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Data and code supporting: From Phenotypic Screening to Target and Compound Prioritization for Autosomal Dominant Polycystic Kidney Disease2026 Zenodo (CERN European Organization for Nuclear Research) dataset Computer Science Computational Drug Discovery Methods Open access
David Alencar Araripe, Margarita Iljin, Hester Bange, Leo Price, Rongfang Liu, Daan van der Es, +3 more
0citations -
Data and code supporting: From Phenotypic Screening to Target and Compound Prioritization for Autosomal Dominant Polycystic Kidney Disease2026 Zenodo (CERN European Organization for Nuclear Research) dataset Computer Science Computational Drug Discovery Methods Open access
David Alencar Araripe, Margarita Iljin, Hester Bange, Leo Price, Rongfang Liu, Daan van der Es, +3 more
0citations -
Novel YAP1/TAZ pathway inhibitors identified through phenotypic screening with potent anti-tumor activity via blockade of GGTase-I / Rho-GTPase signaling2023 bioRxiv (Cold Spring Harbor Laboratory) preprint Biochemistry, Genetics and Molecular Biology Hippo pathway signaling and YAP/TAZ Open access
Keith Graham, Philip Lienau, Benjamin Bader, Stefan Prechtl, Jan Naujoks, Ralf Lesche, +32 more
0citations -
A genome-wide CRISPR/Cas phenotypic screen for modulators of DUX4 cytotoxicity reveals screen complications2020 bioRxiv (Cold Spring Harbor Laboratory) preprint Biochemistry, Genetics and Molecular Biology Muscle Physiology and Disorders Open access
Ator Ashoti, Francesco Limone, Melissa van Kranenburg, Anna Alemany, Mirna Lilian Baak, Judith Vivié, +4 more
2citations -
From phenotypic screening to target and compound prioritization for autosomal dominant polycystic kidney disease2026 SLAS DISCOVERY article Biochemistry, Genetics and Molecular Biology Genetic and Kidney Cyst Diseases Open access
David Alencar Araripe, Margarita Iljin, Hester Bange, Leo Price, Rongfang Liu, Daan van der Es, +3 more
0citations -
A small molecule screen identifies novel inducers of EMT that may increase epicardium-driven repair of the heart2020 European Heart Journal article Biochemistry, Genetics and Molecular Biology Congenital heart defects research
Esther Dronkers, Tessa van Herwaarden, Marie‐José Goumans, Anke M. Smits
1citations -
Systematic assessment of transcriptomic and phenotypic biological profiling for mechanism-based hazard assessment using target-annotated reference chemicals in renal proximal tubular epithelial cells2026 bioRxiv (Cold Spring Harbor Laboratory) preprint Computer Science Computational Drug Discovery Methods Open access
Hugo W van Kessel, Marlene Wedler, Palle Steen Helmke, Dace Zigure, Stephen Ferguson, Joshua Harrill, +5 more
0citations -
An Rcs Stress-Based High-Throughput Screen Reveals Novel Gyrase Inhibitors as Indirect Inducers of Cell Envelope Stress in Gram-Negative Bacteria2025 ACS Infectious Diseases article Biochemistry, Genetics and Molecular Biology Bacterial Genetics and Biotechnology Open access
Laurence Cleenewerk, Willemijn Wouters, Joost J. Willemse, Meiling Gao, Vladyslav Lysenko, Jeroen M. Punt, +4 more
3citations -
Syndromic Inborn Errors of Immunity in TREC-Newborn Screening: 5-year Experience from the German Screening Program2026 Journal of Clinical Immunology article Immunology and Microbiology Immunodeficiency and Autoimmune Disorders Open access
Lea Graafen, Carsten Speckmann, Shahrzad Bakhtiar, Horst von Bernuth, Kai Lehmberg, Peter Bader, +27 more
4citations -
Expanding the genetic and phenotypic spectrum of ACTA2-related vasculopathies in a Dutch cohort2022 Genetics in Medicine article Biochemistry, Genetics and Molecular Biology Connective tissue disorders research Open access
Lisa M. van den Bersselaar, Judith M. A. Verhagen, Jos A. Bekkers, Marlies J. E. Kempers, Arjan C. Houweling, Marieke J.H. Baars, +13 more
6citations -
Second-tier genetics improves newborn screening accuracy for SCID and other T cell deficiencies2026 Journal of Human Immunity article Immunology and Microbiology Immunodeficiency and Autoimmune Disorders Open access
Annelotte J. Duintjer, Maartje Blom, Robbert G. M. Bredius, Ingrid Pico‐Knijnenburg, Adinda Heuperman, Hennie M. Hodemaekers, +13 more
0citations -
A Screening Tool to Quickly Identify Movement Disorders in Patients with Inborn Errors of Metabolism2023 Movement Disorders article Biochemistry, Genetics and Molecular Biology Metabolism and Genetic Disorders Open access
Lisette Henriëtta Koens, Marrit R. Klamer, Deborah A. Sival, Bettina Balint, Kailash P. Bhatia, Maria Fiorella Contarino, +11 more
5citations -
Evaluating the association of biallelic OGDHL variants with significant phenotypic heterogeneity2023 Genome Medicine article Biochemistry, Genetics and Molecular Biology Metabolism and Genetic Disorders Open access
Sheng‐Jia Lin, Barbara Vona, Tracy Lau, Kevin Huang, Maha Saad Zaki, Huda Shujaa Aldeen, +31 more
14citations -
Newborn screening of duchenne muscular dystrophy specifically targeting deletions amenable to exon-skipping therapy2021 Scientific Reports article Biochemistry, Genetics and Molecular Biology Muscle Physiology and Disorders Open access cited by 1 patent
Pablo Beckers, Jean‐Hubert Caberg, Vinciane Dideberg, Tamara Dangouloff, Johan T. den Dunnen, Vincent Bours, +2 more
19citations