluin, Elske Hoitsma
5citations -
Missense variants in ANKRD11 cause KBG syndrome by impairment of stability or transcriptional activity of the encoded protein2023 Genetics in Medicine article Biochemistry, Genetics and Molecular Biology Genetics and Neurodevelopmental Disorders Open access
Elke de Boer, Charlotte W. Ockeloen, Rosalie A. Kampen, Juliet E. Hampstead, Alexander J.M. Dingemans, Dmitrijs Rots, +44 more
5citations -
Expansion of the neurodevelopmental phenotype of individuals with EEF1A2 variants and genotype-phenotype study2024 European Journal of Human Genetics article Biochemistry, Genetics and Molecular Biology Genetics and Neurodevelopmental Disorders Open access
Cavan Bennett-Ness, Faustine Ageorges, Detlef Trost, Andrew Green, David R. Goudie, Rosalyn Jewell, +42 more
5citations -
Systematic study of ophthalmological findings in 10 patients with PEX1 -mediated Zellweger spectrum disorder2024 Ophthalmic Genetics article Biochemistry, Genetics and Molecular Biology Metabolism and Genetic Disorders Open access
Jessica S. Karuntu, Femke C. C. Klouwer, Marc Engelen, Camiel J. F. Boon
5citations -
Alveolar capillary dysplasia without misalignment of pulmonary veins, hyperinflammation, megalocornea and overgrowth – Association with a homozygous 2bp-insertion in LTBP2?2021 European Journal of Medical Genetics article Biochemistry, Genetics and Molecular Biology Genomics and Rare Diseases
Kristina Vollbach, Sonja Trepels‐Kottek, Miriam Elbracht, Ingo Kurth, Norbert Wagner, Thorsten W Orlikowsky, +2 more
5citations -
Clinical, Genotypic, and Imaging Characterization of the Spectrum of ABCA4 Retinopathies2023 Ophthalmology Retina article Biochemistry, Genetics and Molecular Biology Retinal Development and Disorders Open access
Francesco Romano, Camiel J. F. Boon, Alessandro Siligato, Gagan Kalra, Aniruddha Kishandutt Agarwal, Maria Chiara Medori, +5 more
5citations -
Reclassification of a likely pathogenic Dutch founder variant in KCNH2; implications of reduced penetrance2022 Human Molecular Genetics article Medicine Cardiac electrophysiology and arrhythmias Open access
Jaël S. Copier, Marianne Bootsma, Chai‐Ann Ng, Arthur A.M. Wilde, Robin A. Bertels, Hennie Bikker, +12 more
5citations