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American Journal of Human Genetics|December 24, 2013
Mutations in CSPP1 cause primary cilia abnormalities and Joubert syndrome with or without Jeune asphyxiating thoracic dystrophyKarina Tuz, Ruxandra Bachmann-Gagescu, Diana R O'Day, et al.
Nature Communications|December 19, 2023
NEMO reshapes the α-Synuclein aggregate interface and acts as an autophagy adapter by co-condensation with p62Nikolas Furthmann, Verian Bader, Lena Angersbach, et al.
Annals of Neurology|June 22, 2026
Hyperacute Interleukin-1β Production and Neutrophil Extracellular Trap Formation in the Cerebral Circulation of Stroke Patients with Large Vessel OcclusionJustine Münsterberg, Caspar Brekenfeld, Hanna Englert, et al.
European Heart Journal|February 10, 2026
Computed tomography-guided vs conventional catheter ablation for ventricular tachycardia: the InEurHeart trialFrederic Sacher, Tobias Reichlin, Mathieu Le Bloa, et al.
American Journal of Human Genetics|October 12, 2023
Rare de novo gain-of-function missense variants in DOT1L are associated with developmental delay and congenital anomaliesZelha Nil, Ashish R Deshwar, Yan Huang, et al.
Acta Neuropathologica|November 24, 2024
Neuronal and oligodendroglial, but not astroglial, tau translates to in vivo tau PET signals in individuals with primary tauopathiesLuna Slemann, Johannes Gnörich, Selina Hummel, et al.
Scientific Data|October 3, 2018
Free-electron laser data for multiple-particle fluctuation scattering analysisKanupriya Pande, Jeffrey J Donatelli, Erik Malmerberg, et al.
Blood Advances|April 23, 2026
DNA methylation-based classification of hematolymphoid neoplasmsAnnapurna Saksena, Christin Siewert, Rust Turakulov, et al.
Space Science Reviews|March 24, 2021
The Ionospheric Connection Explorer Mission: Mission Goals and DesignT J Immel, S L England, S B Mende, et al.
Genome Research|July 14, 2009
High-resolution mapping and analysis of copy number variations in the human genome: a data resource for clinical and research applicationsTamim H Shaikh, Xiaowu Gai, Juan C Perin, et al.
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