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DARTpaths, an in silico platform to investigate molecular mechanisms of compounds.
Bhalla D, Steijaert MN, Poppelaars ES, Teunis M, van der Voet M, Corradi M, Dévière E, Noothout L, Tomassen W, Rooseboom M, Currie RA, Krul C, Pieters R, van Noort V, Wildwater M. Bhalla D, et al. Among authors: van der voet m. Bioinformatics. 2023 Jan 1;39(1):btac767. doi: 10.1093/bioinformatics/btac767. Bioinformatics. 2023. PMID: 36477801 Free PMC article.
Serum Metabolomic Analysis of Coronary Heart Disease Patients with Stable Angina Pectoris Subtyped by Traditional Chinese Medicine Diagnostics Reveals Biomarkers Relevant to Personalized Treatments.
Guo N, Wang P, Yang J, Yang X, van der Voet M, Wildwater M, Wei J, Tang X, Wang M, Yang H. Guo N, et al. Among authors: van der voet m. Front Pharmacol. 2021 Jun 14;12:664320. doi: 10.3389/fphar.2021.664320. eCollection 2021. Front Pharmacol. 2021. PMID: 34194326 Free PMC article.
From Rare Copy Number Variants to Biological Processes in ADHD.
Harich B, van der Voet M, Klein M, Čížek P, Fenckova M, Schenck A, Franke B. Harich B, et al. Among authors: van der voet m. Am J Psychiatry. 2020 Sep 1;177(9):855-866. doi: 10.1176/appi.ajp.2020.19090923. Epub 2020 Jun 30. Am J Psychiatry. 2020. PMID: 32600152
A homozygous FITM2 mutation causes a deafness-dystonia syndrome with motor regression and signs of ichthyosis and sensory neuropathy.
Zazo Seco C, Castells-Nobau A, Joo SH, Schraders M, Foo JN, van der Voet M, Velan SS, Nijhof B, Oostrik J, de Vrieze E, Katana R, Mansoor A, Huynen M, Szklarczyk R, Oti M, Tranebjærg L, van Wijk E, Scheffer-de Gooyert JM, Siddique S, Baets J, de Jonghe P, Kazmi SA, Sadananthan SA, van de Warrenburg BP, Khor CC, Göpfert MC, Qamar R, Schenck A, Kremer H, Siddiqi S. Zazo Seco C, et al. Among authors: van der voet m. Dis Model Mech. 2017 Feb 1;10(2):105-118. doi: 10.1242/dmm.026476. Epub 2016 Dec 15. Dis Model Mech. 2017. PMID: 28067622 Free PMC article.
25 results