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NPJ Precision Oncology|December 18, 2021
Clonal dynamics of BRAF-driven drug resistance in EGFR-mutant lung cancerDiana Schaufler, David F Ast, Hannah L Tumbrink, et al.American Journal of Human Genetics|September 17, 2013
Mutations in GMPPA cause a glycosylation disorder characterized by intellectual disability and autonomic dysfunctionKatrin Koehler, Meera Malik, Saqib Mahmood, et al.EMBO Molecular Medicine|July 16, 2020
Characterization of circulating breast cancer cells with tumorigenic and metastatic capacityClaudia Koch, Andra Kuske, Simon A Joosse, et al.American Journal of Human Genetics|November 4, 2017
De Novo Mutations in SLC25A24 Cause a Craniosynostosis Syndrome with Hypertrichosis, Progeroid Appearance, and Mitochondrial DysfunctionNadja Ehmke, Luitgard Graul-Neumann, Lukasz Smorag, et al.EMBO Molecular Medicine|June 16, 2021
Long-lived macrophage reprogramming drives spike protein-mediated inflammasome activation in COVID-19Sebastian J Theobald, Alexander Simonis, Theodoros Georgomanolis, et al.Nature Communications|January 28, 2026
Injured epithelial cell states impact kidney allograft survival after T-cell-mediated rejectionAnna Maria Pfefferkorn, Lorenz Jahn, Patrick T Gauthier, et al.American Journal of Human Genetics|February 13, 2018
Mutations in the BAF-Complex Subunit DPF2 Are Associated with Coffin-Siris SyndromeGeorgia Vasileiou, Silvia Vergarajauregui, Sabine Endele, et al.Nature Communications|February 22, 2018
Clonal dynamics towards the development of venetoclax resistance in chronic lymphocytic leukemiaCarmen D Herling, Nima Abedpour, Jonathan Weiss, et al.Annals of Neurology|March 3, 2015
Rare variants in γ-aminobutyric acid type A receptor genes in rolandic epilepsy and related syndromesEva M Reinthaler, Borislav Dejanovic, Dennis Lal, et al.European Journal of Human Genetics : EJHG|January 24, 2018
Exome-wide analysis of mutational burden in patients with typical and atypical Rolandic epilepsyDheeraj R Bobbili, Dennis Lal, Patrick May, et al.Pageof 33